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Showing results (81-90 of 143) with videos related to

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Circulation Research|July 21, 2001
Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular blockJ M Lupoglazoff, T Cheav, G Baroudi, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 28, 2002
[Homozygotous mutation of the SCN5A gene responsible for congenital long QT syndrome with 2/1 atrioventricular block]J M Lupoglazoff, I Denjoy, T Cheav, et al.
American Journal of Human Genetics|March 26, 1999
Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmiasR Mohammad-Panah, S Demolombe, N Neyroud, et al.
Cardiovascular Research|March 23, 2000
Novel mutations in KvLQT1 that affect Iks activation through interactions with IskC Chouabe, N Neyroud, P Richard, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|July 25, 2007
[The Jervell and Lange-Nielsen syndrome. Natural history, molecular basis and clinical outcome]I Denjoy, J-M Lupoglazoff, E Villain, et al.
Human Molecular Genetics|September 1, 1994
Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mappingD Hillaire, A Leclerc, S Fauré, et al.
Fundamental & Clinical Pharmacology|January 1, 1987
Quantitative autoradiographic determination of binding sites for a peripheral benzodiazepine ligand ([3H]PK 11195) in human irisD Valtier, C Malgouris, J C Gilbert, 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.
Journal of Molecular and Cellular Cardiology|September 1, 1994
Identification of a mutation near a functional site of the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathyC Dufour, E Dausse, L Fetler, et al.
Neuropharmacology|June 1, 1987
Binding sites for a peripheral type benzodiazepine antagonist ([3H]PK 11195) in human irisD Valtier, C Malgouris, J C Gilbert, et al.
Pageof 15

Showing results (81-90 of 143) with videos related to

Sort By:
Pageof 15
Circulation Research|July 21, 2001
Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular blockJ M Lupoglazoff, T Cheav, G Baroudi, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 28, 2002
[Homozygotous mutation of the SCN5A gene responsible for congenital long QT syndrome with 2/1 atrioventricular block]J M Lupoglazoff, I Denjoy, T Cheav, et al.
American Journal of Human Genetics|March 26, 1999
Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmiasR Mohammad-Panah, S Demolombe, N Neyroud, et al.
Cardiovascular Research|March 23, 2000
Novel mutations in KvLQT1 that affect Iks activation through interactions with IskC Chouabe, N Neyroud, P Richard, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|July 25, 2007
[The Jervell and Lange-Nielsen syndrome. Natural history, molecular basis and clinical outcome]I Denjoy, J-M Lupoglazoff, E Villain, et al.
Human Molecular Genetics|September 1, 1994
Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mappingD Hillaire, A Leclerc, S Fauré, et al.
Fundamental & Clinical Pharmacology|January 1, 1987
Quantitative autoradiographic determination of binding sites for a peripheral benzodiazepine ligand ([3H]PK 11195) in human irisD Valtier, C Malgouris, J C Gilbert, 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.
Journal of Molecular and Cellular Cardiology|September 1, 1994
Identification of a mutation near a functional site of the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathyC Dufour, E Dausse, L Fetler, et al.
Neuropharmacology|June 1, 1987
Binding sites for a peripheral type benzodiazepine antagonist ([3H]PK 11195) in human irisD Valtier, C Malgouris, J C Gilbert, et al.
Pageof 15