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

Yves Tourmen

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
Comptes Rendus Biologies|January 20, 2005
Mitochondrial diseases preferentially involve proteins with prokaryote homologuesYves Tourmen, Marc Ferré, Yves Malthièry, et al.
Genomics|June 25, 2002
Structure and chromosomal distribution of human mitochondrial pseudogenesYves Tourmen, Olivier Baris, Philippe Dessen, et al.
Human Mutation|April 16, 2005
eOPA1: an online database for OPA1 mutationsMarc Ferré, Patrizia Amati-Bonneau, Yves Tourmen, et al.
International Journal of Cardiology|March 7, 2006
The duo low plasma NT-PRO-BRAIN natriuretic peptide and C-reactive protein indicates a complete remission of peripartum cardiomyopathyArnaud Cénac, Yves Tourmen, Eric Adehossi, et al.
Therapie|March 22, 2007
[Prospective observational study of drug-induced hyperkalemia in hospitalized non dialized adult patients]Céline Onno, Héléna Rémignon, Laurence Lagarce, et al.
Basic Research in Cardiology|October 29, 2010
Diabetes mellitus abrogates erythropoietin-induced cardioprotection against ischemic-reperfusion injury by alteration of the RISK/GSK-3β signalingNehmat Ghaboura, Sophie Tamareille, Pierre-Henri Ducluzeau, et al.
European Journal of Endocrinology|March 12, 2004
Decreased expression of thyrotropin receptor gene suggests a high-risk subgroup for oncocytic adenomaDelphine Mirebeau-Prunier, Serge Guyétant, Patrice Rodien, et al.
Human Mutation|February 13, 2004
Fourteen novel OPA1 mutations in autosomal dominant optic atrophy including two de novo mutations in sporadic optic atrophyOlivier Baris, Cécile Delettre, Patrizia Amati-Bonneau, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Comptes Rendus Biologies|January 20, 2005
Mitochondrial diseases preferentially involve proteins with prokaryote homologuesYves Tourmen, Marc Ferré, Yves Malthièry, et al.
Genomics|June 25, 2002
Structure and chromosomal distribution of human mitochondrial pseudogenesYves Tourmen, Olivier Baris, Philippe Dessen, et al.
Human Mutation|April 16, 2005
eOPA1: an online database for OPA1 mutationsMarc Ferré, Patrizia Amati-Bonneau, Yves Tourmen, et al.
International Journal of Cardiology|March 7, 2006
The duo low plasma NT-PRO-BRAIN natriuretic peptide and C-reactive protein indicates a complete remission of peripartum cardiomyopathyArnaud Cénac, Yves Tourmen, Eric Adehossi, et al.
Therapie|March 22, 2007
[Prospective observational study of drug-induced hyperkalemia in hospitalized non dialized adult patients]Céline Onno, Héléna Rémignon, Laurence Lagarce, et al.
Basic Research in Cardiology|October 29, 2010
Diabetes mellitus abrogates erythropoietin-induced cardioprotection against ischemic-reperfusion injury by alteration of the RISK/GSK-3β signalingNehmat Ghaboura, Sophie Tamareille, Pierre-Henri Ducluzeau, et al.
European Journal of Endocrinology|March 12, 2004
Decreased expression of thyrotropin receptor gene suggests a high-risk subgroup for oncocytic adenomaDelphine Mirebeau-Prunier, Serge Guyétant, Patrice Rodien, et al.
Human Mutation|February 13, 2004
Fourteen novel OPA1 mutations in autosomal dominant optic atrophy including two de novo mutations in sporadic optic atrophyOlivier Baris, Cécile Delettre, Patrizia Amati-Bonneau, et al.
Pageof 1