2
40
93
-
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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April 2018 List
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
April 2018 List
URL Address
<a href="http://doi.org/10.1089/jpm.2017.0092" target="_blank" rel="noreferrer noopener">http://doi.org/10.1089/jpm.2017.0092</a>
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The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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Proxy-Reported Quality of Life and Family Impact for Children Followed Longitudinally by a Pediatric Palliative Care Team
Publisher
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Journal of Palliative Medicine
Date
A point or period of time associated with an event in the lifecycle of the resource
2018
Subject
The topic of the resource
Quality of Life; palliative therapy; Child; Longitudinal Studies; Only Child; Palliative Care; major clinical study; statistical significance; longitudinal study; prospective study; child; attention; human; female; male; quality of life; article; diagnosis; analysis of variance; daily life activity; Metronidazole; minimal clinically important difference; physical model
Creator
An entity primarily responsible for making the resource
Weaver M; Wichman C; Darnall C; Bace S; Vail C; Macfadyen A
Description
An account of the resource
Background: One goal of pediatric palliative care is to maintain quality of life for children and their families. Quality-of-life investigations may be enhanced by considering clinically important metrics in addition to statistical significance. Objective: The purpose of this study was to longitudinally evaluate the effect of time on quality of life and family impact for pediatric palliative care patients across all diagnoses and ages. Design: This prospective quality-of-life study included administration of a 23-item PedsQLTM Measurement Model to evaluate for physical, emotional, social, and cognitive dimensions of the child's quality of life and a 36-item PedsQL Family Impact Module to assess for the familial impact at time of initial palliative care consultation, Month 6, and Month 12. Setting/Subjects: All pediatric patients who received a palliative care consultation in our Midwestern free-standing children's hospital over a five-year period were included in the longitudinal study (n = 87). Measurements: Repeated measures ANOVA was used to investigate how proxy-reported quality of life and family impact changed with time with attentiveness to also follow trends in minimal clinically important difference (MCID) metrics. Results: The emotional domain showed a statistically significant positive trend over the first six months of palliative care involvement (p = 0.049), while the physical domain (p = 0.028) and daily activity (p = 0.039) showed a positive improvement for the full year. In using a standard of MCID, the physical, emotional, and cognitive domains improved in the quality-of-life scale and the communication, worry, and daily activity domains improved in the family impact scale over 12 months. Conclusions: In considering quality-of-life analyses for pediatric palliative care programmatic improvements, providers may consider analyzing not only for statistical significance in collective data sets but also for clinically important difference over time.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1089/jpm.2017.0092" target="_blank" rel="noreferrer noopener">10.1089/jpm.2017.0092</a>
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Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2018
Analysis of Variance
April 2018 List
Article
Attention
Bace S
Child
daily life activity
Darnall C
Diagnosis
Female
Human
Journal of Palliative Medicine
Longitudinal Studies
longitudinal study
Macfadyen A
Major Clinical Study
Male
Metronidazole
minimal clinically important difference
Only Child
Palliative Care
Palliative Therapy
physical model
Prospective Study
Quality Of Life
Statistical Significance
Vail C
Weaver M
Wichman C
-
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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March 2018 List
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
March 2018 List
URL Address
<a href="http://doi.org/10.1111/dmcn.13622" target="_blank" rel="noreferrer">http://doi.org/10.1111/dmcn.13622</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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Prevalence and management of dystonia in a paediatric palliative care cohort
Publisher
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Developmental Medicine And Child Neurology
Date
A point or period of time associated with an event in the lifecycle of the resource
2017
Subject
The topic of the resource
dystonia; palliative therapy; prevalence; 302-17-0 (chloral hydrate); 4205-90-7 (clonidine); 4205-91-8 (clonidine); 57066-25-8 (clonidine); benzodiazepine derivative; Child; chloral hydrate; Clinical Article; clonidine; cohort analysis; cross-sectional study; Diagnosis; documentation; England; Female; Human; joint; Male; neurology; precancer; preschool child; seizure
Creator
An entity primarily responsible for making the resource
Slater T; Laddie J; Hughes G; Lumsden DE
Description
An account of the resource
Objectives: Dystonia and seizures can be common, unpredictable and distressing neurological symptoms in paediatric palliative care. Emergency seizure management is increasingly under joint neurology and palliative care, often incorporated into "passport type" individual plans, as advocated by the Royal College of Paediatrics and Child Health. This is rarer in dystonia. We evaluated the comparative frequency of dystonia and seizures in a cohort of children receiving paediatric palliative care and examined how emergency plans differ between neurology, palliative care and in collaboration. Methods: We performed a cross-sectional analysis of the palliative care database at Evelina London Children's Hospital, a non-malignant caseload covering southeast England. Documentation over 12 months (preceding July 2017) was reviewed to assess the frequency of patients with dystonia and seizures, current relevant therapies and proposed emergency management. Results: In a cohort of 109 children with a complex range of diagnoses (mean age = 6.0 years), 37% (n=40) suffered from seizures, 27% (n=29) from dystonia and 43% (n=47) from both. Emergency dystonia plans were identified in 51.7% (15/29) of patients: 7 by palliative care and 8 by neurology. No collaborative plans were found. Emergency seizure plans were identified in 80% (32/40) of patients: 11 by palliative care, 9 by neurology and 12 in collaboration. Conclusions: Dystonia is almost as common as seizures in children with non-malignant conditions receiving palliative care. Individualised seizures plans were commonly documented, but less for prolonged dystonic episodes. Dystonia management was more often led by neurology, in contrast to clear evidence of joint working in patients with seizures. Medications differed for dystonia: palliative care promoted conservative measures and benzodiazepines, whereas clonidine hydrochloride and chloral hydrate were favoured by neurology. Paediatric palliative care is playing an increasing role in life-limiting and life-threatening neurological conditions. However, increased collaborative working is essential to ensure consistent patient-focussed management.
2017
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1111/dmcn.13622" target="_blank" rel="noreferrer">10.1111/dmcn.13622</a>
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Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2017
302-17-0 (chloral hydrate)
4205-90-7 (clonidine)
4205-91-8 (clonidine)
57066-25-8 (clonidine)
benzodiazepine derivative
Child
chloral hydrate
Clinical Article
clonidine
Cohort Analysis
Cross-sectional Study
Developmental Medicine and Child Neurology
Diagnosis
Documentation
Dystonia
England
Female
Hughes G
Human
joint
Laddie J
Lumsden DE
Male
March 2018 List
Neurology
Palliative Therapy
precancer
Preschool Child
Prevalence
Seizure
Slater T
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1002/mds.21812" target="_blank" rel="noreferrer">http://doi.org/10.1002/mds.21812</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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The natural history of Unverricht-Lundborg disease: a report of eight genetically proven cases
Publisher
An entity responsible for making the resource available
Movement Disorders: Official Journal Of The Movement Disorder Society
Date
A point or period of time associated with an event in the lifecycle of the resource
2008
Subject
The topic of the resource
Child; Female; Humans; Male; Adult; Disease Progression; Age Factors; Severity of Illness Index; Magnetic Resonance Imaging; adolescent; Q3 Literature Search; Diagnosis; Differential; Chromosomes; Human; Electroencephalography; Atrophy/complications/pathology; Auditory; Brain Stem/physiology; Brain/pathology/physiopathology; Cerebellar Ataxia/complications/diagnosis; Cerebellum/pathology/physiopathology; Dementia/complications/diagnosis; Dystonia/complications/diagnosis; Electromyography; Evoked Potentials; Evoked Potentials/physiology; Myoclonus/complications/diagnosis; Neuropsychological Tests; Pair 21/genetics; Seizures/complications/diagnosis; Unverricht-Lundborg Syndrome/diagnosis/genetics/physiopathology
Creator
An entity primarily responsible for making the resource
Chew NK; Mir P; Edwards MJ; Cordivari C; Martino D; Schneider SA; Kim HT; Quinn NP; Bhatia KP
Description
An account of the resource
We report eight cases of genetically proven ULD, with the aim of reassessing the clinical characteristics and natural history of ULD in genetically characterized patients. The eight patients had their first symptoms at mean age of 10.6 years (range: 6-14 years). The main clinical features were action myoclonus, cerebellar ataxia, seizures, and mild intellectual dysfunction. We report three new clinical features of ULD; ocular motor apraxia, dystonia, and rapidly progressive dementia. All patients needed a combination of at least four antimyoclonic drugs, but despite this, all patients were severely disabled by their action myoclonus. After a mean duration of disease of 29.9 years (range: 21-37 years), four patients were walking with aids while another four were wheelchair bound. The clinical phenotypes associated with ULD are more diverse than previously recognized and even though the long term functional outcome and survival have improved, the overall efficacy of antimyoclonic drugs remains unsatisfactory.
2008
Identifier
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<a href="http://doi.org/10.1002/mds.21812" target="_blank" rel="noreferrer">10.1002/mds.21812</a>
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Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2008
Adolescent
Adult
Age Factors
Atrophy/complications/pathology
Auditory
Backlog
Bhatia KP
Brain Stem/physiology
Brain/pathology/physiopathology
Cerebellar Ataxia/complications/diagnosis
Cerebellum/pathology/physiopathology
Chew NK
Child
Chromosomes
Cordivari C
Dementia/complications/diagnosis
Diagnosis
Differential
Disease Progression
Dystonia/complications/diagnosis
Edwards MJ
Electroencephalography
Electromyography
Evoked Potentials
Evoked Potentials/physiology
Female
Human
Humans
Journal Article
Kim HT
Magnetic Resonance Imaging
Male
Martino D
Mir P
Movement Disorders: Official Journal Of The Movement Disorder Society
Myoclonus/complications/diagnosis
Neuropsychological Tests
Pair 21/genetics
Q3 Scoping Review Results
Quinn NP
Schneider SA
Seizures/complications/diagnosis
Severity Of Illness Index
Unverricht-Lundborg Syndrome/diagnosis/genetics/physiopathology
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1002/ppul.20725" target="_blank" rel="noreferrer">http://doi.org/10.1002/ppul.20725</a>
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The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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Lung disease in Niemann-Pick disease
Publisher
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Pediatric Pulmonology
Date
A point or period of time associated with an event in the lifecycle of the resource
2007
Subject
The topic of the resource
Child; Female; Humans; Male; Prognosis; Severity of Illness Index; Biopsy; Preschool; infant; Q3 Literature Search; Diagnosis; Differential; Lung Diseases; Respiratory Function Tests; Bronchoalveolar Lavage; Bronchoalveolar Lavage Fluid/cytology; Interstitial/diagnosis/etiology/physiopathology; Niemann-Pick Diseases/complications; Radiography; Thoracic
Creator
An entity primarily responsible for making the resource
Guillemot N; Troadec C; de Villemeur TB; Clement A; Fauroux B
Description
An account of the resource
BACKGROUND: Lung involvement in children with Niemann-Pick disease has rarely been studied systematically. OBJECTIVE: To assess the involvement of the lung and the value of bronchoalveolar lavage in children with Niemann-Pick diseases. DESIGN: Retrospective analysis of patient records. PATIENTS: Thirteen patients, with type A (n = 1), type B (n = 10), and type C (n = 2) Niemann-Pick disease, aged 2 months to 9 years at diagnosis, were included in the study. INTERVENTIONS: Lung involvement was assessed by clinical evaluation, chest radiograph, lung computed tomography (CT) scan, pulmonary function tests, and bronchoalveolar lavage fluid analysis. RESULTS: Respiratory symptoms were present at diagnosis in 10 patients and developed during follow up in the three other patients. All patients showed signs of interstitial lung disease on chest X-ray and lung CT scan. Bronchoalveolar lavage fluid analysis (n = 7) revealed a marked accumulation of foamy macrophages (Niemann-Pick cells) in all patients. At follow up, one patient died of respiratory failure, five patients required long term oxygen therapy and seven other patients presented a chronic obstructive pulmonary disease (n = 6) or chronic cough (n = 1). CONCLUSION: Lung disease was observed in all the patients included in the present study. Bronchoalveolar lavage may be useful in Niemann-Pick diseases by showing the presence of characteristic Niemann-Pick cells.
