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Vincent Meininger

Showing results (61-70 of 142) with videos related to

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Archives of Neurology|June 15, 2011
Association of long ATXN2 CAG repeat sizes with increased risk of amyotrophic lateral sclerosisHussein Daoud, Véronique Belzil, Sandra Martins, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|March 3, 2010
Quality control of vital capacity as a primary outcome measure during phase III therapeutic clinical trial in amyotrophic lateral sclerosisMohammed Sanjak, Francois Salachas, Elizabeth Frija-Orvoen, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|June 19, 2004
Amyotrophic lateral sclerosis: a consensus viewpoint on designing and implementing a clinical trialP Nigel Leigh, Michael Swash, Yasuo Iwasaki, et al.
Journal of Neurology|January 20, 2012
Improving survival in a large French ALS center cohortPaul H Gordon, François Salachas, Gaelle Bruneteau, et al.
Journal of the Neurological Sciences|February 1, 2011
Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosisHélène Blasco, Patrick Vourc'h, Yann Nadjar, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|September 1, 2011
Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish familyMariusz Berdyński, Magdalena Kuźma-Kozakiewicz, Claudia Ricci, et al.
Acta Neuropathologica|February 19, 2013
Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathologyElisa Teyssou, Takahiro Takeda, Vincent Lebon, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 9, 2011
Abnormalities of satellite cells function in amyotrophic lateral sclerosisPierre-François Pradat, Aude Barani, Julia Wanschitz, et al.
Acta Neuropathologica Communications|December 17, 2014
Mitochondrial abnormalities and low grade inflammation are present in the skeletal muscle of a minority of patients with amyotrophic lateral sclerosis; an observational myopathology studySafa Al-Sarraj, Andrew King, Matt Cleveland, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 9, 2014
The El Escorial criteria: strengths and weaknessesFederica Agosta, Ammar Al-Chalabi, Massimo Filippi, et al.
Pageof 15

Showing results (61-70 of 142) with videos related to

Sort By:
Pageof 15
Archives of Neurology|June 15, 2011
Association of long ATXN2 CAG repeat sizes with increased risk of amyotrophic lateral sclerosisHussein Daoud, Véronique Belzil, Sandra Martins, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|March 3, 2010
Quality control of vital capacity as a primary outcome measure during phase III therapeutic clinical trial in amyotrophic lateral sclerosisMohammed Sanjak, Francois Salachas, Elizabeth Frija-Orvoen, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|June 19, 2004
Amyotrophic lateral sclerosis: a consensus viewpoint on designing and implementing a clinical trialP Nigel Leigh, Michael Swash, Yasuo Iwasaki, et al.
Journal of Neurology|January 20, 2012
Improving survival in a large French ALS center cohortPaul H Gordon, François Salachas, Gaelle Bruneteau, et al.
Journal of the Neurological Sciences|February 1, 2011
Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosisHélène Blasco, Patrick Vourc'h, Yann Nadjar, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|September 1, 2011
Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish familyMariusz Berdyński, Magdalena Kuźma-Kozakiewicz, Claudia Ricci, et al.
Acta Neuropathologica|February 19, 2013
Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathologyElisa Teyssou, Takahiro Takeda, Vincent Lebon, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 9, 2011
Abnormalities of satellite cells function in amyotrophic lateral sclerosisPierre-François Pradat, Aude Barani, Julia Wanschitz, et al.
Acta Neuropathologica Communications|December 17, 2014
Mitochondrial abnormalities and low grade inflammation are present in the skeletal muscle of a minority of patients with amyotrophic lateral sclerosis; an observational myopathology studySafa Al-Sarraj, Andrew King, Matt Cleveland, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 9, 2014
The El Escorial criteria: strengths and weaknessesFederica Agosta, Ammar Al-Chalabi, Massimo Filippi, et al.
Pageof 15