DOI : 10.1055/s-00000041

Neuropediatrics

Ausgabe S 01 · Volume 46 · April 2015 DOI: 10.1055/s-005-28977


Abstracts of the 41st Annual Meeting of the Society of Neuropediatrics
Basel, 23–26 April 2015

Prof. Dr. Peter Weber
Abstracts (HTML) Autorenliste
FV03-01
Schneider, J.; Tacke, U.; Bubl, B.; Datta, A.; Weber, P.: Impact of Advanced MRI Imaging in Acute Stroke-Like Episodes
FV03-02
Boelen, M.; Zsoter, A.; Lidzba, K.; Staudt, M.; Wilke, M.: A Comparison of Language Lateralization as Assessed using Functional MRI using Scanner-Generated versus Externally Calculated Statistical Parameter Maps
FV03-03
Blumberg, J.; LeVan, P.; Körbl, K.; Schulze-Bonhage, A.; Hennig, J.; Jacobs, J.: Fast fMRI Sequence Allows for Analysis of BOLD Responses to Single Interictal Epileptic Spikes
FV03-04
Prehl, I.; Reicherter, K.; Jüngling, J.; Hoffmann, J.; Döcker, M.; Riesch, E.; Puk, O.; Russ, A.; Fehr, S.; Stöbe, P.; Grau, T.; Singh, Y.; Battke, F.; Lemke, J.; Lerche, H.; Biskup, S.; Hörtnagel, K.: Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
FV03-05
Hahn, A.; Hoffmann, J.; Biskup, S.; Reich, B.; Scheer, I.; Mayer, K.; Neubauer, B.: Somatic PIK3CA Mosaic as a Cause of Hemimegalencephaly and Congenital Infiltrating Lipomatosis of the Face
FV03-06
Mohr, J.; Glöckle, N.; Heller, C.; Grau, T.; Gleixner, E.; Bengesser, K.; Wilhelm, C.; Battke, F.; Biskup, S.; Hörtnagel, K.: Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases
FV03-07
Geis, T.; Rödl, T.; Rieß, A.; Schara, U.; Wieczorek, D.; Shamdeen, G.; Hehr, U.; Trippe, H.: Genotype and Phenotype in 34 Families with Genetically Confirmed Walker-Warburg Syndrome or Muscle Eye Brain Disease
FV03-08
Buyse, G.; Meier, T.: Idebenone Reduces Loss of Respiratory Function in Duchenne Muscular Dystrophy: Outcome of a Phase III Double Blind, Randomized, Placebo-Controlled Trial
FV03-09
Poretti, A.; Romani, M.; Mancini, F.; Micalizzi, A.; Miccinilli, E.; Steinlin, M.; Wolf, N.; Boltshauser, E.; Valente, E.: Oral-Facial-Digital Syndrome Type VI: is C5orf42 Really the Major Gene?
FV03-10
Poretti, A.; Mancini, F.; Romani, M.; Micalizzi, A.; Fluss, J.; Koch, J.; Huisman, T.; Valente, E.; Boltshauser, E.: Corpus Callosum Anomalies in Joubert Syndrome: Low Prevalence and Weak Phenotype–Genotype Correlation
FV03-11
Toelle, S.; Poretti, A.; Weber, P.; Seute, T.; Bromberg, J.; Scheer, I.; Boltshauser, E.: Cerebellar Hypoplasia and Dysmorphia in Neurofibromatosis Type 1
FV03-12
Heimgärtner, M.; Granström, S.; Mautner, V.; Lidzba, K.: Executive Dysfunction in Neurofibromatosis Type 1: Comparison to Idiopathic ADHD