2007
Identifier
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<a href="http://doi.org/10.1002/ppul.20725" target="_blank" rel="noreferrer">10.1002/ppul.20725</a>
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Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2007
Backlog
Biopsy
Bronchoalveolar Lavage
Bronchoalveolar Lavage Fluid/cytology
Child
Clement A
de Villemeur TB
Diagnosis
Differential
Fauroux B
Female
Guillemot N
Humans
Infant
Interstitial/diagnosis/etiology/physiopathology
Journal Article
Lung Diseases
Male
Niemann-Pick Diseases/complications
Pediatric Pulmonology
Preschool
Prognosis
Q3 Scoping Review Results
Radiography
Respiratory Function Tests
Severity Of Illness Index
Thoracic
Troadec C
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1016/j.psc.2007.07.009" target="_blank" rel="noreferrer">http://doi.org/10.1016/j.psc.2007.07.009</a>
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The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Late consequences of chronic pediatric illness
Publisher
An entity responsible for making the resource available
The Psychiatric Clinics Of North America
Date
A point or period of time associated with an event in the lifecycle of the resource
2007
Subject
The topic of the resource
Child; Humans; Time Factors; adolescent; Arthritis; Diagnosis; Differential; Heart Defects; Chronic Disease/psychology; Congenital/diagnosis/epidemiology/psychology; Cystic Fibrosis/diagnosis/epidemiology/psychology; Juvenile Rheumatoid/diagnosis/epidemiology/psychology; Mental Disorders/diagnosis/epidemiology/etiology
Creator
An entity primarily responsible for making the resource
Turkel S; Pao M
Description
An account of the resource
There are many challenges in coping with and adapting to life with a chronic disease, and increased survival cannot be assumed to be associated with increased quality of life. A recent systematic review shows there is wide variation in outcomes depending on the definitions and measurements used to estimate the prevalence of chronic health conditions, making the impact of disability on children's health and social functioning difficult to assess; various authors have called for an international consensus about the conceptual definition of chronic health conditions in childhood. It frequently is difficult to determine if problems in psychosocial functioning are caused by the underlying illness, by treatment, or by the resultant effects of either illness or treatment on physical growth or cognitive development. Assessment and treatment of mental health should be an integral component of the comprehensive care of chronically ill children and adolescents. Transition of care is an important process that addresses significant changes from child-oriented to adult-oriented care. Adults who have chronic health conditions should continue to be evaluated periodically for late consequences of the childhood illness and early medical care, and attention should be paid to their ongoing psychosocial, psychiatric, educational, and vocational needs.
2007
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/j.psc.2007.07.009" target="_blank" rel="noreferrer">10.1016/j.psc.2007.07.009</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2007
Adolescent
Arthritis
Backlog
Child
Chronic Disease/psychology
Congenital/diagnosis/epidemiology/psychology
Cystic Fibrosis/diagnosis/epidemiology/psychology
Diagnosis
Differential
Heart Defects
Humans
Journal Article
Juvenile Rheumatoid/diagnosis/epidemiology/psychology
Mental Disorders/diagnosis/epidemiology/etiology
Pao M
The Psychiatric Clinics Of North America
Time Factors
Turkel S
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1016/S1474-4422(09)70271-6" target="_blank" rel="noreferrer">http://doi.org/10.1016/S1474-4422(09)70271-6</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management
Publisher
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Lancet Neurology
Date
A point or period of time associated with an event in the lifecycle of the resource
2010
Subject
The topic of the resource
Female; Humans; Male; Diagnosis; Differential; Duchenne/diagnosis/genetics/therapy; Glucocorticoids/administration & dosage/adverse effects/therapeutic use; Muscular Dystrophy
Creator
An entity primarily responsible for making the resource
Bushby K; Finkel R; Birnkrant DJ; Case LE; Clemens PR; Cripe L; Kaul A; Kinnett K; McDonald C; Pandya S; Poysky J; Shapiro F; Tomezsko J; Constantin C; DMD Care Considerations Working Group
Description
An account of the resource
Duchenne muscular dystrophy (DMD) is a severe, progressive disease that affects 1 in 3600-6000 live male births. Although guidelines are available for various aspects of DMD, comprehensive clinical care recommendations do not exist. The US Centers for Disease Control and Prevention selected 84 clinicians to develop care recommendations using the RAND Corporation-University of California Los Angeles Appropriateness Method. The DMD Care Considerations Working Group evaluated assessments and interventions used in the management of diagnostics, gastroenterology and nutrition, rehabilitation, and neuromuscular, psychosocial, cardiovascular, respiratory, orthopaedic, and surgical aspects of DMD. These recommendations, presented in two parts, are intended for the wide range of practitioners who care for individuals with DMD. They provide a framework for recognising the multisystem primary manifestations and secondary complications of DMD and for providing coordinated multidisciplinary care. In part 1 of this Review, we describe the methods used to generate the recommendations, and the overall perspective on care, pharmacological treatment, and psychosocial management.
2010
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/S1474-4422(09)70271-6" target="_blank" rel="noreferrer">10.1016/S1474-4422(09)70271-6</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2010
Backlog
Birnkrant DJ
Bushby K
Case LE
Clemens PR
Constantin C
Cripe L
Diagnosis
Differential
DMD Care Considerations Working Group
Duchenne/diagnosis/genetics/therapy
Female
Finkel R
Glucocorticoids/administration & dosage/adverse effects/therapeutic use
Humans
Journal Article
Kaul A
Kinnett K
Lancet Neurology
Male
McDonald C
Muscular Dystrophy
Pandya S
Poysky J
Shapiro F
Tomezsko J
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1097/BPO.0b013e3181558bc1" target="_blank" rel="noreferrer">http://doi.org/10.1097/BPO.0b013e3181558bc1</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Diagnostic evaluation using whole-body technetium bone scan in children with cerebral palsy and pain.
Publisher
An entity responsible for making the resource available
Journal Of Pediatric Orthopedics
Date
A point or period of time associated with an event in the lifecycle of the resource
2008
Subject
The topic of the resource
Child; Female; Humans; Male; Pain Measurement; Adult; Severity of Illness Index; Reproducibility of Results; adolescent; Preschool; retrospective studies; Emission-Computed; Tomography; Diagnosis; Differential; Bone and Bones/radionuclide imaging; Cerebral Palsy/complications/radionuclide imaging; Pain/etiology/radionuclide imaging; Single-Photon/methods; Technetium/diagnostic use; Whole Body Imaging/methods
Creator
An entity primarily responsible for making the resource
Bajelidze G; Belthur MV; Littleton AG; Dabney Kirk W; Miller F
Description
An account of the resource
BACKGROUND: Pain in noncommunicative children can be difficult to localize and diagnose. The purpose of this study is to report our experience using a 3-phase whole-body technetium bone scan as a screening tool in identifying the source of persistent pain in children with profound disabilities who cannot communicate. METHODS: We reviewed the medical and imaging records of 45 patients who met the inclusion criteria of the study, which included a diagnosis of spastic quadriplegic cerebral palsy with severe motor and cognitive impairment, persistent pain of more than 1 week in duration with no recognizable source, and a 3-phase whole-body bone scan as part of the pain workup. RESULTS: The study group included 26 females and 19 males with an average age at presentation of 13.5 years (range, 3-20 years). A positive bone scan was seen in 24 patients (53%). The diagnosis and the source of pain were identified in all 24 patients with a positive bone scan, with the bone scan being instrumental in establishing a diagnosis or localization in 22 patients. An orthopaedic diagnosis was not established in the 21 other patients with a negative bone scan. Based on the bone scan results, additional imaging was obtained at the anatomical location indicated. The bone scan was used to establish a diagnosis of fracture in 10 of 24 patients. Other diagnoses included 3 patients with painful internal hardware, 2 with sinusitis, 2 with infections, and 1 with an obstructed kidney. CONCLUSIONS: Whole-body bone scan is a viable imaging option to identify the source of persistent pain in children who are noncommunicative. The bone scan can assist in localizing the source of pain and direct the location for further imaging as needed.
2008-02
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1097/BPO.0b013e3181558bc1" target="_blank" rel="noreferrer">10.1097/BPO.0b013e3181558bc1</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2008
Adolescent
Adult
Backlog
Bajelidze G
Belthur MV
Bone and Bones/radionuclide imaging
Cerebral Palsy/complications/radionuclide imaging
Child
Dabney Kirk W
Diagnosis
Differential
Emission-Computed
Female
Humans
Journal Article
Journal Of Pediatric Orthopedics
Littleton AG
Male
Miller F
Pain Measurement
Pain/etiology/radionuclide imaging
Preschool
Reproducibility of Results
Retrospective Studies
Severity Of Illness Index
Single-Photon/methods
Technetium/diagnostic use
Tomography
Whole Body Imaging/methods
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1097/MPG.0b013e3181cb4309" target="_blank" rel="noreferrer">http://doi.org/10.1097/MPG.0b013e3181cb4309</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Lack of utility of abdominal x-rays in the evaluation of children with constipation: comparison of different scoring methods
Publisher
An entity responsible for making the resource available
Journal Of Pediatric Gastroenterology And Nutrition
Date
A point or period of time associated with an event in the lifecycle of the resource
2010
Subject
The topic of the resource
Child; Female; Humans; Male; Observer Variation; retrospective studies; Diagnosis; Differential; Radiography; ROC Curve; Abdominal/methods; Colon/physiopathology/radiography; Colonic Diseases; Constipation/physiopathology/radiography; Fecal Incontinence/physiopathology/radiography; Feces; Functional/physiopathology/radiography; Gastrointestinal Transit; X-Rays
Creator
An entity primarily responsible for making the resource
Pensabene L; Buonomo C; Fishman L; Chitkara D; Nurko S
Description
An account of the resource
BACKGROUND AND AIM: Abdominal x-rays are used diagnostically in the evaluation of children with constipation. However, their clinical utility has not been established. The aim of the study was to assess the accuracy of different methods in identifying children with functional constipation (FC) or nonretentive fecal incontinence (NRFI). PATIENTS AND METHODS: Retrospective review of abdominal x-rays in which colonic transit (CT), Barr, Leech, and fecal loading (FL) scores were blindly measured by blinded pediatric gastroenterologists and a radiologist. Children were classified a priori as FC or NRFI. RESULTS: One hundred sixty patients (125 FC, 35 NRFI) were studied. There were significant differences (P 50% of NRFI had abnormal scores. CT discriminated better between FC and NRFI. There was a significant correlation (P < 0.05) between CT and Barr (0.45), Leech (0.41) and FL scores (0.36), and between Barr and Leech scores (r = 0.94). There was good intraobserver correlation between Barr, Leech, and FL scores but poor interobserver reproducibility. CONCLUSIONS: Although significant differences in overall FC and NRFI scores exist, the discriminative value is low for all scores. There is poor interobserver reproducibility of the Barr, Leech, and FL scores. These findings confirm the limited value of the plain abdominal x-ray in the evaluation of children with constipation.
