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Page 1
Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction.
Lieb W, Zeller T, Mangino M, Götz A, Braund P, Wenzel JJ, Horn C, Proust C, Linsel-Nitschke P, Amouyel P, Bruse P, Arveiler D, König IR, Ferrières J, Ziegler A, Balmforth AJ, Evans A, Ducimetière P, Cambien F, Hengstenberg C, Stark K, Hall AS, Schunkert H, Blankenberg S, Samani NJ, Erdmann J, Tiret L. Lieb W, et al. Among authors: ferrieres j. J Mol Med (Berl). 2008 Oct;86(10):1163-70. doi: 10.1007/s00109-008-0376-5. Epub 2008 Jul 1. J Mol Med (Berl). 2008. PMID: 18592168
Five frequent polymorphisms of the PAI-1 gene: lack of association between genotypes, PAI activity, and triglyceride levels in a healthy population.
Henry M, Chomiki N, Scarabin PY, Alessi MC, Peiretti F, Arveiler D, Ferrières J, Evans A, Amouyel P, Poirier O, Cambien F, Juhan-Vague I. Henry M, et al. Among authors: ferrieres j. Arterioscler Thromb Vasc Biol. 1997 May;17(5):851-8. doi: 10.1161/01.atv.17.5.851. Arterioscler Thromb Vasc Biol. 1997. PMID: 9157947
Influence of parental history of hypertension on blood pressure.
Lascaux-Lefebvre V, Ruidavets J, Arveiler D, Amouyel P, Haas B, Cottel D, Bingham A, Ducimetière P, Ferrières J. Lascaux-Lefebvre V, et al. Among authors: ferrieres j. J Hum Hypertens. 1999 Sep;13(9):631-6. doi: 10.1038/sj.jhh.1000884. J Hum Hypertens. 1999. PMID: 10482973
Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene. CARDIGENE group.
Charron P, Tesson F, Poirier O, Nicaud V, Peuchmaurd M, Tiret L, Cambien F, Amouyel P, Dubourg O, Bouhour J, 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. Charron P, et al. Among authors: ferrieres j. Eur Heart J. 1999 Nov;20(21):1587-91. doi: 10.1053/euhj.1999.1696. Eur Heart J. 1999. PMID: 10529327
655 results