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

C Desnuelle

Showing results (91-100 of 118) with videos related to

Pageof 12
Sort By:
Diabetologia|December 1, 1995
Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA?P Silvestre-Aillaud, D BenDahan, V Paquis-Fluckinger, et al.
Diabetologia|July 14, 1998
Importance of searching for mtDNA defects in patients with diabetes and hearing deficitV Paquis-Flucklinger, B Vialettes, P Vague, 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.
Archives of Neurology|May 1, 1995
Levorotatory form of 5-hydroxytryptophan in Friedreich's ataxia. Results of a double-blind drug-placebo cooperative studyP Trouillas, G Serratrice, D Laplane, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletionsR Paul, C Desnuelle, J Pouget, et al.
Annals of Physical and Rehabilitation Medicine|April 6, 2012
Pain assessment in Charcot-Marie-Tooth (CMT) diseaseC Ribiere, M Bernardin, S Sacconi, et al.
Gene Therapy|June 24, 2005
Normal growth and regenerating ability of myoblasts from unaffected muscles of facioscapulohumeral muscular dystrophy patientsJ-T Vilquin, J-P Marolleau, S Sacconi, et al.
Journal of the Neurological Sciences|March 1, 1991
Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): a clinical, biochemical and molecular studyL A Bindoff, C Desnuelle, M A Birch-Machin, et al.
American Journal of Physiology. Cell Physiology|July 3, 2009
Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubesS Sacconi, D Simkin, N Arrighi, et al.
European Journal of Neurology|May 23, 2014
Revisiting the spectrum of lower motor neuron diseases with snake eyes appearance on magnetic resonance imagingM-V Lebouteux, J Franques, R Guillevin, et al.
Pageof 12

Showing results (91-100 of 118) with videos related to

Sort By:
Pageof 12
Diabetologia|December 1, 1995
Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA?P Silvestre-Aillaud, D BenDahan, V Paquis-Fluckinger, et al.
Diabetologia|July 14, 1998
Importance of searching for mtDNA defects in patients with diabetes and hearing deficitV Paquis-Flucklinger, B Vialettes, P Vague, 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.
Archives of Neurology|May 1, 1995
Levorotatory form of 5-hydroxytryptophan in Friedreich's ataxia. Results of a double-blind drug-placebo cooperative studyP Trouillas, G Serratrice, D Laplane, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletionsR Paul, C Desnuelle, J Pouget, et al.
Annals of Physical and Rehabilitation Medicine|April 6, 2012
Pain assessment in Charcot-Marie-Tooth (CMT) diseaseC Ribiere, M Bernardin, S Sacconi, et al.
Gene Therapy|June 24, 2005
Normal growth and regenerating ability of myoblasts from unaffected muscles of facioscapulohumeral muscular dystrophy patientsJ-T Vilquin, J-P Marolleau, S Sacconi, et al.
Journal of the Neurological Sciences|March 1, 1991
Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): a clinical, biochemical and molecular studyL A Bindoff, C Desnuelle, M A Birch-Machin, et al.
American Journal of Physiology. Cell Physiology|July 3, 2009
Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubesS Sacconi, D Simkin, N Arrighi, et al.
European Journal of Neurology|May 23, 2014
Revisiting the spectrum of lower motor neuron diseases with snake eyes appearance on magnetic resonance imagingM-V Lebouteux, J Franques, R Guillevin, et al.
Pageof 12