Peyvandi F - Search Results

1

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

2

Reduced circulating FABP2 in patients with moderate to severe COVID-19 may indicate enterocyte functional change rather than cell death.

Assante G, Tourna A, Carpani R, Ferrari F, Prati D, Peyvandi F, Blasi F, Bandera A, Le Guennec A, Chokshi S, Patel VC, Cox IJ, Valenti L, Youngson NA. Assante G, et al. Among authors: peyvandi f. Sci Rep. 2022 Nov 5;12(1):18792. doi: 10.1038/s41598-022-23282-x. Sci Rep. 2022. PMID: 36335131 Free PMC article.

3

Mild and Moderate Hemophilia A: Neglected Conditions, Still with Unmet Needs.

Castaman G, Peyvandi F, De Cristofaro R, Pollio B, Di Minno DMN. Castaman G, et al. Among authors: peyvandi f. J Clin Med. 2023 Feb 8;12(4):1368. doi: 10.3390/jcm12041368. J Clin Med. 2023. PMID: 36835904 Free PMC article.

4

Emicizumab prophylaxis in infants with hemophilia A (HAVEN 7): primary analysis of a phase 3b open-label trial.

Pipe SW, Collins P, Dhalluin C, Kenet G, Schmitt C, Buri M, Jiménez-Yuste V, Peyvandi F, Young G, Oldenburg J, Mancuso ME, Kavakli K, Kiialainen A, Deb S, Niggli M, Chang T, Lehle M, Fijnvandraat K. Pipe SW, et al. Among authors: peyvandi f. Blood. 2024 Apr 4;143(14):1355-1364. doi: 10.1182/blood.2023021832. Blood. 2024. PMID: 38127586 Free PMC article. Clinical Trial.

5

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

6

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.

7

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.

8

Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII.

Peyvandi F, Tuddenham EG, Akhtari AM, Lak M, Mannucci PM. Peyvandi F, et al. Br J Haematol. 1998 Mar;100(4):773-6. doi: 10.1046/j.1365-2141.1998.00620.x. Br J Haematol. 1998. PMID: 9531348 Free article.

9

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.

10

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.

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