Browse Items (99 total)
- Tags: Q3 Scoping Review Results
The natural history of degenerative ataxia: a retrospective study in 466 patients
Tags: 1998, Abele M, Adolescent, Adult, Age of Onset, Aged, Backlog, Boesch S, Brain, Brice A, Burk K, Cerebellar Ataxia/genetics/mortality/physiopathology, Child, Dichgans J, Disease Progression, Female, Friedreich Ataxia/genetics/mortality/physiopathology, Gait, Humans, Inzelberg R, Journal Article, Klockgether T, Kramer B, Laccone F, Lopes-Cendes I, Ludtke R, Male, Middle Aged, Multiple System Atrophy/genetics/mortality/physiopathology, Preschool, Prognosis, Q3 Scoping Review Results, Retrospective Studies, Riess O, Risk Factors, Schols L, Sex Characteristics, Spinocerebellar Degenerations/genetics/mortality/physiopathology, Survival Analysis, Time Factors, Trinucleotide Repeats, Wheelchairs, Zilber N
Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes (MELAS): clinical, radiological, pathological, and genetic observations
Tags: 1993, Annals Of Neurology, Backlog, Base Sequence, Becker LE, Capillaries/pathology, Child, Chuang S, DNA/analysis, Electron, Female, Ho VB, Humans, Infant, Journal Article, Koo B, MacGregor D, Male, McGreal DA, MELAS Syndrome/genetics/pathology/radiography, Merante F, Microscopy, Mitochondria/pathology, Molecular Sequence Data, Muscles/pathology, Preschool, Q3 Scoping Review Results, Robinson BH, Tein I, Tomography, Wherrett JR, X-Ray Computed
Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiency
Tags: 2005, Age of Onset, Aged, Atrophy/enzymology/genetics/physiopathology, Backlog, Bodamer OA, Brain Diseases, Carnitine/therapeutic use, Cerebral Cortex/enzymology/pathology/physiopathology, Cognition Disorders/enzymology/genetics/physiopathology, Disease Progression, DNA Mutational Analysis, Food, Formulated, Glutaryl-CoA Dehydrogenase/deficiency, Gruber S, Harting I, Hoffmann GF, Humans, Inborn/enzymology/genetics/physiopathology, Journal Article, Kolker S, Kulkens S, Lateral Ventricles/pathology, Magnetic Resonance Imaging, Male, Metabolic, Movement Disorders/enzymology/genetics/physiopathology, Mutation/genetics, Myelinated/pathology, Nerve Fibers, Neurology, Q3 Scoping Review Results, Sauer S, Treatment Outcome, Zschocke J
Long-term follow-up, neurological outcome and survival rate in 28 Nordic patients with glutaric aciduria type 1
Tags: 2004, Adolescent, Adult, Amino Acid Metabolism, Backlog, Child, Christensen E, European Journal of Paediatric Neurology, Female, Finland/epidemiology, Follow-up Studies, Glutarates/urine, Glutaryl-CoA Dehydrogenase, Hagberg G, Holme E, Humans, Inborn Errors/complications/diagnosis/mortality, Infant, Journal Article, Kyllerman M, Lonnquist T, Male, Nervous System Diseases/etiology, Newborn, Oxidoreductases Acting on CH-CH Group Donors/deficiency, Preschool, Prognosis, Q3 Scoping Review Results, Rotwelt T, Scandinavia/epidemiology, Skjeldal O, Skov L, Survival Rate, Time Factors, von Dobeln U
Myopathy with mitochondrial changes presenting as respiratory failure in two brothers
Tags: 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
Progressive cerebral vascular degeneration with mitochondrial encephalopathy
Tags: 2008, Acyl-CoA Dehydrogenase/deficiency/genetics, American Journal Of Medical Genetics.Part A, Backlog, Brain/blood supply/physiopathology, Cerebrovascular Circulation, Child, Cowan TM, Enns GM, Ernst SL, Female, Gallagher RC, Hedlund GL, Humans, Journal Article, Leu/genetics, Longo N, Magnetic Resonance Angiography, MELAS Syndrome/ge [Genetics], Pasquali M, Pique LM, Point Mutation, Q3 Scoping Review Results, RNA, Schrijver I, Steinberg GK, Transfer, Vogel H
Disorders of movement in Leigh syndrome
Tags: 1993, Backlog, Basal Ganglia Diseases/complications/enzymology/physiopathology, Basal Ganglia/enzymology/physiopathology, Brain/enzymology/physiopathology/radiography, Burke RE, Child, De Vivo DC, Dystonia/complications/diagnosis/physiopathology, Electron Transport Complex IV/metabolism, Enzyme Repression, Female, Humans, Journal Article, Leigh Disease/complications/diagnosis/physiopathology, Macaya A, Magnetic Resonance Imaging, Male, Mental Disorders/etiology, Mitochondrial Encephalomyopathies/complications/enzymology, Movement Disorders/complications/diagnosis/physiopathology, Munell F, Neuropediatrics, Preschool, Q3 Scoping Review Results, Retrospective Studies
The natural history of juvenile or subacute GM2 gangliosidosis: 21 new cases and literature review of 134 previously reported.
