Mannucci PM - Search Results

1

Von Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS-IPS study.

Pagliari MT, Rosendaal FR, Ahmadinejad M, Badiee Z, Baghaipour MR, Baronciani L, Benítez Hidalgo O, Bodó I, Budde U, Castaman G, Eshghi P, Goudemand J, Karimi M, Keikhaei B, Lassila R, Leebeek FWG, Lopez Fernandez MF, Mannucci PM, Marino R, Oldenburg J, Peake I, Santoro C, Schneppenheim R, Tiede A, Toogeh G, Tosetto A, Trossaert M, Yadegari H, Zetterberg EMK, Peyvandi F, Federici AB, Eikenboom J. Pagliari MT, et al. Among authors: mannucci pm. J Thromb Haemost. 2022 May;20(5):1106-1114. doi: 10.1111/jth.15658. Epub 2022 Feb 22. J Thromb Haemost. 2022. PMID: 35092343 Free PMC article.

2

Advances in the genetics and treatment of von Willebrand disease.

Federici AB, Mannucci PM. Federici AB, et al. Among authors: mannucci pm. Curr Opin Pediatr. 2002 Feb;14(1):23-33. doi: 10.1097/00008480-200202000-00005. Curr Opin Pediatr. 2002. PMID: 11880730 Review.

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. Among authors: mannucci pm. Haematologica. 2002 May;87(5):512-4. Haematologica. 2002. PMID: 12010665

4

The elusive pathogenesis of von Willebrand disease Vicenza.

Castaman G, Rodeghiero F, Mannucci PM. Castaman G, et al. Among authors: mannucci pm. Blood. 2002 Jun 1;99(11):4243-4; author reply 4244. doi: 10.1182/blood.v99.11.4243. Blood. 2002. PMID: 12043692 Free article. No abstract available.

5

Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia.

Asselta R, Spena S, Duga S, Peyvandi F, Malcovati M, Mannucci PM, Tenchini ML. Asselta R, et al. Among authors: mannucci pm. Haematologica. 2002 Aug;87(8):855-9. Haematologica. 2002. PMID: 12161363

6

The thrombogram in rare inherited coagulation disorders: its relation to clinical bleeding.

Al Dieri R, Peyvandi F, Santagostino E, Giansily M, Mannucci PM, Schved JF, Béguin S, Hemker HC. Al Dieri R, et al. Among authors: mannucci pm. Thromb Haemost. 2002 Oct;88(4):576-82. Thromb Haemost. 2002. PMID: 12362226

7

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: mannucci pm. Thromb Haemost. 2002 Oct;88(4):690-1. Thromb Haemost. 2002. PMID: 12362247 No abstract available.

8

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: mannucci pm. 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.

9

Two naturally occurring mutations on FVII gene (S363I-W364C) altering intrinsic catalytic activity.

Peyvandi F, De Cristofaro R, Akhavan S, Carew JA, Landolfi R, Bauer KA, Mannucci PM. Peyvandi F, et al. Among authors: mannucci pm. Thromb Haemost. 2002 Nov;88(5):750-5. Thromb Haemost. 2002. PMID: 12428089

10

Von Willebrand's disease in the year 2003: towards the complete identification of gene defects for correct diagnosis and treatment.

Castaman G, Federici AB, Rodeghiero F, Mannucci PM. Castaman G, et al. Among authors: mannucci pm. Haematologica. 2003 Jan;88(1):94-108. Haematologica. 2003. PMID: 12551832 Free article. Review.

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