DOI : 10.1055/s-00000041

Neuropediatrics

Issue 02 · Volume 36 · April 2005 DOI: 10.1055/s-002-4024


Abstracts of the 31st Annual Meeting of the Society for Neuropediatrics (Gesellschaft für Neuropädiatrie)
Erlangen, Germany, 21 –23, April 2005

Scientific Organisation: R. Trollmann D. Wenzel
Abstracts (HTML) List of Authors
P8
Boda, V.; Fischer, D.; Vlaho, S.; Bauer, K.; Kieslich, M.: A rare differential diagnosis of severe neonatal muscular hypotonia with respiratory distress: Myotubular myopathy (MTM 1) with detection of a new complex mutation in myotubularin gene
P9
von der Hagen, M.; Mitzscherling, P.; Köhler, K.; Kaindl, A.; Stoltenburg-Didinger, G.; Hübner, A.: Acute reversible muscle weakness in two infants with limb girdle muscular dystrophy (LGMD) 2I and identification of a novel missense mutation in the FKRP gene
P10
Schessl, J.; Kirschner, J.; Korinthenberg, R.: Clinical trial 'immunosuppressive treatment in Duchenne muscular dystrophy' – update
P11
Ramelli, G. P.; Hammer, J.: Swiss physicians' practices of long-term mechanical ventilatory support of children and adolescent with Duchenne muscular dystrophy
P12
Smitka, M.; von der Hagen, M.; Kaindl, A.; Gilitzer, C.; Dumontier, J.; Nicolino, M.; Heubner, G.: Cardiac and motor improvement with enzyme replacement therapy in a patient with infantile-onset Pompe disease
P13
Marquard, K.; Rautenstrauss, B.; Huehne, K.; Sasse, B.; Wörle, H.; Keimer, R.: Giant Axonal Neuropathy – a neurodegenerative disorder – a novel mutation in the GAN-Gen
P14
Hasselmann, O.; Künzle, C.; Barben, J.; Huemer, C.: Myopathic sarcoidosis, an interdisciplinary challenge
P15
van Baalen, A.; Wiegand, G.; Stephani, U.: High resolution micro-ultrasound in neuromuscular disorders