2010
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1097/MPG.0b013e3181cb4309" target="_blank" rel="noreferrer">10.1097/MPG.0b013e3181cb4309</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2010
Abdominal/methods
Backlog
Buonomo C
Child
Chitkara D
Colon/physiopathology/radiography
Colonic Diseases
Constipation/physiopathology/radiography
Diagnosis
Differential
Fecal Incontinence/physiopathology/radiography
Feces
Female
Fishman L
Functional/physiopathology/radiography
Gastrointestinal Transit
Humans
Journal Article
Journal Of Pediatric Gastroenterology And Nutrition
Male
Nurko S
Observer Variation
Pensabene L
Radiography
Retrospective Studies
ROC Curve
X-Rays
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1136/adc.2008.150417" target="_blank" rel="noreferrer">http://doi.org/10.1136/adc.2008.150417</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Autopsies in children continue to reveal unanticipated discrepancies between autopsy findings and antemortem clinical diagnoses
Publisher
An entity responsible for making the resource available
Archives Of Disease In Childhood
Date
A point or period of time associated with an event in the lifecycle of the resource
2009
Subject
The topic of the resource
Child; Female; Humans; Male; Intensive Care Units; Preschool; infant; Epidemiologic Methods; Diagnosis; Pediatric/statistics & numerical data; Autopsy/standards/statistics & numerical data
Creator
An entity primarily responsible for making the resource
Narayanan A; Thorburn K; Baines P
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1136/adc.2008.150417" target="_blank" rel="noreferrer">10.1136/adc.2008.150417</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
Description
An account of the resource
2009
2009
Archives of Disease in Childhood
Autopsy/standards/statistics & numerical data
Backlog
Baines P
Child
Diagnosis
Epidemiologic Methods
Female
Humans
Infant
Intensive Care Units
Journal Article
Male
Narayanan A
Pediatric/statistics & Numerical Data
Preschool
Thorburn K
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1177/0883073807309254" target="_blank" rel="noreferrer">http://doi.org/10.1177/0883073807309254</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Diagnostic yield of brain biopsies in children presenting to neurology
Publisher
An entity responsible for making the resource available
Journal Of Child Neurology
Date
A point or period of time associated with an event in the lifecycle of the resource
2008
Subject
The topic of the resource
Child; Female; Humans; Male; Odds Ratio; Predictive Value of Tests; Outcome and Process Assessment (Health Care); Preschool; infant; retrospective studies; Brain/pathology; Diagnosis; Differential; Children W/SNI; Epilepsy/pathology; Likelihood Functions; Decision Trees; Biopsy/statistics & numerical data; Brain Diseases/pathology; Neurodegenerative Diseases/pathology; Vasculitis/pathology
Creator
An entity primarily responsible for making the resource
Venkateswaran S; Hawkins C; Wassmer E
Description
An account of the resource
The role of brain biopsy is well established in patients with neoplastic lesions, with a diagnostic yield approaching 95%. The diagnostic yield of brain biopsy in adults with neurological decline varies from 20% to 43%. Only a few studies have examined the diagnostic yield of brain biopsy in children with idiopathic neurological decline. A retrospective analysis was conducted on all open and closed pediatric brain biopsies performed between January 1988 and May 2003. Biopsies were performed for diagnostic purposes in patients showing a progressively deteriorating neurologic course in whom less-invasive modalities such as neuroimaging, electroencephalography (EEG), and molecular genetic studies were either negative or inconclusive. Immunocompromised patients were included. Patients were excluded if the preoperative diagnosis was a neoplasm or if the patient was undergoing a resection as part of a work-up for intractable epilepsy. Each patient underwent numerous investigations before brain biopsy. The utility of each biopsy was analyzed. Sixty-six children had brain biopsies performed for diagnostic purposes during the study period. Patient ages ranged from 2 months to 16 years and 9 months at the time of biopsy. The diagnostic yield was 48.5% overall, with a yield of 68.8% between 1996 and 2003. Of the total, 26 (39.4%) biopsies were both diagnostic and useful. Patients most frequently presented with seizures (56.1%) and encephalopathy (33%). The most frequently diagnosed disease was vasculitis (18.2%). A total of 71.9% of patients with diagnostic biopsies improved with appropriate treatment. Brain biopsy in children had a diagnostic yield of 48.5% in our series. A specific diagnosis may help in management and outcome, especially with a diagnosis of vasculitis.
2008
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1177/0883073807309254" target="_blank" rel="noreferrer">10.1177/0883073807309254</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2008
Backlog
Biopsy/statistics & numerical data
Brain Diseases/pathology
Brain/pathology
Child
Children W/SNI
Decision Trees
Diagnosis
Differential
Epilepsy/pathology
Female
Hawkins C
Humans
Infant
Journal Article
Journal of Child Neurology
Likelihood Functions
Male
Neurodegenerative Diseases/pathology
Odds Ratio
Outcome And Process Assessment (health Care)
Predictive Value of Tests
Preschool
Retrospective Studies
Vasculitis/pathology
Venkateswaran S
Wassmer E
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1542/pir.28-3-101" target="_blank" rel="noreferrer">http://doi.org/10.1542/pir.28-3-101</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Gastroesophageal reflux
Publisher
An entity responsible for making the resource available
Pediatrics In Review / American Academy Of Pediatrics
Date
A point or period of time associated with an event in the lifecycle of the resource
2007
Subject
The topic of the resource
Child; Humans; Prognosis; adolescent; Preschool; infant; Nervous System Diseases/complications; Nutritional Failure; Diagnosis; Differential; Digestive System; Pediatrics/methods; Proton Pumps/antagonists & inhibitors; Enzyme Inhibitors/therapeutic use; Diagnostic Techniques; Gastroesophageal Reflux/complications/diagnosis/physiopathology/therapy; Histamine H2 Antagonists/therapeutic use; Medical History Taking/methods; Respiratory Tract Diseases/etiology/prevention & control; Vomiting/diagnosis/etiology
Creator
An entity primarily responsible for making the resource
Michail S
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1542/pir.28-3-101" target="_blank" rel="noreferrer">10.1542/pir.28-3-101</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
Description
An account of the resource
2007
2007
Adolescent
Backlog
Child
Diagnosis
Diagnostic Techniques
Differential
Digestive System
Enzyme Inhibitors/therapeutic use
Gastroesophageal Reflux/complications/diagnosis/physiopathology/therapy
Histamine H2 Antagonists/therapeutic use
Humans
Infant
Journal Article
Medical History Taking/methods
Michail S
Nervous System Diseases/complications
Nutritional Failure
Pediatrics In Review / American Academy Of Pediatrics
Pediatrics/methods
Preschool
Prognosis
Proton Pumps/antagonists & inhibitors
Respiratory Tract Diseases/etiology/prevention & control
Vomiting/diagnosis/etiology
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1007/s10545-006-0193-3" target="_blank" rel="noreferrer">http://doi.org/10.1007/s10545-006-0193-3</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
An unusual clinical and biochemical presentation of ornithine transcarbamylase deficiency in a male patient
Publisher
An entity responsible for making the resource available
Journal Of Inherited Metabolic Disease
Date
A point or period of time associated with an event in the lifecycle of the resource
2006
Subject
The topic of the resource
Child; Humans; Male; Fatal Outcome; Preschool; Q3 Literature Search; Diagnosis; Differential; Amino Acid Metabolism; Amino Acids/blood; Inborn Errors/diagnosis; Ornithine Carbamoyltransferase Deficiency Disease/blood/diagnosis; Ornithine Carbamoyltransferase/deficiency; Orotic Acid/urine
Creator
An entity primarily responsible for making the resource
Burlina AB; Peduto A; Di Palma A; Bellizzi A; Sperli D; Morrone A; Burlina AP
Description
An account of the resource
We report a male patient with a history of recurrent idiopathic vomiting, normal plasma ammonia and glutamine concentrations in acute phase, who died at 3 years of age. Ornithine transcarbamylase deficiency was diagnosed after detecting elevated urinary orotate concentrations in a sample collected just before death, and the diagnosis was confirmed by DNA analysis.
2006
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1007/s10545-006-0193-3" target="_blank" rel="noreferrer">10.1007/s10545-006-0193-3</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2006
Amino Acid Metabolism
Amino Acids/blood
Backlog
Bellizzi A
Burlina AB
Burlina AP
Child
Di Palma A
Diagnosis
Differential
Fatal Outcome
Humans
Inborn Errors/diagnosis
Journal Article
Journal Of Inherited Metabolic Disease
Male
Morrone A
Ornithine Carbamoyltransferase Deficiency Disease/blood/diagnosis
Ornithine Carbamoyltransferase/deficiency
Orotic Acid/urine
Peduto A
Preschool
Q3 Scoping Review Results
Sperli D
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1016/j.jpeds.2004.11.034" target="_blank" rel="noreferrer">http://doi.org/10.1016/j.jpeds.2004.11.034</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Decisions in diagnosing and managing chronic gastroesophageal reflux disease in children
Publisher
An entity responsible for making the resource available
The Journal Of Pediatrics
Date
A point or period of time associated with an event in the lifecycle of the resource
2005
Subject
The topic of the resource
Child; Humans; Biopsy; Esophagoscopy; Fundoplication; Medical History Taking; Diagnosis; Differential; Anti-Ulcer Agents/therapeutic use; Gastroesophageal Reflux/diagnosis/therapy; Proton Pumps/antagonists & inhibitors
Creator
An entity primarily responsible for making the resource
Hassall E
Description
An account of the resource
Gastroesophageal reflux disease (GERD) presents in different ways in children, most commonly with vomiting, or with esophageal symptoms such as regurgitation, heartburn, or dysphagia. Extraesophageal symptoms and signs also frequently occur. Less well recognized is that abdominal pain is a relatively common mode of presentation. Although abdominal pain is common in school-aged children, GERD and other acid-related disorders such as peptic ulcer disease are relatively uncommon causes of such. A careful history will usually determine whether an acid-related disorder is in the differential diagnosis of abdominal pain. Early detection and treatment of GERD in children may prevent, attenuate, or heal complications such as failure to thrive or feeding refusal as well as pulmonary, ear-nose-and-throat disorders, erosive esophagitis, and peptic stricture. In children with persistent or severe symptoms and/or complications of GERD such as erosive esophagitis, the major treatment options are pharmacologic management with acid-suppressing medication, specifically proton pump inhibitors (PPIs), or antireflux surgery. For many patients, PPI treatment offers advantages over surgery. When given in adequate doses, PPIs can safely effect relief of GERD symptoms and healing of esophagitis in children. Antireflux surgery may work well in selected patients, but it carries significant risk of morbidity, including high failure rates, even in the short term. Some postoperative studies report that more than 60% of patients are back on medical treatment with proton pump inhibitors for recurrence of GERD symptoms, and a similar percentage have new symptoms that were not present before surgery. Death is uncommon but does occur and is an unacceptable risk in an otherwise healthy, low-risk individual. Laparoscopic surgery may have some disadvantages compared with open surgery, including a higher rate of redo operations. Studies show that many children undergo surgery for unclear indications, often with few preoperative diagnostic studies. The availability of highly effective medical therapy, together with more careful selection of patients for surgery, may result in better patient outcomes, with much lower operative rates.
