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

Brigitte Chabrol

Showing results (11-20 of 147) with videos related to

Pageof 15
Sort By:
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 5, 2025
Mitochondrial Leigh syndrome: the state of the artGauthier Toutain, Célia Hoebeke, Marguerite Gastaldi, et al.
Gene|November 6, 2012
Novel PTEN germline mutation in a family with mild phenotype: difficulties in genetic counselingTiffany Busa, Brigitte Chabrol, Odile Perret, et al.
Muscle & Nerve|July 13, 2021
Motor unit number index: A potential electrophysiological biomarker for pediatric spinal muscular atrophyChristophe Boulay, Emilien Delmont, Frédérique Audic, et al.
Neuroscience Letters|June 6, 2006
Anticipatory postural adjustments in a bimanual load-lifting task in children with Duchenne muscular dystrophyMarianne Jover, Christina Schmitz, Emmanuelle Bosdure, et al.
Developmental Medicine and Child Neurology|February 6, 2010
Anticipatory postural adjustments in a bimanual load-lifting task in children with developmental coordination disorderMarianne Jover, Christina Schmitz, Laurie Centelles, et al.
Clinical Dysmorphology|July 9, 2016
Large in-frame intragenic deletion of OPHN1 in a male patient with a normal intelligence quotient scoreTiffany Busa, Emilie Caietta, Brigitte Chabrol, et al.
European Journal of Medical Genetics|September 11, 2025
Innovative treatments of pediatric spinal muscular atrophy: The decision-making process in FranceMaelle Biotteau, Juliette Ropars, Brigitte Chabrol, et al.
Muscle & Nerve|September 7, 2017
Clinical features and evolution of juvenile myasthenia gravis in a French cohortColine Barraud, Isabelle Desguerre, Christine Barnerias, et al.
Orphanet Journal of Rare Diseases|April 19, 2015
Diagnosis, quality of life, and treatment of patients with Hunter syndrome in the French healthcare system: a retrospective observational studyNathalie Guffon, Bénédicte Heron, Brigitte Chabrol, et al.
The Journal of Pediatrics|February 21, 2012
Resistant Kawasaki disease treated with anti-CD20Emilie Sauvaget, Béatrice Bonello, Marion David, et al.
Pageof 15

Showing results (11-20 of 147) with videos related to

Sort By:
Pageof 15
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 5, 2025
Mitochondrial Leigh syndrome: the state of the artGauthier Toutain, Célia Hoebeke, Marguerite Gastaldi, et al.
Gene|November 6, 2012
Novel PTEN germline mutation in a family with mild phenotype: difficulties in genetic counselingTiffany Busa, Brigitte Chabrol, Odile Perret, et al.
Muscle & Nerve|July 13, 2021
Motor unit number index: A potential electrophysiological biomarker for pediatric spinal muscular atrophyChristophe Boulay, Emilien Delmont, Frédérique Audic, et al.
Neuroscience Letters|June 6, 2006
Anticipatory postural adjustments in a bimanual load-lifting task in children with Duchenne muscular dystrophyMarianne Jover, Christina Schmitz, Emmanuelle Bosdure, et al.
Developmental Medicine and Child Neurology|February 6, 2010
Anticipatory postural adjustments in a bimanual load-lifting task in children with developmental coordination disorderMarianne Jover, Christina Schmitz, Laurie Centelles, et al.
Clinical Dysmorphology|July 9, 2016
Large in-frame intragenic deletion of OPHN1 in a male patient with a normal intelligence quotient scoreTiffany Busa, Emilie Caietta, Brigitte Chabrol, et al.
European Journal of Medical Genetics|September 11, 2025
Innovative treatments of pediatric spinal muscular atrophy: The decision-making process in FranceMaelle Biotteau, Juliette Ropars, Brigitte Chabrol, et al.
Muscle & Nerve|September 7, 2017
Clinical features and evolution of juvenile myasthenia gravis in a French cohortColine Barraud, Isabelle Desguerre, Christine Barnerias, et al.
Orphanet Journal of Rare Diseases|April 19, 2015
Diagnosis, quality of life, and treatment of patients with Hunter syndrome in the French healthcare system: a retrospective observational studyNathalie Guffon, Bénédicte Heron, Brigitte Chabrol, et al.
The Journal of Pediatrics|February 21, 2012
Resistant Kawasaki disease treated with anti-CD20Emilie Sauvaget, Béatrice Bonello, Marion David, et al.
Pageof 15