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Revue Neurologique|February 29, 2000
[True neurological thoracic outlet syndrome]N Le Forestier, P Mouton, T Maisonobe, et al.Annals of Neurology|January 1, 1997
Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A diseaseE LeGuern, R Gouider, D Mabin, et al.Cytogenetics and Cell Genetics|January 1, 1996
Microsatellite mapping of the deletion in patients with hereditary neuropathy with liability to pressure palsies (HNPP): new molecular tools for the study of the region 17p12 --> p11 and for diagnosisE LeGuern, N Ravise, R Gouider, et al.Revue Neurologique|January 1, 1993
[Paraneoplastic myasthenic syndrome]J M Léger, A C Bachoud-Lévi, B Eymard, et al.Revue Neurologique|January 1, 1986
[Chloroquine neuromyopathies: 4 cases during antimalarial prevention]J M Léger, H Puifoulloux, S Dancea, et al.Revue Neurologique|January 1, 1988
[Pigmentary orthochromatic leukodystrophy. Van Bogaert and Nyssen disease]L Belec, F Gray, F Louarn, et al.Revue Neurologique|January 1, 1981
[Mutations affecting myelination in the mouse; their correlation to human diseases (author's transl)]N Baumann, J M Bourre, C Jacque, et al.Human Molecular Genetics|October 1, 1994
Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosisD A Figlewicz, A Krizus, M G Martinoli, et al.Journal of Medical Genetics|October 22, 2008
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosisH Daoud, P N Valdmanis, E Kabashi, et al.Neurology|December 1, 1996
A confirmatory dose-ranging study of riluzole in ALS. ALS/Riluzole Study Group-IIL Lacomblez, G Bensimon, P N Leigh, et al.Pageof 32