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

Yann Pereon

Showing results (11-20 of 38) with videos related to

Pageof 4
Sort By:
Plos One|November 19, 2011
Immune response and mitochondrial metabolism are commonly deregulated in DMD and aging skeletal muscleDaniel Baron, Armelle Magot, Gérard Ramstein, et al.
Plos One|September 14, 2016
Muscle Activation during Gait in Children with Duchenne Muscular DystrophyJuliette Ropars, Mathieu Lempereur, Carole Vuillerot, et al.
Muscle & Nerve|March 27, 2015
Muscle magnetic resonance imaging abnormalities in X-linked myopathy with excessive autophagySandra Mercier, Armelle Magot, Florence Caillon, et al.
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.
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.
Journal of Neurology|June 9, 2023
Clinical features and maternal and fetal outcomes in women with Guillain-Barré syndrome in pregnancyNolwenn Krief, René Gabriel, Cécile Cauquil, et al.
Journal of Neurology|March 22, 2024
Phenotype variability and natural history of X-linked myopathy with excessive autophagyGorka Fernández-Eulate, Girolamo Alfieri, Marco Spinazzi, et al.
European Heart Journal|December 13, 2016
Incidence and predictors of sudden death, major conduction defects and sustained ventricular tachyarrhythmias in 1388 patients with myotonic dystrophy type 1Karim Wahbi, Dominique Babuty, Vincent Probst, et al.
European Journal of Neurology|August 15, 2022
Anti-disialosyl-immunoglobulin M chronic autoimmune neuropathies: a nationwide multicenter retrospective studyClaire Peillet, David Adams, Shahram Attarian, et al.
JAMA Cardiology|September 24, 2025
Electrocardiogram vs Electrophysiological Study and Major Conduction Delays in Myotonic Dystrophy Type 1Nicolas Clementy, Fabien Labombarda, François Grolleau, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Plos One|November 19, 2011
Immune response and mitochondrial metabolism are commonly deregulated in DMD and aging skeletal muscleDaniel Baron, Armelle Magot, Gérard Ramstein, et al.
Plos One|September 14, 2016
Muscle Activation during Gait in Children with Duchenne Muscular DystrophyJuliette Ropars, Mathieu Lempereur, Carole Vuillerot, et al.
Muscle & Nerve|March 27, 2015
Muscle magnetic resonance imaging abnormalities in X-linked myopathy with excessive autophagySandra Mercier, Armelle Magot, Florence Caillon, et al.
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.
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.
Journal of Neurology|June 9, 2023
Clinical features and maternal and fetal outcomes in women with Guillain-Barré syndrome in pregnancyNolwenn Krief, René Gabriel, Cécile Cauquil, et al.
Journal of Neurology|March 22, 2024
Phenotype variability and natural history of X-linked myopathy with excessive autophagyGorka Fernández-Eulate, Girolamo Alfieri, Marco Spinazzi, et al.
European Heart Journal|December 13, 2016
Incidence and predictors of sudden death, major conduction defects and sustained ventricular tachyarrhythmias in 1388 patients with myotonic dystrophy type 1Karim Wahbi, Dominique Babuty, Vincent Probst, et al.
European Journal of Neurology|August 15, 2022
Anti-disialosyl-immunoglobulin M chronic autoimmune neuropathies: a nationwide multicenter retrospective studyClaire Peillet, David Adams, Shahram Attarian, et al.
JAMA Cardiology|September 24, 2025
Electrocardiogram vs Electrophysiological Study and Major Conduction Delays in Myotonic Dystrophy Type 1Nicolas Clementy, Fabien Labombarda, François Grolleau, et al.
Pageof 4