Akhavan S - Search Results

1

Two naturally occurring mutations on FVII gene (S363I-W364C) altering intrinsic catalytic activity.

Peyvandi F, De Cristofaro R, Akhavan S, Carew JA, Landolfi R, Bauer KA, Mannucci PM. Peyvandi F, et al. Among authors: akhavan s. Thromb Haemost. 2002 Nov;88(5):750-5. Thromb Haemost. 2002. PMID: 12428089

2

Molecular and functional characterization of a natural homozygous Arg67His mutation in the prothrombin gene of a patient with a severe procoagulant defect contrasting with a mild hemorrhagic phenotype.

Akhavan S, De Cristofaro R, Peyvandi F, Lavoretano S, Landolfi R, Mannucci PM. Akhavan S, et al. Blood. 2002 Aug 15;100(4):1347-53. doi: 10.1182/blood-2002-01-0243. Blood. 2002. PMID: 12149217 Free article.

3

The P303T mutation in the human factor VII (FVII) gene alters the conformational state of the enzyme and causes a severe functional deficiency.

Peyvandi F, De Cristofaro R, Garagiola I, Palla R, Akhavan S, Landolfi R, Mannucci PM. Peyvandi F, et al. Among authors: akhavan s. Br J Haematol. 2004 Dec;127(5):576-84. doi: 10.1111/j.1365-2141.2004.05241.x. Br J Haematol. 2004. PMID: 15566361 Free article.

4

Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency.

Peyvandi F, Menegatti M, Santagostino E, Akhavan S, Uprichard J, Perry DJ, Perkins SJ, Mannucci PM. Peyvandi F, et al. Among authors: akhavan s. Br J Haematol. 2002 Jun;117(3):685-92. doi: 10.1046/j.1365-2141.2002.03486.x. Br J Haematol. 2002. PMID: 12028042 Free article.

5

Plasma prothrombin levels are not associated with mutations in the promoter region of the prothrombin gene.

Akhavan S, Lavoretano S, Chantarangkul V, Mannucci PM. Akhavan S, et al. Thromb Haemost. 2002 Nov;88(5):877-8. Thromb Haemost. 2002. PMID: 12428112 No abstract available.

6

Laboratory screening of thrombophilia. Evaluation of the diagnostic efficacy of a global test to detect congenital deficiencies of the protein C anticoagulant pathway.

Tripodi A, Akhavan S, Asti D, Faioni EM, Mannucci PM. Tripodi A, et al. Among authors: akhavan s. Blood Coagul Fibrinolysis. 1998 Sep;9(6):485-9. doi: 10.1097/00001721-199809000-00005. Blood Coagul Fibrinolysis. 1998. PMID: 9818998

7

Interaction between the G20210A mutation of the prothrombin gene and oral contraceptive use in deep vein thrombosis.

Martinelli I, Taioli E, Bucciarelli P, Akhavan S, Mannucci PM. Martinelli I, et al. Among authors: akhavan s. Arterioscler Thromb Vasc Biol. 1999 Mar;19(3):700-3. doi: 10.1161/01.atv.19.3.700. Arterioscler Thromb Vasc Biol. 1999. PMID: 10073976

8

Identification and three-dimensional structural analysis of nine novel mutations in patients with prothrombin deficiency.

Akhavan S, Mannucci PM, Lak M, Mancuso G, Mazzucconi MG, Rocino A, Jenkins PV, Perkins SJ. Akhavan S, et al. Thromb Haemost. 2000 Dec;84(6):989-97. Thromb Haemost. 2000. PMID: 11154146

9

Rare coagulation deficiencies.

Peyvandi F, Duga S, Akhavan S, Mannucci PM. Peyvandi F, et al. Among authors: akhavan s. Haemophilia. 2002 May;8(3):308-21. doi: 10.1046/j.1365-2516.2002.00633.x. Haemophilia. 2002. PMID: 12010428 Review.

10

A critical role for Gly25 in the B chain of human thrombin.

Akhavan S, Miteva MA, Villoutreix BO, Venisse L, Peyvandi F, Mannucci PM, Guillin MC, Bezeaud A. Akhavan S, et al. J Thromb Haemost. 2005 Jan;3(1):139-45. doi: 10.1111/j.1538-7836.2004.01086.x. J Thromb Haemost. 2005. PMID: 15634277 Free article.

We have recently identified (Akhavan S et al., Thromb Haemost 2000; 84: 989-97) a patient with a mild bleeding diathesis associated to an homozygous mutation in the thrombin B chain (Gly25Ser, chymotrypsinogen numbering, i.e. position 330 in human prothrombin number …

We have recently identified (Akhavan S et al., Thromb Haemost 2000; 84: 989-97) a patient with a mild bleeding diathesis assoc …

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