Tags: 2006, Acute Disease, Adolescent, Adult, Backlog, Banwell B, Blaser S, Child, Clarke JT, Female, Gangliosidoses, Giugliani R, GM2/diagnosis, Humans, Infant, Journal Article, Kok F, Longitudinal Studies, Maegawa GH, Mahuran D, Male, Pediatrics, Preschool, Prospective Studies, Q3 Scoping Review Results, Retrospective Studies, Stockley T, Tropak M
Leigh's syndrome
Tags: 2004, Autopsy, Backlog, Basal Ganglia/pathology, Behari M, Biopsy, Disease Progression, Fatal Outcome, Female, Gupta V, Humans, Immunohistochemistry, Indian Journal Of Pediatrics, Infant, Journal Article, Leigh Disease/diagnosis/physiopathology/therapy, Magnetic Resonance Imaging, Mannan AA, Needle, Q3 Scoping Review Results, Ralte AM, Risk Assessment, Sarkar C, Severity Of Illness Index, Sharma MC, Shrivastava P
Sleep disorders in Sanfilippo syndrome: a polygraphic study
Tags: 2003, Adolescent, Adult, Backlog, Child, Clinical Eeg (electroencephalography), Della Marca G, Female, Humans, Iuvone L, Journal Article, Male, Mariotti P, Mazza S, Mennuni GF, Mucopolysaccharidosis III/complications, Polysomnography, Q3 Scoping Review Results, Ricci R, Sleep Disorders/etiology/physiopathology, Vernacotola S
Natural history of Type A Niemann-Pick disease: possible endpoints for therapeutic trials
Tags: 2006, Aron A, Backlog, Brodie SE, Child Development, Desnick RJ, Female, Humans, Infant, Infant Behavior, Journal Article, Language Development, Longevity, Male, McGovern MM, Motor Skills, Muscle Hypotonia/etiology/physiopathology, Neurodegenerative Diseases/complications/physiopathology/psychology, Neurology, Niemann-Pick Diseases/classification/complications/physiopathology/psychology, Q3 Scoping Review Results, Reflex, Respiratory Insufficiency/etiology/mortality, Stretch, Wasserstein MP
Sleep-disordered breathing and respiratory failure in acid maltase deficiency
Tags: 2001, Adolescent, Adult, Backlog, Child, Diaphragm/physiopathology, et al, Glycogen Storage Disease Type II/complications, Humans, Journal Article, Mellies U, Middle Aged, Neurology, Polysomnography, Predictive Value of Tests, Preschool, Q3 Scoping Review Results, Ragette R, REM, Respiratory Insufficiency/diagnosis/etiology/physiopathology, Schwake C, Sensitivity and Specificity, Sleep, Sleep Apnea Syndromes/diagnosis/etiology/physiopathology, Vital Capacity
Scoring evaluation of the natural course of mucopolysaccharidosis type IIIA (Sanfilippo syndrome type A)
Tags: 2007, Adolescent, Adult, Backlog, Braulke T, Child, Cohort Studies, Disease Progression, Female, Gal A, Humans, Infant, Journal Article, Kossow K, Longitudinal Studies, Male, Meyer A, Mucopolysaccharidosis III/classification/diagnosis/pathology, Muhlhausen C, Muschol N, Newborn, Pediatrics, Preschool, Q3 Scoping Review Results, Questionnaires, Research Design, Ullrich K
Neurological presentation in pediatric patients with congenital disorders of glycosylation type Ia
Tags: 2003, Adolescent, Adult, Age of Onset, Backlog, Carbohydrate-Deficient Glycoprotein Syndrome/complications/diagnosis/genetics, Child, Cormier-Daire V, De Lonlay P, Female, Heron D, Humans, Infant, Journal Article, Male, Matthijs G, Mental Disorders/diagnosis/etiology/genetics, Merzoug V, Mikaeloff Y, Miossec-Chauvet E, Nervous System Diseases/diagnosis/etiology/genetics, Neuropediatrics, Ponsot G, Preschool, Q3 Scoping Review Results, Retrospective Studies, Seta N, Severity Of Illness Index, Van Hulle C
