DOI : 10.1055/s-00000041

Neuropediatrics

Issue S 01 · Volume 45 · September 2014 DOI: 10.1055/s-004-27711


Abstracts of the 40th Annual Meeting of the Society of Neuropediatrics
Munich, 17–19 September 2014

Prof. Dr. Med. Martin Staudt
Abstracts (HTML) List of Authors
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Kirschner, J.; Dessaud, E.; André, C.; Scherrer, B.; Pruss, R.; Cuvier, V.; Hauke, W.; Müller-Felber, W.; Schara, U.; Walter, M.; Bertini, E.: Results of a Phase II Study to Assess Safety and Efficacy of Olesoxime (TRO19622) in 3- to 25-Year-Old Spinal Muscular Atrophy Patients
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Della Marina, A.; Lutz, S.; Trippe, H.; Schweiger, B.; Neudorf, U.; Schara, U.: Juvenile Dermatomyositis: Analysis of a Single Muscular Center Cohort
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Geis, T.; Müller-Felber, W.; Schirmer, S.; Topaloglu, H.; Hehr, U.: Broad Phenotypic Spectrum of A-Dystroglycanopathies due to POMT1 Mutations in 16 Families
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Giarrana, M.; Joset, P.; Robb, S.; Steindl, K.; Rauch, A.; Klein, A.: Severe Case of Congenital Myasthenic Syndrome with Novel Mutations in MUSK
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Korenke, G.; Marquardt, I.; Leiphold, E.; Bergmann, M.; Kurth, I.: Sensory Autonomic Neuropathy with Analgesia and Gastroenterological Symptoms due to a Mutation in the SCN11A Gene
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Opladen, T.: iNTD: Deep Phenotyping of Inborn Errors of BH4 and Neurotransmitter Metabolism and Evidence-Based International Treatment Guidelines
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Boy, N.; Heringer, J.; Haege, G.; Glahn, E.; Hoffmann, G.; Burgard, P.; Kölker, S.: Development of Neuropsychological Functions in Patients with Glutaric Aciduria Type I
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Waldmeier, S.; Slotbloom, J.; El-Koussy, M.; Springer, E.; Weisstanner, C.; Steinlin, M.: Ataxia in Creatine Deficiency Syndrome
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Makowski, C.; Haack, T.; Prokisch, H.; Burdach, S.: Brown-Vialetto-Van Laere Syndrome: Clinical Course under High-Dose Riboflavin over 2 Years
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Mechler, K.; Mountford, W.; Hoffmann, G.; Ries, M.: Natural History of Molybdenum Cofactor Deficiency
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Brockmann, K.: Erhebung Seltener Neurologischer Erkrankungen im Kindesalter