Palla R - Search Results

1

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

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

Role of chloride ions in modulation of the interaction between von Willebrand factor and ADAMTS-13.

De Cristofaro R, Peyvandi F, Palla R, Lavoretano S, Lombardi R, Merati G, Romitelli F, Di Stasio E, Mannucci PM. De Cristofaro R, et al. Among authors: palla r. J Biol Chem. 2005 Jun 17;280(24):23295-302. doi: 10.1074/jbc.M501143200. Epub 2005 Apr 4. J Biol Chem. 2005. PMID: 15809291 Free article.

5

The natural mutation by deletion of Lys9 in the thrombin A-chain affects the pKa value of catalytic residues, the overall enzyme's stability and conformational transitions linked to Na+ binding.

De Cristofaro R, Carotti A, Akhavan S, Palla R, Peyvandi F, Altomare C, Mannucci PM. De Cristofaro R, et al. Among authors: palla r. FEBS J. 2006 Jan;273(1):159-69. doi: 10.1111/j.1742-4658.2005.05052.x. FEBS J. 2006. PMID: 16367756 Free article.

6

Molecular mapping of the chloride-binding site in von Willebrand factor (VWF): energetics and conformational effects on the VWF/ADAMTS-13 interaction.

De Cristofaro R, Peyvandi F, Baronciani L, Palla R, Lavoretano S, Lombardi R, Di Stasio E, Federici AB, Mannucci PM. De Cristofaro R, et al. Among authors: palla r. J Biol Chem. 2006 Oct 13;281(41):30400-11. doi: 10.1074/jbc.M603321200. Epub 2006 Aug 9. J Biol Chem. 2006. PMID: 16899464 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. 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.

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: 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.

9

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.

10

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

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