Supportive and palliative care needs of families of children with life-threatening illnesses in Western Australia: evidence to guide the development of a palliative care service
Tags: 2007, Aoun S, Backlog, Child, Community Health Nursing/organization & administration/standards, Critical Illness, Family Health, Humans, Journal Article, Kristjanson LJ, Monterosso L, Palliative Care/organization & administration/psychology/standards, Palliative Medicine, Parents/psychology, Patient Care Team, Phillips MB, Q3 Scoping Review Results, Quality of Health Care/organization & administration/standards, Social Support, Terminally Ill, Western Australia
Late onset Pompe disease: clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients
Tags: 2007, Adolescent, Adult, Age of Onset, Backlog, Baethmann M, Child, Disease Progression, Electromyography, Female, Gempel K, Glycogen Storage Disease Type II/diagnosis/physiopathology, Horvath R, Humans, Journal Article, Limb-Girdle, Lochmuller H, Longitudinal Studies, Male, Middle Aged, Mueller-Felber W, Muscle Weakness, Muscular Dystrophies, Neuromuscular Disorders, Podskarbi T, Pongratz D, Preschool, Q3 Scoping Review Results, Respiration Disorders/etiology, Retrospective Studies, Schlotter-Weigel B, Schoser B, Shin Y, Walter MC
Liver involvement in Alpers disease
Tags: 1991, Backlog, Beckwith B, Biopsy, Brain/pathology, Child, Diffuse Cerebral Sclerosis of Schilder/diagnosis/metabolism/pathology, Female, Humans, Infant, Journal Article, Liver Function Tests, Liver/metabolism/pathology, Male, Narkewicz MR, Preschool, Q3 Scoping Review Results, Silverman A, Sokol RJ, Sondheimer J, Status Epilepticus/diagnosis/metabolism/pathology, Syndrome, The Journal Of Pediatrics
Corneal surface irregularities and episodic pain in a patient with mucolipidosis IV
Tags: 1990, Archives Of Ophthalmology, Backlog, Cataract Extraction, Child, Conjunctiva/pathology, Cornea/pathology, Epithelium/pathology, Fish I, Humans, Journal Article, Kenyon KR, Kolodny EH, Lessell S, Male, Mucolipidoses/pathology, Newman NJ, Pain/etiology, Preschool, Q3 Scoping Review Results, Starck T, Tears/secretion
Neurologic presentations of mitochondrial disorders
Tags: 2000, Backlog, Barash V, Brain Diseases, Child, Deafness/diagnosis/genetics, Developmental Disabilities/diagnosis/genetics, Fattal-Valevski A, Female, Follow-up Studies, Gutman A, Harel S, Humans, Inborn/diagnosis/genetics, Journal Article, Journal of Child Neurology, Lerman-Sagie T, Lev D, Male, MELAS Syndrome/diagnosis/genetics, Mental Retardation/diagnosis/genetics, MERRF Syndrome/diagnosis/genetics, Metabolic, Mitochondrial Myopathies/diagnosis/genetics, Neurologic Examination, Nissenkorn A, Q3 Scoping Review Results, Watemberg N, Zeharia A
Seizures in children with congenital hydrocephalus: long-term outcome
Coping with Dravet syndrome: parental experiences with a catastrophic epilepsy
Tags: 2006, Adaptation, Adolescent, Adult, Backlog, Camfield CS, Camfield PR, Caregivers/psychology, Child, Chronic Disease, Developmental Medicine and Child Neurology, Epilepsy/nursing/psychology, Family Health, Female, Humans, Journal Article, Male, Middle Aged, Nolan KJ, Parent-child Relations, Parents/psychology, Preschool, Psychological, Psychological/psychology, Q3 Scoping Review Results, Seizures/nursing/psychology, Severity Of Illness Index, Social Isolation, Social Support, Stress, Syndrome
