Results 241 to 250 of about 49,167 (262)

Charcot-Marie-Tooth disease and sleep apnoea syndrome: a family study

Lancet, The, 2001
Jean Louis Pepin
exaly  

Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene

New England Journal of Medicine, 1993
Ueli Suter, Deanna A Kulpa, James R Lupski   +2 more
exaly  

Central sleep apnoeas in patients with Charcot-Marie-Tooth disease

Lancet, The, 2001
exaly   +2 more sources

Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network

Journal of Cell Biology, 2005
Axel Niemann, Angelo Schenone, Ueli Suter   +2 more
exaly  

Intermediate Charcot–Marie–Tooth disease: an electrophysiological reappraisal and systematic review

Journal of Neurology, 2017
J. Berciano, Antonio G. García, E. Gallardo, K. Peeters, A. Pelayo-Negro, S. Álvarez-Paradelo, J. Gazulla, Miriam Martínez-Tames, J. Infante, A. Jordanova   +9 more
semanticscholar   +1 more source

Soluble neuregulin-1 modulates disease pathogenesis in rodent models of Charcot-Marie-Tooth disease 1A

Nature Medicine, 2014
Robert Fledrich, Ruth M Stassart, Thomas Prukop   +2 more
exaly  

Dynamin 2 mutations in Charcot–Marie–Tooth neuropathy highlight the importance of clathrin-mediated endocytosis in myelination

Brain, 2012
Thomas Bock, Elisa Tinelli, Dies Meijer
exaly  

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

Nature Genetics, 2004
Stephan Zuchner, Maria Muglia, Alessandra M Patitucci   +2 more
exaly  

Diagnosis, natural history, and management of Charcot-Marie-Tooth disease.

Lancet Neurology, 2009
D. Pareyson, C. Marchesi
semanticscholar   +1 more source

Charcot‐Marie‐Tooth Disorders

Neurology, 1990
openaire   +1 more source