DOI : 10.1055/s-00000041

Neuropediatrics

Issue S 01 · Volume 48 · April 2017 DOI: 10.1055/s-007-33900


Abstracts of the 43rd Annual Meeting of the Society for Neuropediatrics
Bad Nauheim, 27. to 30.04.2017

Chair: Prof. Dr. Bernd A. Neubauer, MD, Department of Pediatric Neurology, University Hospital Giessen, Giessen, Germany
Abstracts (HTML) List of Authors
OP01
Brockmann, K.; Warthemann, Rita; Schröder, Simone: The Acquisition of Rare Neurological Disorders in Childhood (”ESNEK”): First Interim Results after 2 Years
OP02
Bonikowski, M.; Dursun, N.; Carranza, J.; Tilton, A.; Aydin, R.; Unlu, E.; Erhan, B.; Rodriguez, M. L.; Picaut, P.; Grandoulier, A. S.; Delgado, M. R.: Time to Retreatment after AbobotulinumtoxinA (Dysport) Injections in Children with Dynamic Equinus Foot Deformity
OP03
Rosewich, H.; Ohlenbusch, A.; Weise, D.; Brockmann, K.; Gärtner, J.: Acute and Episodic Movement Disorders: ATP1A3-Related Disorders as Differential Diagnosis
OP04
Wallmeier, J.; Weichert, J.; Omram, H.: Ciliogenesis Defect of Multiple Motile Cilia Causes Hydrocephalus
OP05
Reihle, C.; Eitel, H.; Nasko, M.; Schilling, F.; Uhlemann, F.; AlMatter, M.; Henkes, H.; Blankenburg, M.: Time Is Brain: Thrombectomy after Pediatric Stroke in Two Previously Healthy Girls
OP06
Cattani, A.; Kunze, F.; Marquardt, G.; Schubert-Bast, S.; Bartels, Baz M.; Seifert, V.; Freiman, T. M.: What Is the Right Pressure of Shunt Valves in Newborns?
OP07
Hochstein, J.; Nickel, M.; Löbel, U.; Grosser, M.; Sedlacik, J.; Schulz, A.: Longitudinal 8-year Brain Volumetric Analysis in 35 CLN3 Patients: Successful Development of a Sensitive Marker to Measure Clinical Outcome
OP08
Beschle, J.; Groeschel, S.; Kehrer, C.; Strölin, M.; Raabe, C.; Bayha, U.; Bevot, A.; Döring, M.; Grimm, A.; Bender, B.; Krägeloh-Mann, I.: Early Effects after Hematopoietic Stem Cell Transplantation in 13 Children with Juvenile Metachromatic Leukodystrophy
OP09
Distelmaier, F.; Kremer, L.; Danhauser, K.; Herebian, D.; Müller-Felber, W.; Haack, T.; Mayatepek, E.; Strom, T.; Meitinger, T.; Klopstock, T.; Pronicka, E.; Mayr, J.; Baric, I.; Prokisch, H.: NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood
OP10
Zsoter, A.; Hessenauer, M.; Jelesch, E.; Hartlieb, T.; Pieper, T.; Kudernatsch, M.; Staudt, M.: Worsening of Hand Function but Significant Improvement of Abilities Measured in PEDI in a Child with Sturge-Weber Syndrome
OP11
Goebel, A.-M.; Koustenis, E.; Rückriegel, S. M.; Schuelke, M.; Pfuhlmann, L.; Brandsma, R.; Sival, D.; Driever, Hernáiz P.: Motor Function in Pediatric ALL Survivors after Chemotherapy-Only
OP12
Schroeder, A. S.; Berweck, S.; Vill, K.; Gerstl, L.; Jansen, C.; Kappl, S.; Wissel, J.; Fietzek, U.; Heinen, F.; Müller-Felber, W.: Improving the Quality of Care in the Specialization: The Benefits of “Hands-on” Courses for Learning Neuromuscular Ultrasound
