Gandrille S - 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. 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.

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

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

4

Identification of mutations in 90 of 121 consecutive symptomatic French patients with a type I protein C deficiency. The French INSERM Network on Molecular Abnormalities Responsible for Protein C and Protein S deficiencies.

Gandrille S, Aiach M. Gandrille S, et al. Blood. 1995 Oct 1;86(7):2598-605. Blood. 1995. PMID: 7670104 Free article.

5

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.

6

First frameshift mutation in the active protein S gene associated with a quantitative hereditary deficiency.

Borgel D, Gandrille S, Gouault-Heilmann M, Aiach M. Borgel D, et al. Among authors: gandrille s. Blood Coagul Fibrinolysis. 1994 Aug;5(4):593-600. Blood Coagul Fibrinolysis. 1994. PMID: 7841316

7

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.

8

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. Among authors: gandrille s. Thromb Haemost. 1994 Jun;71(6):748-54. Thromb Haemost. 1994. PMID: 7974343

9

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. Thromb Haemost. 1993 Nov 15;70(5):747-52. Thromb Haemost. 1993. PMID: 8128429

10

A review of mutations causing deficiencies of antithrombin, protein C and protein S.

Aiach M, Gandrille S, Emmerich J. Aiach M, et al. Among authors: gandrille s. Thromb Haemost. 1995 Jul;74(1):81-9. Thromb Haemost. 1995. PMID: 8578531 Review.

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