2005
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/j.jpeds.2004.11.034" target="_blank" rel="noreferrer">10.1016/j.jpeds.2004.11.034</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2005
Anti-Ulcer Agents/therapeutic use
Backlog
Biopsy
Child
Diagnosis
Differential
Esophagoscopy
Fundoplication
Gastroesophageal Reflux/diagnosis/therapy
Hassall E
Humans
Journal Article
Medical History Taking
Proton Pumps/antagonists & inhibitors
The Journal Of Pediatrics
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1016/j.jpeds.2004.11.035" target="_blank" rel="noreferrer">http://doi.org/10.1016/j.jpeds.2004.11.035</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Care at the front line: Clinical decisions in the management of pediatric acid-related disorders
Publisher
An entity responsible for making the resource available
The Journal Of Pediatrics
Date
A point or period of time associated with an event in the lifecycle of the resource
2005
Subject
The topic of the resource
Child; Humans; Primary Health Care; Diagnosis; Differential; Abdominal Pain/etiology; Asthma/diagnosis; Gastroesophageal Reflux/diagnosis; Helicobacter Infections/diagnosis; Helicobacter pylori
Creator
An entity primarily responsible for making the resource
Gold BD
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/j.jpeds.2004.11.035" target="_blank" rel="noreferrer">10.1016/j.jpeds.2004.11.035</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
Description
An account of the resource
2005
2005
Abdominal Pain/etiology
Asthma/diagnosis
Backlog
Child
Diagnosis
Differential
Gastroesophageal Reflux/diagnosis
Gold BD
Helicobacter Infections/diagnosis
Helicobacter pylori
Humans
Journal Article
Primary Health Care
The Journal Of Pediatrics
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1097/01.ajp.0000130160.40974.f5" target="_blank" rel="noreferrer">http://doi.org/10.1097/01.ajp.0000130160.40974.f5</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Psychological, behavioral, and family characteristics of pediatric patients with chronic pain: a 1-year retrospective study and cluster analysis
Publisher
An entity responsible for making the resource available
The Clinical Journal Of Pain
Date
A point or period of time associated with an event in the lifecycle of the resource
2005
Subject
The topic of the resource
PedPal Lit; Adolescent Child Chronic Disease Cluster Analysis Comorbidity; another with relatively low scores on distress and disability; as well as demographic and pain characteristic information. A cluster analysis was conducted to identify 3 distinct subgroups of patients to replicate similar studies of adult chronic pain sufferers. RESULTS: Overall; Diagnosis; epidemiology/psychology Pain/classification/; epidemiology/psychology Prevalence Retrospective Studies Risk Assessment/; Family Relations Female Humans Male Massachusetts/epidemiology Mental Disorders/; mean scores were within population norms on measures of distress and family functioning; with somatic symptoms at a level of clinical significance. The cluster analysis identified the 3 subgroups that were strikingly similar to those identified in adult chronic pain populations: one with high levels of distress and disability
Creator
An entity primarily responsible for making the resource
Scharff L; Langan N; Rotter N; Scott-Sutherland J; Schenck C; Tayor N; McDonald-Nolan L; Masek B
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1097/01.ajp.0000130160.40974.f5" target="_blank" rel="noreferrer">10.1097/01.ajp.0000130160.40974.f5</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
Description
An account of the resource
2005
2005
Adolescent Child Chronic Disease Cluster Analysis Comorbidity
another with relatively low scores on distress and disability
as well as demographic and pain characteristic information. A cluster analysis was conducted to identify 3 distinct subgroups of patients to replicate similar studies of adult chronic pain sufferers. RESULTS: Overall
Backlog
Diagnosis
epidemiology/psychology Pain/classification/
epidemiology/psychology Prevalence Retrospective Studies Risk Assessment/
Family Relations Female Humans Male Massachusetts/epidemiology Mental Disorders/
Journal Article
Langan N
Masek B
McDonald-Nolan L
mean scores were within population norms on measures of distress and family functioning
PedPal Lit
Rotter N
Scharff L
Schenck C
Scott-Sutherland J
Tayor N
The Clinical Journal Of Pain
with somatic symptoms at a level of clinical significance. The cluster analysis identified the 3 subgroups that were strikingly similar to those identified in adult chronic pain populations: one with high levels of distress and disability
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1111/j.1088-145x.2005.00002.x" target="_blank" rel="noreferrer">http://doi.org/10.1111/j.1088-145x.2005.00002.x</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Utilizing an oral sucrose solution to minimize neonatal pain
Publisher
An entity responsible for making the resource available
Journal for Specialists in Pediatric Nursing
Date
A point or period of time associated with an event in the lifecycle of the resource
2005
Subject
The topic of the resource
Nursing; PedPal Lit; Administration; Newborn; Diagnosis; Newborn Infant; Diseases; administration & dosage; Drug Therapy; nursing Pain Measurement Randomized Controlled Trials Risk Assessment Severity of Illness Index Sucrose; adverse effects Treatment Outcome; etiology; methods Pain; Oral Comparative Study Evidence-Based Medicine Female Follow-Up Studies Humans Infant; therapy Intensive Care Units Male Neonatal Nursing
Creator
An entity primarily responsible for making the resource
Thompson DG
Description
An account of the resource
ISSUES AND PURPOSE: To present an evidence-based practice protocol for oral sucrose administration to minimize neonatal procedural pain. CONCLUSION: Examination of published research may provide additional modalities to expand an established pediatric pain-management program. PRACTICAL IMPLICATIONS: The extensive research evaluating oral sucrose supports its inclusion in a pediatric pain-management program. A thorough implementation plan will allow new modalities to be included to optimize procedural pain relief for hospitalized neonates with minimal staff resistance and improved patient outcomes.
2005
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1111/j.1088-145x.2005.00002.x" target="_blank" rel="noreferrer">10.1111/j.1088-145x.2005.00002.x</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2005
Administration
administration & dosage
adverse effects Treatment Outcome
Backlog
Diagnosis
Diseases
Drug Therapy
etiology
Journal Article
Journal for Specialists in Pediatric Nursing
methods Pain
Newborn
Newborn Infant
Nursing
nursing Pain Measurement Randomized Controlled Trials Risk Assessment Severity of Illness Index Sucrose
Oral Comparative Study Evidence-Based Medicine Female Follow-Up Studies Humans Infant
PedPal Lit
therapy Intensive Care Units Male Neonatal Nursing
Thompson DG
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1503/cmaj.1040302" target="_blank" rel="noreferrer">http://doi.org/10.1503/cmaj.1040302</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Fetal alcohol spectrum disorder: Canadian guidelines for diagnosis
Publisher
An entity responsible for making the resource available
Canadian Medical Association Journal
Date
A point or period of time associated with an event in the lifecycle of the resource
2005
Subject
The topic of the resource
Child; Female; Humans; infant; Pregnancy; Adult; Risk Factors; Non-U.S. Gov't; Research Support; Newborn; Diagnosis; Differential; Abnormalities; Multiple/diagnosis; Canada/epidemiology; Alcohol Drinking/prevention & control; Alcoholism/diagnosis/prevention & control; Ethanol; Fetal Alcohol Syndrome/diagnosis/epidemiology/prevention & control; Mass Screening/standards; Medical History Taking/standards; Nervous System Diseases/diagnosis; Physical Examination/standards; Pregnancy Complications/diagnosis/prevention & control; Prenatal Exposure Delayed Effects; Referral and Consultation/standards
Creator
An entity primarily responsible for making the resource
Chudley AE; Conry J; Cook JL; Loock C; Rosales T; LeBlanc N; Public Health Agency of Canada's National Advisory Committee on Fetal Alcohol Spectrum Disorder
Description
An account of the resource
The diagnosis of fetal alcohol spectrum disorder (FASD) is complex and guidelines are warranted. A subcommittee of the Public Health Agency of Canada's National Advisory Committee on Fetal Alcohol Spectrum Disorder reviewed, analysed and integrated current approaches to diagnosis to reach agreement on a standard in Canada. The purpose of this paper is to review and clarify the use of current diagnostic systems and make recommendations on their application for diagnosis of FASD-related disabilities in people of all ages. The guidelines are based on widespread consultation of expert practitioners and partners in the field. The guidelines have been organized into 7 categories: screening and referral; the physical examination and differential diagnosis; the neurobehavioural assessment; and treatment and follow-up; maternal alcohol history in pregnancy; diagnostic criteria for fetal alcohol syndrome (FAS), partial FAS and alcohol-related neurodevelopmental disorder; and harmonization of Institute of Medicine and 4-Digit Diagnostic Code approaches. The diagnosis requires a comprehensive history and physical and neurobehavioural assessments; a multidisciplinary approach is necessary. These are the first Canadian guidelines for the diagnosis of FAS and its related disabilities, developed by broad-based consultation among experts in diagnosis.
2005
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1503/cmaj.1040302" target="_blank" rel="noreferrer">10.1503/cmaj.1040302</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2005
Abnormalities
Adult
Alcohol Drinking/prevention & control
Alcoholism/diagnosis/prevention & control
Backlog
Canada/epidemiology
Canadian Medical Association Journal
Child
Chudley AE
Conry J
Cook JL
Diagnosis
Differential
Ethanol
Female
Fetal Alcohol Syndrome/diagnosis/epidemiology/prevention & control
Humans
Infant
Journal Article
LeBlanc N
Loock C
Mass Screening/standards
Medical History Taking/standards
Multiple/diagnosis
Nervous System Diseases/diagnosis
Newborn
Non-U.S. Gov't
Physical Examination/standards
Pregnancy
Pregnancy Complications/diagnosis/prevention & control
Prenatal Exposure Delayed Effects
Public Health Agency of Canada's National Advisory Committee on Fetal Alcohol Spectrum Disorder
Referral and Consultation/standards
Research Support
Risk Factors
Rosales T
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1016/j.adnc.2004.05.006" target="_blank" rel="noreferrer">http://doi.org/10.1016/j.adnc.2004.05.006</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Discerning differences: gastroesophageal reflux and gastroesophageal reflux disease in infants
Publisher
An entity responsible for making the resource available
Advances In Neonatal Care
Date
A point or period of time associated with an event in the lifecycle of the resource
2004
Subject
The topic of the resource
Nursing; PedPal Lit; Premature; Diagnosis; Newborn Infant; Diagnosis; Differential Directories Gastroesophageal Reflux; physiology Internet Nursing Assessment%X Gastroesophageal reflux (GER) is a frequently encountered problem in infancy; physiopathology; therapy Health Education Humans Infant Infant
Creator
An entity primarily responsible for making the resource
Henry SM
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/j.adnc.2004.05.006" target="_blank" rel="noreferrer">10.1016/j.adnc.2004.05.006</a>
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Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
Description
An account of the resource
2004
2004
Advances in Neonatal Care
Backlog
Diagnosis
Differential Directories Gastroesophageal Reflux
Henry SM
Journal Article
Newborn Infant
Nursing
PedPal Lit
physiology Internet Nursing Assessment%X Gastroesophageal reflux (GER) is a frequently encountered problem in infancy
physiopathology
Premature
therapy Health Education Humans Infant Infant
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1016/s0749-0690(02)00032-0" target="_blank" rel="noreferrer">http://doi.org/10.1016/s0749-0690(02)00032-0</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Distinguishing starvation from cachexia
Publisher
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Clinics In Geriatric Medicine
Date
A point or period of time associated with an event in the lifecycle of the resource
2002
Subject
The topic of the resource
Humans; Aged; Nutritional Status; Diagnosis; Differential; Nutrition Assessment; Energy Intake; Cachexia/diagnosis; Starvation/diagnosis
Creator
An entity primarily responsible for making the resource
Thomas DR
Description
An account of the resource
The poor response to hypercaloric feeding in ill adults may be caused by failure to distinguish cachexia from starvation (Table 1). The chief difference between starvation and cachexia is that refeeding reverses starvation but is less effective for cachexia. The ineffectiveness of refeeding in treating cachexia may explain some of the poor results from direct nutritional interventions in clinical trials. Simple starvation should respond to voluntary or involuntary hypercaloric feedings. The failure to demonstrate a more positive response may be caused by underlying cachexic states.
