Rossi E - Search Results

1

Interaction between hyperhomocysteinemia and inherited thrombophilic factors in venous thromboembolism.

De Stefano V, Casorelli I, Rossi E, Zappacosta B, Leone G. De Stefano V, et al. Among authors: rossi e. Semin Thromb Hemost. 2000;26(3):305-11. doi: 10.1055/s-2000-8473. Semin Thromb Hemost. 2000. PMID: 11011848 Review.

2

Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients.

De Stefano V, Chiusolo P, Paciaroni K, Casorelli I, Rossi E, Molinari M, Servidei S, Tonali PA, Leone G. De Stefano V, et al. Among authors: rossi e. Blood. 1998 May 15;91(10):3562-5. Blood. 1998. PMID: 9572989 Free article.

3

Prevalence of mild hyperhomocysteinaemia and association with thrombophilic genotypes (factor V Leiden and prothrombin G20210A) in Italian patients with venous thromboembolic disease.

De Stefano V, Zappacosta B, Persichilli S, Rossi E, Casorelli I, Paciaroni K, Chiusolo P, Leone AM, Giardina B, Leone G. De Stefano V, et al. Among authors: rossi e. Br J Haematol. 1999 Aug;106(2):564-8. doi: 10.1046/j.1365-2141.1999.01613.x. Br J Haematol. 1999. PMID: 10460623 Free article.

4

The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation.

De Stefano V, Martinelli I, Mannucci PM, Paciaroni K, Chiusolo P, Casorelli I, Rossi E, Leone G. De Stefano V, et al. Among authors: rossi e. N Engl J Med. 1999 Sep 9;341(11):801-6. doi: 10.1056/NEJM199909093411104. N Engl J Med. 1999. PMID: 10477778 Free article.

5

The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutation.

De Stefano V, Martinelli I, Mannucci PM, Paciaroni K, Rossi E, Chiusolo P, Casorelli I, Leone G. De Stefano V, et al. Among authors: rossi e. Br J Haematol. 2001 Jun;113(3):630-5. doi: 10.1046/j.1365-2141.2001.02827.x. Br J Haematol. 2001. PMID: 11380448 Free article.

6

Prevalence of the factor II G20210A mutation in symptomatic patients with inherited thrombophilia.

De Stefano V, Chiusolo P, Paciaroni K, Casorelli I, Di Mario A, Rossi E, Leone G. De Stefano V, et al. Among authors: rossi e. Thromb Haemost. 1998 Aug;80(2):342-3. Thromb Haemost. 1998. PMID: 9716164 No abstract available.

7

The C807T/G873A polymorphism in the platelet glycoprotein Ia gene and the risk of acute coronary syndrome in the Italian population.

Casorelli I, De Stefano V, Leone AM, Chiusolo P, Burzotta F, Paciaroni K, Rossi E, Andreotti F, Leone G, Maseri A. Casorelli I, et al. Among authors: rossi e. Br J Haematol. 2001 Jul;114(1):150-4. doi: 10.1046/j.1365-2141.2001.02868.x. Br J Haematol. 2001. PMID: 11472360 Free article.

8

Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease.

Burzotta F, Paciaroni K, De Stefano V, Chiusolo P, Manzoli A, Casorelli I, Leone AM, Rossi E, Leone G, Maseri A, Andreotti F. Burzotta F, et al. Among authors: rossi e. Eur Heart J. 2002 Jan;23(1):26-30. doi: 10.1053/euhj.2001.2685. Eur Heart J. 2002. PMID: 11741359

9

The risk of thrombosis in patients with acute leukemia: occurrence of thrombosis at diagnosis and during treatment.

De Stefano V, Sorà F, Rossi E, Chiusolo P, Laurenti L, Fianchi L, Zini G, Pagano L, Sica S, Leone G. De Stefano V, et al. Among authors: rossi e. J Thromb Haemost. 2005 Sep;3(9):1985-92. doi: 10.1111/j.1538-7836.2005.01467.x. J Thromb Haemost. 2005. PMID: 16102104 Free article.

10

Incidence of the JAK2 V617F mutation among patients with splanchnic or cerebral venous thrombosis and without overt chronic myeloproliferative disorders.

De Stefano V, Fiorini A, Rossi E, Za T, Farina G, Chiusolo P, Sica S, Leone G. De Stefano V, et al. Among authors: rossi e. J Thromb Haemost. 2007 Apr;5(4):708-14. doi: 10.1111/j.1538-7836.2007.02424.x. Epub 2007 Jan 29. J Thromb Haemost. 2007. PMID: 17263783 Free article.

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