Abstracts (HTML) Autorenliste

Lampe, C.

Challenges in Interdisciplinary Communication
Health-Related Quality of Life in Children and Adolescents with Spinal Dysraphic Disorders
Two Siblings with D-Bifunctional Protein Deficiency and Unusual Clinical Course

Lampe, Ch.

Autoimmunencephalitis and Psychiatric Symptoms: The Example “SREAT”

Lange, J.

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

Langenbach, A.

Unbalanced Translocation Affecting the Long Arms of Chromosome 10 and 22 Causes Complex Syndromes with Very Severe Neurodevelopmental Delay, Speech Impairment, Autistic Behavior, and Epilepsy

Langer, T.

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

Lebek, S.

Pathological Fractures in Patients with Myelomeningocele

Lechner, C.

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

Lechner, Ch.

Neuromyelitis Optica Spectrum Disorders in Pediatric Patients

Lee-Kirsch, M. A.

Interferonopathies of the Nervous System
Effects of Janus Kinase Inhibition in Two Children with Aicardi-Goutières Syndrome
The Enemy Within: Deleterious Consequences of an Inappropriate Antiviral Response for the Central Nervous System

Leenen, A.

Unbalanced Translocation Affecting the Long Arms of Chromosome 10 and 22 Causes Complex Syndromes with Very Severe Neurodevelopmental Delay, Speech Impairment, Autistic Behavior, and Epilepsy

Leis, Th.

BNS Epilepsy, Global Developmental Delay, Optic Coloboma, and Vesicoureteral Reflux as Leading Symptoms of COL4A1 Mutation: A Case Report

Leiz, S.

Reversible Epileptic Encephalopathy upon Uridine Treatment in Patients with CAD Mutations

Lemke, J. R.

Recommendations for Diagnostic Genetic Testing in Epilepsies

Lessel, D.

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

Lester, T.

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

Leypoldt, F.

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

Lidzba, K.

ADHD Is a Risk Factor for Cognitive Development in NF1

Liehr, T.

Unbalanced Translocation Affecting the Long Arms of Chromosome 10 and 22 Causes Complex Syndromes with Very Severe Neurodevelopmental Delay, Speech Impairment, Autistic Behavior, and Epilepsy

Lim, D.

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

Linner, E.

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

Lipp, J.

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

Lippert, L.

Autoimmunencephalitis and Psychiatric Symptoms: The Example “SREAT”

Löbel, U.

Compassionate Use of Simvastatin for a Patient with Juvenile Metachromatic Leukodystrophy
Longitudinal 8-year Brain Volumetric Analysis in 35 CLN3 Patients: Successful Development of a Sensitive Marker to Measure Clinical Outcome

Lorenz, B.

Juvenile Ceroid Lipofuscinosis CLN3: A Fatal Disease with Primary Ocular Manifestation

Lorenz, I.

Toxic Rapidly Progressive Myelopathy Induced by Nelarabine in an Adolescent with Relapsed Pre-T-ALL

Lücke, T.

Plasmapheresis as at Treatment Option in Anti-MOG–Related Neurological Disorders with Fulminant Progress
The L-Arginine/NO Pathway in Children with Attention-Deficit/Hyperactivity Disorder (ADHD)
Difficulties in the Acquisition of Literacy in Children with Rolandic Epilepsy or Rolandic EEG Pattern
Lunch and Cognitive Performance in School Children: The Crossover Intervention Trial CogniDo
Long-Term Neurodevelopmental Outcome of Patients with Mucopolysaccharidosis-1H (MPS-1H) following Hematopoietic Stem Cell Transplantation (HSCT)
Novel Homozygous Missense Mutation in ALDH7A1 Causes Neonatal Pyridoxine-Dependent Epilepsy
Unexpected Cause of Progressive Decrease in Sensorimotor Function of the Left Leg
Unbalanced Translocation Affecting the Long Arms of Chromosome 10 and 22 Causes Complex Syndromes with Very Severe Neurodevelopmental Delay, Speech Impairment, Autistic Behavior, and Epilepsy
Globotriaosylsphingosine (Lyso-GB3 bzw. Lyso-GL3), an Excellent Biomarker for Children with Fabry Disease

Lücke, Th.

CAPOS-Syndrome: A Rare Differential Diagnosis to Friedreich’s Ataxia

Luo, X.

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

Lüsebrink, N.

Posttraumatic Encephalocele as a Rare but Relevant Complication of Frontobasal Fractures
MEF2C Mutations: The Cause of an Epileptic Encephalopathy Syndrome with Pathognomonic Fidgetiness and Myoclonias

Lüttgen, S.

The Potential of Whole-Exome Sequencing (WES) in Neuropediatric Patients: Single-Center Experience at the University Hospital Hamburg Eppendorf