2002
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/s0749-0690(02)00032-0" target="_blank" rel="noreferrer">10.1016/s0749-0690(02)00032-0</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2002
Aged
Backlog
Cachexia/diagnosis
Clinics In Geriatric Medicine
Diagnosis
Differential
Energy Intake
Humans
Journal Article
Nutrition Assessment
Nutritional Status
Starvation/diagnosis
Thomas DR
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1016/s0887-8994(02)00489-7" target="_blank" rel="noreferrer">http://doi.org/10.1016/s0887-8994(02)00489-7</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Early peripheral nervous system manifestations of infantile Krabbe disease
Publisher
An entity responsible for making the resource available
Pediatric Neurology
Date
A point or period of time associated with an event in the lifecycle of the resource
2003
Subject
The topic of the resource
Female; Humans; Male; Biopsy; Family Health; infant; retrospective studies; Diagnosis; Differential; Demyelinating Diseases/pathology/physiopathology; Globoid Cell/pathology/physiopathology; Inclusion Bodies/pathology; Leukodystrophy; Peripheral Nervous System/pathology/physiopathology; Schwann Cells/pathology
Creator
An entity primarily responsible for making the resource
Korn-Lubetzki I; Dor-Wollman T; Soffer D; Raas-Rothschild A; Hurvitz H; Nevo Y
Description
An account of the resource
Early infantile Krabbe disease is relatively frequent in the Muslim-Arab population in Israel. It can be easily diagnosed when it presents with the classic clinical picture characterized by central nervous system manifestations of spasticity, irritability, motor regression and seizures associated with a positive family history. We studied eight children diagnosed with Krabbe disease. In two of these children (25%), peripheral neuropathy was the single initial symptom and the only neurologic finding noted for a period of months. In these patients, diagnosis of Krabbe's disease was delayed and established only 9-11 months after the initial symptoms. In two other children with "classical picture" Krabbe disease, areflexia was noted on admission. The occurrence of peripheral neuropathy as an initial symptom in early infantile Krabbe disease may be underestimated. Krabbe disease should be considered in the differential diagnosis of early infantile peripheral neuropathy. Early diagnosis of affected children might be important for genetic counseling for families at risk.
2003
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/s0887-8994(02)00489-7" target="_blank" rel="noreferrer">10.1016/s0887-8994(02)00489-7</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2003
Backlog
Biopsy
Demyelinating Diseases/pathology/physiopathology
Diagnosis
Differential
Dor-Wollman T
Family Health
Female
Globoid Cell/pathology/physiopathology
Humans
Hurvitz H
Inclusion Bodies/pathology
Infant
Journal Article
Korn-Lubetzki I
Leukodystrophy
Male
Nevo Y
Pediatric Neurology
Peripheral Nervous System/pathology/physiopathology
Raas-Rothschild A
Retrospective Studies
Schwann Cells/pathology
Soffer D
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1080/09638280412331280280" target="_blank" rel="noreferrer">http://doi.org/10.1080/09638280412331280280</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Facilitating communication in children with multiple disabilities: three case studies of girls with Rett syndrome
Publisher
An entity responsible for making the resource available
Disability And Rehabilitation
Date
A point or period of time associated with an event in the lifecycle of the resource
2004
Subject
The topic of the resource
PedPal Lit; Abnormalities; however; Diagnosis; rehabilitation Risk Factors Sampling Studies Severity of Illness Index Sickness Impact Profile Treatment Outcome; increased communication opportunities provided by caregivers did not elicit increased responses from the girls. CONCLUSION: There is a difference in cueing by teachers in their interactions with children with multiple disabilities. Also; means findings should be viewed cautiously and that more research is indicated.; more frequent communicative interactions did not necessarily lead to increased student responses. It is suggest ed that amount and type of cueing may need to be considered to be effective in generating student responses. The small number of participants; Multiple/diagnosis/rehabilitation Child Behavior/physiology Child; Non-U.S. Gov't Rett Syndrome; Preschool Communication Disorders/diagnosis/rehabilitation Female Follow-Up Studies Humans Infant Interpersonal Relations Language Development Disorders/diagnosis/rehabilitation Research Support
Creator
An entity primarily responsible for making the resource
Ryan D; McGregor F; Akermanis M; Southwell K; Ramke M; Woodyatt G
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1080/09638280412331280280" target="_blank" rel="noreferrer">10.1080/09638280412331280280</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
Description
An account of the resource
2004
2004
Abnormalities
Akermanis M
Backlog
Diagnosis
Disability And Rehabilitation
however
increased communication opportunities provided by caregivers did not elicit increased responses from the girls. CONCLUSION: There is a difference in cueing by teachers in their interactions with children with multiple disabilities. Also
Journal Article
McGregor F
means findings should be viewed cautiously and that more research is indicated.
more frequent communicative interactions did not necessarily lead to increased student responses. It is suggest ed that amount and type of cueing may need to be considered to be effective in generating student responses. The small number of participants
Multiple/diagnosis/rehabilitation Child Behavior/physiology Child
Non-U.S. Gov't Rett Syndrome
PedPal Lit
Preschool Communication Disorders/diagnosis/rehabilitation Female Follow-Up Studies Humans Infant Interpersonal Relations Language Development Disorders/diagnosis/rehabilitation Research Support
Ramke M
rehabilitation Risk Factors Sampling Studies Severity of Illness Index Sickness Impact Profile Treatment Outcome
Ryan D
Southwell K
Woodyatt G
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1097/00002508-200207000-00008" target="_blank" rel="noreferrer">http://doi.org/10.1097/00002508-200207000-00008</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Peripheral blood mononuclear cell beta-endorphin concentration is decreased in chronic fatigue syndrome and fibromyalgia but not in depression: preliminary report
Publisher
An entity responsible for making the resource available
The Clinical Journal Of Pain
Date
A point or period of time associated with an event in the lifecycle of the resource
2002
Subject
The topic of the resource
Female; Humans; Male; Adult; Sensitivity and Specificity; Reproducibility of Results; Biomarkers of Pain; Diagnosis; Differential; Leukocytes; Mononuclear/immunology/metabolism; Fatigue Syndrome; beta-Endorphin/blood/immunology/metabolism; Chronic/blood/diagnosis/immunology; Depression/blood/diagnosis; Fibromyalgia/blood/diagnosis/immunology
Creator
An entity primarily responsible for making the resource
Panerai AE; Vecchiet J; Panzeri P; Meroni P; Scarone S; Pizzigallo E; Giamberardino MA; Sacerdote P
Description
An account of the resource
OBJECTIVE: The aim of this study was to examine the possible role of the immune system in the pathophysiology of chronic fatigue syndrome and fibromyalgia syndrome and in the differential diagnosis of depression by investigating changes in peripheral blood mononuclear cell levels of beta-endorphin, an endogenous opioid known to be involved in regulation of the immune system function. DESIGN: Beta-endorphin concentrations were measured by radioimmunoassay in peripheral blood mononuclear cells from healthy controls (n = 8) and patients with chronic fatigue syndrome (n = 17), fibromyalgia syndrome (n = 5), or depression (n = 10). RESULTS: Beta-endorphin concentrations were significantly lower in patients with chronic fatigue syndrome or fibromyalgia syndrome than in normal subjects and depressed patients (p <0.001 and p <0.01, respectively). They were significantly higher in depressed patients than in controls (p <0.01). CONCLUSIONS: Evaluation of peripheral blood mononuclear cell beta-endorphin concentrations could represent a diagnostic tool for chronic fatigue syndrome and fibromyalgia and help with differential diagnosis of these syndromes versus depression. The results obtained are also consistent with the hypothesis that the immune system is activated in both chronic fatigue syndrome and fibromyalgia syndrome.
2002
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1097/00002508-200207000-00008" target="_blank" rel="noreferrer">10.1097/00002508-200207000-00008</a>
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Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2002
Adult
Backlog
beta-Endorphin/blood/immunology/metabolism
Biomarkers of Pain
Chronic/blood/diagnosis/immunology
Depression/blood/diagnosis
Diagnosis
Differential
Fatigue Syndrome
Female
Fibromyalgia/blood/diagnosis/immunology
Giamberardino MA
Humans
Journal Article
Leukocytes
Male
Meroni P
Mononuclear/immunology/metabolism
Panerai AE
Panzeri P
Pizzigallo E
Reproducibility of Results
Sacerdote P
Scarone S
Sensitivity and Specificity
The Clinical Journal Of Pain
Vecchiet J
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1111/j.0736-8046.2004.21214.x" target="_blank" rel="noreferrer">http://doi.org/10.1111/j.0736-8046.2004.21214.x</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Infantile systemic hyalinosis or juvenile hyaline fibromatosis?
Publisher
An entity responsible for making the resource available
Pediatric Dermatology
Date
A point or period of time associated with an event in the lifecycle of the resource
2004
Subject
The topic of the resource
Child; Humans; Male; Preschool; Diagnosis; Differential; Hyalin; Fibroma/pathology; Skin Neoplasms/pathology
Creator
An entity primarily responsible for making the resource
Urbina F; Sazunic I; Murray G
Description
An account of the resource
Infantile systemic hyalinosis and juvenile hyaline fibromatosis are presumably autosomal recessive inherited diseases of unknown origin in which accumulation of an amorphous, hyaline material occurs in the skin and other organs. Both disorders may show clinical overlapping, suggesting that they might represent different variants of the same disease spectrum. We describe a 6-year-old boy with such overlap. Salient features included papular skin lesions on his face and neck, gingival hyperplasia, perianal nodules, large subcutaneous tumors on the scalp, hyperpigmented plaques over the metacarpophalangeal joints and malleoli, limited joint movement, diffuse osteopenia, short stature, and persistent diarrhea. Histopathologic and ultrastructural studies confirmed the presence of hyalin material in the dermis. The term systemic hyalinosis involves both conditions and should be preferred until a clear distinction can be made between them.
2004
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1111/j.0736-8046.2004.21214.x" target="_blank" rel="noreferrer">10.1111/j.0736-8046.2004.21214.x</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2004
Backlog
Child
Diagnosis
Differential
Fibroma/pathology
Humans
Hyalin
Journal Article
Male
Murray G
Pediatric Dermatology
Preschool
Sazunic I
Skin Neoplasms/pathology
Urbina F
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1111/j.1469-8749.2002.tb00776.x" target="_blank" rel="noreferrer">http://doi.org/10.1111/j.1469-8749.2002.tb00776.x</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Infantile neuroaxonal dystrophy (Seitelberger's disease)
Publisher
An entity responsible for making the resource available
Developmental Medicine And Child Neurology
Date
A point or period of time associated with an event in the lifecycle of the resource
2002
Subject
The topic of the resource
Humans; Magnetic Resonance Imaging; Diagnosis; Differential; Electroencephalography; Auditory; Brain Stem/physiology; Brain/pathology/physiopathology; Evoked Potentials; Disease Specific; Neuroaxonal Dystrophies/complications/diagnosis; Pantothenate Kinase-Associated Neurodegeneration/diagnosis; Seizures/diagnosis/etiology; Visual/physiology
Creator
An entity primarily responsible for making the resource
Gordon N
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1111/j.1469-8749.2002.tb00776.x" target="_blank" rel="noreferrer">10.1111/j.1469-8749.2002.tb00776.x</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
Description
An account of the resource
2002
2002
Auditory
Backlog
Brain Stem/physiology
Brain/pathology/physiopathology
Developmental Medicine and Child Neurology
Diagnosis
Differential
Disease Specific
Electroencephalography
Evoked Potentials
Gordon N
Humans
Journal Article
Magnetic Resonance Imaging
Neuroaxonal Dystrophies/complications/diagnosis
Pantothenate Kinase-Associated Neurodegeneration/diagnosis
Seizures/diagnosis/etiology
Visual/physiology
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1185/030079902125001164" target="_blank" rel="noreferrer">http://doi.org/10.1185/030079902125001164</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
New guidelines for the management of migraine in primary care
Publisher
An entity responsible for making the resource available
Current Medical Research And Opinion
Date
A point or period of time associated with an event in the lifecycle of the resource
2002
Subject
The topic of the resource
Humans; Questionnaires; Medical History Taking; Primary Health Care; Non-U.S. Gov't; Research Support; patient care team; referral and consultation; algorithms; Diagnosis; Differential; Patient Education; Migraine Disorders/diagnosis/prevention & control/therapy
Creator
An entity primarily responsible for making the resource
Dowson AJ; Lipscombe S; Sender J; Rees T; Watson D; Migraine In Primary Care Advisors (MIPCA) - Migraine Guidelines Development Group
Description
An account of the resource
Despite repeated initiatives over the past decade, migraine remains under-recognised, under-diagnosed and under-treated in everyday clinical practice. The Migraine in Primary Care Advisors (MIPCA) group has produced new guidelines for migraine management to attempt to rectify this situation. MIPCA is a group of physicians, nurses, pharmacists and other healthcare professionals dedicated to the improvement of headache management in primary care, who have also worked closely with the Migraine Action Association (the UK patients' group) in the development of these guidelines. The principles of the new MIPCA guidelines are: To arrange specific consultations for headache. To institute a system of detailed history taking, patient education and buy-in at the outset of the consultation. To utilise a new screening algorithm for the differential diagnosis of headache, which can be confirmed by further questioning, if necessary. To institute a process of management that is individualised for each patient, using a new algorithm. Assessing the impact on the patient's daily life is a key aspect of diagnosis and management. To prescribe only treatments that have objective evidence of favourable efficacy and tolerability. To utilise prospective follow-up procedures to monitor the success of treatment. To organise a team approach to headache management in primary care.
