Davignon J - Search Results

1

Response to HMG CoA reductase inhibitors in heterozygous familial hypercholesterolemia due to the 10-kb deletion ("French Canadian mutation") of the LDL receptor gene.

Karayan L, Qiu S, Betard C, Dufour R, Roederer G, Minnich A, Davignon J, Genest J Jr. Karayan L, et al. Among authors: davignon j. Arterioscler Thromb. 1994 Aug;14(8):1258-63. doi: 10.1161/01.atv.14.8.1258. Arterioscler Thromb. 1994. PMID: 8049186

2

PCSK9 R46L, lower LDL, and cardiovascular disease risk in familial hypercholesterolemia: a cross-sectional cohort study.

Saavedra YG, Dufour R, Davignon J, Baass A. Saavedra YG, et al. Among authors: davignon j. Arterioscler Thromb Vasc Biol. 2014 Dec;34(12):2700-5. doi: 10.1161/ATVBAHA.114.304406. Epub 2014 Oct 2. Arterioscler Thromb Vasc Biol. 2014. PMID: 25278291

3

Phenotypic heterogeneity associated with defective apolipoprotein B-100 and occurrence of the familial hypercholesterolemia phenotype in the absence of an LDL-receptor defect within a Canadian kindred.

Davignon J, Dufour R, Roy M, Bétard C, Ma Y, Ouellette S, Boulet L, Lussier-Cacan S. Davignon J, et al. Eur J Epidemiol. 1992 May;8 Suppl 1:10-7. doi: 10.1007/BF00145344. Eur J Epidemiol. 1992. PMID: 1505645

4

Identification of a second "French Canadian" LDL receptor gene deletion and development of a rapid method to detect both deletions.

Ma YH, Bétard C, Roy M, Davignon J, Kessling AM. Ma YH, et al. Among authors: davignon j. Clin Genet. 1989 Oct;36(4):219-28. doi: 10.1111/j.1399-0004.1989.tb03194.x. Clin Genet. 1989. PMID: 2805380

5

G-->A substitution at position -75 of the apolipoprotein A-I gene promoter. Evidence against a direct effect on HDL cholesterol levels.

Minnich A, DeLangavant G, Lavigne J, Roederer G, Lussier-Cacan S, Davignon J. Minnich A, et al. Among authors: davignon j. Arterioscler Thromb Vasc Biol. 1995 Oct;15(10):1740-5. doi: 10.1161/01.atv.15.10.1740. Arterioscler Thromb Vasc Biol. 1995. PMID: 7583551

6

Impact of a common mutation of the LDL receptor gene, in French-Canadian patients with familial hypercholesterolemia, on means, variances and correlations among traits of lipid metabolism.

Roy M, Sing CF, Betard C, Davignon J. Roy M, et al. Among authors: davignon j. Clin Genet. 1995 Feb;47(2):59-67. doi: 10.1111/j.1399-0004.1995.tb03925.x. Clin Genet. 1995. PMID: 7606845 Free article.

7

Severe familial HDL deficiency in French-Canadian kindreds. Clinical, biochemical, and molecular characterization.

Marcil M, Boucher B, Krimbou L, Solymoss BC, Davignon J, Frohlich J, Genest J Jr. Marcil M, et al. Among authors: davignon j. Arterioscler Thromb Vasc Biol. 1995 Aug;15(8):1015-24. doi: 10.1161/01.atv.15.8.1015. Arterioscler Thromb Vasc Biol. 1995. PMID: 7627690

8

Influence of probucol on enhanced LDL oxidation after fish oil treatment of hypertriglyceridemic patients.

Lussier-Cacan S, Dubreuil-Quidoz S, Roederer G, Leboeuf N, Boulet L, de Langavant GC, Davignon J, Naruszewicz M. Lussier-Cacan S, et al. Among authors: davignon j. Arterioscler Thromb. 1993 Dec;13(12):1790-7. doi: 10.1161/01.atv.13.12.1790. Arterioscler Thromb. 1993. PMID: 8241099

9

Influence of genetic variability in the nondeletion LDL-receptor allele on phenotypic variation in French-Canadian familial hypercholesterolemia heterozygotes sharing a 'null' LDL-receptor gene defect.

Bétard C, Kessling AM, Roy M, Davignon J. Bétard C, et al. Among authors: davignon j. Atherosclerosis. 1996 Jan 5;119(1):43-55. doi: 10.1016/0021-9150(95)05627-0. Atherosclerosis. 1996. PMID: 8929255

10

New methods for rapid detection of low-density lipoprotein receptor and apolipoprotein B gene mutations causing familial hypercholesterolemia.

Minnich A, Roy M, Chamberland A, Lavigne J, Davignon J. Minnich A, et al. Among authors: davignon j. Clin Biochem. 1995 Jun;28(3):277-84. doi: 10.1016/0009-9120(94)00072-4. Clin Biochem. 1995. PMID: 7554246

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