Search research articles
Contact Us
Filters
Showing results (61-70 of 80) with videos related to
Page
of 8
Sort By:
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 Study
O 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 survey
P de Groote, R Isnard, P Assyag, et al.
European Heart Journal
|
October 3, 2003
Clinical applications of B-type natriuretic peptide (BNP) testing
M 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 patients
S 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 failure
C 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 cardiomyopathy
J 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 cardiomyopathy
P Richard, R Isnard, L Carrier, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 80) with videos related to
Sort By:
Page
of 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 Study
O 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 survey
P de Groote, R Isnard, P Assyag, et al.
European Heart Journal
|
October 3, 2003
Clinical applications of B-type natriuretic peptide (BNP) testing
M 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 patients
S 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 failure
C 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 cardiomyopathy
J 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 cardiomyopathy
P Richard, R Isnard, L Carrier, et al.
Page
of 8