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European Journal of Neurology|January 5, 2011
Non-anti-MAG DADS neuropathy as a variant of CIDP: clinical, electrophysiological, laboratory features and response to treatment in 10 casesS Larue, F Bombelli, K Viala, et al.
Revue Medicale De Liege|July 13, 2004
[The hypolossal-facial anastomosis in man. A model for studying peripheral and central nervous system plasticity]F Tankéré, I Bernat, E Vitte, et al.
Neuromuscular Disorders : NMD|September 1, 1994
Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11-Xq21 microsatellites in a new large family: three new markers are closely linked to the geneE Le Guern, N Ravise, M Gugenheim, et al.
Journal of the Neurological Sciences|October 6, 2000
Blood oxidative stress in amyotrophic lateral sclerosisD Bonnefont-Rousselot, L Lacomblez, M Jaudon, et al.
Revue Neurologique|January 1, 1984
[Methylation of erythrocyte membrane phospholipids: correlation with membrane viscosity. Study of normal and parkinsonian subjects]V Meininger, T Phan, J C Camelin, et al.
Neurology|June 14, 2006
The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type VO Dubourg, H Azzedine, R Ben Yaou, et al.
The European Respiratory Journal|March 8, 2000
Diaphragmatic dysfunction and dyspnoea in amyotrophic lateral sclerosisT Similowski, V Attali, G Bensimon, et al.
Human Molecular Genetics|January 1, 1996
A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2?E LeGuern, R Gouider, N Ravisé, et al.
Neurology|December 1, 1994
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entitiesR Gouider, E LeGuern, J Emile, et al.
American Journal of Human Genetics|June 1, 1996
Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research GroupJ Lopes, E LeGuern, R Gouider, et al.
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