2002
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1185/030079902125001164" target="_blank" rel="noreferrer">10.1185/030079902125001164</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2002
algorithms
Backlog
Current Medical Research And Opinion
Diagnosis
Differential
Dowson AJ
Humans
Journal Article
Lipscombe S
Medical History Taking
Migraine Disorders/diagnosis/prevention & control/therapy
Migraine In Primary Care Advisors (MIPCA) - Migraine Guidelines Development Group
Non-U.S. Gov't
Patient Care Team
Patient Education
Primary Health Care
Questionnaires
Rees T
Referral And Consultation
Research Support
Sender J
Watson D
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1542/peds.111.1.e89" target="_blank" rel="noreferrer">http://doi.org/10.1542/peds.111.1.e89</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Classification and definition of disorders causing hypertonia in childhood
Publisher
An entity responsible for making the resource available
Pediatrics
Date
A point or period of time associated with an event in the lifecycle of the resource
2003
Subject
The topic of the resource
Child; Humans; Severity of Illness Index; Reproducibility of Results; Preschool; infant; Diagnosis; Differential; Dystonia/complications/diagnosis; Muscle Hypertonia/classification/etiology/physiopathology; Muscle Rigidity/complications/diagnosis; Muscle Spasticity/complications/diagnosis
Creator
An entity primarily responsible for making the resource
Sanger TD; Delgado MR; Gaebler-Spira D; Hallett M; Mink JW; Task Force on Childhood Motor Disorders
Description
An account of the resource
OBJECTIVE: This report describes the consensus outcome of an interdisciplinary workshop that was held at the National Institutes of Health in April 2001. The purpose of the workshop and this article are to define the terms "spasticity," "dystonia," and "rigidity" as they are used to describe clinical features of hypertonia in children. The definitions presented here are designed to allow differentiation of clinical features even when more than 1 is present simultaneously. METHODS: A consensus agreement was obtained on the best current definitions and their application in clinical situations. RESULTS: "Spasticity" is defined as hypertonia in which 1 or both of the following signs are present: 1) resistance to externally imposed movement increases with increasing speed of stretch and varies with the direction of joint movement, and/or 2) resistance to externally imposed movement rises rapidly above a threshold speed or joint angle. "Dystonia" is defined as a movement disorder in which involuntary sustained or intermittent muscle contractions cause twisting and repetitive movements, abnormal postures, or both. "Rigidity" is defined as hypertonia in which all of the following are true: 1) the resistance to externally imposed joint movement is present at very low speeds of movement, does not depend on imposed speed, and does not exhibit a speed or angle threshold; 2) simultaneous co-contraction of agonists and antagonists may occur, and this is reflected in an immediate resistance to a reversal of the direction of movement about a joint; 3) the limb does not tend to return toward a particular fixed posture or extreme joint angle; and 4) voluntary activity in distant muscle groups does not lead to involuntary movements about the rigid joints, although rigidity may worsen. CONCLUSION: We have provided a set of definitions for the purpose of identifying different components of childhood hypertonia. We encourage the development of clinical rating scales that are based on these definitions, and we encourage research to relate the degree of hypertonia to the degree of functional ability, change over time, and societal participation in children with motor disorders.
2003
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1542/peds.111.1.e89" target="_blank" rel="noreferrer">10.1542/peds.111.1.e89</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2003
Backlog
Child
Delgado MR
Diagnosis
Differential
Dystonia/complications/diagnosis
Gaebler-Spira D
Hallett M
Humans
Infant
Journal Article
Mink JW
Muscle Hypertonia/classification/etiology/physiopathology
Muscle Rigidity/complications/diagnosis
Muscle Spasticity/complications/diagnosis
Pediatrics
Preschool
Reproducibility of Results
Sanger TD
Severity Of Illness Index
Task Force on Childhood Motor Disorders
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1002/ana.410120313" target="_blank" rel="noreferrer">http://doi.org/10.1002/ana.410120313</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Cataplexy in variant forms of Niemann-Pick disease
Publisher
An entity responsible for making the resource available
Annals Of Neurology
Date
A point or period of time associated with an event in the lifecycle of the resource
1982
Subject
The topic of the resource
Child; Female; Humans; Male; Adult; Preschool; Diagnosis; Differential; Cataplexy/complications/diagnosis; Electroencephalography; Epilepsy/diagnosis; Niemann-Pick Diseases/complications/diagnosis; Ophthalmoplegia/complications; REM; Sleep; Splenomegaly/complications
Creator
An entity primarily responsible for making the resource
Kandt RS; Emerson RG; Singer HS; Valle DL; Moser HW
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1002/ana.410120313" target="_blank" rel="noreferrer">10.1002/ana.410120313</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
Description
An account of the resource
1982
1982
Adult
Annals Of Neurology
Backlog
Cataplexy/complications/diagnosis
Child
Diagnosis
Differential
Electroencephalography
Emerson RG
Epilepsy/diagnosis
Female
Humans
Journal Article
Kandt RS
Male
Moser HW
Niemann-Pick Diseases/complications/diagnosis
Ophthalmoplegia/complications
Preschool
REM
Singer HS
Sleep
Splenomegaly/complications
Valle DL
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1016/s0022-3476(65)80303-1" target="_blank" rel="noreferrer">http://doi.org/10.1016/s0022-3476(65)80303-1</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Observations on Huntington's Chorea in Childhood
Publisher
An entity responsible for making the resource available
The Journal Of Pediatrics
Date
A point or period of time associated with an event in the lifecycle of the resource
1965
Subject
The topic of the resource
Child; Prognosis; Mental Disorders; Movement Disorders; Medical; Q3 Literature Search; Diagnosis; Radiography; Pathology; CHOREA; CHOREA; Genetics; Genetics; HEREDITARY; Human; VENTRICULOGRAPHY
Creator
An entity primarily responsible for making the resource
MARKHAM CH; JWKNOX
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/s0022-3476(65)80303-1" target="_blank" rel="noreferrer">10.1016/s0022-3476(65)80303-1</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
Description
An account of the resource
1965
1965
Backlog
Child
CHOREA
Diagnosis
Genetics
HEREDITARY
Human
Journal Article
JWKNOX
MARKHAM CH
Medical
Mental Disorders
Movement Disorders
Pathology
Prognosis
Q3 Scoping Review Results
Radiography
The Journal Of Pediatrics
VENTRICULOGRAPHY
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1056/nejm198012113032403" target="_blank" rel="noreferrer">http://doi.org/10.1056/nejm198012113032403</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndrome
Publisher
An entity responsible for making the resource available
The New England Journal Of Medicine
Date
A point or period of time associated with an event in the lifecycle of the resource
1980
Subject
The topic of the resource
Child; Humans; Male; Preschool; Q3 Literature Search; Diagnosis; Differential; Lipid Metabolism; Inborn Errors/diagnosis; Liver/metabolism; Carnitine/deficiency/metabolism/therapeutic use; Muscles/metabolism; Reye Syndrome/diagnosis
Creator
An entity primarily responsible for making the resource
Chapoy PR; Angelini C; Brown WJ; Stiff JE; Shug AL; Cederbaum SD
Description
An account of the resource
A 3 1/2-year-old boy presented at three months of age with an acute episode of lethargy, somnolence, hypoglycemia, hepatomegaly, and cardiomegaly, which responded poorly to restoration of the blood sugar level to normal. The absence of ketonuria during subsequent episodes of severe hypoglycemia prompted a search for a defect in fatty acid oxidation. Plasma carnitine (2.0 to 5.0 mumol per liter), muscle carnitine (0.01 to 0.02 mumol per gram, wet weight) and liver carnitine (0.021 to 0.065 mumol per gram, wet weight) were all less than 5 per cent of the normal mean. During a 36-hour fast, ketones were barely detectable. Prolonged treatment with oral carnitine over a six-month period resulted in increased muscle strength, a dramatic reduction in cardiac size, relief of cardiomyopathy, partial repletion of carnitine levels in plasma and muscle, and complete repletion in the liver. Systemic carnitine deficiency is an easily treatable cause of recurrent Reye's-like syndrome. Its diagnosis requires measurement of carnitine levels.
1980
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1056/nejm198012113032403" target="_blank" rel="noreferrer">10.1056/nejm198012113032403</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
1980
Angelini C
Backlog
Brown WJ
Carnitine/deficiency/metabolism/therapeutic use
Cederbaum SD
Chapoy PR
Child
Diagnosis
Differential
Humans
Inborn Errors/diagnosis
Journal Article
Lipid Metabolism
Liver/metabolism
Male
Muscles/metabolism
Preschool
Q3 Scoping Review Results
Reye Syndrome/diagnosis
Shug AL
Stiff JE
The New England Journal Of Medicine
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1002/(sici)1099-0496(199903)27:3%3C213::aid-ppul11%3E3.0.co" target="_blank" rel="noreferrer">http://doi.org/10.1002/(sici)1099-0496(199903)27:3%3C213::aid-ppul11%3E3.0.co</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Myopathy with mitochondrial changes presenting as respiratory failure in two brothers
Publisher
An entity responsible for making the resource available
Pediatric Pulmonology
Date
A point or period of time associated with an event in the lifecycle of the resource
1999
Subject
The topic of the resource
Child; Humans; Male; Biopsy; Fatal Outcome; Q3 Literature Search; Diagnosis; Differential; Interstitial/diagnosis/pathology; Lung Diseases; Mitochondrial Myopathies/diagnosis/genetics/pathology; Needle; Nuclear Family; Respiratory Function Tests; Respiratory Insufficiency/etiology
Creator
An entity primarily responsible for making the resource
Lemos AB; Mosquera J; Mate A; Sirvent J
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1002/(sici)1099-0496(199903)27:3%3C213::aid-ppul11%3E3.0.co" target="_blank" rel="noreferrer">10.1002/(sici)1099-0496(199903)27:3%3C213::aid-ppul11%3E3.0.co</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
1999
Backlog
Biopsy
Child
Diagnosis
Differential
Fatal Outcome
Humans
Interstitial/diagnosis/pathology
Journal Article
Lemos AB
Lung Diseases
Male
Mate A
Mitochondrial Myopathies/diagnosis/genetics/pathology
Mosquera J
Needle
Nuclear Family
Pediatric Pulmonology
Q3 Scoping Review Results
Respiratory Function Tests
Respiratory Insufficiency/etiology
Sirvent J
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1002/1531-8257(200011)15:6%3C1199::aid-mds1020%3E3.0.co" target="_blank" rel="noreferrer">http://doi.org/10.1002/1531-8257(200011)15:6%3C1199::aid-mds1020%3E3.0.co</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Niemann-Pick disease type C: Two cases and an update.
