Peyvandi F - Search Results

1

An international registry of patients with plasminogen deficiency (HISTORY).

Shapiro AD, Menegatti M, Palla R, Boscarino M, Roberson C, Lanzi P, Bowen J, Nakar C, Janson IA, Peyvandi F. Shapiro AD, et al. Among authors: peyvandi f. Haematologica. 2020 Mar;105(3):554-561. doi: 10.3324/haematol.2019.241158. Epub 2020 Jan 30. Haematologica. 2020. PMID: 32001536 Free PMC article. Review.

2

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

3

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.

4

Pitfalls in molecular diagnosis in a family with severe factor VII (FVII) deficiency--misdiagnosis by direct sequence analysis using a PCR product.

Garagiola I, Palla R, Peyvandi F. Garagiola I, et al. Among authors: peyvandi f. Prenat Diagn. 2003 Sep;23(9):731-4. doi: 10.1002/pd.679. Prenat Diagn. 2003. PMID: 12975783

5

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

6

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.

7

Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patients.

Zadra G, Asselta R, Malcovati M, Santagostino E, Peyvandi F, Mannucci PM, Tenchini ML, Duga S. Zadra G, et al. Among authors: peyvandi f. Haematologica. 2004 Nov;89(11):1332-40. Haematologica. 2004. PMID: 15531455 Free article.

8

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.

9

Role of the 2 adenine (g.11293_11294insAA) insertion polymorphism in the 3' untranslated region of the factor VII (FVII) gene: molecular characterization of a patient with severe FVII deficiency.

Peyvandi F, Garagiola I, Palla R, Marziliano N, Mannucci PM. Peyvandi F, et al. Hum Mutat. 2005 Nov;26(5):455-61. doi: 10.1002/humu.20241. Hum Mutat. 2005. PMID: 16173031

10

Mechanisms of the interaction between two ADAMTS13 gene mutations leading to severe deficiency of enzymatic activity.

Peyvandi F, Lavoretano S, Palla R, Valsecchi C, Merati G, De Cristofaro R, Rossi E, Mannuccio Mannucci P. Peyvandi F, et al. Hum Mutat. 2006 Apr;27(4):330-6. doi: 10.1002/humu.20267. Hum Mutat. 2006. PMID: 16453338

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