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Emilien Bernard

Showing results (41-50 of 50) with videos related to

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Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|August 29, 2021
Assessing the upper motor neuron in amyotrophic lateral sclerosis using the triple stimulation technique: A multicenter prospective studyAude-Marie Grapperon, Annie Verschueren, Elisabeth Jouve, et al.
BMJ Neurology Open|February 23, 2026
Bi-allelic intermediate ATXN2 repeat expansions are associated with slow progressing, leg-onset familial ALSKoen Cedric Demaegd, Wouter Koole, Joke Jfa van Vugt, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 31, 2021
Impact of a frequent nearsplice <i>SOD1</i> variant in amyotrophic lateral sclerosis: optimising <i>SOD1</i> genetic screening for gene therapy opportunitiesFrançois Muratet, Elisa Teyssou, Aude Chiot, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 7, 2021
Effect of familial clustering in the genetic screening of 235 French ALS familiesPhilippe Corcia, William Camu, Celine Brulard, et al.
Brain : a Journal of Neurology|December 11, 2023
The new missense G376V-TDP-43 variant induces late-onset distal myopathy but not amyotrophic lateral sclerosisJulia Zibold, Lola E R Lessard, Flavien Picard, et al.
European Journal of Neurology|March 21, 2023
SORD-related peripheral neuropathy in a French and Swiss cohort: Clinical features, genetic analyses, and sorbitol dosagesNicolas Pons, Gorka Fernández-Eulate, Antoine Pegat, et al.
Brain : a Journal of Neurology|July 12, 2025
Brain atrophy patterns in anti-IgLON5 diseaseSelina M Yogeshwar, Frederik Bartels, Thomas Grüter, et al.
Nature Neuroscience|March 25, 2015
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementiaAxel Freischmidt, Thomas Wieland, Benjamin Richter, et al.
Lancet (London, England)|May 12, 2025
Efficacy and safety of low-dose IL-2 as an add-on therapy to riluzole (MIROCALS): a phase 2b, double-blind, randomised, placebo-controlled trialGilbert Bensimon, P Nigel Leigh, Timothy Tree, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2021
High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 familiesMehdi Benkirane, Cecilia Marelli, Claire Guissart, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|August 29, 2021
Assessing the upper motor neuron in amyotrophic lateral sclerosis using the triple stimulation technique: A multicenter prospective studyAude-Marie Grapperon, Annie Verschueren, Elisabeth Jouve, et al.
BMJ Neurology Open|February 23, 2026
Bi-allelic intermediate ATXN2 repeat expansions are associated with slow progressing, leg-onset familial ALSKoen Cedric Demaegd, Wouter Koole, Joke Jfa van Vugt, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 31, 2021
Impact of a frequent nearsplice <i>SOD1</i> variant in amyotrophic lateral sclerosis: optimising <i>SOD1</i> genetic screening for gene therapy opportunitiesFrançois Muratet, Elisa Teyssou, Aude Chiot, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 7, 2021
Effect of familial clustering in the genetic screening of 235 French ALS familiesPhilippe Corcia, William Camu, Celine Brulard, et al.
Brain : a Journal of Neurology|December 11, 2023
The new missense G376V-TDP-43 variant induces late-onset distal myopathy but not amyotrophic lateral sclerosisJulia Zibold, Lola E R Lessard, Flavien Picard, et al.
European Journal of Neurology|March 21, 2023
SORD-related peripheral neuropathy in a French and Swiss cohort: Clinical features, genetic analyses, and sorbitol dosagesNicolas Pons, Gorka Fernández-Eulate, Antoine Pegat, et al.
Brain : a Journal of Neurology|July 12, 2025
Brain atrophy patterns in anti-IgLON5 diseaseSelina M Yogeshwar, Frederik Bartels, Thomas Grüter, et al.
Nature Neuroscience|March 25, 2015
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementiaAxel Freischmidt, Thomas Wieland, Benjamin Richter, et al.
Lancet (London, England)|May 12, 2025
Efficacy and safety of low-dose IL-2 as an add-on therapy to riluzole (MIROCALS): a phase 2b, double-blind, randomised, placebo-controlled trialGilbert Bensimon, P Nigel Leigh, Timothy Tree, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2021
High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 familiesMehdi Benkirane, Cecilia Marelli, Claire Guissart, et al.
Pageof 5