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

I Denjoy

Showing results (61-70 of 78) with videos related to

Pageof 8
Sort By:
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1994
[Long term course of catecholaminergic polymorphic ventricular tachycardia in children. Apropos of 20 cases with an 8 year-follow-up]V Lucet, F Grau, I Denjoy, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndromeN Neyroud, I Denjoy, C Donger, et al.
Nature Genetics|October 1, 1994
Exclusion of HRAS from long QT locusN Roy, P Kahlem, E Dausse, et al.
Circulation|December 31, 1997
KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndromeC Donger, I Denjoy, M Berthet, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|July 4, 2001
[T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)]J M Lupoglazoff, I Denjoy, M Berthet, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 15, 1999
[Congenital long QT syndrome. The value of genetics in prognostic evaluation]I Denjoy, J M Lupoglazoff, C Donger, et al.
Journal of Molecular and Cellular Cardiology|August 1, 1996
A mutation in HERG associated with notched T waves in long QT syndromeE Dausse, M Berthet, I Denjoy, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 25, 2004
[Neonatal forms of congenital long QT syndrome]J M Lupoglazoff, I Denjoy, E Villain, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|September 28, 1998
[QT interval and drugs. Recommendation for drug prescription for patients with long QT syndrome. Clinical Research Group of INSERM 4940 12: Diagnostic Clinic of Congenital Long QT Syndrome]J Y Le Heuzey, J M Davy, J Weissenburger, et al.
Nature Genetics|February 1, 1997
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndromeN Neyroud, F Tesson, I Denjoy, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1994
[Long term course of catecholaminergic polymorphic ventricular tachycardia in children. Apropos of 20 cases with an 8 year-follow-up]V Lucet, F Grau, I Denjoy, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndromeN Neyroud, I Denjoy, C Donger, et al.
Nature Genetics|October 1, 1994
Exclusion of HRAS from long QT locusN Roy, P Kahlem, E Dausse, et al.
Circulation|December 31, 1997
KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndromeC Donger, I Denjoy, M Berthet, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|July 4, 2001
[T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)]J M Lupoglazoff, I Denjoy, M Berthet, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 15, 1999
[Congenital long QT syndrome. The value of genetics in prognostic evaluation]I Denjoy, J M Lupoglazoff, C Donger, et al.
Journal of Molecular and Cellular Cardiology|August 1, 1996
A mutation in HERG associated with notched T waves in long QT syndromeE Dausse, M Berthet, I Denjoy, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 25, 2004
[Neonatal forms of congenital long QT syndrome]J M Lupoglazoff, I Denjoy, E Villain, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|September 28, 1998
[QT interval and drugs. Recommendation for drug prescription for patients with long QT syndrome. Clinical Research Group of INSERM 4940 12: Diagnostic Clinic of Congenital Long QT Syndrome]J Y Le Heuzey, J M Davy, J Weissenburger, et al.
Nature Genetics|February 1, 1997
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndromeN Neyroud, F Tesson, I Denjoy, et al.
Pageof 8