Peyvandi F - Search Results

1

Peyvandi F, Artoni A, Novembrino C, Aliberti S, Panigada M, Boscarino M, Gualtierotti R, Rossi F, Palla R, Martinelli I, Grasselli G, Blasi F, Tripodi A. Peyvandi F, et al. Haematologica. 2021 May 1;106(5):1472-1475. doi: 10.3324/haematol.2020.262634. Haematologica. 2021. PMID: 32855280 Free PMC article. No abstract available.

2

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

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. 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

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

5

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

6

Molecular characterization of an Italian patient with plasminogen deficiency and ligneous conjunctivitis.

Siboni SM, Spreafico M, Menegatti M, Martinelli I, Peyvandi F. Siboni SM, et al. Among authors: peyvandi f. Blood Coagul Fibrinolysis. 2007 Jan;18(1):81-4. doi: 10.1097/MBC.0b013e3280124f17. Blood Coagul Fibrinolysis. 2007. PMID: 17179833 Free article.

7

ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission.

Peyvandi F, Lavoretano S, Palla R, Feys HB, Vanhoorelbeke K, Battaglioli T, Valsecchi C, Canciani MT, Fabris F, Zver S, Réti M, Mikovic D, Karimi M, Giuffrida G, Laurenti L, Mannucci PM. Peyvandi F, et al. Haematologica. 2008 Feb;93(2):232-9. doi: 10.3324/haematol.11739. Epub 2008 Jan 26. Haematologica. 2008. PMID: 18223285 Free article.

8

Mechanistic studies on ADAMTS13 catalysis.

Di Stasio E, Lancellotti S, Peyvandi F, Palla R, Mannucci PM, De Cristofaro R. Di Stasio E, et al. Among authors: peyvandi f. Biophys J. 2008 Sep;95(5):2450-61. doi: 10.1529/biophysj.108.131532. Epub 2008 May 23. Biophys J. 2008. PMID: 18502798 Free PMC article.

9

Second international collaborative study evaluating performance characteristics of methods measuring the von Willebrand factor cleaving protease (ADAMTS-13).

Tripodi A, Peyvandi F, Chantarangkul V, Palla R, Afrasiabi A, Canciani MT, Chung DW, Ferrari S, Fujimura Y, Karimi M, Kokame K, Kremer Hovinga JA, Lämmle B, de Meyer SF, Plaimauer B, Vanhoorelbeke K, Varadi K, Mannucci PM. Tripodi A, et al. Among authors: peyvandi f. J Thromb Haemost. 2008 Sep;6(9):1534-41. doi: 10.1111/j.1538-7836.2008.03099.x. Epub 2008 Jul 26. J Thromb Haemost. 2008. PMID: 18662260 Free PMC article.

10

The first deletion mutation in the TSP1-6 repeat domain of ADAMTS13 in a family with inherited thrombotic thrombocytopenic purpura.

Palla R, Lavoretano S, Lombardi R, Garagiola I, Karimi M, Afrasiabi A, Ramzi M, De Cristofaro R, Peyvandi F. Palla R, et al. Among authors: peyvandi f. Haematologica. 2009 Feb;94(2):289-93. doi: 10.3324/haematol.13524. Epub 2008 Dec 30. Haematologica. 2009. PMID: 19116307 Free PMC article.

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