Abstracts (HTML) List of Authors

Haack, T.

NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood
The Potential of Whole-Exome Sequencing (WES) in Neuropediatric Patients: Single-Center Experience at the University Hospital Hamburg Eppendorf

Haack, T. B.

Reversible Epileptic Encephalopathy upon Uridine Treatment in Patients with CAD Mutations
Congenital Myasthenic Syndrome Caused by Isolated PREPL Deficiency

Haaga, M.

Explorative Saccade Training in Children with Homonymous Hemianopia

Haas, D.

Successfully Completed Pregnancy in a Patient with SLC25A19-Associated Form of a Treatable Leigh-Like Syndrome

Haber, B.

Severe Course of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) with Detection of an Unknown Antineuronal Antibody

Haber, E.

4H Leukodystrophy: A Rare Movement Disorder

Haberlandt, E.

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

Häberle, J.

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

Hahn, A.

The Impact of Morphometric Skin Punch Biopsy Analysis for a Small Nerve Fiber Involvement in Children with Pain Syndrome
Myositis-Associated Autoantibodies in Juvenile Dermatomyositis
Mutations in KIF14, Encoding Kinesin-Like Protein KIF14, Cause Primary and Syndromic Microcephaly
STAC3-Associated Congenital Myopathy in a Boy of Turkish Ancestry with Severe Scoliosis and Early-Onset Respiratory Insufficiency
Congenital Hyperekplexia: A Visual Diagnosis

Hanebeck, B.

Severe Course of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) with Detection of an Unknown Antineuronal Antibody

Hanff, E.

The L-Arginine/NO Pathway in Children with Attention-Deficit/Hyperactivity Disorder (ADHD)

Härtel, Ch.

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

Hartlieb, T.

Worsening of Hand Function but Significant Improvement of Abilities Measured in PEDI in a Child with Sturge-Weber Syndrome

Hartmann, H.

Hyperkinetic Movement Disorder as First Manifestation of an Autoimmune Disease
Long-Term Neurodevelopmental Outcome of Patients with Mucopolysaccharidosis-1H (MPS-1H) following Hematopoietic Stem Cell Transplantation (HSCT)
Transcobalamin II Deficiency: Rare Differential Diagnosis in a Neonate with Hematological Disease and Failure to Thrive

Haßlberger, T.

Development of a Classification System for Wheelchair Maintenance and Seat Positioning

Haubenberger, D.

Validation of Digital Spiral Analysis in Pediatric Tremor

Heidenreich, Y.

The Impact of Morphometric Skin Punch Biopsy Analysis for a Small Nerve Fiber Involvement in Children with Pain Syndrome

Heimgärtner, M.

ADHD Is a Risk Factor for Cognitive Development in NF1

Heinemeyer, J.

A Novel Nonsense Mutation in TRIP4 Gene Causes Severe Muscular Weakness with Respiratory Failure and Cardiomyopathy but without Skin, Joint, and/or Bone Abnormalities

Heinen, F.

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

Heinrich, B.

Homozygous Splice Mutation in CWF19L1 in Two Brothers with Autosomal Recessive Cerebellar Ataxia

Heinz-Erian, E.

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
Neuromyelitis Optica Spectrum Disorders in Pediatric Patients

Hempel, M.

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

Henkes, H.

Time Is Brain: Thrombectomy after Pediatric Stroke in Two Previously Healthy Girls

Hennes, E. M.

Neuromyelitis Optica Spectrum Disorders in Pediatric Patients

Hennig, B.

Reintegration to School after Craniocerebral Injury: Results of a Survey

Hentschel, F.

Rehabilitative Outcome after Selective Dorsal Rhizotomy (SDR)

Henzi, B.

Northern Epilepsy: Not So Northern Anymore

Herberhold, T.

A Technical Neuro-Orthopedic and Neuropediatric Report on Requirements Needed for a Successful Rehabilitation of a Disabled Adolescent

Herebian, D.

NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood

Herting, A.

Dramatic Onset of Focal Seizures: Differentiating Structural Focal Epilepsy from Ring Chromosome 20

Hertzberg, C.

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

Herzig, N.

GOAL: Gait Outcome Assessment List

Heß, K.

Emery-Dreifuss Muscular Dystrophy Type 1 in a 15-Year-Old Patient Due to a Novel Putative Splice-Site Mutation

Hessenauer, M.

Long-Term Outcome after Vegetative State Due to Near-Drowning and Quality of Life of the Families
Early-Phase Rehabilitation of Children and Adolescents with Chronic Disorders of Consciousness: Standardized, Ability-Based Registration of Remission (RemiPro) Supports Goal-Finding and Establishing a Prognosis
Learning to Cope with Mirror Movements in Activities of Daily Living: Effects of Targeted Bimanual Therapy in Children with Unilateral Spastic CP
Worsening of Hand Function but Significant Improvement of Abilities Measured in PEDI in a Child with Sturge-Weber Syndrome

Hethey, S.

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

Hinrichs, R.

Reintegration to School after Craniocerebral Injury: Results of a Survey

Hinze, C.

The Enemy Within: Deleterious Consequences of an Inappropriate Antiviral Response for the Central Nervous System

Hischke, S.

The Natural History of Canavan Disease: Description of 23 New Cases and Comparison with Literature

Hochstein, J.

Longitudinal 8-year Brain Volumetric Analysis in 35 CLN3 Patients: Successful Development of a Sensitive Marker to Measure Clinical Outcome

Hoffmann, G.

Severe Course of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) with Detection of an Unknown Antineuronal Antibody

Hoffmann, G. F.

Biochemical Investigations for Neurometabolic Diseases in the Future: Biochemistry versus Molecular Genetics
Niemann-Pick Type C Disease: A Challenge in Diagnostics, Therapy, and Care for Affected Families
Successfully Completed Pregnancy in a Patient with SLC25A19-Associated Form of a Treatable Leigh-Like Syndrome
Quantitative Clinical Characteristics of 53 Patients with MPS VII: A Cross-Sectional Analysis

Hofmann-Peters, A.

Dramatic Onset of Focal Seizures: Differentiating Structural Focal Epilepsy from Ring Chromosome 20

Holinski-Feder, E.

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

Höll, T.

Everolimus Reduces Seizure Frequency in Tuberous Sclerosis Complex

Holterhus, P.

Type 1 Diabetes and Epilepsy in Children: Is There a Pathogenetic Association between Frequency, Manifestation, and Antibodies?

Holzinger, D.

When It Is Not MS…—Differential Diagnosis of Optic Neuritis and Multifocal Inflammatory Cerebral Lesions in an Adolescent

Horneff, G.

Acute Flaccid Myelitis (AFM) Associated with Enterovirus: A Distinct Clinical Entity?

Hörning, A.

Learning to Cope with Mirror Movements in Activities of Daily Living: Effects of Targeted Bimanual Therapy in Children with Unilateral Spastic CP

Hörtnagel, K.

Emery-Dreifuss Muscular Dystrophy Type 1 in a 15-Year-Old Patient Due to a Novel Putative Splice-Site Mutation

Horvath, T.

Transient Ischemic Attack (TIA): A Problem Not to Miss

Huemer, M.

Biotin Thiamine Responsive Basal Ganglia Disease: Clinical Improvement after Initiation of Biotin and Thiamine Therapy

Hummel, H.

Effect of Modern Therapy on Disease Progression in Pediatric MS

Huppke, B.

Effect of Modern Therapy on Disease Progression in Pediatric MS

Huppke, P.

Effect of Modern Therapy on Disease Progression in Pediatric MS

Hussain, M. S.

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