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Neuromolecular Medicine|June 16, 2006
Molecular diagnostics of Charcot-Marie-Tooth disease and related peripheral neuropathiesKinga Szigeti, Eva Nelis, James R Lupski
BMC Cell Biology|November 27, 2002
Tracing myelin protein zero (P0) in vivo by construction of P0-GFP fusion proteinsArif B Ekici, Sevinc Oezbey, Christina Fuchs, et al.
Journal of the Peripheral Nervous System : JPNS|July 2, 2002
Mutation analysis of 12 candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3Joy Irobi, Eva Nelis, Kristien Verhoeven, et al.
Journal of Neurology|June 19, 2008
Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutationElena Gallardo, Kristl G Claeys, Eva Nelis, et al.
Neuromuscular Disorders : NMD|October 17, 2003
Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth diseaseNadia Ammar, Eva Nelis, Luciano Merlini, et al.
Muscle & Nerve|March 31, 2004
Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophyGert Hünermund, Anja Schirmacher, Bernd Ringelstein, et al.
Neuromuscular Disorders : NMD|January 27, 2009
Peripheral neuropathy and 46XY gonadal dysgenesis: a heterogeneous entityJonathan Baets, Ines Dierick, Chantal Ceuterick-de Groote, et al.
Brain : a Journal of Neurology|February 5, 2003
Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathyJan Senderek, Carsten Bergmann, Vincent T Ramaekers, et al.
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