Mannucci PM - Search Results

1

Pattern of comorbidities and 1-year mortality in elderly patients with COPD hospitalized in internal medicine wards: data from the RePoSI Registry.

Argano C, Scichilone N, Natoli G, Nobili A, Corazza GR, Mannucci PM, Perticone F, Corrao S; REPOSI Investigators. Argano C, et al. Among authors: mannucci pm. Intern Emerg Med. 2021 Mar;16(2):389-400. doi: 10.1007/s11739-020-02412-1. Epub 2020 Jul 27. Intern Emerg Med. 2021. PMID: 32720248 Free PMC article.

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

3

Von Willebrand factor cleaving protease (ADAMTS-13) in 123 patients with connective tissue diseases (systemic lupus erythematosus and systemic sclerosis).

Mannucci PM, Vanoli M, Forza I, Canciani MT, Scorza R. Mannucci PM, et al. Haematologica. 2003 Aug;88(8):914-8. Haematologica. 2003. PMID: 12935979

4

Recessively inherited coagulation disorders.

Mannucci PM, Duga S, Peyvandi F. Mannucci PM, et al. Blood. 2004 Sep 1;104(5):1243-52. doi: 10.1182/blood-2004-02-0595. Epub 2004 May 11. Blood. 2004. PMID: 15138162 Free article. Review.

5

von Willebrand factor cleaving protease (ADAMTS-13) and ADAMTS-13 neutralizing autoantibodies in 100 patients with thrombotic thrombocytopenic purpura.

Peyvandi F, Ferrari S, Lavoretano S, Canciani MT, Mannucci PM. Peyvandi F, et al. Among authors: mannucci pm. Br J Haematol. 2004 Nov;127(4):433-9. doi: 10.1111/j.1365-2141.2004.05217.x. Br J Haematol. 2004. PMID: 15521921 Free article.

6

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: mannucci pm. 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.

7

Clinical and laboratory patterns of the haemolytic uraemic syndrome and thrombotic thrombocytopenic purpura in southern Iran.

Karimi M, Sabzi A, Peyvandi F, Mannucci PM. Karimi M, et al. Among authors: mannucci pm. Intern Emerg Med. 2006;1(1):35-9. doi: 10.1007/BF02934718. Intern Emerg Med. 2006. PMID: 16941811

8

TTP and ADAMTS13: When Is Testing Appropriate?

Mannucci PM, Peyvandi F. Mannucci PM, et al. Hematology Am Soc Hematol Educ Program. 2007:121-6. doi: 10.1182/asheducation-2007.1.121. Hematology Am Soc Hematol Educ Program. 2007. PMID: 18024619 Review.

9

Thrombophilia screening: little role for the JAK2V617F mutation.

Mannucci PM, Peyvandi F. Mannucci PM, et al. Mayo Clin Proc. 2008 Apr;83(4):398-9. doi: 10.4065/83.4.398. Mayo Clin Proc. 2008. PMID: 18380984 No abstract available.

10

The genetic basis of coronary artery disease: from candidate genes to whole genome analysis.

Franchini M, Peyvandi F, Mannucci PM. Franchini M, et al. Among authors: mannucci pm. Trends Cardiovasc Med. 2008 Jul;18(5):157-62. doi: 10.1016/j.tcm.2008.04.003. Trends Cardiovasc Med. 2008. PMID: 18790385 Review.

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