Neonatal-onset propionic acidemia: neurologic and developmental profiles, and implications for management
Tags: 1995, Backlog, Brazelton TB, Carboxy-Lyases/deficiency, Child, Cognition Disorders/etiology, Developmental Disabilities/etiology, Enteral Nutrition, Female, Gastrostomy, Gopal YR, Humans, Infant, Journal Article, Korson MS, Male, Methylmalonyl-CoA Decarboxylase, Muscle Tonus, North KN, Nutritional Status, Preschool, Propionic Acids/blood, Prospective Studies, Q3 Scoping Review Results, Rohr FJ, The Journal Of Pediatrics, Waisbren SE, Warman ML
A follow up study of myocardial involvement in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS)
Tags: 1998, Adolescent, Adult, Aotsuka H, Backlog, Child, Echocardiography, Electrocardiography, Female, Follow-up Studies, Heart (british Cardiac Society), Humans, Hypertrophy, Journal Article, Left Ventricular/physiopathology/ultrasonography, Male, MELAS Syndrome/physiopathology/ultrasonography, Okajima Y, Q3 Scoping Review Results, Stroke Volume, Takayanagi M, Tanabe Y
Infantile type of sialic acid storage disease with sialuria
Tags: 1986, Backlog, Carbohydrate Metabolism, Clinical Genetics, Erwa W, Fibroblasts/metabolism/ultrastructure, Humans, Inborn Errors/metabolism/pathology, Infant, Journal Article, Leukocytes/metabolism/ultrastructure, Male, Mutz I, Paschke E, Pavelka M, Q3 Scoping Review Results, Roscher A, Sialic Acids/metabolism/urine, Trinkl G, Vacuoles/metabolism/ultrastructure
Miglustat for treatment of Niemann-Pick C disease: a randomised controlled study
Tags: 1-Deoxynojirimycin/analogs & derivatives/therapeutic use, 2007, Abel L, Adolescent, Adult, Age Factors, Analysis of Variance, Backlog, Child, Cohort Studies, Deglutition/drug effects, Double-Blind Method, Drug Administration Schedule, Enzyme Inhibitors/therapeutic use, Female, Humans, Journal Article, Lancet Neurology, Male, Niemann-Pick Disease, Patterson MC, Prady H, Preschool, Q3 Scoping Review Results, Retrospective Studies, Saccades/drug effects, Severity Of Illness Index, Type C/drug therapy/physiopathology, Vecchio D, Wraith JE
Neurologic course of congenital disorders of glycosylation
Tags: 2001, Aspartic Acid/analogs & derivatives/metabolism, Backlog, Brain Diseases, Brain/pathology/physiopathology, Carbohydrate-Deficient Glycoprotein Syndrome/diagnosis, Child, Developmental Disabilities/diagnosis, Epilepsy/diagnosis, Female, Humans, Inborn/diagnosis, Infant, Journal Article, Journal of Child Neurology, Krasnewich D, Lactic Acid/metabolism, Magnetic Resonance Imaging, Magnetic Resonance Spectroscopy, Male, Metabolic, Nerve Degeneration/diagnosis, Neurologic Examination, Pearl PL, Preschool, Q3 Scoping Review Results, Stroke/diagnosis
Mitochondrial neurogastrointestinal encephalomyopathy: diagnosis by rectal biopsy
Tags: 1998, Adolescent, Anthony DA, Backlog, Biopsy/methods, Cox GF, DNA, Electron, Fadic R, Female, Fox V, Humans, Intestinal Pseudo-Obstruction/pathology, Johns DR, Journal Article, Kalsner L, Microscopy, Mitochondrial Myopathies/pathology, Mitochondrial/analysis, Muscles/pathology, Perez-Atayde AR, Q3 Scoping Review Results, Rectum/innervation/pathology, Rivkin M, Teitelbaum JE, The American Journal Of Surgical Pathology
A scale to monitor progression and treatment of mitochondrial disease in children.