OP13
Staudt, M.; Ivanov, I.; Küster, S.; Krumm, A.; Haaga, M.; Cordey, A.; Gehrlich, C.; Trauzettel-Klosinski, S.: Explorative Saccade Training in Children with Homonymous Hemianopia
OP14
Reutlinger, C.; Gebhard, B.; Hennig, B.; Hinrichs, R.: Reintegration to School after Craniocerebral Injury: Results of a Survey
OP15a
Finkel, R.; Kuntz, N.; Mercuri, E.; Muntoni, F.; Chiriboga, C. A.; Darras, B.; Topaloglu, H.; Montes, J.; Su, J.; Zhong, Z. J.; Gheuens, S.; Bennett, C. F.; Schneider, E.; Farwell, W.: Interim Efficacy and Safety Results from the Phase 3 ENDEAR Study of Nusinersen in Infants Diagnosed with Spinal Muscular Atrophy (SMA)
OP15b
Kirschner, Jan; Mercuri, Eugenio; Finkel, Richard S.; Chiriboga, Claudia A.; Kuntz, Nancy; Darras, Basil T.; Shieh, Perry B.; Saito, Kayoko; De Vivo, Darryl C.; Mazzone, Elena S.; Montes, Jacqueline; Yang, Qingqing; Zhong, Zhenshao John; Gheuens, Sarah; Bennett, C Frank; Schneider, Eugene; Farwell, Wildon; on behalf of the CHERISH Study Group: Efficacy and safety of nusinersen in children with later-onset spinal muscular atrophy (SMA): results of the phase 3 CHERISH study
OP16
Mitter, D.; Pringsheim, M.; Kaulisch, M.; Plümacher, K.; Schröder, S.; Warthemann, R.; Malzahn, D.; Zirn, B.; Brockmann, K.: FOXG1 Syndrome: Genotype–Phenotype Association in 84 Patients with FOXG1 Variants
OP17
Zielonka, M.; Garbade, S. F.; Kölker, S.; Hoffmann, G. F.; Ries, M.: Quantitative Clinical Characteristics of 53 Patients with MPS VII: A Cross-Sectional Analysis
OP18
Heimgärtner, M.; Granström, S.; Mautner, V.-F.; Lidzba, K.: ADHD Is a Risk Factor for Cognitive Development in NF1
OP19
Huppke, P.; Huppke, B.; Hummel, H.; Stark, W.; Gärtner, J.: Effect of Modern Therapy on Disease Progression in Pediatric MS
OP20
Straßburg, H. M.: The Foundation of the Society for Neuropediatrics
OP21
Methling, B.; Köhler, C.; Thiels, Ch.; Lücke, Th.: CAPOS-Syndrome: A Rare Differential Diagnosis to Friedreich’s Ataxia
OP22
Slavc, I.; Cohen-Pfeffer, J. L.; Gururangan, S.; Jurecki, E.; Krauser, J.; Lester, T.; Lim, D.; Maldaun, M.; Schwering, C.; Shaywitz, A. J.; Westphal, M.: Expert Opinion on the Management of Intracerebroventricular (ICV) Drug Delivery
OP23
Denecke, J.; Johannsen, J.; Neu, A.; Santer, R.; Kloth, K.; Lüttgen, S.; Strom, T.; Haack, T.; Mahler, E.; Kubisch, C.; Lessel, D.; Hempel, M.: The Potential of Whole-Exome Sequencing (WES) in Neuropediatric Patients: Single-Center Experience at the University Hospital Hamburg Eppendorf
OP24
Deba, T.; Althaus, J.; Fiedler, B.; Groß, C.; Hinze, C.; Sträter, R.; Lee-Kirsch, M. A.; Omran, H.; Kurlemann, G.: The Enemy Within: Deleterious Consequences of an Inappropriate Antiviral Response for the Central Nervous System
OP25
Oster, I.; Horneff, G.; Stücklin, A.; Müller, K.: Acute Flaccid Myelitis (AFM) Associated with Enterovirus: A Distinct Clinical Entity?