Paciaroni K - Search Results

1

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: paciaroni k. 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.

2

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: paciaroni k. Haematologica. 2004 Sep;89(9):1134-8. Haematologica. 2004. PMID: 15377476

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: paciaroni k. 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 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: paciaroni k. 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.

5

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

6

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: paciaroni k. Heart. 2004 Jan;90(1):82-6. doi: 10.1136/heart.90.1.82. Heart. 2004. PMID: 14676252 Free PMC article.

7

Screening for inherited thrombophilia: indications and therapeutic implications.

De Stefano V, Rossi E, Paciaroni K, Leone G. De Stefano V, et al. Among authors: paciaroni k. Haematologica. 2002 Oct;87(10):1095-108. Haematologica. 2002. PMID: 12368166 Review.

8

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: paciaroni k. Haematologica. 2003 Jan;88(1):61-6. Haematologica. 2003. PMID: 12551828

9

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

10

Epidemiology of factor V Leiden: clinical implications.

De Stefano V, Chiusolo P, Paciaroni K, Leone G. De Stefano V, et al. Among authors: paciaroni k. Semin Thromb Hemost. 1998;24(4):367-79. doi: 10.1055/s-2007-996025. Semin Thromb Hemost. 1998. PMID: 9763354 Review.

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