Gandrille S - Search Results

1

Mechanism of protein C deficiency in a patient with arginine 358 alpha 1-antitrypsin (Pittsburgh mutation): role in the maintenance of hemostatic balance.

Emmerich J, Alhenc-Gelas M, Gandrille S, Guichet C, Fiessinger JN, Aiach M. Emmerich J, et al. Among authors: gandrille s. J Lab Clin Med. 1995 Apr;125(4):531-9. J Lab Clin Med. 1995. PMID: 7706910

2

Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S Deficiencies.

Borgel D, Duchemin J, Alhenc-Gelas M, Matheron C, Aiach M, Gandrille S. Borgel D, et al. Among authors: gandrille s. J Lab Clin Med. 1996 Aug;128(2):218-27. doi: 10.1016/s0022-2143(96)90015-3. J Lab Clin Med. 1996. PMID: 8765219 Clinical Trial.

3

Cleaved protein S (PS), total PS, free PS, and activated protein C cofactor activity as risk factors for venous thromboembolism.

Borgel D, Reny JL, Fischelis D, Gandrille S, Emmerich J, Fiessinger JN, Aiach M. Borgel D, et al. Among authors: gandrille s. Clin Chem. 2003 Apr;49(4):575-80. doi: 10.1373/49.4.575. Clin Chem. 2003. PMID: 12651809

4

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

5

Molecular basis for hereditary antithrombin III quantitative deficiencies: a stop codon in exon IIIa and a frameshift in exon VI.

Gandrille S, Vidaud D, Emmerich J, Clauser E, Sié P, Fiessinger JN, Alhenc-Gelas M, Priollet P, Aiach M. Gandrille S, et al. Br J Haematol. 1991 Jul;78(3):414-20. doi: 10.1111/j.1365-2141.1991.tb04457.x. Br J Haematol. 1991. PMID: 1873224

6

Important role of arginine 129 in heparin-binding site of antithrombin III. Identification of a novel mutation arginine 129 to glutamine.

Gandrille S, Aiach M, Lane DA, Vidaud D, Molho-Sabatier P, Caso R, de Moerloose P, Fiessinger JN, Clauser E. Gandrille S, et al. J Biol Chem. 1990 Nov 5;265(31):18997-9001. J Biol Chem. 1990. PMID: 2229057 Free article.

7

A study of fibrinogen and fibrinolysis in 10 adults with nephrotic syndrome.

Gandrille S, Jouvin MH, Toulon P, Remy P, Fiessinger JN, Roncato M, Moatti N, Aiach M. Gandrille S, et al. Thromb Haemost. 1988 Jun 16;59(3):445-50. Thromb Haemost. 1988. PMID: 3142081

8

Association of inherited dysfibrinogenaemia and protein C deficiency in two unrelated families.

Gandrille S, Priollet P, Capron L, Roncato M, Fiessinger JN, Aiach M. Gandrille S, et al. Br J Haematol. 1988 Mar;68(3):329-37. doi: 10.1111/j.1365-2141.1988.tb04210.x. Br J Haematol. 1988. PMID: 3355791

9

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

10

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

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