Abstracts (HTML) List of Authors

Wagner, M.

Muscle Dystrophy Differential Diagnosis: Manifestation of Anti-HMG-CoA Reductase Antibody Myositis in Infancy

Wallmeier, J.

Ciliogenesis Defect of Multiple Motile Cilia Causes Hydrocephalus

Walter, J.

X-ALD as the Cause of Autistic Behavior

Walter, M. C.

Titinopathies in Human Genetics Diagnostics
CNV Detection from Targeted Next-Generation Panel Sequencing Data Increases the Diagnostic Yield in Patients with Neuromuscular Diseases

Wandinger, K.

A Five-Year-Old Boy Diagnosed with an Anti-mGluR1 Positive Post–Streptococcal-Associated Cerebellitis

Warthemann, R.

FOXG1 Syndrome: Genotype–Phenotype Association in 84 Patients with FOXG1 Variants

Warthemann, Rita

The Acquisition of Rare Neurological Disorders in Childhood (”ESNEK”): First Interim Results after 2 Years

Waseem, S. S.

Mutations in KIF14, Encoding Kinesin-Like Protein KIF14, Cause Primary and Syndromic Microcephaly

Weber, C.

Assessment of Anthropometric Measures and Hand Muscle Strength in Children to Establish Standardized Parameters for Pediatric Neurorehabilitation

Weber, H.

Assessment of Anthropometric Measures and Hand Muscle Strength in Children to Establish Standardized Parameters for Pediatric Neurorehabilitation

Weber, P.

Developmental Disorders and Cerebral Visual Impairment
Biotin Thiamine Responsive Basal Ganglia Disease: Clinical Improvement after Initiation of Biotin and Thiamine Therapy
Infantile Dystonia Parkinsonism Caused by a Mutation in SLC6A3: Case Report of Three Siblings

Weber, Y. G.

Recommendations for Diagnostic Genetic Testing in Epilepsies

Weichert, J.

Ciliogenesis Defect of Multiple Motile Cilia Causes Hydrocephalus

Weidemann, J.

Acute Flaccid Paralysis of Unknown Cause: A Report of Three Unusual Cases Mimicking Poliomyelitis

Weinberger, R.

GOAL: Gait Outcome Assessment List

Weiner, V.

Acute Flaccid Paralysis of Unknown Cause: A Report of Three Unusual Cases Mimicking Poliomyelitis

Weir, S.

GOAL: Gait Outcome Assessment List

Weise, D.

Acute and Episodic Movement Disorders: ATP1A3-Related Disorders as Differential Diagnosis

Weise, S.

Pharmacological Treatment of Stimulus-Induced Drop Episodes in Children with Coffin-Lowry Syndrome: Case Experience and an Overview of the Literature

Weisner, Th.

A Five-Year-Old Boy Diagnosed with an Anti-mGluR1 Positive Post–Streptococcal-Associated Cerebellitis

Weiss, D.

Respiratory Distress and Encephalopathy: Fat Embolism Syndrome in Duchenne Muscular Dystrophy

Wellmer, J.

Stereotactic Radiofrequency Thermocoagulation (L-RFTC) of Focal Cortical Dysplasias: Applicable to Children?

Werner, C.

Meta-analyses of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy
Lung Function in Ataluren-Treated, Nonambulatory Patients with Nonsense Mutation Duchenne Muscular Dystrophy from a Long-Term Extension Trial

Weschke, B.

Lacosamide Lowers Valproate and Levetiracetam Levels

Westphal, M.

Expert Opinion on the Management of Intracerebroventricular (ICV) Drug Delivery

Wicht, S.

Autoimmunencephalitis and Psychiatric Symptoms: The Example “SREAT”

Wider, S.

Single-Center Experience with Intrathecal Administration of Nusinersen in Children with Spinal Muscular Atrophy Type I

Wiegand, G.

Predictors of Efficacy in Patients with Adjunctive Everolimus Therapy for Treatment-Resistant Seizures Associated with Tuberous Sclerosis Complex

Wiemer-Kruel, A.

Autoimmunencephalitis and Psychiatric Symptoms: The Example “SREAT”
Predictors of Efficacy in Patients with Adjunctive Everolimus Therapy for Treatment-Resistant Seizures Associated with Tuberous Sclerosis Complex

Wildbolz, M.

Northern Epilepsy: Not So Northern Anymore

Wilker, M.

Acute Flaccid Paralysis of Unknown Cause: A Report of Three Unusual Cases Mimicking Poliomyelitis

Wille, D.

Clinical Presentation and Molecular Findings in Two Index Patients with GM2 Gangliosidosis/Mb. Sandhoff

Winkler, S.

Perampanel Add-on Therapy for the Treatment of Children and Adolescents with Partial and Primary Generalized Seizures: A Report from the University Hospital of Innsbruck

Wissel, J.

Improving the Quality of Care in the Specialization: The Benefits of “Hands-on” Courses for Learning Neuromuscular Ultrasound

Witt, O.

Everolimus as a Therapy of a Benign, Infiltrative Growing Bone Tumor of the Mandibula: A Rare Manifestation with Tuberous Sclerosis

Wittmack, E.

Rehabilitative Outcome after Selective Dorsal Rhizotomy (SDR)

Wolf, N. I.

Hypomyelination: Lessons from Genetic Testing

Wolter, S.

Rehabilitative Outcome after Selective Dorsal Rhizotomy (SDR)

Wortmann, S. B.

Reversible Epileptic Encephalopathy upon Uridine Treatment in Patients with CAD Mutations

Wunderlich, S.

Health-Related Quality of Life in Children and Adolescents with Spinal Dysraphic Disorders

Wusthoff, C.

High-Frequency Oscillations in Surface EEG Recorded from Neonates with Perinatally Acquired Hypoxic Ischemic Encephalopathy: A Retrospective Study

Wyschkon, A.

Innovation on the BUEVA-III: Basic Diagnostics of Developmental Disorders in Preschool Age—Version III