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M Vallat

Showing results (331-340 of 370) with videos related to

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Neuroepidemiology|January 1, 1996
Survival prediction in sporadic amyotrophic lateral sclerosis. Age and clinical form at onset are independent risk factorsP M Preux, P Couratier, F Boutros-Toni, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1M Tazir, J M Vallat, P Bomont, et al.
European Journal of Neurology|November 27, 2019
Antibody- and macrophage-mediated segmental demyelination in chronic inflammatory demyelinating polyneuropathy: clinical, electrophysiological, immunological and pathological correlatesJ-M Vallat, S Mathis, E Vegezzi, et al.
Neurology|April 23, 2003
Interferon beta-1a as an investigational treatment for CIDPJ-M Vallat, A F Hahn, J-M Léger, et al.
Headache|November 1, 1993
Prevalence of headache in a representative sample of the population in a French department (Haute-Vienne-Limousin)M Munoz, M Dumas, F Boutros-Toni, et al.
Journal of Medical Genetics|July 5, 2003
Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutationsA De Sandre-Giovannoli, M Chaouch, I Boccaccio, et al.
Annales De Medecine Interne|January 1, 1993
[Spastic paraplegia and polymyositis associated with HTLV-1 in a Togolese patient]K E Grunitzky, M Mijiyawa, A Vovor, et al.
Revue Neurologique|January 1, 1988
[A neuro-epidemiologic survey in a Limousin town]M Munoz, M Dumas, F Boutros-Toni, et al.
Revue Neurologique|May 26, 1999
[Cerebral miliary granulomatosis with Histoplasma capsulatum in an HIV seronegative patient]M Hadi, M P Boncoeur-Martel, B Bouteille, et al.
Human Molecular Genetics|September 1, 1995
Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. The French CMT Collaborative Research GroupE LeGuern, R Gouider, J Lopes, et al.
Pageof 37

Showing results (331-340 of 370) with videos related to

Sort By:
Pageof 37
Neuroepidemiology|January 1, 1996
Survival prediction in sporadic amyotrophic lateral sclerosis. Age and clinical form at onset are independent risk factorsP M Preux, P Couratier, F Boutros-Toni, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1M Tazir, J M Vallat, P Bomont, et al.
European Journal of Neurology|November 27, 2019
Antibody- and macrophage-mediated segmental demyelination in chronic inflammatory demyelinating polyneuropathy: clinical, electrophysiological, immunological and pathological correlatesJ-M Vallat, S Mathis, E Vegezzi, et al.
Neurology|April 23, 2003
Interferon beta-1a as an investigational treatment for CIDPJ-M Vallat, A F Hahn, J-M Léger, et al.
Headache|November 1, 1993
Prevalence of headache in a representative sample of the population in a French department (Haute-Vienne-Limousin)M Munoz, M Dumas, F Boutros-Toni, et al.
Journal of Medical Genetics|July 5, 2003
Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutationsA De Sandre-Giovannoli, M Chaouch, I Boccaccio, et al.
Annales De Medecine Interne|January 1, 1993
[Spastic paraplegia and polymyositis associated with HTLV-1 in a Togolese patient]K E Grunitzky, M Mijiyawa, A Vovor, et al.
Revue Neurologique|January 1, 1988
[A neuro-epidemiologic survey in a Limousin town]M Munoz, M Dumas, F Boutros-Toni, et al.
Revue Neurologique|May 26, 1999
[Cerebral miliary granulomatosis with Histoplasma capsulatum in an HIV seronegative patient]M Hadi, M P Boncoeur-Martel, B Bouteille, et al.
Human Molecular Genetics|September 1, 1995
Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. The French CMT Collaborative Research GroupE LeGuern, R Gouider, J Lopes, et al.
Pageof 37