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

Emmanuelle C Genin

Showing results (21-30 of 28) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 28 results.
Brain : a Journal of Neurology|January 1, 2016
Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from ChinaSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|August 13, 2014
Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron diseaseSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|September 29, 2014
Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosisSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|June 18, 2014
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvementSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|February 15, 2015
Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutationSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|October 29, 2014
Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|October 31, 2024
Nifuroxazide rescues the deleterious effects due to CHCHD10-associated MICOS defects in disease modelsBaptiste Ropert, Sylvie Bannwarth, Emmanuelle C Genin, et al.
American Journal of Human Genetics|December 20, 2016
Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe EncephalopathySamira Ait-El-Mkadem, Manal Dayem-Quere, Mirjana Gusic, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Brain : a Journal of Neurology|January 1, 2016
Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from ChinaSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|August 13, 2014
Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron diseaseSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|September 29, 2014
Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosisSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|June 18, 2014
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvementSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|February 15, 2015
Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutationSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|October 29, 2014
Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|October 31, 2024
Nifuroxazide rescues the deleterious effects due to CHCHD10-associated MICOS defects in disease modelsBaptiste Ropert, Sylvie Bannwarth, Emmanuelle C Genin, et al.
American Journal of Human Genetics|December 20, 2016
Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe EncephalopathySamira Ait-El-Mkadem, Manal Dayem-Quere, Mirjana Gusic, et al.
Pageof 3