Sié P - Search Results

1

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. Among authors: sie p. Blood. 1991 Nov 1;78(9):2305-9. Blood. 1991. PMID: 1932746 Free article.

2

Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene.

Picard V, Bura A, Emmerich J, Alhenc-Gelas M, Biron C, Houbouyan-Reveillard LL, Molho P, Labatide-Alanore A, Sié P, Toulon P, Verdy E, Aiach M. Picard V, et al. Among authors: sie p. Br J Haematol. 2000 Sep;110(3):731-4. doi: 10.1046/j.1365-2141.2000.02245.x. Br J Haematol. 2000. PMID: 10997988 Free article.

3

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. Among authors: sie p. Br J Haematol. 1991 Jul;78(3):414-20. doi: 10.1111/j.1365-2141.1991.tb04457.x. Br J Haematol. 1991. PMID: 1873224

4

[Biological monitoring of treatment with low molecular weight heparin].

Aiach M, Sié P. Aiach M, et al. Among authors: sie p. Ann Biol Clin (Paris). 1988;46(9):715-8. Ann Biol Clin (Paris). 1988. PMID: 2851948 Review. French.

5

Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene.

Gandrille S, Borgel D, Eschwege-Gufflet V, Aillaud M, Dreyfus M, Matheron C, Gaussem P, Abgrall JF, Jude B, Sie P, et al. Gandrille S, et al. Among authors: sie p. Blood. 1995 Jan 1;85(1):130-8. Blood. 1995. PMID: 7803790 Free article.

6

[Treatment of deep venous thrombosis. Comparative study of a low molecular weight heparin fragment (Fragmin) by the subcutaneous route and standard heparin by the continuous intravenous route. A multicenter study].

Aiach M, Fiessinger JN, Vitoux JF, Derlon A, Grollier G, Le Querrec A, Gouault-Heilmann M, Huet Y, Franco A, Polack B, Pouzol P, Dubois A, Schved JF, Boneu B, Guittard J, Sie P, Heilmann JJ, Kher A, Haye I. Aiach M, et al. Among authors: sie p. Rev Med Interne. 1989 Jul-Aug;10(4):375-81. Rev Med Interne. 1989. PMID: 2552552 Clinical Trial. French.

7

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: sie p. Thromb Haemost. 1995 Apr;73(4):734-5. Thromb Haemost. 1995. PMID: 7495093 No abstract available.

8

Pharmacodynamics and pharmacokinetics of dermatan sulfate in humans.

Dol F, Houin G, Rostin M, Montastruc JL, Dupouy D, Gianese F, Sie P, Boneu B. Dol F, et al. Among authors: sie p. Blood. 1989 Oct;74(5):1577-82. Blood. 1989. PMID: 2790187 Free article.

9

Antithrombotic properties of a dermatan sulfate hexadecasaccharide fractionated by affinity for heparin cofactor II.

Sie P, Dupouy D, Caranobe C, Petitou M, Boneu B. Sie P, et al. Blood. 1993 Apr 1;81(7):1771-7. Blood. 1993. PMID: 8461463 Free article.

10

Role of 4 platelet membrane glycoprotein polymorphisms on experimental arterial thrombus formation in men.

Cadroy Y, Sakariassen KS, Charlet JP, Thalamas C, Boneu B, Sie P. Cadroy Y, et al. Among authors: sie p. Blood. 2001 Nov 15;98(10):3159-61. doi: 10.1182/blood.v98.10.3159. Blood. 2001. PMID: 11698306 Free article.

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