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Jean Pouget

Showing results (51-60 of 113) with videos related to

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Annals of Neurology|October 27, 2011
Molecular combing reveals allelic combinations in facioscapulohumeral dystrophyKarine Nguyen, Pierre Walrafen, Rafaëlle Bernard, et al.
Medecine Sciences : M/S|November 13, 2018
[Towards an harmonization of diagnosis by NGS of neuromuscular diseases - Actions of the Molecular Genetics sub-group of FILNEMUS]Aurélien Perrin, Philippe Latour, Vincent Procaccio, et al.
The Journal of Rheumatology|August 2, 2006
Platelet-endothelial cell adhesion molecule-1 and CD146: soluble levels and in situ expression of cellular adhesion molecules implicated in the cohesion of endothelial cells in idiopathic inflammatory myopathiesDominique Figarella-Branger, Nicolas Schleinitz, Brigitte Boutière-Albanèse, 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.
Journal of the Neurological Sciences|March 4, 2015
Letter to the Editor on a paper by Hsiao C-T, Tsai P-C, Liao Y-C, Lee Y-C, Soong B-W. C9ORF72 repeat expansion is not a significant cause of late-onset cerebellar ataxia syndrome. J Neurol Sci 2014;347:322-324Morgane Plutino, Annabelle Chaussenot, Samira Ait-El-Mkadem, et al.
Neurology and Therapy|March 24, 2019
Efficacy and Safety of Octagam® in Patients With Chronic Inflammatory Demyelinating PolyneuropathyChafké Belmokhtar, Pierre Lozeron, David Adams, et al.
Muscle & Nerve|July 23, 2013
Association between structural and functional corticospinal involvement in amyotrophic lateral sclerosis assessed by diffusion tensor MRI and triple stimulation techniqueAude-Marie Grapperon, Annie Verschueren, Yann Duclos, et al.
Human Mutation|July 13, 2005
Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathiesKarine Nguyen, Guillaume Bassez, Rafaëlle Bernard, et al.
Medicine|December 28, 2012
Correlation of clinicoserologic and pathologic classifications of inflammatory myopathies: study of 178 cases and guidelines for diagnosisCarla Fernandez, Nathalie Bardin, André Maues De Paula, et al.
Archives of Physical Medicine and Rehabilitation|October 3, 2007
Development of a French isometric strength normative database for adults using quantitative muscle testingJean-Yves Hogrel, Christine A Payan, Gwenn Ollivier, et al.
Pageof 12

Showing results (51-60 of 113) with videos related to

Sort By:
Pageof 12
Annals of Neurology|October 27, 2011
Molecular combing reveals allelic combinations in facioscapulohumeral dystrophyKarine Nguyen, Pierre Walrafen, Rafaëlle Bernard, et al.
Medecine Sciences : M/S|November 13, 2018
[Towards an harmonization of diagnosis by NGS of neuromuscular diseases - Actions of the Molecular Genetics sub-group of FILNEMUS]Aurélien Perrin, Philippe Latour, Vincent Procaccio, et al.
The Journal of Rheumatology|August 2, 2006
Platelet-endothelial cell adhesion molecule-1 and CD146: soluble levels and in situ expression of cellular adhesion molecules implicated in the cohesion of endothelial cells in idiopathic inflammatory myopathiesDominique Figarella-Branger, Nicolas Schleinitz, Brigitte Boutière-Albanèse, 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.
Journal of the Neurological Sciences|March 4, 2015
Letter to the Editor on a paper by Hsiao C-T, Tsai P-C, Liao Y-C, Lee Y-C, Soong B-W. C9ORF72 repeat expansion is not a significant cause of late-onset cerebellar ataxia syndrome. J Neurol Sci 2014;347:322-324Morgane Plutino, Annabelle Chaussenot, Samira Ait-El-Mkadem, et al.
Neurology and Therapy|March 24, 2019
Efficacy and Safety of Octagam® in Patients With Chronic Inflammatory Demyelinating PolyneuropathyChafké Belmokhtar, Pierre Lozeron, David Adams, et al.
Muscle & Nerve|July 23, 2013
Association between structural and functional corticospinal involvement in amyotrophic lateral sclerosis assessed by diffusion tensor MRI and triple stimulation techniqueAude-Marie Grapperon, Annie Verschueren, Yann Duclos, et al.
Human Mutation|July 13, 2005
Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathiesKarine Nguyen, Guillaume Bassez, Rafaëlle Bernard, et al.
Medicine|December 28, 2012
Correlation of clinicoserologic and pathologic classifications of inflammatory myopathies: study of 178 cases and guidelines for diagnosisCarla Fernandez, Nathalie Bardin, André Maues De Paula, et al.
Archives of Physical Medicine and Rehabilitation|October 3, 2007
Development of a French isometric strength normative database for adults using quantitative muscle testingJean-Yves Hogrel, Christine A Payan, Gwenn Ollivier, et al.
Pageof 12