Madonna P - 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: madonna p. 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: madonna p. 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. 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: madonna p. Haematologica. 1997 Mar-Apr;82(2):189-90. Haematologica. 1997. PMID: 9175326

5

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: madonna p. 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.

6

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. 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.

7

Oxidative stress and platelet activation in homozygous homocystinuria.

Davì G, Di Minno G, Coppola A, Andria G, Cerbone AM, Madonna P, Tufano A, Falco A, Marchesani P, Ciabattoni G, Patrono C. Davì G, et al. Among authors: madonna p. Circulation. 2001 Sep 4;104(10):1124-8. doi: 10.1161/hc3501.095287. Circulation. 2001. PMID: 11535567 Clinical Trial.

8

G20210A PRTH gene mutation and other trombophilic polymorphisms in patients with cerebral vein thrombosis.

Madonna P, De Stefano V, Coppola A, Albisinni R, Cerbone AM. Madonna P, et al. Stroke. 2000 Jul;31(7):1787-8. doi: 10.1161/01.str.31.7.1785-c. Stroke. 2000. PMID: 10884490 No abstract available.

9

G20210A prothrombin gene mutation and other trombophilic polymorphisms in patients with portal or hepatic venous thrombosis.

Madonna P, De Stefano V, Coppola A, Cerbone AM, Di Minno G. Madonna P, et al. Gastroenterology. 2001 Mar;120(4):1059-60. doi: 10.1053/gast.2001.23083. Gastroenterology. 2001. PMID: 11265667 No abstract available.

10

Severe pancytopenia and intrahepatic cholestasis in a patient with a history of Hodgkin's disease. Responsiveness to high-dose pulse steroid therapy and diagnosis of a late relapse.

Coppola A, Camera A, Pagano A, Madonna P, Albisinni R, Pezzullo L, Maria Cerbone A, Di Minno G. Coppola A, et al. Among authors: madonna p. Eur J Intern Med. 2001 Dec;12(6):515-7. doi: 10.1016/s0953-6205(01)00166-2. Eur J Intern Med. 2001. PMID: 11711275

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