Browse Items (7 total)
- Tags: AIM
The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature
Tags: 2003, AIM, alpha-Glucosidases/ge [Genetics], alpha-Glucosidases/me [Metabolism], Backlog, Bakker HD, Blood Chemical Analysis, Brain/pa [Pathology], Cardiomegaly/di [Diagnosis], Cardiomegaly/et [Etiology], Child Development, de Klerk JB, Disease Progression, Glycogen Storage Disease Type II/co [Complications], Glycogen Storage Disease Type II/mo [Mortality], Glycogen Storage Disease Type II/pp [Physiopathology], Hop W, Humans, IM, Infant, Journal Article, Loonen MC, Mutation, Netherlands/ep [Epidemiology], Newborn/gd [Growth & Development], Pediatrics, Poll-The BT, Premature, Reuser AJ, Smeitink JA, Smit GP, Survival Analysis, van den Hout HM, Van der Ploeg AT, van Diggelen OP
The clinical and demographic characteristics of nonneuronopathic Gaucher disease in 887 children at diagnosis
Tags: 2006, Adolescent, AIM, Andersson HC, Anemia/et [Etiology], Archives Of Pediatrics & Adolescent Medicine, Backlog, Bone Diseases/et [Etiology], Child, Female, Gaucher Disease/co [Complications], Gaucher Disease/di [Diagnosis], Growth Disorders/et [Etiology], Hepatomegaly/et [Etiology], Humans, IM, Infant, Journal Article, Kacena KA, Kaplan P, Longitudinal Studies, Male, Newborn, Preschool, Q3 Scoping Review Results, Splenomegaly/et [Etiology], Thrombocytopenia/et [Etiology], Yee JD
Supporting the family after the death of a child.
Tags: 2012, Adolescent, AIM, Backlog, Child, Chronic Disease, Counseling, Death, Disabled Children, Grief, Guidelines As Topic, Guilt, HEALTH COMMITTEE ON PSYCHOSOCIAL ASPECTS OF CHILD AND FAMILY, Humans, IM, Infant, Journal Article, Mortality, Parenting, Parents, Pediatrics, Physician's Role, Premature, Preschool, Professional-family Relations, sibling bereavement, Siblings, Social Support, Substance-Related Disorders, Sudden, Sudden Infant Death, Suicide, Wender E
Outcome at age 4 years in offspring of women with maternal phenylketonuria: the Maternal PKU Collaborative Study
Tags: 2000, AIM, Allred E, Azen C, Backlog, Chang PN, Child, Child Behavior, Cipcic-Schmidt S, Cognition, de la Cruz F, Developmental Disabilities, Developmental Disabilities/di [Diagnosis], Developmental Disabilities/et [Etiology], Female, Hall R, Hanley W, Humans, IM, JAMA, Journal Article, Koch R, Levy HL, Logistic Models, Longitudinal Studies, Male, Matalon R, Nanson J, Phenylketonurias/dh [Diet Therapy], Phenylketonurias/pp [Physiopathology], Pregnancy, Pregnancy Complications/dh [Diet Therapy], Pregnancy Outcome, Preschool, Psychological Tests, Rouse B, Shifrin H, Trefz F, Waisbren SE
Natural history of nonketotic hyperglycinemia in 65 patients
Tags: 2004, Adolescent, Age of Onset, AIM, Anticonvulsants/tu [Therapeutic Use], Apnea/et [Etiology], Apnea/th [Therapy], Applegarth D, Artificial, Backlog, Child, Corpus Callosum/ab [Abnormalities], Disease Progression, Female, Glycine/bl [Blood], Glycine/cf [Cerebrospinal Fluid], Hamosh A, Health Surveys, Hoover-Fong JE, Humans, Hydrocephalus/ep [Epidemiology], Hydrocephalus/et [Etiology], Hyperglycinemia, IM, Infant, Journal Article, Juvenile/dt [Drug Therapy], Juvenile/ep [Epidemiology], Juvenile/et [Etiology], Male, Myoclonic Epilepsy, Neurology, Newborn, Nonketotic/co [Complications], Nonketotic/ep [Epidemiology], Nonketotic/me [Metabolism], Nonketotic/mo [Mortality], Nystagmus, Pathologic/ep [Epidemiology], Pathologic/et [Etiology], Pregnancy, Pregnancy Complications/ep [Epidemiology], Preschool, Psychomotor Disorders/ep [Epidemiology], Psychomotor Disorders/et [Etiology], Questionnaires, Registries, Respiration, Retrospective Studies, Seizures/dt [Drug Therapy], Seizures/ep [Epidemiology], Seizures/et [Etiology], Sex Factors, Shah S, Survival Analysis, Toone J, Van Hove JL
Long-term outcome and clinical spectrum of 73 pediatric patients with mitochondrial diseases
Tags: 2007, AIM, Backlog, Cause Of Death, Chevalier I, Child, Cohort Studies, Debray FG, Decarie JC, DNA, DNA Fragmentation, Female, Follow-up Studies, HEREDITARY, Humans, IM, Infant, Journal Article, Lambert M, Leber/di [Diagnosis], Leber/ge [Genetics], Leber/mo [Mortality], Longitudinal Studies, Male, MELAS Syndrome/di [Diagnosis], MELAS Syndrome/mo [Mortality], MELAS Syndrome/th [Therapy], Mitchell GA, Mitochondrial Diseases/di [Diagnosis], Mitochondrial Diseases/ge [Genetics], Mitochondrial Diseases/mo [Mortality], Mitochondrial Encephalomyopathies/di [Diagnosis], Mitochondrial Encephalomyopathies/mo [Mortality], Mitochondrial Encephalomyopathies/th [therapy], Mitochondrial Myopathies/di [Diagnosis], Mitochondrial Myopathies/ge [Genetics], Mitochondrial Myopathies/mo [Mortality], Mitochondrial/ge [Genetics], Newborn, Optic Atrophy, Pediatrics, Preschool, Probability, Proportional Hazards Models, Q3 Scoping Review Results, Retrospective Studies, Robinson BH, Robitaille Y, Severity Of Illness Index, Shoubridge EA, Survival Analysis, Time Factors