De Stefano V - Search Results

1

The G20210A prothrombin mutation and the Physicians' Health Study.

Andreotti F, Burzotta F, De Stefano V, Maseri A, Iacoviello L. Andreotti F, et al. Among authors: de stefano v. Circulation. 2000 May 30;101(21):E207-8. doi: 10.1161/01.cir.101.21.e207. Circulation. 2000. PMID: 10831536 No abstract available.

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. 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. 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. 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

G20210A prothrombin gene polymorphism and extent of coronary disease.

Burzotta F, Paciaroni K, Andreotti F, Casorelli I, De Stefano V. Burzotta F, et al. Among authors: de stefano v. Thromb Haemost. 2000 Jul;84(1):142-3. Thromb Haemost. 2000. PMID: 10928489 No abstract available.

6

Prevalence of factor V Leiden and the G20210A prothrombin-gene mutation in inflammatory bowel disease.

Papa A, De Stefano V, Gasbarrini A, Chiusolo P, Cianci R, Casorelli I, Paciaroni K, Cammarota G, Leone G, Gasbarrini G. Papa A, et al. Among authors: de stefano v. Blood Coagul Fibrinolysis. 2000 Jul;11(5):499-503. doi: 10.1097/00001721-200007000-00013. Blood Coagul Fibrinolysis. 2000. PMID: 10937811

7

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. 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.

8

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: de stefano v. 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.

9

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: de stefano v. Eur Heart J. 2002 Jan;23(1):26-30. doi: 10.1053/euhj.2001.2685. Eur Heart J. 2002. PMID: 11741359

10

Different circumstances of the first venous thromboembolism among younger or older heterozygous carriers of the G20210A polymorphism in the prothrombin gene.

De Stefano V, Rossi E, Paciaroni K, D'Orazio A, Cina G, Marchitelli E, Pepe R, Leone G. De Stefano V, et al. Haematologica. 2003 Jan;88(1):61-6. Haematologica. 2003. PMID: 12551828

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