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F Kyndt

Showing results (1-10 of 11) with videos related to

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Archives Des Maladies Du Coeur Et Des Vaisseaux|December 26, 2003
[Genetic aspects of cardiac conduction defects]V Probst, F Kyndt, M Allouis, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|December 26, 2003
[Genetics and cardiac arrhythmias]V Probst, F Kyndt, M Allouis, et al.
European Heart Journal|February 24, 2001
Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotypeG Lande, F Kyndt, I Baró, et al.
Journal of the American College of Cardiology|June 7, 2000
Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28J N Trochu, F Kyndt, J J Schott, 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.
Heart Rhythm|November 6, 2008
Sodium channel blocker tests allow a clear distinction of electrophysiological characteristics and prognosis in patients with a type 2 or 3 Brugada electrocardiogram patternS Evain, F Briec, F Kyndt, et al.
Nature Genetics|September 2, 1999
Cardiac conduction defects associate with mutations in SCN5AJ J Schott, C Alshinawi, F Kyndt, et al.
Circulation|December 19, 2001
Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French familyF Kyndt, V Probst, F Potet, et al.
Prenatal Diagnosis|December 17, 2008
Prenatal diagnosis of Larsen syndrome caused by a mutation in the filamin B geneN Winer, F Kyndt, A Paumier, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|January 29, 2008
[Genetic aspects of valvulopathies]F Kyndt, S Le Scouarnec, P Jaafar, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Archives Des Maladies Du Coeur Et Des Vaisseaux|December 26, 2003
[Genetic aspects of cardiac conduction defects]V Probst, F Kyndt, M Allouis, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|December 26, 2003
[Genetics and cardiac arrhythmias]V Probst, F Kyndt, M Allouis, et al.
European Heart Journal|February 24, 2001
Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotypeG Lande, F Kyndt, I Baró, et al.
Journal of the American College of Cardiology|June 7, 2000
Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28J N Trochu, F Kyndt, J J Schott, 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.
Heart Rhythm|November 6, 2008
Sodium channel blocker tests allow a clear distinction of electrophysiological characteristics and prognosis in patients with a type 2 or 3 Brugada electrocardiogram patternS Evain, F Briec, F Kyndt, et al.
Nature Genetics|September 2, 1999
Cardiac conduction defects associate with mutations in SCN5AJ J Schott, C Alshinawi, F Kyndt, et al.
Circulation|December 19, 2001
Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French familyF Kyndt, V Probst, F Potet, et al.
Prenatal Diagnosis|December 17, 2008
Prenatal diagnosis of Larsen syndrome caused by a mutation in the filamin B geneN Winer, F Kyndt, A Paumier, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|January 29, 2008
[Genetic aspects of valvulopathies]F Kyndt, S Le Scouarnec, P Jaafar, et al.
Pageof 2