Peyvandi F - Search Results

1

Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs.

Asselta R, Duga S, Spena S, Santagostino E, Peyvandi F, Piseddu G, Targhetta R, Malcovati M, Mannucci PM, Tenchini ML. Asselta R, et al. Among authors: peyvandi f. Blood. 2001 Dec 15;98(13):3685-92. doi: 10.1182/blood.v98.13.3685. Blood. 2001. PMID: 11739173 Free article.

2

Factor V (Arg 506-->Gln) mutation in young survivors of myocardial infarction.

Ardissino D, Peyvandi F, Merlini PA, Colombi E, Mannucci PM. Ardissino D, et al. Among authors: peyvandi f. Thromb Haemost. 1996 May;75(5):701-2. Thromb Haemost. 1996. PMID: 8725707

3

Frequency of factor V Arg506 Gln in Italians.

Mannucci PM, Duca F, Peyvandi F, Tagliabue L, Merati G, Martinelli I, Cattaneo M. Mannucci PM, et al. Among authors: peyvandi f. Thromb Haemost. 1996 Apr;75(4):694. Thromb Haemost. 1996. PMID: 8743202 No abstract available.

4

The G1456 to T mutation in the thrombomodulin gene is not frequent in patients with venous thrombosis.

Faioni EM, Merati G, Peyvandi F, Bettini PM, Mannucci PM. Faioni EM, et al. Among authors: peyvandi f. Blood. 1997 Feb 15;89(4):1467. Blood. 1997. PMID: 9028975 Free article. No abstract available.

5

Gene polymorphisms predicting high plasma levels of coagulation and fibrinolysis proteins. A study in centenarians.

Mannucci PM, Mari D, Merati G, Peyvandi F, Tagliabue L, Sacchi E, Taioli E, Sansoni P, Bertolini S, Franceschi C. Mannucci PM, et al. Among authors: peyvandi f. Arterioscler Thromb Vasc Biol. 1997 Apr;17(4):755-9. doi: 10.1161/01.atv.17.4.755. Arterioscler Thromb Vasc Biol. 1997. PMID: 9108791

6

Symptoms of inherited factor V deficiency in 35 Iranian patients.

Lak M, Sharifian R, Peyvandi F, Mannucci PM. Lak M, et al. Among authors: peyvandi f. Br J Haematol. 1998 Dec;103(4):1067-9. doi: 10.1046/j.1365-2141.1998.01077.x. Br J Haematol. 1998. PMID: 9886321 Free article.

7

Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency.

Neerman-Arbez M, Johnson KM, Morris MA, McVey JH, Peyvandi F, Nichols WC, Ginsburg D, Rossier C, Antonarakis SE, Tuddenham EG. Neerman-Arbez M, et al. Among authors: peyvandi f. Blood. 1999 Apr 1;93(7):2253-60. Blood. 1999. PMID: 10090934 Free article.

8

Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia.

Lak M, Keihani M, Elahi F, Peyvandi F, Mannucci PM. Lak M, et al. Among authors: peyvandi f. Br J Haematol. 1999 Oct;107(1):204-6. doi: 10.1046/j.1365-2141.1999.01681.x. Br J Haematol. 1999. PMID: 10520042 Free article.

9

Rare coagulation disorders.

Peyvandi F, Mannucci PM. Peyvandi F, et al. Thromb Haemost. 1999 Oct;82(4):1207-14. Thromb Haemost. 1999. PMID: 10544899 Review.

10

Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiency.

Peyvandi F, Jenkins PV, Mannucci PM, Billio A, Zeinali S, Perkins SJ, Perry DJ. Peyvandi F, et al. Thromb Haemost. 2000 Aug;84(2):250-7. Thromb Haemost. 2000. PMID: 10959697

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