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Documents dont l'auteur est "Bouchard, G."

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Nombre de documents: 5

Article de revue

Hamet, P., Seda, O., Merlo, E., Tremblay, J., Broeckel, U., Gaudet, D., Bouchard, G., Gagnon, F., Antoniol, G., Wan, R., Pausova, Z., Gossard, F., Kotchen, T. A., Pintos, J., & Cowley, A. W. (2005). Partitioning of Extra/Intracellular Body Water Plays a Role in Specific Subsets of Hypertension Featuring Metabolic Syndrome and Premature Death. Journal of Hypertension, 23, S264-S264. Non disponible

Hamet, P., Merlo, E., Šeda, O., Broeckel, U., Tremblay, J., Kaldunski, M., Gaudet, D., Bouchard, G., Deslauriers, B., Gagnon, F., Antoniol, G., Pausová, Z., Labuda, M., Jomphe, M., Gossard, F., Tremblay, G., Kirova, R., Tonellato, P., Orlov, S. N., ... Cowley, A. W. (2005). Quantitative founder effect analysis of French-Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension. American Journal on Human Genetics, 76(5), 815-832. Lien externe

Hamet, P., Seda, O., Merlo, E., Gaudet, D., Broeckel, U., Gagnon, F., Antoniol, G., Bouchard, G., Kotchen, T. A., & Cowley, A. W. (2004). Resolution of Complex Trait of Hypertension by Linkage, Systematic Allelic Contribution Analysis and Ancestral Data in French-Canadian Families. Journal of Hypertension, 22, S5-S5. Lien externe

Merlo, E., Seda, O., Antoniol, G., Gaudet, D., Deslauriers, B., Tremblay, J., Cowley, A. W., Bouchard, G., & Hamet, P. (2003). Differential Genetic Contribution Density of Separable Layered Founders in Saguenay (Québec) Population. Journal of Hypertension, 21, S305-S305. Non disponible

Résumé

Seda, O., Merlo, E., Tremblay, J., Broeckel, U., Kaldunski, M., Gaudet, D., Bouchard, G., Gagnon, F., Antoniol, G., Brunelle, P. L., Gurau, A., Gossard, F., Kotchen, T. A., Pausova, Z., Orlov, S. N., Wan, R., Jomphe, M., Pintos, J., Cowley, A. W., & Hamet, P. (mai 2005). Hypertension with and without metabolic syndrome presents as distinct clinical and genetic entities in French-Canadians [Résumé]. European Human Genetics Conference, Prague, Czech Republic. Publié dans European Journal of Human Genetics, 13(S1). Lien externe

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