Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Christophe Vial

Showing results (51-60 of 61) with videos related to

Pageof 7
Sort By:
Muscle & Nerve|April 14, 2017
Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteriaFlorence Robert-Varvat, Guillemette Jousserand, Françoise Bouhour, et al.
Neurology|October 25, 2013
Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutationsKarine Auré, Odile Dubourg, Claude Jardel, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 25, 2012
Regional difference and similarity of familial amyloidosis with polyneuropathy in FranceDavid Adams, Pierre Lozeron, Marie Theaudin, et al.
Parkinsonism & Related Disorders|November 6, 2017
Incobotulinum toxin A in Parkinson's disease with foot dystonia: A double blind randomized trialIsabelle Rieu, Bertrand Degos, Giovanni Castelnovo, et al.
Respiratory Care|January 17, 2013
Absence of airway secretion accumulation predicts tolerance of noninvasive ventilation in subjects with amyotrophic lateral sclerosisNadia Vandenberghe, Anne-Evelyne Vallet, Thierry Petitjean, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 27, 2017
Anti-MAG antibodies in 202 patients: clinicopathological and therapeutic featuresJuliette Svahn, Philippe Petiot, Jean-Christophe Antoine, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|December 15, 2022
Immune-Mediated Rippling Muscle Disease Associated With Thymoma and Anti-MURC/Cavin-4 AutoantibodiesJuliette Svahn, Laurent Coudert, Nathalie Streichenberger, et al.
Orphanet Journal of Rare Diseases|January 22, 2015
Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter studyEmmanuelle Salort-Campana, Karine Nguyen, Rafaelle Bernard, et al.
Neurology|April 14, 2019
FSHD1 and FSHD2 form a disease continuumSabrina Sacconi, Audrey Briand-Suleau, Marilyn Gros, et al.
Nature Communications|March 29, 2019
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusionsMontse Olivé, Martin Engvall, Gianina Ravenscroft, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Muscle & Nerve|April 14, 2017
Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteriaFlorence Robert-Varvat, Guillemette Jousserand, Françoise Bouhour, et al.
Neurology|October 25, 2013
Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutationsKarine Auré, Odile Dubourg, Claude Jardel, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 25, 2012
Regional difference and similarity of familial amyloidosis with polyneuropathy in FranceDavid Adams, Pierre Lozeron, Marie Theaudin, et al.
Parkinsonism & Related Disorders|November 6, 2017
Incobotulinum toxin A in Parkinson's disease with foot dystonia: A double blind randomized trialIsabelle Rieu, Bertrand Degos, Giovanni Castelnovo, et al.
Respiratory Care|January 17, 2013
Absence of airway secretion accumulation predicts tolerance of noninvasive ventilation in subjects with amyotrophic lateral sclerosisNadia Vandenberghe, Anne-Evelyne Vallet, Thierry Petitjean, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 27, 2017
Anti-MAG antibodies in 202 patients: clinicopathological and therapeutic featuresJuliette Svahn, Philippe Petiot, Jean-Christophe Antoine, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|December 15, 2022
Immune-Mediated Rippling Muscle Disease Associated With Thymoma and Anti-MURC/Cavin-4 AutoantibodiesJuliette Svahn, Laurent Coudert, Nathalie Streichenberger, et al.
Orphanet Journal of Rare Diseases|January 22, 2015
Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter studyEmmanuelle Salort-Campana, Karine Nguyen, Rafaelle Bernard, et al.
Neurology|April 14, 2019
FSHD1 and FSHD2 form a disease continuumSabrina Sacconi, Audrey Briand-Suleau, Marilyn Gros, et al.
Nature Communications|March 29, 2019
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusionsMontse Olivé, Martin Engvall, Gianina Ravenscroft, et al.
Pageof 7