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

Abstracts (HTML) List of Authors

Laine, M.

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

Lampe, R.

Cerebral Blood Circulation in Premature Infants by Means of Mathematical Modeling

Lang-Dullenkopf, A.

Developmental Profile of 3-Year-Old Girl with Atypical Rett Syndrome with Detection of a Currently Unpublished Mutation in the MECP2 Gen

Langhagen, T.

Clinical Neurophysiology in Dizzy Children: Which Tests do I Need?
Health-Related Quality of Life of Children with Vertigo: Retrospective Study at the German Center for Vertigo and Balance Disorders

Lassay, L.

Spinal Hemorrhage: An Interdisciplinary Emergency

Lava, S.

High Prevalence of Pathologic Copy Number Variations Detected by Array Comparative Genomic Hybridization in Children with Autism Spectrum Disorders: The Experience of Southern Switzerland

Ledergerber, K.

The Impact of Infectious Diseases on Sleeping Behavior in Preterm Infants

Leis, T.

Rare Variant of GM2 Gangliosidosis due to Activator Protein Deficiency: A Case Report

Leitz, S.

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

Leiz, S.

Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Heterozygous Mutation in the KCNMA1 Gene with “Loss of Function” Phenotype in a Patient with Generalized Epilepsy

Lemberg, K.

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

Lemke, J.

Pontocerebellar Hypoplasia Type 9: A New Subtype
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Video-Documented Long-Term Follow-Up of a 10 Years' Old Girl with Severe Dyskinesia and Paroxysmal Choreoathetosis: A Variant Ataxia-Telangiectasia (A-T)

Lerche, H.

Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy

LeVan, P.

Fast fMRI Sequence Allows for Analysis of BOLD Responses to Single Interictal Epileptic Spikes

Lidzba, K.

Executive Dysfunction in Neurofibromatosis Type 1: Comparison to Idiopathic ADHD
A Comparison of Language Lateralization as Assessed using Functional MRI using Scanner-Generated versus Externally Calculated Statistical Parameter Maps

Limburg, K.

Transcranial Biphasic Quadro-Pulse Stimulation with One but not Two Full-Sine Cycles Induces Long-Term Depression-Like Changes in Corticomotor Excitability

Linder-Lucht, M.

Neurogenic Thoracic Outlet Syndrome: A Rare Differential Diagnosis of upper Extremity Paresthesia in a Pediatric Patient
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations

Löbel, U.

Optic Atrophy in an Iron Storage Disorder Reducing Tissue Iron Load in a Child with MPAN Disease
Hypomyelination without Hypogonadotropic Hypogonadism and Hypodontia as a Variant of 4H Syndrome
Hematopoietic Stem Cell Transplantation for Late-Onset Krabbe Disease

Loddenkemper, T.

Therapy and Clinical Course in 52 Patients with PCDH19 Mutations

Loges, N.

Subcellular Analysis of the Motor Protein Apparatus in Ependymal Cilia

Lotte, J.

Therapy and Clinical Course in 52 Patients with PCDH19 Mutations

Lücke, T.

Infantile Manifestation of a Mitochondriopathy due to a Homozygous Mutation in DARS2 Gene
Rolandic Epilepsy: Retrospective Analysis of Neuropsychological and Clinical Data
Cognitive Development in Children with Rolandic Epilepsy: Results of a Current PubMed Search
Therapeutic Options in Treatment of Juvenile Huntington Disease: Difference to Adult Patients

Luntz, S.

Neurological Multicenter Clinical Research in Vulnerable Populations: Variability in Institutional Review Boards' Responses

Lustenberger, A.

Pontocerebellar Hypoplasia Type 9: A New Subtype

Lütschg, J.

Spinal Cord Monitoring in Patients with SMA Type III: A Case Report

Lutz, N.

Neurological Multicenter Clinical Research in Vulnerable Populations: Variability in Institutional Review Boards' Responses

Lutz, S.

Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Growth and Endocrinological Evaluation in Autosomal Recessive Proximal Spinal Muscular Atrophies Type I–III
X-Linked Myotubular Myopathy Clinical Improvement by Use of Pyridostigmine in an Infant