DOI : 10.1055/s-00000041

Neuropediatrics

Ausgabe S 01 · Volume 47 · April 2016 DOI: 10.1055/s-006-31610


Abstracts of the 42nd Annual Meeting of the Society for Neuropediatrics
Bochum, 21–24 April 2016

Chair: Prof. Dr. med. Ulrike Schara, Department of Neuropediatrics, Developmental Medicine and Social Pediatrics, University Children's Hospital Essen, University Duisburg-Essen, Essen, Germany; Co-Chair: Prof. Dr. med. Thomas Lüke, Department of Neuropediatrics, University Children's Hospital, Ruhr-University Bochum, Bochum, Germany
Abstracts (HTML) Autorenliste
PS01-01
Tibussek, D.; Harmsen, S.; Klee, D.; Horn, A.; Karenfort, M.; Distelmaier, F.; Mayatepek, E.: Rare Causes of Childhood Stroke: A Single-Center Experience
PS01-02
Korinthenberg, R.; Klemann, C.; Sacco, E.; Kirschner, J.: Chronic Hemolysis, Steroid-Dependent CIDP, and Progressive Moya-Moya Disease Due to Hereditary Immune Dysregulation
PS01-03
Sträter, R.; Althaus, J.; Fiedler, B.; Groll, A.; Schwindt, W.; Omran, H.; Rössig, C.: Attention after Thrombectomy in Pediatric Stroke: Keep in Mind the Possibility of a Progressive Stenosing Cerebral Vasculopathy
PS01-04
Feder, L.; Nissen, A.; Bulst, S.; Dusl, M.; Senderek, J.; Walter, M. C.; Schara, U.; Della, Marina A.; Kölbel, Heike; Lochmüller, H.; Benet-Pagès, A.; Abicht, A.: Congenital Myasthenic Syndromes: Efficiency and Pitfalls of Phenotype-Based Gene Panel Testing
PS01-05
Wibbeler, E.; Della, Marina A.; Abicht, A.; Lochmüller, H.; Schara, U.: Long-Term Follow-Up of Patients with Congenital Myasthenic Syndromes: What Do We Learn?
PS01-06
Schorling, D.; Rost, S.; Korinthenberg, R.; Krüger, M.; Beytia, M.; Müller, C. R.; Bönnemann, C.; Kirschner, J.: Early Lethal Neurodegeneration with Myasthenic and Myopathic Features: A New Genetic Syndrome Due to Previously Undescribed ALG14 Mutations
PS01-07
Methling, B.; Thiels, C.; Heyer, C.; Mengel, E.; Lücke, T.: α-Fucosidase Deficiency: A Rare Differential Diagnosis of the Eye-of-the-Tiger Sign and Extrapyramidal Movement Disorders
PS01-08
Hackenberg, A.; Joset, P.; Schmitt, B.; Plecko, B.: Severe Intellectual Disability with Speech Delay, Clumsiness, and Drug Responsive Epilepsy in a Boy with GAMT Deficiency
PS01-10
Korenke, G. C.; Nuoffer, J-M.; Alhaddad, B.; Mayr, H.; Prokisch, H.; Haack, T. B.: Paroxysmal Dyskinesia in ECHS1 Defect with Globus Pallidus Lesions
PS01-11
Thiels, Ch.; Hoffjan, S.; Köhler, C.; Wolff, M.; Lücke, T.: SCN2A A Sequence Variant in Mosaic State in a Patient with Infantile Epileptic Encephalopathy
PS01-12
Wilichowski, E.; Erdlenbruch, B.; Ohlenbusch, A.; Gärtner, J.: A New Mitochondrial tRNA(Met)—Gene Mutation in a 12-Year-Old Boy with MELAS: Clinical Presentation and Effects of Arginine Treatment
PS01-13
Fischer, M.; Steinert, M.; Köhler, C.; Thiels, Ch.; Lücke, T.: Cockayne Syndrome: Two Siblings with Neurodegenerative Disease and Infection-Associated Deterioration
PS01-17
Hennes, E.; Baumann, M.; Schimmel, M.; Karenfort, M.; Häusler, M.; Bajer-Kornek, B.; Blaschek, A.; Leiz, S.; Gotwald, T.; Berger, T.; Reindl, M.; Rostasy, K.: Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children