Palla R - Search Results

1

Genetic risk stratification to reduce inhibitor development in the early treatment of hemophilia A: a SIPPET analysis.

Rosendaal FR, Palla R, Garagiola I, Mannucci PM, Peyvandi F; SIPPET Study Group. Rosendaal FR, et al. Among authors: palla r. Blood. 2017 Oct 12;130(15):1757-1759. doi: 10.1182/blood-2017-06-791756. Epub 2017 Aug 2. Blood. 2017. PMID: 28768627 Free article. Clinical Trial.

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: palla r. 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. Among authors: palla r. 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

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. Among authors: palla r. Hum Mutat. 2006 Apr;27(4):330-6. doi: 10.1002/humu.20267. Hum Mutat. 2006. PMID: 16453338

5

The thrombospondin-1 N700S polymorphism is associated with early myocardial infarction without altering von Willebrand factor multimer size.

Zwicker JI, Peyvandi F, Palla R, Lombardi R, Canciani MT, Cairo A, Ardissino D, Bernardinelli L, Bauer KA, Lawler J, Mannucci P. Zwicker JI, et al. Among authors: palla r. Blood. 2006 Aug 15;108(4):1280-3. doi: 10.1182/blood-2006-04-015701. Epub 2006 May 9. Blood. 2006. PMID: 16684956 Free PMC article.

6

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. Among authors: palla r. Haematologica. 2008 Feb;93(2):232-9. doi: 10.3324/haematol.11739. Epub 2008 Jan 26. Haematologica. 2008. PMID: 18223285 Free article.

7

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: palla r. 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.

8

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. Haematologica. 2009 Feb;94(2):289-93. doi: 10.3324/haematol.13524. Epub 2008 Dec 30. Haematologica. 2009. PMID: 19116307 Free PMC article.

9

Introduction. Rare bleeding disorders: general aspects of clinical features, diagnosis, and management.

Peyvandi F, Palla R, Menegatti M, Mannucci PM. Peyvandi F, et al. Among authors: palla r. Semin Thromb Hemost. 2009 Jun;35(4):349-55. doi: 10.1055/s-0029-1225757. Epub 2009 Jul 13. Semin Thromb Hemost. 2009. PMID: 19598063

10

ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura.

Lotta LA, Garagiola I, Palla R, Cairo A, Peyvandi F. Lotta LA, et al. Among authors: palla r. Hum Mutat. 2010 Jan;31(1):11-9. doi: 10.1002/humu.21143. Hum Mutat. 2010. PMID: 19847791 Review.

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