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

Pascal Cintas

Showing results (51-60 of 80) with videos related to

Pageof 8
Sort By:
Neurology. Genetics|April 11, 2025
Spectrum of Phenotypes in SMA Patients With 4 <i>SMN2</i> Copies in the French Population: Registre SMA FranceLorène Gerin, Juliette Ropars, Rocío Garcia-Uzquiano, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|October 19, 2023
Hereditary transthyretin amyloidosis in middle-aged and elderly patients with idiopathic polyneuropathy: a nationwide prospective studyGuillaume Fargeot, Andoni Echaniz-Laguna, Céline Labeyrie, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|July 25, 2020
Motor unit number index as an individual biomarker: Reference limits of intra-individual variability over time in healthy subjectsEmilien Delmont, François Wang, Jean-Pascal Lefaucheur, et al.
European Journal of Neurology|November 21, 2024
Phenotype-genotype correlation in X-linked Charcot-Marie-Tooth disease: A French cohort studyLuce Barbat du Closel, Nathalie Bonello-Palot, Emilien Delmont, et al.
Autoimmunity Reviews|May 24, 2026
Subtype-specific mortality in idiopathic inflammatory myopathies: A hospital-based cohortAurore Larrauffie, Chloé Bost, Claire Barrier, et al.
European Journal of Neurology|June 19, 2023
Clinical and electrophysiological characteristics of women with X-linked Charcot-Marie-Tooth diseaseLuce Barbat du Closel, Nathalie Bonello-Palot, Yann Péréon, et al.
The Journal of Molecular Diagnostics : JMD|May 25, 2018
A Reliable Targeted Next-Generation Sequencing Strategy for Diagnosis of Myopathies and Muscular Dystrophies, Especially for the Giant Titin and Nebulin GenesReda Zenagui, Delphine Lacourt, Henri Pegeot, et al.
European Journal of Neurology|August 7, 2024
Bulbar muscle impairment in patients with late onset Pompe disease: Insight from the French Pompe registryEmilie Retailleau, Claire Lefeuvre, Marie De Antonio, et al.
Journal of Neurology|March 2, 2026
Electrophysiological assessment of motor unit loss in adult spinal muscular atrophy types III and IV: a multicenter national study comparing MUNIX, CMAP, and MUSIXEva Sole-Cruz, Emmanuelle Salort-Campana, Timothee Lenglet, et al.
European Journal of Neurology|October 27, 2025
Causes of Death and Comorbidities in Adult Patients With Late-Onset Pompe Disease: A French Pompe Registry Retrospective StudyDiana Maria Chitimus, Céline Tard, Maxime Fournier, et al.
Pageof 8

Showing results (51-60 of 80) with videos related to

Sort By:
Pageof 8
Neurology. Genetics|April 11, 2025
Spectrum of Phenotypes in SMA Patients With 4 <i>SMN2</i> Copies in the French Population: Registre SMA FranceLorène Gerin, Juliette Ropars, Rocío Garcia-Uzquiano, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|October 19, 2023
Hereditary transthyretin amyloidosis in middle-aged and elderly patients with idiopathic polyneuropathy: a nationwide prospective studyGuillaume Fargeot, Andoni Echaniz-Laguna, Céline Labeyrie, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|July 25, 2020
Motor unit number index as an individual biomarker: Reference limits of intra-individual variability over time in healthy subjectsEmilien Delmont, François Wang, Jean-Pascal Lefaucheur, et al.
European Journal of Neurology|November 21, 2024
Phenotype-genotype correlation in X-linked Charcot-Marie-Tooth disease: A French cohort studyLuce Barbat du Closel, Nathalie Bonello-Palot, Emilien Delmont, et al.
Autoimmunity Reviews|May 24, 2026
Subtype-specific mortality in idiopathic inflammatory myopathies: A hospital-based cohortAurore Larrauffie, Chloé Bost, Claire Barrier, et al.
European Journal of Neurology|June 19, 2023
Clinical and electrophysiological characteristics of women with X-linked Charcot-Marie-Tooth diseaseLuce Barbat du Closel, Nathalie Bonello-Palot, Yann Péréon, et al.
The Journal of Molecular Diagnostics : JMD|May 25, 2018
A Reliable Targeted Next-Generation Sequencing Strategy for Diagnosis of Myopathies and Muscular Dystrophies, Especially for the Giant Titin and Nebulin GenesReda Zenagui, Delphine Lacourt, Henri Pegeot, et al.
European Journal of Neurology|August 7, 2024
Bulbar muscle impairment in patients with late onset Pompe disease: Insight from the French Pompe registryEmilie Retailleau, Claire Lefeuvre, Marie De Antonio, et al.
Journal of Neurology|March 2, 2026
Electrophysiological assessment of motor unit loss in adult spinal muscular atrophy types III and IV: a multicenter national study comparing MUNIX, CMAP, and MUSIXEva Sole-Cruz, Emmanuelle Salort-Campana, Timothee Lenglet, et al.
European Journal of Neurology|October 27, 2025
Causes of Death and Comorbidities in Adult Patients With Late-Onset Pompe Disease: A French Pompe Registry Retrospective StudyDiana Maria Chitimus, Céline Tard, Maxime Fournier, et al.
Pageof 8