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Vincent Meininger

Showing results (101-110 of 142) with videos related to

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Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|October 26, 2011
Diaphragm pacing improves sleep in patients with amyotrophic lateral sclerosisJesus Gonzalez-Bermejo, Capucine Morélot-Panzini, François Salachas, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 27, 2010
Impaired glucose tolerance in patients with amyotrophic lateral sclerosisPierre-Francois Pradat, Gaelle Bruneteau, Paul H Gordon, et al.
Neuro-Degenerative Diseases|September 22, 2011
Muscle gene expression is a marker of amyotrophic lateral sclerosis severityPierre-François Pradat, Odile Dubourg, Marc de Tapia, et al.
Annals of Neurology|April 8, 2009
TARDBP mutations in motoneuron disease with frontotemporal lobar degenerationLina Benajiba, Isabelle Le Ber, Agnès Camuzat, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 25, 2018
The motor unit number index (MUNIX) profile of patients with adult spinal muscular atrophyGiorgia Querin, Timothée Lenglet, Rabab Debs, et al.
Neurobiology of Aging|January 12, 2011
Screening of OPTN in French familial amyotrophic lateral sclerosisStéphanie Millecamps, Séverine Boillée, Elodie Chabrol, et al.
International Journal of Molecular Sciences|May 28, 2022
The Amyotrophic Lateral Sclerosis M114T PFN1 Mutation Deregulates Alternative Autophagy Pathways and Mitochondrial HomeostasisElisa Teyssou, Laura Chartier, Delphine Roussel, et al.
Human Mutation|April 10, 2013
A rare motor neuron deleterious missense mutation in the DPYSL3 (CRMP4) gene is associated with ALSHélène Blasco, Nathalie Bernard-Marissal, Patrick Vourc'h, et al.
Journal of Medical Genetics|April 14, 2012
Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genesStéphanie Millecamps, Séverine Boillée, Isabelle Le Ber, et al.
Human Molecular Genetics|March 1, 2013
Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosisEdor Kabashi, Hajer El Oussini, Valérie Bercier, et al.
Pageof 15

Showing results (101-110 of 142) with videos related to

Sort By:
Pageof 15
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|October 26, 2011
Diaphragm pacing improves sleep in patients with amyotrophic lateral sclerosisJesus Gonzalez-Bermejo, Capucine Morélot-Panzini, François Salachas, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 27, 2010
Impaired glucose tolerance in patients with amyotrophic lateral sclerosisPierre-Francois Pradat, Gaelle Bruneteau, Paul H Gordon, et al.
Neuro-Degenerative Diseases|September 22, 2011
Muscle gene expression is a marker of amyotrophic lateral sclerosis severityPierre-François Pradat, Odile Dubourg, Marc de Tapia, et al.
Annals of Neurology|April 8, 2009
TARDBP mutations in motoneuron disease with frontotemporal lobar degenerationLina Benajiba, Isabelle Le Ber, Agnès Camuzat, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 25, 2018
The motor unit number index (MUNIX) profile of patients with adult spinal muscular atrophyGiorgia Querin, Timothée Lenglet, Rabab Debs, et al.
Neurobiology of Aging|January 12, 2011
Screening of OPTN in French familial amyotrophic lateral sclerosisStéphanie Millecamps, Séverine Boillée, Elodie Chabrol, et al.
International Journal of Molecular Sciences|May 28, 2022
The Amyotrophic Lateral Sclerosis M114T PFN1 Mutation Deregulates Alternative Autophagy Pathways and Mitochondrial HomeostasisElisa Teyssou, Laura Chartier, Delphine Roussel, et al.
Human Mutation|April 10, 2013
A rare motor neuron deleterious missense mutation in the DPYSL3 (CRMP4) gene is associated with ALSHélène Blasco, Nathalie Bernard-Marissal, Patrick Vourc'h, et al.
Journal of Medical Genetics|April 14, 2012
Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genesStéphanie Millecamps, Séverine Boillée, Isabelle Le Ber, et al.
Human Molecular Genetics|March 1, 2013
Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosisEdor Kabashi, Hajer El Oussini, Valérie Bercier, et al.
Pageof 15