Tags: 2006, Adolescent, Backlog, Bugiani M, Child, Disability Evaluation, Disease Progression, Elson JL, Female, Great Britain, Humans, Infant, Journal Article, Longitudinal Studies, Male, McFarland R, Mitochondrial Diseases/diagnosis/therapy, Mitochondrial Encephalomyopathies/diagnosis/therapy, Morava E, Neurology/methods, Neuromuscular Disorders, Newborn, Observer Variation, Pediatrics/methods, Phoenix C, Predictive Value of Tests, Preschool, Prognosis, Q3 Scoping Review Results, Reproducibility of Results, Schaefer AM, Smeitink JA, Turnbull DM, Uziel G
Neuroanatomy of holoprosencephaly as predictor of function: beyond the face predicting the brain
Tags: 2002, Adolescent, Adult, Backlog, Barkovich AJ, Brain/pathology, Chi-Square Distribution, Child, Clegg NJ, Delgado MR, Face/pathology, Female, Forecasting, Hahn JS, Holoprosencephaly/pathology/physiopathology, Humans, Infant, Journal Article, Kinsman SL, Levey EB, Linear Models, Magnetic Resonance Imaging, Male, Miller VS, Neurology, Nonparametric, Plawner LL, Preschool, Prospective Studies, Q3 Scoping Review Results, Seizures/pathology/physiopathology, Simon EM, Stashinko EE, Statistics, Sweet VT, Tomography, X-Ray Computed
Neurologically impaired children and digestive problems
Tags: 2006, Adolescent, Archives de Pediatrie, Backlog, Botulinum Toxin Type A/administration & dosage, Brain Damage, Capito C, Child, Chronic/complications/therapy, Disabled Children, Enteral Nutrition, Follow-up Studies, France, Fundoplication, Gastric Acidity Determination, Gastroesophageal Reflux/complications/therapy, Gastroscopy, Heloury Y, Humans, Infant, Injections, Intramuscular, Journal Article, Leclair MD, Podevin G, Preschool, Prospective Studies, Protein-Energy Malnutrition/etiology/therapy, Q3 Scoping Review Results, Treatment Outcome
Peroxisome biogenesis disorders with prolonged survival: phenotypic expression in a cohort of 31 patients
Tags: 2004, Admiraal RJ, Adolescent, Adult, American Journal Of Medical Genetics.Part A, Backlog, Barth PG, Child, Cohort Studies, de Klerk JB, Developmental Disabilities/pathology, Duran M, Eye Diseases/pathology, Face/abnormalities, Female, Follow-up Studies, Gootjes J, Growth Disorders/pathology, Humans, Infant, Journal Article, Kidney/pathology, Liver/pathology, Male, Membrane Proteins/genetics, Mutation, Peroxisomal Disorders/genetics/mortality/pathology, Phenotype, Poll-The BT, Preschool, Q3 Scoping Review Results, Seizures/pathology, Spleen/pathology, Survival Rate, Time Factors, Wanders RJ, Waterham HR, Wenniger-Prick LJ
Clinical manifestations of Fabry disease in children: data from the Fabry Outcome Survey
Tags: 2006, Acta Paediatrica, Adolescent, Age of Onset, alpha-Galactosidase/metabolism/therapeutic use, Backlog, Beck M, Child, DNA Mutational Analysis, Fabry Disease/diagnosis/drug therapy/physiopathology, Female, FOS European Investigators, Heterozygote, Humans, Isoenzymes/therapeutic use, Journal Article, Male, Mehta A, Outcome Assessment (health Care), Parini R, Pintos-Morell G, Preschool, Q3 Scoping Review Results, Ramaswami U, Sunder-Plassmann G, Whybra C, Widmer U
Ocular findings in Norwegian patients with ataxia-telangiectasia: a 5 year prospective cohort study
