Cerbone AM - Search Results

1

The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene. A case-control study of patients with early-onset thrombotic events.

D'Angelo A, Coppola A, Madonna P, Fermo I, Pagano A, Mazzola G, Galli L, Cerbone AM. D'Angelo A, et al. Among authors: cerbone am. Thromb Haemost. 2000 Apr;83(4):563-70. Thromb Haemost. 2000. PMID: 10780318

2

Homozygous C677T mutation of the 5,10 methylenetetrahydrofolate reductase gene and hyperhomocysteinemia in Italian patients with a history of early-onset ischemic stroke.

Soriente L, Coppola A, Madonna P, Cerbone AM, Di Minno G, Orefice G, D'Angelo A. Soriente L, et al. Among authors: cerbone am. Stroke. 1998 Apr;29(4):869-71. doi: 10.1161/01.str.29.4.869. Stroke. 1998. PMID: 9550528 No abstract available.

3

Hyperhomocysteinemia and other inherited prothrombotic conditions in young adults with a history of ischemic stroke.

Madonna P, de Stefano V, Coppola A, Cirillo F, Cerbone AM, Orefice G, Di Minno G. Madonna P, et al. Among authors: cerbone am. Stroke. 2002 Jan;33(1):51-6. doi: 10.1161/hs0102.100483. Stroke. 2002. PMID: 11779888

4

Platelet and monocyte variables in homocystinuria due to cystathionine-beta-synthase deficiency.

Coppola A, Albisinni R, Madonna P, Pagano A, Cerbone AM, Di Minno G. Coppola A, et al. Among authors: cerbone am. Haematologica. 1997 Mar-Apr;82(2):189-90. Haematologica. 1997. PMID: 9175326

5

Homocysteine, coagulation, platelet function, and thrombosis.

Coppola A, Davi G, De Stefano V, Mancini FP, Cerbone AM, Di Minno G. Coppola A, et al. Among authors: cerbone am. Semin Thromb Hemost. 2000;26(3):243-54. doi: 10.1055/s-2000-8469. Semin Thromb Hemost. 2000. PMID: 11011842 Review.

6

Idiopathic Budd-Chiari syndrome in a patient with homozygous Factor V Leiden and heterozygous Factor II G20210A mutations.

De Stefano V, Madonna P, Giannino A, Coppola A, Cerbone AM, Pauciullo P, Di Minno G. De Stefano V, et al. Among authors: cerbone am. Thromb Res. 2000 Dec 15;100(6):567-8. doi: 10.1016/s0049-3848(00)00355-8. Thromb Res. 2000. PMID: 11197916 No abstract available.

7

Coexistence of thrombophilic gene polymorphisms among 559 unrelated consecutive patients with a history of thrombosis.

Madonna P, Piemontino U, De Stefano V, Albisinni R, Cerbone AM, Di Minno G. Madonna P, et al. Among authors: cerbone am. Thromb Res. 2001 Feb 15;101(4):317-9. doi: 10.1016/s0049-3848(00)00416-3. Thromb Res. 2001. PMID: 11320983 No abstract available.

8

Inherited thrombophilia: implications for prevention and treatment of venous thromboembolism.

Coppola A, Tufano A, Cerbone AM, Di Minno G. Coppola A, et al. Among authors: cerbone am. Semin Thromb Hemost. 2009 Oct;35(7):683-94. doi: 10.1055/s-0029-1242722. Semin Thromb Hemost. 2009. PMID: 20013535 Review.

9

Cardiovascular risk factors and outcome in patients with retinal vein occlusion.

Di Capua M, Coppola A, Albisinni R, Tufano A, Guida A, Di Minno MN, Cirillo F, Loffredo M, Cerbone AM. Di Capua M, et al. Among authors: cerbone am. J Thromb Thrombolysis. 2010 Jul;30(1):16-22. doi: 10.1007/s11239-009-0388-1. J Thromb Thrombolysis. 2010. PMID: 19705255

10

Risk factors and recurrent thrombotic episodes in patients with cerebral venous thrombosis.

Tufano A, Guida A, Coppola A, Nardo A, Di Capua M, Quintavalle G, Di Minno MN, Cerbone AM, Di Minno G. Tufano A, et al. Among authors: cerbone am. Blood Transfus. 2014 Jan;12 Suppl 1(Suppl 1):s337-42. doi: 10.2450/2013.0196-12. Epub 2013 Feb 6. Blood Transfus. 2014. PMID: 23399370 Free PMC article.

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