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

David Moore

Showing results (501-510 of 540) with videos related to

Pageof 54
Sort By:
Brain : a Journal of Neurology|January 11, 2015
Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosisSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
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.
Proceedings (Baylor University. Medical Center)|March 16, 2026
Insights from a multidisciplinary heart team for highest-risk valve diseaseTaylor Pickering, John Eisenga, Kyle McCullough, 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|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.
Influenza and Other Respiratory Viruses|November 19, 2021
Epidemiology of SARS-CoV-2 infection and SARS-CoV-2 positive hospital admissions among children in South AfricaTendesayi Kufa, Waasila Jassat, Cheryl Cohen, et al.
Journal of the International AIDS Society|January 16, 2018
Increased non-AIDS mortality among persons with AIDS-defining events after antiretroviral therapy initiationApril C Pettit, Mark J Giganti, Suzanne M Ingle, et al.
Journal of Medicinal Chemistry|July 20, 2012
Discovery of piragliatin--first glucokinase activator studied in type 2 diabetic patientsRamakanth Sarabu, Fred T Bizzarro, Wendy L Corbett, et al.
Pageof 54

Showing results (501-510 of 540) with videos related to

Sort By:
Pageof 54
Brain : a Journal of Neurology|January 11, 2015
Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosisSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
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.
Proceedings (Baylor University. Medical Center)|March 16, 2026
Insights from a multidisciplinary heart team for highest-risk valve diseaseTaylor Pickering, John Eisenga, Kyle McCullough, 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|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.
Influenza and Other Respiratory Viruses|November 19, 2021
Epidemiology of SARS-CoV-2 infection and SARS-CoV-2 positive hospital admissions among children in South AfricaTendesayi Kufa, Waasila Jassat, Cheryl Cohen, et al.
Journal of the International AIDS Society|January 16, 2018
Increased non-AIDS mortality among persons with AIDS-defining events after antiretroviral therapy initiationApril C Pettit, Mark J Giganti, Suzanne M Ingle, et al.
Journal of Medicinal Chemistry|July 20, 2012
Discovery of piragliatin--first glucokinase activator studied in type 2 diabetic patientsRamakanth Sarabu, Fred T Bizzarro, Wendy L Corbett, et al.
Pageof 54