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R Isnard

Showing results (61-70 of 80) with videos related to

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Archives Des Maladies Du Coeur Et Des Vaisseaux|February 1, 1993
[French familial multicenter survey of hypertrophic cardiomyopathy. Initial Doppler echocardiographic results]O Dubourg, M Komajda, R Isnard, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|April 1, 1995
[Clinico-pathological polymorphism of hypertrophic cardiomyopathy in echocardiography]O Dubourg, R Isnard, L Fetler, et al.
Echocardiography (Mount Kisco, N.Y.)|April 8, 1995
Doppler echocardiography in familial hypertrophic cardiomyopathy: the French Cooperative StudyO Dubourg, R Isnard, A Hagège, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|December 1, 1994
[Demonstration of a fifth locus implicated in familial hypertrophic cardiomyopathies]C Hengstenberg, P Charron, R Isnard, et al.
European Journal of Heart Failure|November 21, 2007
Is the gap between guidelines and clinical practice in heart failure treatment being filled? Insights from the IMPACT RECO surveyP de Groote, R Isnard, P Assyag, et al.
European Heart Journal|October 3, 2003
Clinical applications of B-type natriuretic peptide (BNP) testingM R Cowie, P Jourdain, A Maisel, et al.
Diabetes & Metabolism|September 14, 2010
A randomized study comparing isotope and echocardiography stress testing in the screening of silent myocardial ischaemia in type 2 diabetic patientsS Jacqueminet, O Barthelemy, F Rouzet, et al.
The Journal of Endocrinology|January 1, 1996
Plasma levels and molecular forms of proatrial natriuretic peptides in healthy subjects and in patients with congestive heart failureC Azizi, G Maistre, H Kalotka, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 16, 1998
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathyJ Flavigny, P Richard, R Isnard, et al.
Journal of Medical Genetics|July 29, 1999
Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathyP Richard, R Isnard, L Carrier, et al.
Pageof 8

Showing results (61-70 of 80) with videos related to

Sort By:
Pageof 8
Archives Des Maladies Du Coeur Et Des Vaisseaux|February 1, 1993
[French familial multicenter survey of hypertrophic cardiomyopathy. Initial Doppler echocardiographic results]O Dubourg, M Komajda, R Isnard, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|April 1, 1995
[Clinico-pathological polymorphism of hypertrophic cardiomyopathy in echocardiography]O Dubourg, R Isnard, L Fetler, et al.
Echocardiography (Mount Kisco, N.Y.)|April 8, 1995
Doppler echocardiography in familial hypertrophic cardiomyopathy: the French Cooperative StudyO Dubourg, R Isnard, A Hagège, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|December 1, 1994
[Demonstration of a fifth locus implicated in familial hypertrophic cardiomyopathies]C Hengstenberg, P Charron, R Isnard, et al.
European Journal of Heart Failure|November 21, 2007
Is the gap between guidelines and clinical practice in heart failure treatment being filled? Insights from the IMPACT RECO surveyP de Groote, R Isnard, P Assyag, et al.
European Heart Journal|October 3, 2003
Clinical applications of B-type natriuretic peptide (BNP) testingM R Cowie, P Jourdain, A Maisel, et al.
Diabetes & Metabolism|September 14, 2010
A randomized study comparing isotope and echocardiography stress testing in the screening of silent myocardial ischaemia in type 2 diabetic patientsS Jacqueminet, O Barthelemy, F Rouzet, et al.
The Journal of Endocrinology|January 1, 1996
Plasma levels and molecular forms of proatrial natriuretic peptides in healthy subjects and in patients with congestive heart failureC Azizi, G Maistre, H Kalotka, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 16, 1998
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathyJ Flavigny, P Richard, R Isnard, et al.
Journal of Medical Genetics|July 29, 1999
Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathyP Richard, R Isnard, L Carrier, et al.
Pageof 8