Genetic factors in familial hypertrophic cardiomyopathy: does molecular cardiology offer new perspectives?

ανά Komajda, M.
Έκδοση 1996

Genetics of dilated cardiomyopathy: a molecular maze?

ανά KOMAJDA, M
Έκδοση 2000

Are angiotensin II receptor blockers indicated in chronic heart failure?

ανά Komajda, M
Έκδοση 2002

How will the human genome project change cardiovascular medicine?

ανά KOMAJDA, M., CHARRON, P.
Έκδοση 2001

Angiotensin converting enzyme inhibition: from viper to patient

ανά Komajda, M., Wimart, M.
Έκδοση 2000

The COX8 gene is not the disease gene of the CMH4 locus in familial hypertrophic cardiomyopathy.

ανά Bonne, G, Carrier, L, Schwartz, K, Komajda, M
Έκδοση 1995

The role of the neurohormonal system in heart failure

ανά Komajda, M., Pousset, F., Isnard, R., Lechat, P.
Έκδοση 1998

Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families.

ανά McKenna, W. J., Spirito, P., Desnos, M., Dubourg, O., Komajda, M.
Έκδοση 1997

Intracardiac conduction defects in dystrophia myotonica. Electrophysiological study of 12 cases.

ανά Komajda, M, Frank, R, Vedel, J, Fontaine, G, Petitot, J C, Grosgogeat, Y
Έκδοση 1980

Long-term treatment of congestive heart failure with captopril(SQ14, 225)

ανά Komajda, M., Eugene, M., Evans, J., Drobinski, G., Laurenceau, J. L., Grosgogeat, Y.
Έκδοση 1982

Skeletal actin mRNA increases in the human heart during ontogenic development and is the major isoform of control and failing adult hearts.

ανά Boheler, K R, Carrier, L, de la Bastie, D, Allen, P D, Komajda, M, Mercadier, J J, Schwartz, K
Έκδοση 1991

Rosiglitazone RECORD study: glucose control outcomes at 18 months

ανά Home, P D, Jones, N P, Pocock, S J, Beck-Nielsen, H, Gomis, R, Hanefeld, M, Komajda, M, Curtis, P
Έκδοση 2007

Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.

ανά Dausse, E, Komajda, M, Fetler, L, Dubourg, O, Dufour, C, Carrier, L, Wisnewsky, C, Bercovici, J, Hengstenberg, C, al-Mahdawi, S
Έκδοση 1993

Idiopathic dilated cardiomyopathy: lack of association with haemochromatosis gene in the CARDIGENE study

ανά HETET, G, GRANDCHAMP, B, BOUCHIER, C, NICAUD, V, TIRET, L, ROIZES, G, DESNOS, M, SCHWARTZ, K, DORENT, R, KOMAJDA, M, GROUP, F. T.
Έκδοση 2001

Altered sarcoplasmic reticulum Ca2(+)-ATPase gene expression in the human ventricle during end-stage heart failure.

ανά Mercadier, J J, Lompré, A M, Duc, P, Boheler, K R, Fraysse, J B, Wisnewsky, C, Allen, P D, Komajda, M, Schwartz, K
Έκδοση 1990

A New Locus for Autosomal Dominant Dilated Cardiomyopathy Identified on Chromosome 6q12-q16

ανά Sylvius, N., Tesson, F., Gayet, C., Charron, P., Bénaïche, A., Peuchmaurd, M., Duboscq-Bidot, L., Feingold, J., Beckmann, J. S., Bouchier, C., Komajda, M.
Έκδοση 2001

First description of germline mosaicism in familial hypertrophic cardiomyopathy

ανά Forissier, J., Richard, P., Briault, S., Ledeuil, C., Dubourg, O., Charbonnier, B., Carrier, L., Moraine, C., Bonne, G., Komajda, M., Schwartz, K., Hainque, B.
Έκδοση 2000

Relation between QT duration and maximal wall thickness in familial hypertrophic cardiomyopathy

ανά Jouven, X, Hagege, A, Charron, P, Carrier, L, Dubourg, O, Langlard, J M, Aliaga, S, Bouhour, J B, Schwartz, K, Desnos, M, Komajda, M
Έκδοση 2002

Relation between severity of left ventricular systolic dysfunction and repolarisation abnormalities on the surface ECG: a report from the Euro heart failure survey

ανά Velavan, P, Khan, NK, Rigby, A S, Goode, K, Komajda, M, Follath, F, Swedberg, K, Madeira, H, Clark, A L, Cleland, J G F
Έκδοση 2006

Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic survey

ανά Charron, P, Villard, E, Sebillon, P, Laforet, P, Maisonobe, T, Duboscq-Bidot, L, Romero, N, Drouin-Garraud, V, Frebourg, T, Richard, P, Eymard, B, Komajda, M
Έκδοση 2004