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Dabke, P.
Transcobalamin II Deficiency: Rare Differential Diagnosis in a Neonate with Hematological Disease and Failure to Thrive
Danhauser, K.
NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood
Darras, B.
Interim Efficacy and Safety Results from the Phase 3 ENDEAR Study of Nusinersen in Infants Diagnosed with Spinal Muscular Atrophy (SMA)
Darras, Basil T.
Efficacy and safety of nusinersen in children with later-onset spinal muscular atrophy (SMA): results of the phase 3 CHERISH study
Das, A.
Transcobalamin II Deficiency: Rare Differential Diagnosis in a Neonate with Hematological Disease and Failure to Thrive
Das, A. M.
Long-Term Neurodevelopmental Outcome of Patients with Mucopolysaccharidosis-1H (MPS-1H) following Hematopoietic Stem Cell Transplantation (HSCT)
Datta, A. N.
Infantile Dystonia Parkinsonism Caused by a Mutation in SLC6A3: Case Report of Three Siblings
Deba, T.
When It Is Not MS…—Differential Diagnosis of Optic Neuritis and Multifocal Inflammatory Cerebral Lesions in an Adolescent
The Enemy Within: Deleterious Consequences of an Inappropriate Antiviral Response for the Central Nervous System
Decker, C.
Unexpected Cause of Progressive Decrease in Sensorimotor Function of the Left Leg
De Geyter, J.
Homozygous Splice Mutation in CWF19L1 in Two Brothers with Autosomal Recessive Cerebellar Ataxia
Delgado, M. R.
Time to Retreatment after AbobotulinumtoxinA (Dysport) Injections in Children with Dynamic Equinus Foot Deformity
Abobotulinumtoxin-A (DYSPORT) Injection Doses per Muscle in Pediatric Patients with Lower Limb Spasticity
Phase 3 Trial to Evaluate AbobotulinumtoxinA (Dysport) Injections in Children with Upper Limb Spasticity Due to Cerebral Palsy: A Study Design
Demirbas, S.
Early Radiologic Pattern in a Patient with Megaloencephalic Leukoencephalopathy Due to Homozygous MLC1 Mutation
Denecke, J.
Compassionate Use of Simvastatin for a Patient with Juvenile Metachromatic Leukodystrophy
Respiratory Distress and Encephalopathy: Fat Embolism Syndrome in Duchenne Muscular Dystrophy
The Natural History of Canavan Disease: Description of 23 New Cases and Comparison with Literature
The Potential of Whole-Exome Sequencing (WES) in Neuropediatric Patients: Single-Center Experience at the University Hospital Hamburg Eppendorf
A Novel Nonsense Mutation in TRIP4 Gene Causes Severe Muscular Weakness with Respiratory Failure and Cardiomyopathy but without Skin, Joint, and/or Bone Abnormalities
De Vivo, Darryl C.
Efficacy and safety of nusinersen in children with later-onset spinal muscular atrophy (SMA): results of the phase 3 CHERISH study
de Vries, P.
Predictors of Efficacy in Patients with Adjunctive Everolimus Therapy for Treatment-Resistant Seizures Associated with Tuberous Sclerosis Complex
Diepold, M.
Transient Ischemic Attack (TIA): A Problem Not to Miss
Dillenberger, S.
Midaortic Syndrome in TSC
Distelmaier, F.
Reversible Epileptic Encephalopathy upon Uridine Treatment in Patients with CAD Mutations
Congenital Myasthenic Syndrome Caused by Isolated PREPL Deficiency
NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood
Doege, C.
Evaluation of the Effects of Anticonvulsive Therapy in Children with Symptomatic Epilepsy by a State Space Modeling Approach
Domscheit, S.
Type 1 Diabetes and Epilepsy in Children: Is There a Pathogenetic Association between Frequency, Manifestation, and Antibodies?
Döring, M.
Early Effects after Hematopoietic Stem Cell Transplantation in 13 Children with Juvenile Metachromatic Leukodystrophy
Drenckhahn, A.
Dilatative Cardiomyopathy and Severe Cardiac Dysfunction in a Patient with CCFDN Syndrome
Driever, Hernáiz P.
Motor Function in Pediatric ALL Survivors after Chemotherapy-Only
Duckwitz, H.
Pharmacological Treatment of Stimulus-Induced Drop Episodes in Children with Coffin-Lowry Syndrome: Case Experience and an Overview of the Literature
Dufke, A.
Remarkable Genetic Finding in a Girl with Phenotype of Classic Pelizäus-Merzbacher Disease: Xq22.2 Microdeletion Including PLP1 and Other Genes
Dursun, N.
Time to Retreatment after AbobotulinumtoxinA (Dysport) Injections in Children with Dynamic Equinus Foot Deformity
Abobotulinumtoxin-A (DYSPORT) Injection Doses per Muscle in Pediatric Patients with Lower Limb Spasticity
Phase 3 Trial to Evaluate AbobotulinumtoxinA (Dysport) Injections in Children with Upper Limb Spasticity Due to Cerebral Palsy: A Study Design