Leone G - Search Results

1

G20210A prothrombin gene polymorphism and coronary ischaemic syndromes: a phenotype-specific meta-analysis of 12 034 subjects.

Burzotta F, Paciaroni K, De Stefano V, Crea F, Maseri A, Leone G, Andreotti F. Burzotta F, et al. Among authors: leone g. Heart. 2004 Jan;90(1):82-6. doi: 10.1136/heart.90.1.82. Heart. 2004. PMID: 14676252 Free PMC article.

2

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. Among authors: leone g. Haematologica. 2003 Jan;88(1):61-6. Haematologica. 2003. PMID: 12551828

3

G20210A prothrombin gene variant and clinical outcome in patients with a first acute coronary syndrome.

Burzotta F, Leone AM, Paciaroni K, De Stefano V, Rossi E, Testa L, Giannico F, Leone G, Maseri A, Crea F, Andreotti F. Burzotta F, et al. Among authors: leone am, leone g. Haematologica. 2004 Sep;89(9):1134-8. Haematologica. 2004. PMID: 15377476

4

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: leone g. Blood. 1998 May 15;91(10):3562-5. Blood. 1998. PMID: 9572989 Free article.

5

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: leone g. N Engl J Med. 1999 Sep 9;341(11):801-6. doi: 10.1056/NEJM199909093411104. N Engl J Med. 1999. PMID: 10477778 Free article.

6

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: leone g. 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.

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: leone am, leone g. 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: leone am, leone g. Eur Heart J. 2002 Jan;23(1):26-30. doi: 10.1053/euhj.2001.2685. Eur Heart J. 2002. PMID: 11741359

9

Glycoprotein Ia C807T gene polymorphism and increased risk of recurrent acute coronary syndromes: a five year follow up.

Leone AM, De Stefano V, Burzotta F, Chiusolo P, Casorelli I, Paciaroni K, Rossi E, Sciahbasi A, Testa L, Leone G, Crea F, Andreotti F. Leone AM, et al. Among authors: leone g. Heart. 2004 May;90(5):567-9. doi: 10.1136/hrt.2003.017624. Heart. 2004. PMID: 15084564 Free PMC article. No abstract available.

10

In families with inherited thrombophilia the risk of venous thromboembolism is dependent on the clinical phenotype of the proband.

Rossi E, Ciminello A, Za T, Betti S, Leone G, De Stefano V. Rossi E, et al. Among authors: leone g. Thromb Haemost. 2011 Oct;106(4):646-54. doi: 10.1160/TH11-02-0080. Epub 2011 Aug 11. Thromb Haemost. 2011. PMID: 21833444

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