Peyvandi F - Search Results

1

Frequency of the p.Gly262Asp mutation in congenital Factor X deficiency.

Epcacan S, Menegatti M, Akbayram S, Cairo A, Peyvandi F, Oner AF. Epcacan S, et al. Among authors: peyvandi f. Eur J Clin Invest. 2015 Oct;45(10):1087-91. doi: 10.1111/eci.12511. Epub 2015 Sep 2. Eur J Clin Invest. 2015. PMID: 26222694

2

Apparently dominant transmission of a recessive disease: deficiency of factor VII in Iranian Jews.

Tagliabue L, Duca F, Peyvandi F. Tagliabue L, et al. Among authors: peyvandi f. Ann Ital Med Int. 2000 Oct-Dec;15(4):263-6. Ann Ital Med Int. 2000. PMID: 11202627

3

Factor XI deficiency in Iranians: its clinical manifestations in comparison with those of classic hemophilia.

Peyvandi F, Lak M, Mannucci PM. Peyvandi F, et al. Haematologica. 2002 May;87(5):512-4. Haematologica. 2002. PMID: 12010665

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. 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

Relatively poor performance of clinical laboratories for DNA analyses in the detection of two thrombophilic mutations--a cause for concern.

Tripodi A, Peyvandi F, Chantarangkul V, Menegatti M, Mannucci PM. Tripodi A, et al. Among authors: peyvandi f. Thromb Haemost. 2002 Oct;88(4):690-1. Thromb Haemost. 2002. PMID: 12362247 No abstract available.

6

Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency: molecular characterization by expression of the recombinant protein.

Duga S, Montefusco MC, Asselta R, Malcovati M, Peyvandi F, Santagostino E, Mannucci PM, Tenchini ML. Duga S, et al. Among authors: peyvandi f. Blood. 2003 Jan 1;101(1):173-7. doi: 10.1182/blood-2002-06-1928. Epub 2002 Aug 15. Blood. 2003. PMID: 12393490 Free article.

7

Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: Broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutations.

Montefusco MC, Duga S, Asselta R, Malcovati M, Peyvandi F, Santagostino E, Mannucci PM, Tenchini ML. Montefusco MC, et al. Among authors: peyvandi f. Blood. 2003 Nov 1;102(9):3210-6. doi: 10.1182/blood-2003-03-0922. Epub 2003 Jun 19. Blood. 2003. PMID: 12816860 Free article.

8

Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency.

Peyvandi F, Tagliabue L, Menegatti M, Karimi M, Komáromi I, Katona E, Muszbek L, Mannucci PM. Peyvandi F, et al. Hum Mutat. 2004 Jan;23(1):98. doi: 10.1002/humu.9206. Hum Mutat. 2004. PMID: 14695539

9

A rare inherited coagulation disorder: combined homozygous factor VII and factor X deficiency.

Menegatti M, Karimi M, Garagiola I, Mannucci P, Peyvandi F. Menegatti M, et al. Among authors: peyvandi f. Am J Hematol. 2004 Sep;77(1):90-1. doi: 10.1002/ajh.20132. Am J Hematol. 2004. PMID: 15307115 Free article.

10

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. 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.

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