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P Bouche

Showing results (71-80 of 158) with videos related to

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Brain : a Journal of Neurology|January 3, 2001
Intravenous immunoglobulin therapy in multifocal motor neuropathy: a double-blind, placebo-controlled studyJ M Léger, B Chassande, L Musset, et al.
Revue Neurologique|January 3, 2009
[Multifocal motor neuropathy: a retrospective study of sensory nerve conduction velocities in long-term follow-up of 21 patients]I Lievens, E Fournier, K Viala, et al.
Neurology|January 1, 1994
Genetic expression of a transthyretin mutation in a case of amyloidotic polyneuropathy occurring in an AfricanJ M Léger, G Grateau, M Gugenheim, et al.
Journal of Medical Genetics|November 1, 1992
Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research GroupA Brice, N Ravisé, G Stevanin, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|October 1, 1989
Cervical magnetic stimulation: a new painless method for bilateral phrenic nerve stimulation in conscious humansT Similowski, B Fleury, S Launois, et al.
Presse Medicale (Paris, France : 1983)|October 10, 1987
[Peripheral neuropathies in relation to HIV infection]J M Leger, P Chaine, P Bouche, et al.
European Journal of Neurology|December 4, 2003
Polyneuropathy associated with IgG/IgA monoclonal gammopathy: a clinical and electrophysiological study of 15 casesL Magy, B Chassande, T Maisonobe, et al.
Revue Des Maladies Respiratoires|January 1, 1988
[Cervical magnetic stimulation. A new method of bilateral phrenic nerve stimulation for use in clinical practice]T Similowski, B Fleury, S Launois, et al.
Muscle & Nerve|September 26, 2000
Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weaknessO Dubourg, C Barhoumi, H Azzedine, et al.
Muscle & Nerve|June 12, 1999
Polyneuropathy in autosomal dominant cerebellar ataxias: phenotype-genotype correlationN Kubis, A Dürr, M Gugenheim, et al.
Pageof 16

Showing results (71-80 of 158) with videos related to

Sort By:
Pageof 16
Brain : a Journal of Neurology|January 3, 2001
Intravenous immunoglobulin therapy in multifocal motor neuropathy: a double-blind, placebo-controlled studyJ M Léger, B Chassande, L Musset, et al.
Revue Neurologique|January 3, 2009
[Multifocal motor neuropathy: a retrospective study of sensory nerve conduction velocities in long-term follow-up of 21 patients]I Lievens, E Fournier, K Viala, et al.
Neurology|January 1, 1994
Genetic expression of a transthyretin mutation in a case of amyloidotic polyneuropathy occurring in an AfricanJ M Léger, G Grateau, M Gugenheim, et al.
Journal of Medical Genetics|November 1, 1992
Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research GroupA Brice, N Ravisé, G Stevanin, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|October 1, 1989
Cervical magnetic stimulation: a new painless method for bilateral phrenic nerve stimulation in conscious humansT Similowski, B Fleury, S Launois, et al.
Presse Medicale (Paris, France : 1983)|October 10, 1987
[Peripheral neuropathies in relation to HIV infection]J M Leger, P Chaine, P Bouche, et al.
European Journal of Neurology|December 4, 2003
Polyneuropathy associated with IgG/IgA monoclonal gammopathy: a clinical and electrophysiological study of 15 casesL Magy, B Chassande, T Maisonobe, et al.
Revue Des Maladies Respiratoires|January 1, 1988
[Cervical magnetic stimulation. A new method of bilateral phrenic nerve stimulation for use in clinical practice]T Similowski, B Fleury, S Launois, et al.
Muscle & Nerve|September 26, 2000
Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weaknessO Dubourg, C Barhoumi, H Azzedine, et al.
Muscle & Nerve|June 12, 1999
Polyneuropathy in autosomal dominant cerebellar ataxias: phenotype-genotype correlationN Kubis, A Dürr, M Gugenheim, et al.
Pageof 16