Lapecorella M - Search Results

1

Severe venous thromboembolism in a young man with Klinefelter's syndrome and heterozygosis for both G20210A prothrombin and factor V Leiden mutations.

Lapecorella M, Marino R, De Pergola G, Scaraggi FA, Speciale V, De Mitrio V. Lapecorella M, et al. Blood Coagul Fibrinolysis. 2003 Jan;14(1):95-8. doi: 10.1097/00001721-200301000-00017. Blood Coagul Fibrinolysis. 2003. PMID: 12544736

2

Beneficial effects of postmenopausal hormone replacement therapy with transdermal estradiol on sensitivity to activated protein C.

De Mitrio V, Marino R, Cicinelli E, Galantino P, Di Bari L, Giannoccaro F, De Pergola G, Lapecorella M, Schonauer S, Schiraldi O. De Mitrio V, et al. Among authors: lapecorella m. Blood Coagul Fibrinolysis. 2000 Mar;11(2):175-82. Blood Coagul Fibrinolysis. 2000. PMID: 10759011

3

Upper extremity deep vein thrombosis after suspension of progesterone-only oral treatment.

Lapecorella M, Orecchioni A, Dell'Orso L, Mariani G. Lapecorella M, et al. Blood Coagul Fibrinolysis. 2007 Jul;18(5):513-7. doi: 10.1097/MBC.0b013e3281a3bed8. Blood Coagul Fibrinolysis. 2007. PMID: 17581329

4

Evidence-based recommendations on the treatment of von Willebrand disease in Italy.

Mannucci PM, Franchini M, Castaman G, Federici AB; Italian Association of Hemophilia Centers. Mannucci PM, et al. Blood Transfus. 2009 Apr;7(2):117-26. doi: 10.2450/2008.0052-08. Blood Transfus. 2009. PMID: 19503633 Free PMC article.

5

Unusual onset of venous thromboembolism and heparin-induced thrombocytopenia in a patient with essential thrombocythemia.

Lapecorella M, Lucchesi A, Di Ianni M, Napolitano M, Coletti G, Di Leonardo G, Dell'Orso L, Barnabei R, Mariani G. Lapecorella M, et al. Blood Coagul Fibrinolysis. 2010 Jan;21(1):85-90. doi: 10.1097/MBC.0b013e32832f2b08. Blood Coagul Fibrinolysis. 2010. PMID: 19923984

6

Evidence of jak2 val617phe positive essential thrombocythemia with splanchnic thrombosis during estroprogestinic treatment.

Lapecorella M, Tabilio A, Lucchesi A, Napolitano M, Colagrande M, Di Ianni M, Mariani G. Lapecorella M, et al. Blood Coagul Fibrinolysis. 2008 Jul;19(5):453-7. doi: 10.1097/MBC.0b013e3283079e46. Blood Coagul Fibrinolysis. 2008. PMID: 18600099

7

Factor VII deficiency: defining the clinical picture and optimizing therapeutic options.

Lapecorella M, Mariani G; International Registry on Congenital Factor VII Deficiency. Lapecorella M, et al. Haemophilia. 2008 Nov;14(6):1170-5. doi: 10.1111/j.1365-2516.2008.01844.x. Haemophilia. 2008. PMID: 19141157 Review.

8

Vitamin K-induced modification of coagulation phenotype in VKORC1 homozygous deficiency.

Marchetti G, Caruso P, Lunghi B, Pinotti M, Lapecorella M, Napolitano M, Canella A, Mariani G, Bernardi F. Marchetti G, et al. Among authors: lapecorella m. J Thromb Haemost. 2008 May;6(5):797-803. doi: 10.1111/j.1538-7836.2008.02934.x. Epub 2008 Feb 25. J Thromb Haemost. 2008. PMID: 18315553 Free article.

9

Effective hemostasis during minor surgery in a case of hereditary combined deficiency of vitamin K-dependent clotting factors.

Lapecorella M, Napolitano M, Bernardi F, Pinotti M, Sbrighi PS, Marchetti G, Canella A, Caruso P, Orecchioni A, Mariani G. Lapecorella M, et al. Clin Appl Thromb Hemost. 2010 Apr;16(2):221-3. doi: 10.1177/1076029608330473. Epub 2009 Jan 13. Clin Appl Thromb Hemost. 2010. PMID: 19144654 Free article.

10

Hereditary hemorrhagic teleangectasia with celiac disease and atrial fibrillation.

Lapecorella M, Napolitano M, Mariani G. Lapecorella M, et al. Eur J Intern Med. 2007 Jul;18(4):349. doi: 10.1016/j.ejim.2006.10.005. Eur J Intern Med. 2007. PMID: 17574120 No abstract available.

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