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Christophe Vial

Showing results (31-40 of 61) with videos related to

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Muscle & Nerve|October 28, 2006
Granulomatous myositis: a clinical study of thirteen casesKarine Le Roux, Nathalie Streichenberger, Christophe Vial, et al.
American Journal of Epidemiology|June 10, 2011
Guillain-Barre syndrome, influenzalike illnesses, and influenza vaccination during seasons with and without circulating A/H1N1 virusesLamiae Grimaldi-Bensouda, Annick Alpérovitch, Gérard Besson, et al.
Annals of Surgery|March 21, 2014
Outcomes after bilateral hand allotransplantation: a risk/benefit ratio analysisPalmina Petruzzo, Aram Gazarian, Jean Kanitakis, et al.
Journal of Neurology|December 20, 2011
Clinical and electrophysiological characteristics of neuropathy associated with Tangier diseaseJulie Zyss, Anthony Béhin, Philippe Couvert, et al.
Journal of the Peripheral Nervous System : JPNS|June 22, 2006
SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutationsPhilippe Latour, Pierre-Marie Gonnaud, Elisabeth Ollagnon, et al.
Annals of Neurology|June 21, 2006
Cold extends electromyography distinction between ion channel mutations causing myotoniaEmmanuel Fournier, Karine Viala, Hélène Gervais, et al.
Neurology|May 14, 2013
Placebo-controlled trial of rituximab in IgM anti-myelin-associated glycoprotein neuropathyJean-Marc Léger, Karine Viala, Guillaume Nicolas, et al.
European Journal of Endocrinology|December 15, 2017
Triple-A syndrome: a wide spectrum of adrenal dysfunctionFlorence Roucher-Boulez, Aude Brac de la Perriere, Aude Jacquez, et al.
Journal of Neurology|August 17, 2023
Myasthenia gravis treatment in the elderly presents with a significant iatrogenic risk: a multicentric retrospective studyJean-Baptiste Chanson, Françoise Bouhour, Anne-Catherine Aubé-Nathier, et al.
Orphanet Journal of Rare Diseases|April 12, 2020
The French national protocol for Kennedy's disease (SBMA): consensus diagnostic and management recommendationsPierre-François Pradat, Emilien Bernard, Philippe Corcia, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Muscle & Nerve|October 28, 2006
Granulomatous myositis: a clinical study of thirteen casesKarine Le Roux, Nathalie Streichenberger, Christophe Vial, et al.
American Journal of Epidemiology|June 10, 2011
Guillain-Barre syndrome, influenzalike illnesses, and influenza vaccination during seasons with and without circulating A/H1N1 virusesLamiae Grimaldi-Bensouda, Annick Alpérovitch, Gérard Besson, et al.
Annals of Surgery|March 21, 2014
Outcomes after bilateral hand allotransplantation: a risk/benefit ratio analysisPalmina Petruzzo, Aram Gazarian, Jean Kanitakis, et al.
Journal of Neurology|December 20, 2011
Clinical and electrophysiological characteristics of neuropathy associated with Tangier diseaseJulie Zyss, Anthony Béhin, Philippe Couvert, et al.
Journal of the Peripheral Nervous System : JPNS|June 22, 2006
SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutationsPhilippe Latour, Pierre-Marie Gonnaud, Elisabeth Ollagnon, et al.
Annals of Neurology|June 21, 2006
Cold extends electromyography distinction between ion channel mutations causing myotoniaEmmanuel Fournier, Karine Viala, Hélène Gervais, et al.
Neurology|May 14, 2013
Placebo-controlled trial of rituximab in IgM anti-myelin-associated glycoprotein neuropathyJean-Marc Léger, Karine Viala, Guillaume Nicolas, et al.
European Journal of Endocrinology|December 15, 2017
Triple-A syndrome: a wide spectrum of adrenal dysfunctionFlorence Roucher-Boulez, Aude Brac de la Perriere, Aude Jacquez, et al.
Journal of Neurology|August 17, 2023
Myasthenia gravis treatment in the elderly presents with a significant iatrogenic risk: a multicentric retrospective studyJean-Baptiste Chanson, Françoise Bouhour, Anne-Catherine Aubé-Nathier, et al.
Orphanet Journal of Rare Diseases|April 12, 2020
The French national protocol for Kennedy's disease (SBMA): consensus diagnostic and management recommendationsPierre-François Pradat, Emilien Bernard, Philippe Corcia, et al.
Pageof 7