Elbaz A - Search Results

1

Association between the Glu298Asp polymorphism in the endothelial constitutive nitric oxide synthase gene and brain infarction. The GENIC Investigators.

Elbaz A, Poirier O, Moulin T, Chédru F, Cambien F, Amarenco P. Elbaz A, et al. Stroke. 2000 Jul;31(7):1634-9. doi: 10.1161/01.str.31.7.1634. Stroke. 2000. PMID: 10884465

2

Genetic susceptibility and ischaemic stroke.

Elbaz A, Amarenco P. Elbaz A, et al. Curr Opin Neurol. 1999 Feb;12(1):47-55. doi: 10.1097/00019052-199902000-00009. Curr Opin Neurol. 1999. PMID: 10097885 Review.

3

Familial aggregation of Parkinson's disease: a population-based case-control study in Europe. EUROPARKINSON Study Group.

Elbaz A, Grigoletto F, Baldereschi M, Breteler MM, Manubens-Bertran JM, Lopez-Pousa S, Dartigues JF, Alpérovitch A, Tzourio C, Rocca WA. Elbaz A, et al. Neurology. 1999 Jun 10;52(9):1876-82. doi: 10.1212/wnl.52.9.1876. Neurology. 1999. PMID: 10371537

4

The association between the Val34Leu polymorphism in the factor XIII gene and brain infarction.

Elbaz A, Poirier O, Canaple S, Chédru F, Cambien F, Amarenco P. Elbaz A, et al. Blood. 2000 Jan 15;95(2):586-91. Blood. 2000. PMID: 10627467 Free article.

5

Common carotid artery intima-media thickness and brain infarction : the Etude du Profil Génétique de l'Infarctus Cérébral (GENIC) case-control study. The GENIC Investigators.

Touboul PJ, Elbaz A, Koller C, Lucas C, Adraï V, Chédru F, Amarenco P. Touboul PJ, et al. Among authors: elbaz a. Circulation. 2000 Jul 18;102(3):313-8. doi: 10.1161/01.cir.102.3.313. Circulation. 2000. PMID: 10899095

6

Parkinson's disease, smoking, and family history. EUROPARKINSON Study Group.

Elbaz A, Manubens-Bertran JM, Baldereschi M, Breteler MM, Grigoletto F, Lopez-Pousa S, Dartigues JF, Alpérovitch A, Rocca WA, Tzourio C. Elbaz A, et al. J Neurol. 2000 Oct;247(10):793-8. doi: 10.1007/s004150070095. J Neurol. 2000. PMID: 11127536

7

Plasminogen activator inhibitor genotype and brain infarction.

Elbaz A, Cambien F, Amarenco P; GENIC investigators. Elbaz A, et al. Circulation. 2001 Jan 16;103(2):e13-4; author reply e13-4. doi: 10.1161/01.cir.103.2.e13. Circulation. 2001. PMID: 11208705 No abstract available.

8

Association studies between haemochromatosis gene mutations and the risk of cardiovascular diseases.

Hetet G, Elbaz A, Gariepy J, Nicaud V, Arveiler D, Morrison C, Kee F, Evans A, Simon A, Amarenco P, Cambien F, Grandchamp B. Hetet G, et al. Among authors: elbaz a. Eur J Clin Invest. 2001 May;31(5):382-8. doi: 10.1046/j.1365-2362.2001.00829.x. Eur J Clin Invest. 2001. PMID: 11380589

9

Characterization of polymorphic structure of cathepsin G gene: role in cardiovascular and cerebrovascular diseases.

Herrmann SM, Funke-Kaiser H, Schmidt-Petersen K, Nicaud V, Gautier-Bertrand M, Evans A, Kee F, Arveiler D, Morrison C, Orzechowski HD, Elbaz A, Amarenco P, Cambien F, Paul M. Herrmann SM, et al. Among authors: elbaz a. Arterioscler Thromb Vasc Biol. 2001 Sep;21(9):1538-43. doi: 10.1161/hq0901.095555. Arterioscler Thromb Vasc Biol. 2001. PMID: 11557685

10

Association between Parkinson's disease and polymorphisms in the nNOS and iNOS genes in a community-based case-control study.

Levecque C, Elbaz A, Clavel J, Richard F, Vidal JS, Amouyel P, Tzourio C, Alpérovitch A, Chartier-Harlin MC. Levecque C, et al. Among authors: elbaz a. Hum Mol Genet. 2003 Jan 1;12(1):79-86. doi: 10.1093/hmg/ddg009. Hum Mol Genet. 2003. PMID: 12490535

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