Tags: 2007, Accommodation, Acta Ophthalmologica, Adolescent, Adult, Apraxias/diagnosis, Ataxia Telangiectasia/diagnosis, Backlog, Bek T, Capillaries/pathology, Child, Conjunctiva/blood supply, Conjunctival Diseases/diagnosis, Female, Genotype, Heiberg A, Humans, Journal Article, Lindman C, Male, Norway, Ocular, Ocular Motility Disorders/diagnosis, Phenotype, Photography, Preschool, Prospective Studies, Q3 Scoping Review Results, Riise R, Rodningen OK, Saccades, Stray-Pedersen A, Ygge J
Mitochondrial respiratory chain disease presenting as progressive bulbar paralysis of childhood
Tags: 2004, Backlog, Braun KP, Bulbar Palsy, Child, de Koning TJ, Dorland L, Fatal Outcome, Humans, Infant, Journal Article, Journal Of Inherited Metabolic Disease, Male, Mitochondrial Diseases/complications/diagnosis, Preschool, Progressive/diagnosis/etiology, Q3 Scoping Review Results, Roeleveld-Versteegh AB, Siblings, Smeitink JA
Links between abnormal brain structure and cognition in holoprosencephaly
Tags: 2006, Adolescent, Age Factors, Backlog, Benasich AA, Brain/abnormalities, Child, Cognition, Cognition Disorders/pathology, Corpus Striatum/abnormalities, Epilepsy/pathology, Female, Flax J, Hahn JS, Holoprosencephaly/pathology, Humans, Hypothalamus/abnormalities, Infant, Jing H, Journal Article, Kovar C, Male, Motor Skills Disorders/pathology, Neuropsychological Tests, Paterson SJ, Pediatric Neurology, Predictive Value of Tests, Preschool, Q3 Scoping Review Results, Roesler CP, Severity Of Illness Index, Sex Factors, Stashinko EE, Thalamic Nuclei/abnormalities
Melatonin treatment for sleep disorders in children with neurodevelopmental disorders: an observational study
Tags: 2002, Adolescent, Child, Child Preschool, Davies P, Developmental Disabilities, Developmental Disabilities/complications, Developmental Medicine and Child Neurology, Dose-Response Relationship Drug, Epilepsy, Epilepsy/complications, Female, Humans, Infant, Lennox-Gastaut syndrome, Leukodystrophy, Male, Medical Records, melatonin, Melatonin/therapeutic use, MPSII, MPSIII, Nervous System Diseases, Nervous System Diseases/complications, Outpatients, pharmacologic intervention, Q3 Scoping Review Results, Ross C, Sex Factors, Sleep Disorders/complications/drug therapy, sleep disturbance/disorders, Sleep Wake Disorders, Vision Disorders, Vision Disorders/complications, Whitehouse W
Melatonin treatment for sleep disorders in children with neurodevelopmental disorders: an observational study
Tags: 2002, Adolescent, Backlog, Child, Davies P, Developmental Disabilities/complications, Developmental Medicine and Child Neurology, Dose-Response Relationship, Drug, Epilepsy/complications, Female, Humans, Infant, Journal Article, Male, Medical Records, Melatonin/therapeutic use, Nervous System Diseases/complications, Outpatients, Preschool, Q3 Scoping Review Results, Ross C, Sex Factors, Sleep Disorders/complications/drug therapy, Vision Disorders/complications, Whitehouse W
Clinical and genetic spectrum of Sanfilippo type C (MPS IIIC) disease in The Netherlands
Tags: 2008, Acetyltransferases/chemistry/deficiency/genetics, Adolescent, Adult, Age of Onset, Backlog, Child, DNA Mutational Analysis, DNA/genetics, Durand S, Female, Genotype, Humans, Infant, Journal Article, Male, Middle Aged, Missense, Models, Molecular, Molecular Genetics and Metabolism, Mucopolysaccharidosis III/classification/enzymology/genetics/physiopathology, Mutation, Netherlands, Phenotype, Poorthuis BJ, Preschool, Pshezhetsky AV, Q3 Scoping Review Results, Ruijter GJ, Valstar MJ, van de Kamp JM, van der Helm RM, van Diggelen OP, Wevers RA, Wijburg FA