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

N Bahi-Buisson

Showing results (41-50 of 44) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 44 results.
Molecular Genetics and Metabolism|June 12, 2013
Renal transplantation in 4 patients with methylmalonic aciduria: a cell therapy for metabolic diseaseA Brassier, O Boyer, V Valayannopoulos, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 27, 2021
Electro-clinical features in epileptic children with chromosome 15q duplication syndromeM-T Dangles, V Malan, G Dumas, et al.
Neurology|March 26, 2008
Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutationsE Roze, E Apartis, F Clot, et al.
Journal of Medical Genetics|June 5, 2010
Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speechC Bonnet, J Andrieux, M Béri-Dexheimer, et al.
Pageof 5

Showing results (41-50 of 44) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 44 results.
Molecular Genetics and Metabolism|June 12, 2013
Renal transplantation in 4 patients with methylmalonic aciduria: a cell therapy for metabolic diseaseA Brassier, O Boyer, V Valayannopoulos, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 27, 2021
Electro-clinical features in epileptic children with chromosome 15q duplication syndromeM-T Dangles, V Malan, G Dumas, et al.
Neurology|March 26, 2008
Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutationsE Roze, E Apartis, F Clot, et al.
Journal of Medical Genetics|June 5, 2010
Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speechC Bonnet, J Andrieux, M Béri-Dexheimer, et al.
Pageof 5