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 Birouk

Showing results (31-40 of 36) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 36 results.
Neurology|May 5, 1998
X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic studyN Birouk, E LeGuern, T Maisonobe, et al.
Revue Neurologique|July 31, 1998
[Multifocal motor neuropathies with conduction blocks. 39 cases]N Le Forestier, B Chassande, A Moulonguet, et al.
Human Mutation|January 1, 1997
Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 familiesH Rouger, E LeGuern, N Birouk, et al.
American Journal of Human Genetics|April 11, 2003
Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucomaH Azzedine, A Bolino, T Taïeb, et al.
Neuromolecular Medicine|June 16, 2006
Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth diseaseO Dubourg, H Azzedine, C Verny, et al.
Neurology|August 23, 2006
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutationsH Azzedine, N Ravisé, C Verny, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Neurology|May 5, 1998
X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic studyN Birouk, E LeGuern, T Maisonobe, et al.
Revue Neurologique|July 31, 1998
[Multifocal motor neuropathies with conduction blocks. 39 cases]N Le Forestier, B Chassande, A Moulonguet, et al.
Human Mutation|January 1, 1997
Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 familiesH Rouger, E LeGuern, N Birouk, et al.
American Journal of Human Genetics|April 11, 2003
Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucomaH Azzedine, A Bolino, T Taïeb, et al.
Neuromolecular Medicine|June 16, 2006
Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth diseaseO Dubourg, H Azzedine, C Verny, et al.
Neurology|August 23, 2006
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutationsH Azzedine, N Ravisé, C Verny, et al.
Pageof 4