Alhenc-Gelas M - Search Results

1

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. Blood Coagul Fibrinolysis. 1995 Feb;6(1):35-41. doi: 10.1097/00001721-199502000-00006. Blood Coagul Fibrinolysis. 1995. PMID: 7795152 Review.

2

Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresis.

Gandrille S, Vidaud M, Aiach M, Alhenc-Gelas M, Fischer AM, Gouault-Heilman M, Toulon P, Fiessinger JN, Goossens M. Gandrille S, et al. Hum Mutat. 1992;1(6):491-500. doi: 10.1002/humu.1380010607. Hum Mutat. 1992. PMID: 1301959

3

Met 358 to Arg mutation of alpha 1-antitrypsin associated with protein C deficiency in a patient with mild bleeding tendency.

Vidaud D, Emmerich J, Alhenc-Gelas M, Yvart J, Fiessinger JN, Aiach M. Vidaud D, et al. J Clin Invest. 1992 May;89(5):1537-43. doi: 10.1172/JCI115746. J Clin Invest. 1992. PMID: 1569192 Free PMC article.

4

Molecular basis for antithrombin III type I deficiency: three novel mutations located in exon IV.

Vidaud D, Emmerich J, Sirieix ME, Sié P, Alhenc-Gelas M, Aiach M. Vidaud D, et al. Blood. 1991 Nov 1;78(9):2305-9. Blood. 1991. PMID: 1932746 Free article.

5

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

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

6

Incidence of activated protein C resistance caused by the ARG 506 GLN mutation in factor V in 113 unrelated symptomatic protein C-deficient patients. The French Network on the behalf of INSERM.

Gandrille S, Greengard JS, Alhenc-Gelas M, Juhan-Vague I, Abgrall JF, Jude B, Griffin JH, Aiach M. Gandrille S, et al. Blood. 1995 Jul 1;86(1):219-24. Blood. 1995. PMID: 7795227 Free article.

7

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. Thromb Haemost. 1994 Oct;72(4):534-9. Thromb Haemost. 1994. PMID: 7878627

8

First de novo mutations in the protein C gene of two patients with type I deficiency: a missense mutation and a splice site deletion.

Gandrille S, Jude B, Alhenc-Gelas M, Emmerich J, Aiach M. Gandrille S, et al. Blood. 1994 Oct 15;84(8):2566-70. Blood. 1994. PMID: 7919373 Free article.

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. Thromb Haemost. 1994 Jun;71(6):698-702. Thromb Haemost. 1994. PMID: 7974334 Clinical Trial.

10

Influence of six mutations of the protein C gene on the Gla domain conformation and calcium affinity.

Gaussem P, Gandrille S, Duchemin J, Emmerich J, Alhenc-Gelas M, Aillaud MF, Aiach M. Gaussem P, et al. Thromb Haemost. 1994 Jun;71(6):748-54. Thromb Haemost. 1994. PMID: 7974343

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