Publisher
An entity responsible for making the resource available
Movement Disorders: Official Journal Of The Movement Disorder Society
Date
A point or period of time associated with an event in the lifecycle of the resource
2000
Subject
The topic of the resource
Female; Humans; Male; Middle Aged; Disease Progression; Longitudinal Studies; adolescent; Age of Onset; Cholesterol/metabolism; Esterification; Diagnosis; Differential; Cells; Cultured; Fibroblasts/metabolism; Niemann-Pick Diseases/diagnosis/physiopathology; Skin/pathology
Creator
An entity primarily responsible for making the resource
Uc EY; Wenger DA; Jankovic J
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1002/1531-8257(200011)15:6%3C1199::aid-mds1020%3E3.0.co" target="_blank" rel="noreferrer">10.1002/1531-8257(200011)15:6%3C1199::aid-mds1020%3E3.0.co</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
Description
An account of the resource
We describe two patients with juvenile-onset Niemann-Pick disease type C (NPC) to illustrate the variable neurologic features of this condition. One presented with hypersplenism at age 10 and was misdiagnosed with Gaucher disease. He developed complex partial seizures in his teens but remained otherwise neurologically asymptomatic until his mid 30s. At age 45, he had mild dementia and dysarthria, vertical supranuclear ophthalmoplegia, axonal sensorimotor polyneuropathy, and cerebellar ataxia. The second patient presented with rapidly progressive dystonia at age 8, and mild hepatosplenomegaly, vertical supranuclear ophthalmoplegia, severe behavioral disorder, and dementia by age 14. The diagnosis of NPC was based on deficient cholesterol esterification and excessive lysosomal filipin staining in cultured skin fibroblasts. Current notions about diagnosis and pathogenesis of NPC are reviewed.
2000
Adolescent
Age of Onset
Backlog
Cells
Cholesterol/metabolism
Cultured
Diagnosis
Differential
Disease Progression
Esterification
Female
Fibroblasts/metabolism
Humans
Jankovic J
Journal Article
Longitudinal Studies
Male
Middle Aged
Movement Disorders: Official Journal Of The Movement Disorder Society
Niemann-Pick Diseases/diagnosis/physiopathology
Skin/pathology
Uc EY
Wenger DA
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1016/0387-7604(94)90077-9" target="_blank" rel="noreferrer">http://doi.org/10.1016/0387-7604(94)90077-9</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Acute onset of X-linked adrenoleukodystrophy mimicking encephalitis
Publisher
An entity responsible for making the resource available
Brain & Development
Date
A point or period of time associated with an event in the lifecycle of the resource
1994
Subject
The topic of the resource
Humans; Male; Acute Disease; infant; Q3 Literature Search; Tomography; Diagnosis; Differential; X-Ray Computed; Adrenoleukodystrophy/diagnosis/drug therapy/genetics; Encephalitis/diagnosis; Erucic Acids/therapeutic use; Fatty Acids/blood; Linkage (Genetics); X Chromosome
Creator
An entity primarily responsible for making the resource
Zammarchi E; Donati MA; Tucci F; Fonda C; Fanelli F; Pazzaglia R
Description
An account of the resource
We report the case of a 6-year-old boy with X-linked adrenoleukodystrophy (ALD). In view of the acute onset of vomiting, fever, and coma, encephalitis was initially suspected. However, brain magnetic resonance imaging demonstrated a pattern of demyelination that was consistent with ALD; this diagnosis was confirmed by the finding of elevated plasma very long-chain fatty acids levels. At presentation, the patient was hyponatremic. That this metabolic disturbance and the coma resolved within hours of the initiation of corticosteroid therapy suggests that the presenting symptoms were secondary to adrenal cortical insufficiency. Primary adrenal failure was confirmed by endocrinologic evaluation. Thrombocytopenia, hepatic transaminase abnormalities, anemia and leukopenia developed during the subsequent course of therapy with oleic acid and erucic acid.
1994
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/0387-7604(94)90077-9" target="_blank" rel="noreferrer">10.1016/0387-7604(94)90077-9</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
1994
Acute Disease
Adrenoleukodystrophy/diagnosis/drug therapy/genetics
Backlog
Brain & Development
Diagnosis
Differential
Donati MA
Encephalitis/diagnosis
Erucic Acids/therapeutic use
Fanelli F
Fatty Acids/blood
Fonda C
Humans
Infant
Journal Article
Linkage (Genetics)
Male
Pazzaglia R
Q3 Scoping Review Results
Tomography
Tucci F
X Chromosome
X-Ray Computed
Zammarchi E
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1016/s0887-8994(00)00232-0" target="_blank" rel="noreferrer">http://doi.org/10.1016/s0887-8994(00)00232-0</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Update on genetic disorders affecting white matter
Publisher
An entity responsible for making the resource available
Pediatric Neurology
Date
A point or period of time associated with an event in the lifecycle of the resource
2001
Subject
The topic of the resource
Child; Humans; Magnetic Resonance Imaging; Brain/pathology; Diagnosis; Differential; Brain Diseases/diagnosis/genetics/metabolism/pathology; Hereditary Central Nervous System Demyelinating Diseases/diagnosis/genetics/pathology
Creator
An entity primarily responsible for making the resource
Kaye EM
Description
An account of the resource
The classification of diseases affecting white matter has changed dramatically with the use of magnetic resonance imaging. Classical leukodystrophies, such as metachromatic leukodystrophy and Krabbe's disease, account for only a small number of inherited diseases that affect white matter. Magnetic resonance imaging has clarified genetic disorders that result in white matter changes or leukoencephalopathies. The term leukoencephalopathy is used to reflect the broader number of diseases that may cause as either primary or secondary changes in myelin development. This review attempts to categorize white matter disorders into classes such as lipid, myelin protein, organic acids, and defects in energy metabolism, in addition to other causes.
2001
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/s0887-8994(00)00232-0" target="_blank" rel="noreferrer">10.1016/s0887-8994(00)00232-0</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2001
Backlog
Brain Diseases/diagnosis/genetics/metabolism/pathology
Brain/pathology
Child
Diagnosis
Differential
Hereditary Central Nervous System Demyelinating Diseases/diagnosis/genetics/pathology
Humans
Journal Article
Kaye EM
Magnetic Resonance Imaging
Pediatric Neurology
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1053/spen.2001.29477" target="_blank" rel="noreferrer">http://doi.org/10.1053/spen.2001.29477</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Sleep disorders in children with neurologic diseases
Publisher
An entity responsible for making the resource available
Seminars In Pediatric Neurology
Date
A point or period of time associated with an event in the lifecycle of the resource
2001
Subject
The topic of the resource
Child; Humans; Preschool; Q3 Literature Search; Nervous System Diseases/complications; Diagnosis; Differential; Anticonvulsants/therapeutic use; Sleep Disorders/etiology; Blindness/complications; Epilepsy/complications; Headache/complications; Melatonin/therapeutic use; Mental Retardation/complications; Muscular Dystrophies/complications
Creator
An entity primarily responsible for making the resource
Zucconi M; Bruni O
Description
An account of the resource
Pediatric neurologic diseases are often associated with different kinds of sleep disruption (mainly insomnia, less frequently hypersomnia or parasomnias). Due to the key-role of sleep for development, the effort to ameliorate sleep patterns in these children could have important prognostic benefits. Study of sleep architecture and organization in neurologic disorders could lead to a better comprehension of the pathogenesis and a better treatment of the disorders. This article focuses on the following specific neurologic diseases: nocturnal frontal lobe epilepsy and abnormal motor behaviors of epileptic origin, evaluating differential diagnosis with parasomnias; achondroplasia, confirming the crucial role of craniofacial deformity in determining sleep-disordered breathing; neuromuscular diseases, mainly Duchenne's muscular dystrophy and myotonic dystrophy; cerebral palsy, evaluating either the features of sleep architecture and the importance of the respiratory problems associated; headaches, confirming the strict relationships with sleep in terms of neurochemical and neurobehavioral substrates; and finally a review on the effectiveness of melatonin for sleep problems in children with neurologic syndromes and mental retardation, blindness, and epilepsy.
2001
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1053/spen.2001.29477" target="_blank" rel="noreferrer">10.1053/spen.2001.29477</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2001
Anticonvulsants/therapeutic use
Backlog
Blindness/complications
Bruni O
Child
Diagnosis
Differential
Epilepsy/complications
Headache/complications
Humans
Journal Article
Melatonin/therapeutic use
Mental Retardation/complications
Muscular Dystrophies/complications
Nervous System Diseases/complications
Preschool
Q3 Scoping Review Results
Seminars In Pediatric Neurology
Sleep Disorders/etiology
Zucconi M
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1212/wnl.55.4.468" target="_blank" rel="noreferrer">http://doi.org/10.1212/wnl.55.4.468</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society
Publisher
An entity responsible for making the resource available
Neurology
Date
A point or period of time associated with an event in the lifecycle of the resource
2000
Subject
The topic of the resource
Child; Humans; Risk Assessment; Predictive Value of Tests; Nervous System; Preschool; Non-U.S. Gov't; P.H.S.; Research Support; U.S. Gov't; infant; Diagnosis; Differential; Neuropsychological Tests; Disease Management; Developmental Disabilities/diagnosis; Electrophysiology; Asperger Syndrome/diagnosis; Autistic Disorder/diagnosis/genetics; Childhood/diagnosis; Lead Poisoning; Mass Screening/methods/standards
Creator
An entity primarily responsible for making the resource
Filipek PA; Accardo PJ; Ashwal S; Baranek GT; Cook EH; Dawson G; Gordon B; Gravel JS; Johnson CP; Kallen RJ; Levy SE; Minshew NJ; Ozonoff S; Prizant BM; Rapin I; Rogers SJ; Stone WL; Teplin SW; Tuchman RF; Volkmar FR
Description
An account of the resource
Autism is a common disorder of childhood, affecting 1 in 500 children. Yet, it often remains unrecognized and undiagnosed until or after late preschool age because appropriate tools for routine developmental screening and screening specifically for autism have not been available. Early identification of children with autism and intensive, early intervention during the toddler and preschool years improves outcome for most young children with autism. This practice parameter reviews the available empirical evidence and gives specific recommendations for the identification of children with autism. This approach requires a dual process: 1) routine developmental surveillance and screening specifically for autism to be performed on all children to first identify those at risk for any type of atypical development, and to identify those specifically at risk for autism; and 2) to diagnose and evaluate autism, to differentiate autism from other developmental disorders.
2000
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1212/wnl.55.4.468" target="_blank" rel="noreferrer">10.1212/wnl.55.4.468</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2000
Accardo PJ
Ashwal S
Asperger Syndrome/diagnosis
Autistic Disorder/diagnosis/genetics
Backlog
Baranek GT
Child
Childhood/diagnosis
Cook EH
Dawson G
Developmental Disabilities/diagnosis
Diagnosis
Differential
Disease Management
Electrophysiology
Filipek PA
Gordon B
Gravel JS
Humans
Infant
Johnson CP
Journal Article
Kallen RJ
Lead Poisoning
Levy SE
Mass Screening/methods/standards
Minshew NJ
Nervous System
Neurology
Neuropsychological Tests
Non-U.S. Gov't
Ozonoff S
P.H.S.
