Torres AL - Search Results

1

Detection of a novel mutation (stop 468) in exon 10 of the low-density lipoprotein receptor gene causing familial hypercholesterolemia among French Canadians.

Simard J, Moorjani S, Vohl MC, Couture P, Torres AL, Gagné C, Després JP, Labrie F, Lupien PJ. Simard J, et al. Among authors: torres al. Hum Mol Genet. 1994 Sep;3(9):1689-91. doi: 10.1093/hmg/3.9.1689. Hum Mol Genet. 1994. PMID: 7833932 No abstract available.

2

Mutations of low-density-lipoprotein-receptor gene, variation in plasma cholesterol, and expression of coronary heart disease in homozygous familial hypercholesterolaemia.

Moorjani S, Roy M, Torres A, Bétard C, Gagné C, Lambert M, Brun D, Davignon J, Lupien P. Moorjani S, et al. Lancet. 1993 May 22;341(8856):1303-6. doi: 10.1016/0140-6736(93)90815-x. Lancet. 1993. PMID: 8098448

3

Rapid restriction fragment analysis for screening four point mutations of the low-density lipoprotein receptor gene in French Canadians.

Vohl MC, Couture P, Moorjani S, Torres AL, Gagné C, Després JP, Lupien PJ, Labrie F, Simard J. Vohl MC, et al. Among authors: torres al. Hum Mutat. 1995;6(3):243-6. doi: 10.1002/humu.1380060307. Hum Mutat. 1995. PMID: 8535443

4

Heterozygous familial hypercholesterolemia in children: low-density lipoprotein receptor mutational analysis and variation in the expression of plasma lipoprotein-lipid concentrations.

Torres AL, Moorjani S, Vohl MC, Gagné C, Lamarche B, Brun LD, Lupien PJ, Després JP. Torres AL, et al. Atherosclerosis. 1996 Sep 27;126(1):163-71. doi: 10.1016/0021-9150(96)05907-2. Atherosclerosis. 1996. PMID: 8879444

5

Geographic distribution of French-Canadian low-density lipoprotein receptor gene mutations in the Province of Quebec.

Vohl MC, Moorjani S, Roy M, Gaudet D, Torres AL, Minnich A, Gagné C, Tremblay G, Lambert M, Bergeron J, Couture P, Perron P, Blaichman S, Brun LD, Davignon J, Lupien PJ, Després JP. Vohl MC, et al. Among authors: torres al. Clin Genet. 1997 Jul;52(1):1-6. doi: 10.1111/j.1399-0004.1997.tb02506.x. Clin Genet. 1997. PMID: 9272705

6

Identification of three mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia among French Canadians.

Couture P, Vohl MC, Gagné C, Gaudet D, Torres AL, Lupien PJ, Després JP, Labrie F, Simard J, Moorjani S. Couture P, et al. Among authors: torres al. Hum Mutat. 1998;Suppl 1:S226-31. doi: 10.1002/humu.1380110173. Hum Mutat. 1998. PMID: 9452094 No abstract available.

7

Prevention of raised low-density lipoprotein cholesterol in a patient with familial hypercholesterolaemia and lipoprotein lipase deficiency.

Zambon A, Torres A, Bijvoet S, Gagne C, Moorjani S, Lupien PJ, Hayden MR, Brunzell JD. Zambon A, et al. Lancet. 1993 May 1;341(8853):1119-21. doi: 10.1016/0140-6736(93)93129-o. Lancet. 1993. PMID: 8097805

8

Homozygous familial hypercholesterolaemia.

Gagné C, Moorjani S, Torres AL, Brun D, Lupien PJ. Gagné C, et al. Among authors: torres al. Lancet. 1994 Jan 15;343(8890):177. doi: 10.1016/s0140-6736(94)90968-7. Lancet. 1994. PMID: 7904025 No abstract available.

9

Molecular genetic analysis of severe protein C deficiency.

Millar DS, Johansen B, Berntorp E, Minford A, Bolton-Maggs P, Wensley R, Kakkar V, Schulman S, Torres A, Bosch N, Cooper DN. Millar DS, et al. Hum Genet. 2000 Jun;106(6):646-53. doi: 10.1007/s004390000315. Hum Genet. 2000. PMID: 10942114

10

Coumarin/β-Cyclodextrin Inclusion Complexes Promote Acceleration and Improvement of Wound Healing.

Dutra FVA, Francisco CS, Carneiro Pires B, Borges MMC, Torres ALH, Resende VA, Mateus MFM, Cipriano DF, Miguez FB, Freitas JCC, Teixeira JP, Borges WS, Guimarães L, da Cunha EFF, Ramalho TC, Nascimento CS Jr, De Sousa FB, Costa RA, Lacerda V Junior, Borges KB. Dutra FVA, et al. Among authors: torres alh. ACS Appl Mater Interfaces. 2024 Jun 19;16(24):30900-30914. doi: 10.1021/acsami.4c05069. Epub 2024 Jun 7. ACS Appl Mater Interfaces. 2024. PMID: 38848495

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