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

B Eymard

Showing results (91-100 of 160) with videos related to

Pageof 16
Sort By:
Neurology|March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.
Revue Neurologique|April 1, 2000
[Miyoshi distal myopathy: specific signs and incidence]B Eymard, P Laforêt, F M Tomé, et al.
Immunologic Research|January 1, 1988
Cellular aspects of myasthenia gravisS Berrih-Aknin, S Cohen-Kaminsky, D Neumann, et al.
Revue Neurologique|January 1, 1991
[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy]C Marsac, F Degoul, G Bonne, et al.
Journal of the Neurological Sciences|October 1, 1991
Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF)P Seibel, F Degoul, G Bonne, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutationsE Plassart, J Reboul, C S Rime, et al.
European Journal of Neurology|November 29, 2013
Intrafamilial heterogeneous clinical presentation of the mitochondrial 3243 MELAS mutation; molecular investigations among four generationsF Degoul, M Diry, F Viader, et al.
Journal of the Neurological Sciences|February 1, 1991
Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studiesF Degoul, I Nelson, P Lestienne, et al.
Neurology|May 5, 1998
Novel muscle chloride channel (CLCN1) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetranceE Plassart-Schiess, A Gervais, B Eymard, et al.
Revue Neurologique|August 27, 2013
Attitudes and expectations of patients with neuromuscular diseases about their participation in a clinical trialM Gargiulo, A Herson, C C Michon, et al.
Pageof 16

Showing results (91-100 of 160) with videos related to

Sort By:
Pageof 16
Neurology|March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.
Revue Neurologique|April 1, 2000
[Miyoshi distal myopathy: specific signs and incidence]B Eymard, P Laforêt, F M Tomé, et al.
Immunologic Research|January 1, 1988
Cellular aspects of myasthenia gravisS Berrih-Aknin, S Cohen-Kaminsky, D Neumann, et al.
Revue Neurologique|January 1, 1991
[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy]C Marsac, F Degoul, G Bonne, et al.
Journal of the Neurological Sciences|October 1, 1991
Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF)P Seibel, F Degoul, G Bonne, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutationsE Plassart, J Reboul, C S Rime, et al.
European Journal of Neurology|November 29, 2013
Intrafamilial heterogeneous clinical presentation of the mitochondrial 3243 MELAS mutation; molecular investigations among four generationsF Degoul, M Diry, F Viader, et al.
Journal of the Neurological Sciences|February 1, 1991
Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studiesF Degoul, I Nelson, P Lestienne, et al.
Neurology|May 5, 1998
Novel muscle chloride channel (CLCN1) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetranceE Plassart-Schiess, A Gervais, B Eymard, et al.
Revue Neurologique|August 27, 2013
Attitudes and expectations of patients with neuromuscular diseases about their participation in a clinical trialM Gargiulo, A Herson, C C Michon, et al.
Pageof 16