Aiach M - Search Results

1

Portal vein thrombosis and factor V Arg 506 to Gln mutation.

Levoir D, Emmerich J, Alhenc-Gelas M, Dumontier I, Petite JP, Fiessinger JN, Aiach M. Levoir D, et al. Among authors: aiach m. Thromb Haemost. 1995 Mar;73(3):550-1. Thromb Haemost. 1995. PMID: 7667842 No abstract available.

2

Clinical features in 36 patients homozygous for the ARG 506-->GLN factor V mutation.

Emmerich J, Alhenc-Gelas M, Aillaud MF, Juhan-Vague I, Jude B, Garcin JM, Dreyfus M, de Moerloose P, Le Querrec A, Priollet P, Berruyer M, Vallantin X, Wolf M, Aiach M, Fiessinger JN. Emmerich J, et al. Among authors: aiach m. Thromb Haemost. 1997 Apr;77(4):620-3. Thromb Haemost. 1997. PMID: 9134631

3

The factor V gene A4070G mutation and the risk of venous thrombosis.

Alhenc-Gelas M, Nicaud V, Gandrille S, van Dreden P, Amiral J, Aubry ML, Fiessinger JN, Emmerich J, Aiach M. Alhenc-Gelas M, et al. Among authors: aiach m. Thromb Haemost. 1999 Feb;81(2):193-7. Thromb Haemost. 1999. PMID: 10063990

4

Evaluation of APC resistance in the plasma of patients with Q506 mutation of factor V (factor V Leiden) and treated by oral anticoagulants.

Cadroy Y, Sié P, Alhenc-Gelas M, Aiach M. Cadroy Y, et al. Among authors: aiach m. Thromb Haemost. 1995 Apr;73(4):734-5. Thromb Haemost. 1995. PMID: 7495093 No abstract available.

5

Mutation in the factor V gene and the risk of myocardial infarction.

Emmerich J, Aiach M. Emmerich J, et al. Among authors: aiach m. N Engl J Med. 1995 Sep 28;333(13):880-1. N Engl J Med. 1995. PMID: 7651494 No abstract available.

6

A rapid screening method for the factor V Arg506-->Gln mutation.

Gandrille S, Alhenc-Gelas M, Aiach M. Gandrille S, et al. Among authors: aiach m. Blood Coagul Fibrinolysis. 1995 May;6(3):245-8. doi: 10.1097/00001721-199505000-00008. Blood Coagul Fibrinolysis. 1995. PMID: 7654939

7

Protein C infusion in a patient with inherited protein C deficiency caused by two missense mutations: Arg 178 to Gln and Arg-1 to His.

Alhenc-Gelas M, Emmerich J, Gandrille S, Aubry ML, Benaily N, Fiessinger JN, Aiach M. Alhenc-Gelas M, et al. Among authors: aiach m. Blood Coagul Fibrinolysis. 1995 Feb;6(1):35-41. doi: 10.1097/00001721-199502000-00006. Blood Coagul Fibrinolysis. 1995. PMID: 7795152 Review.

8

Molecular basis of antithrombin type I deficiency: the first large in-frame deletion and two novel mutations in exon 6.

Emmerich J, Chadeuf G, Alhenc-Gelas M, Gouault-Heilman M, Toulon P, Fiessinger JN, Aiach M. Emmerich J, et al. Among authors: aiach m. Thromb Haemost. 1994 Oct;72(4):534-9. Thromb Haemost. 1994. PMID: 7878627

9

Adjusted versus fixed doses of the low-molecular-weight heparin fragmin in the treatment of deep vein thrombosis. Fragmin-Study Group.

Alhenc-Gelas M, Jestin-Le Guernic C, Vitoux JF, Kher A, Aiach M, Fiessinger JN. Alhenc-Gelas M, et al. Among authors: aiach m. Thromb Haemost. 1994 Jun;71(6):698-702. Thromb Haemost. 1994. PMID: 7974334 Clinical Trial.

10

Compound heterozygosity in a family with protein C deficiency illustrating the complexity of the underlying molecular mechanism.

Gandrille S, Jude B, Alhenc-Gelas M, Millaire A, Aiach M. Gandrille S, et al. Among authors: aiach m. Thromb Haemost. 1993 Nov 15;70(5):747-52. Thromb Haemost. 1993. PMID: 8128429

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