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

H Hammouda

Showing results (11-20 of 14) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 14 results.
Archives of Physical Medicine and Rehabilitation|July 7, 2009
Periodic salbutamol in facioscapulohumeral muscular dystrophy: a randomized controlled trialC A Payan, J Y Hogrel, E H Hammouda, et al.
Pacing and Clinical Electrophysiology : PACE|January 4, 2001
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutationH M Bécane, G Bonne, S Varnous, et al.
Nature Genetics|March 18, 1999
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophyG Bonne, M R Di Barletta, S Varnous, et al.
Nature Genetics|December 2, 2000
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia)S Nicole, C S Davoine, H Topaloglu, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Archives of Physical Medicine and Rehabilitation|July 7, 2009
Periodic salbutamol in facioscapulohumeral muscular dystrophy: a randomized controlled trialC A Payan, J Y Hogrel, E H Hammouda, et al.
Pacing and Clinical Electrophysiology : PACE|January 4, 2001
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutationH M Bécane, G Bonne, S Varnous, et al.
Nature Genetics|March 18, 1999
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophyG Bonne, M R Di Barletta, S Varnous, et al.
Nature Genetics|December 2, 2000
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia)S Nicole, C S Davoine, H Topaloglu, et al.
Pageof 2