Mapping of a gene for long QT syndrome to chromosome 4q25-27 von SCHOTT, J.-J, CHARPENTIER, F, LE MAREC, H, PASCAL, O, PELTIER, S, FOLEY, P, DROUIN, E, BOUHOUR, J.-B, DONNELLY, P, VERGNAUD, G, BACHNER, L, MOISAN, J.-P

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Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience von Charron, P, Héron, D, Gargiulo, M, Richard, P, Dubourg, O, Desnos, M, Bouhour, J-B, Feingold, J, Carrier, L, Hainque, B, Schwartz, K, Komajda, M

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Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene von CHARRON, P, DUBOURG, O, RICHARD, P, HAINQUE, B, BOUHOUR, J.-B, SCHWARTZ, K, KOMAJDA, M, DESNOS, M, BENNACEUR, M, CARRIER, L, CAMPROUX, A.-C, ISNARD, R, HAGEGE, A, LANGLARD, J. M, BONNE, G

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Organization and Sequence of Human Cardiac Myosin Binding Protein C Gene (MYBPC3) and Identification of Mutations Predicted to Produce Truncated Proteins in Familial Hypertrophic C... von Carrier, Lucie, Bonne, Gisele, Bahrend, Ellen, Yu, Bing, Richard, Pascale, Niel, Florence, Hainque, Bernard, Cruaud, Corinne, Gary, Francoise, Labeit, Siegfried, Bouhour, Jean-Brieuc, Dubourg, Olivier, Desnos, Michel, Hagege, Albert A, Trent, Ronald J, Komajda, Michel, Fiszman, Marc, Schwartz, Ketty

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Lack of association between polymorphisms of eight candidate genes and Idiopathic dilated cardiomyopathy : The CARDIGENE study von TIRET, L, MALLET, C, CAMBIEN, F, KOMAJDA, M, POIRIER, O, NICAUD, V, MILLAIRE, A, BOUHOUR, J.-B, ROIZES, G, DESNOS, M, DORENT, R, SCHWARTZ, K

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Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population von CHARRON, P, DUBOURG, O, BOUHOUR, J.-B, SCHWARTZ, K, KOMAJDA, M, DESNOS, M, ISNARD, R, HAGEGE, A, MILLAIRE, A, CARRIER, L, BONNE, G, TESSON, F, RICHARD, P

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Relation between QT duration and maximal wall thickness in familial hypertrophic cardiomyopathy von Jouven, X, Hagege, A, Charron, P, Carrier, L, Dubourg, O, Langlard, J M, Aliaga, S, Bouhour, J B, Schwartz, K, Desnos, M, Komajda, M

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Accuracy of European diagnostic criteria for familial hypertrophic cardiomyopathy in a genotyped population von Charron, P., Forissier, J.F., Amara, M.E., Dubourg, O., Desnos, M., Bouhour, J-B., Isnard, R., Hagege, A., Bénaı&#x0308, che, A., Richard, P., Schwartz, K., Komajda, M.

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Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children von Charron, Ph, Dubourg, O., Desnos, M., Bouhour, J-B., Isnard, R., Hagege, A., Carrier, L., Bonne, G., Tesson, F., Richard, P., Hainque, B., Schwartz, K., Komajda, M.

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Familial hypertrophic cardiomyopathy. Cardiac ultrasonic abnormalities in genetically affected subjects without echocardiographic evidence of left ventricular hypertrophy von Hagège, A.A., Dubourg, O., Desnos, M., Mirochnik, R., Isnard, G., Bonne, G., Carrier, L., Guicheney, P., Bouhour, J-B., Schwartz, K., Komajda, M.

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Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28 von Kyndt, Florence, Schott, Jean-Jacques, Trochu, Jean-Noël, Baranger, Florence, Herbert, Odile, Scott, Valérie, Fressinaud, Edith, David, Albert, Moisan, Jean-Paul, Bouhour, Jean-Brieuc, Le Marec, Hervé, Bénichou, Bernard

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Role of Endothelium-Derived Nitric Oxide in the Regulation of Cardiac Oxygen Metabolism: Implications in Health and Disease von Trochu, Jean-Noël, Bouhour, Jean-Brieuc, Kaley, Gabor, Hintze, Thomas H

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Genotype-phenotype correlations in familial hypertrophic cardiomyopathy a comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes von CHARRON, P, DUBOURG, O, FEINGOLD, J, SCHWARTZ, K, KOMAJDA, M, DESNOS, M, ISNARD, R, HAGEGE, A, BONNE, G, CARRIER, L, TESSON, F, BOUHOUR, J. B, BUZZI, J.-C

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Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene von Charron, Ph, Tesson, F, Poirier, O, Nicaud, V, Peuchmaurd, M, Tiret, L, Cambien, F, Amouyel, P, Dubourg, O, Bouhour, J.-B, Millaire, A, Juilliere, Y, Bareiss, P, André-Fouët, X, Pouillart, F, Arveiler, D, Ferrières, J, Dorent, R, Roizès, G, Schwartz, K, Desnos, M, Komajda, M

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Ambulatory heart failure management in private practice in France von Komajda, M., Bouhour, J.B., Amouyel, P., Delahaye, F., Vicaut, E., Croce, I., Rougemond, E., Vuittenez, F., Leutenegger, E.

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Factors predicting mortality in idiopathic dilated cardiomyopathy von KOMAJDA, M., JAIS, J. P., REEVES, F., GOLDFARB, B., BOUHOUR, J. B., JUILLIERES, Y., LANFRANCHI, J., PEYCELON, P., GESLIN, PH, CARRIE, D., GROSGOGEAT, Y.

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Familial hypertrophic cardiomyopathy : microsatellite haplotyping and identification of a hot spot for mutations in the β-myosin heavy chain gene von DAUSSE, E, KOMAJDA, M, ISNARD, R, HAGEGE, A, BOUHOUR, J.-B, DESNOS, M, BECKMANN, J, WEISSENBACH, J, SCHWARTZ, K, GUICHENEY, P, FETLER, L, DUBOURG, O, DUFOUR, C, CARRIER, L, WISNEWSKY, C, BERCOVICI, J, HENGSTENBERG, C, SAHAR AL-MAHDAWI

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Detection of enteroviruses in endomyocardial biopsy by molecular approach von Petitjean, J., Kopecka, H., Freymuth, F., Langlard, J. M., Scanu, P., Galateau, F., Bouhour, J. B., Ferriere, M., Charbonneau, P., Komajda, M.

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The management of patients with heart failure in France von Cohen-Solal, A., Bouhour, J.B., Thebaut, J.F.

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Prognostic value of neurohormonal activation and cardiopulmonary exercise testing in patients with chronic heart failure von Isnard, Richard, Pousset, Françoise, Trochu, Jean-Noël, Chafirovskaı̈a, Olga, Carayon, Alain, Golmard, Jean-Louis, Lechat, Philippe, Thomas, Daniel, Bouhour, Jean-Brieuc, Komajda, Michel

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