Predictive Value of Tests
Preschool
Prizant BM
Rapin I
Research Support
Risk Assessment
Rogers SJ
Stone WL
Teplin SW
Tuchman RF
U.S. Gov't
Volkmar FR
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=10590906" target="_blank" rel="noreferrer">http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=10590906</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Neuromuscular disorders of childhood
Publisher
An entity responsible for making the resource available
Current Opinion In Pediatrics
Date
A point or period of time associated with an event in the lifecycle of the resource
1999
Subject
The topic of the resource
Child; Diagnosis; Differential; Human; Neuromuscular Diseases/diagnosis/physiopathology/therapy; Charcot-Marie-Tooth Disease/diagnosis/physiopathology; Muscular Dystrophies/diagnosis/genetics; Myasthenia Gravis/diagnosis; Peripheral Nervous System Diseases/diagnosis; Spinal Muscular Atrophies of Childhood/diagnosis
Creator
An entity primarily responsible for making the resource
Andersson PB; Rando TA
Description
An account of the resource
Neuromuscular disorders are common causes of weakness and hypotonia in the infantile period and in childhood. Accurate diagnosis of specific neuromuscular disorders depends first on identification of which aspect of the peripheral neuromuscular system is affected--the motor neuron in the spinal cord, the nerve root or peripheral nerve, the neuromuscular junction, or the muscle--and then on the determination of the etiology and specific clinical entity. This review provides an overview of the major neuromuscular disorders of childhood with attention to recent advances and emerging areas of research.
1999
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
1999
Andersson PB
Backlog
Charcot-Marie-Tooth Disease/diagnosis/physiopathology
Child
Current Opinion In Pediatrics
Diagnosis
Differential
Human
Journal Article
Muscular Dystrophies/diagnosis/genetics
Myasthenia Gravis/diagnosis
Neuromuscular Diseases/diagnosis/physiopathology/therapy
Peripheral Nervous System Diseases/diagnosis
Rando TA
Spinal Muscular Atrophies of Childhood/diagnosis
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=10590907" target="_blank" rel="noreferrer">http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=10590907</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Cerebral palsy and neurodegenerative disease
Publisher
An entity responsible for making the resource available
Current Opinion In Pediatrics
Date
A point or period of time associated with an event in the lifecycle of the resource
1999
Subject
The topic of the resource
Child; Disease Progression; Diagnosis; Differential; Human; Cerebral Palsy/diagnosis; Mitochondrial Myopathies/diagnosis; Neurodegenerative Diseases/diagnosis
Creator
An entity primarily responsible for making the resource
Bass N
Description
An account of the resource
Cerebral palsy refers to a neurologic disorder of motor skills that is static in nature and is the result of injury to the brain before its development is complete. Many neurodegenerative or metabolic disorders have a slow rate of progression and can be misdiagnosed as cerebral palsy. Diseases that have been misdiagnosed as cerebral palsy are presented here to provide the clinician with framework for the complex evaluation of these patients.
1999
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
1999
Backlog
Bass N
Cerebral Palsy/diagnosis
Child
Current Opinion In Pediatrics
Diagnosis
Differential
Disease Progression
Human
Journal Article
Mitochondrial Myopathies/diagnosis
Neurodegenerative Diseases/diagnosis
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=11723390" target="_blank" rel="noreferrer">http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=11723390</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
An update on the leukodsytrophies
Publisher
An entity responsible for making the resource available
Current Opinion In Neurology
Date
A point or period of time associated with an event in the lifecycle of the resource
2001
Subject
The topic of the resource
Child; Adult; P.H.S.; U.S. Gov't; Brain Diseases; Diagnosis; Differential; Human; Metabolic; Support; Diseases/diagnosis/genetics; Glial Fibrillary Acidic Protein/genetics; Hereditary Central Nervous System Demyelinating; Inborn/diagnosis/genetics; Myelin Proteolipid Protein/genetics
Creator
An entity primarily responsible for making the resource
Schiffmann R; Boespflug-Tanguy O
Description
An account of the resource
This review centers on important recent advances in the understanding of the role of glial fibrillary acidic protein in Alexander disease and of proteolipid protein in hypomyelinating disorders such as Pelizaeus-Merzbacher and spastic paraplegia. We also describe seven novel leukodystrophies. These include childhood ataxia with central nervous system hypomyelination, a relatively common leukodystrophy syndrome with linkage to chromosome 3 in some patients, and megalencephalic leukoencephalopathy with subcortical cysts whose gene has recently been cloned. These, along with five other disorders, including leukodystrophy with polyol metabolism abnormality, demonstrate that an increasing number of protein and metabolic abnormalities can cause primary myelin disorders.
2001
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Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2001
Adult
Backlog
Boespflug-Tanguy O
Brain Diseases
Child
Current Opinion in Neurology
Diagnosis
Differential
Diseases/diagnosis/genetics
Glial Fibrillary Acidic Protein/genetics
Hereditary Central Nervous System Demyelinating
Human
Inborn/diagnosis/genetics
Journal Article
Metabolic
Myelin Proteolipid Protein/genetics
P.H.S.
Schiffmann R
Support
U.S. Gov't
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1176/appi.ajp.2011.11060886" target="_blank" rel="noreferrer">http://doi.org/10.1176/appi.ajp.2011.11060886</a>
<a href="http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000300121100017" target="_blank" rel="noreferrer">http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000300121100017</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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Attention Bias Modification Treatment for Pediatric Anxiety Disorders: A Randomized Controlled Trial
Publisher
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American Journal Of Psychiatry
Date
A point or period of time associated with an event in the lifecycle of the resource
2012
Subject
The topic of the resource
Depression; Management; Children; Diagnosis; Adolescents; Anxieties; Attentional bias; Care and treatment; PSYCHIATRY; THREAT; Anxiety in children; Child & adolescent psychiatry; childhood; Clinical outcomes; FACIAL EXPRESSIONS; INDIVIDUALS; Influence; MANIPULATION; VULNERABILITY
Creator
An entity primarily responsible for making the resource
Eldar S; Apter A; Lotan D; Perez-Edgar K; Naim R; Fox NA; Pine DS; Bar-Haim Y
Description
An account of the resource
Objective: While attention bias modification (ABM) is a promising novel treatment for anxiety disorders, clinical trial data remain restricted to adults. The authors examined whether ABM induces greater reductions in pediatric anxiety symptoms and symptom severity than multiple control training interventions. Method: From a target sample of 186 treatment-seeking children at a hospital-based child anxiety clinic, 40 patients with an ongoing anxiety disorder who met all inclusion criteria were enrolled in the study. Children were randomly assigned to one of three conditions: ABM designed to shift attention away from threat; placebo attention training using stimuli identical to those in the ABM condition; and placebo attention training using only neutral stimuli. All participants completed four weekly 480-trial sessions (1,920 total trials). Before and after the attention training sessions, children's clinical status was determined via semi-structured interviews and questionnaires. Reduction in the number of anxiety symptoms and their severity was compared across the three groups. Results: Change in the number of anxiety symptoms and their severity differed across the three conditions. This reflected significant reductions in the number of anxiety symptoms and symptom severity in the ABM condition but not in the placebo attention training or placebo-neutral condition. Conclusions: ABM, compared with two control conditions, reduces pediatric anxiety symptoms and severity. Further study of efficacy and underlying mechanisms is warranted. (Am J Psychiatry 2012; 169:213-220)
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1176/appi.ajp.2011.11060886" target="_blank" rel="noreferrer">10.1176/appi.ajp.2011.11060886</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2012
Adolescents
American Journal Of Psychiatry
Anxieties
Anxiety in children
Apter A
Attentional bias
Backlog
Bar-Haim Y
Care And Treatment
Child & adolescent psychiatry
childhood
Children
Clinical outcomes
Depression
Diagnosis
Eldar S
FACIAL EXPRESSIONS
Fox NA
INDIVIDUALS
Influence
Journal Article
Lotan D
Management
MANIPULATION
Naim R
Perez-Edgar K
Pine DS
Psychiatry
THREAT
VULNERABILITY
-
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
January 2018 List
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
January 2018 List
URL Address
<a href="http://doi.org/10.1016/j.ejpn.2017.04.1310" target="_blank" rel="noreferrer">http://doi.org/10.1016/j.ejpn.2017.04.1310</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Palliative care in children with spinal muscular atrophy type 1: How do they die? Results from a French multicentric study (National Hospital clinical Research Program)
Publisher
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European Journal Of Paediatric Neurology
Date
A point or period of time associated with an event in the lifecycle of the resource
2017
Subject
The topic of the resource
clinical research; palliative therapy; Werdnig Hoffmann disease; 50-48-6 (amitriptyline); 52-26-6 (morphine); 57-27-2 (morphine); 549-18-8 (amitriptyline); Amitriptyline; benzodiazepine derivative; Child; Clinical Article; clinical practice; Diagnosis; Drug Therapy; Female; follow up; Human; infant; Intensive care unit; Interview; Male; Morphine; multicenter study; nasogastric tube; Noninvasive Ventilation; psychologist; quantitative analysis; Resuscitation; time of death
Creator
An entity primarily responsible for making the resource
Hully M; Barnerias C; Vanesse S; Viallard ML; Desguerre I
Description
An account of the resource
Objective: The national Hospital Clinical Research Program (PHRC) called Assessment of clinical practices of palliative care in children with Spinal Muscular Atrophy Type 1 (SMA 1) was conducted to depict palliative practices in that fatal disease, in which death up to now occurs few weeks or months after the diagnosis. We here report data about the conditions of death for the patients included. Methods: In this French multicentric study, patients were included from june 2012 to june 2016. Parents and physicians filled in a specific health book during the follow up, the physician in charge filled in a survey concerning the patient's management over the last 48 hours before death, then a semidirected interview of the parents was conducted by a trained psychologist 6 to 18 months after the child's death. We here report the quantitative analysis of data obtained from the survey about patient's management around death. Results: 38 patients were included in the study (17 centres), data were available for 36 dead patients. Median age at inclusion was 3 months (0,6-10,4), death occurred at a median 5,5 month of age (1,5-16,4), i.e a median follow-up of 2 months (0,2-12,8). 39% of patients died at home, 6% in an intensive care unit. At the time of death, patients received morphine (56%), benzodiazepines (39%), amitriptyline (39%). Treatments were given through a nasogastric tube (83%), and oxygenotherapy was delivered (76%). 6% patients received noninvasive ventilation at the time of death. No resuscitation recommendations had been prepared for most patients (97%), written in 85%, after a multidisciplinary meeting in most cases (79%). Conclusion: Our data confirm current knowledge about natural outcome in SMA 1, death occurring very soon after the diagnosis, claiming for an effective palliative management of the patients, including the involvement of parents in medical care at home.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/j.ejpn.2017.04.1310" target="_blank" rel="noreferrer">10.1016/j.ejpn.2017.04.1310</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2017
50-48-6 (amitriptyline)
52-26-6 (morphine)
549-18-8 (amitriptyline)
57-27-2 (morphine)
Amitriptyline
Barnerias C
benzodiazepine derivative
Child
Clinical Article
Clinical Practice
Clinical Research
Desguerre I
Diagnosis
Drug Therapy
European Journal of Paediatric Neurology
Female
Follow Up
Hully M
Human
Infant
Intensive Care Unit
Interview
January 2018 List
Male
Morphine
Multicenter Study
nasogastric tube
Noninvasive Ventilation
Palliative Therapy
Psychologist
quantitative analysis
Resuscitation
time of death
Vanesse S
Viallard ML
Werdnig Hoffmann disease