Abstracts of the 41st Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) List of Authors

Waibel, J.

Intrafamilial Variability of Natural Disease Course in Metachromatic Leukodystrophy

Wallmeier, J.

Subcellular Analysis of the Motor Protein Apparatus in Ependymal Cilia

Weber, P.

Attention Problems in Children with Epilepsy. How is the Long-Term Outcome?
The Impact of Infectious Diseases on Sleeping Behavior in Preterm Infants
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Cerebellar Hypoplasia and Dysmorphia in Neurofibromatosis Type 1
Impact of Advanced MRI Imaging in Acute Stroke-Like Episodes
Internetwork Connectivity Alterations in Children with Benign Epilepsy with Centrotemporal Spikes
Immediate Effects of Phototherapy on Sleep of Very Preterm Neonates: An Observational Study

Wegener, J.

Bone Marrow Transplantation in a Mouse Model for Rett Syndrome

Weigt-Usinger, K.

Rolandic Epilepsy: Retrospective Analysis of Neuropsychological and Clinical Data
Cognitive Development in Children with Rolandic Epilepsy: Results of a Current PubMed Search

Weisbrod, T.

Therapy and Clinical Course in 52 Patients with PCDH19 Mutations

Weissert, R.

Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study

Weisstanner, C.

Longitudinal Functional Reorganization after Pediatric Stroke: A Descriptive Case Study

Wenner, K.

Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study

Wieczorek, D.

Genotype and Phenotype in 34 Families with Genetically Confirmed Walker-Warburg Syndrome or Muscle Eye Brain Disease

Wiemer-Kruel, A.

Modified Atkins Diet, an Alternative Treatment of Glucose Transporter Type 1 Deficiency Syndrome

Wiesel, T.

ADEM-Like Presentation as the Main Manifestation of X-Linked Lymphoproliferative Disease in a 4-Year-Old Male Patient

Wiesmann, C.

Design of a Confirmatory Phase 3, Multicenter, Randomized, Double Blind, Placebo-Controlled Study (ACT DMD) of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy

Wiest, R.

Longitudinal Functional Reorganization after Pediatric Stroke: A Descriptive Case Study

Wilhelm, C.

Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases

Wilichowski, E.

Novel Mutation in the Inverted Formin 2 Gene in a Family with Hereditary Motor and Sensory Neuropathy, and Nephropathy

Wilke, M.

A Comparison of Language Lateralization as Assessed using Functional MRI using Scanner-Generated versus Externally Calculated Statistical Parameter Maps

Wilken, B.

Therapy and Clinical Course in 52 Patients with PCDH19 Mutations

Wilkens, B.

Cerebral Palsy and Breathing: More than Prophylaxis of Pneumonia

Will, B.

Clinical and Imaging Findings and Postoperative Esthetic Results in Patients with Single or Bilateral Coronal Synostosis

William, R.

The DEM-CHILD Neuronal Ceroid Lipofuscinoses Patient Database: A Tool for the Evaluation of Therapies in Neuronal Ceroid Lipofuscinoses

Winkler, P.

Hemispheric Dissociation between Ipsilateral Motor and Contralateral Somatosensory Representation of the Paretic Hand: Deterioration of Hand Function after Hemispherotomy in a Case of Hemispheric Polymicrogyria
Focal Cortical Dysplasia in a Family with KCNQ3 Mutation

Wittmann, W.

Mutation Spectrum and Infantile Manifestation in Hereditary Spastic Paraplegia

Wolf, N.

Intrafamilial Variability of Natural Disease Course in Metachromatic Leukodystrophy
Oral-Facial-Digital Syndrome Type VI: is C5orf42 Really the Major Gene?
Hypomyelination without Hypogonadotropic Hypogonadism and Hypodontia as a Variant of 4H Syndrome

Wolf, P.

Therapy and Clinical Course in 52 Patients with PCDH19 Mutations

Wolf, S.

The Objective Measurement of Diadochokinesis in Children with Bilateral Spastic Cerebral Palsy

Wolff, M.

Quinidine: A Targeted Drug Treatment for Patients with the Syndrome of Malignant Migrating Partial Seizures in Infancy and KCNT1 Mutation

Wörle, H.

MERS: Mild Encephalopathy/Encephalitis with Reversible Lesions in the Splenium Another Three Cases
Manganese Storage Disease as a Rare Cause of Dystonia with Bilateral Changes in Basal Ganglia and Polycythemia