De Stefano V - Search Results

1

The Aspirin Regimens in Essential Thrombocythemia (ARES) phase II randomized trial design: Implementation of the serum thromboxane B₂ assay as an evaluation tool of different aspirin dosing regimens in the clinical setting.

De Stefano V, Rocca B, Tosetto A, Soldati D, Petrucci G, Beggiato E, Bertozzi I, Betti S, Carli G, Carpenedo M, Cattaneo D, Cavalca V, Dragani A, Elli E, Finazzi G, Iurlo A, Lanzarone G, Lissandrini L, Palandri F, Paoli C, Rambaldi A, Ranalli P, Randi ML, Ricco A, Rossi E, Ruggeri M, Specchia G, Timillero A, Turnu L, Vianelli N, Vannucchi AM, Rodeghiero F, Patrono C. De Stefano V, et al. Blood Cancer J. 2018 Jun 1;8(6):49. doi: 10.1038/s41408-018-0078-3. Blood Cancer J. 2018. PMID: 29880847 Free PMC article. Clinical Trial.

2

Clinical manifestations and management of inherited thrombophilia: retrospective analysis and follow-up after diagnosis of 238 patients with congenital deficiency of antithrombin III, protein C, protein S.

De Stefano V, Leone G, Mastrangelo S, Tripodi A, Rodeghiero F, Castaman G, Barbui T, Finazzi G, Bizzi B, Mannucci PM. De Stefano V, et al. Thromb Haemost. 1994 Sep;72(3):352-8. Thromb Haemost. 1994. PMID: 7855783

3

Inherited thrombophilia: pathogenesis, clinical syndromes, and management.

De Stefano V, Finazzi G, Mannucci PM. De Stefano V, et al. Blood. 1996 May 1;87(9):3531-44. Blood. 1996. PMID: 8611675 Free article. Review. No abstract available.

4

Natural history and risk factors for thrombosis in 360 patients with antiphospholipid antibodies: a four-year prospective study from the Italian Registry.

Finazzi G, Brancaccio V, Moia M, Ciaverella N, Mazzucconi MG, Schinco PC, Ruggeri M, Pogliani EM, Gamba G, Rossi E, Baudo F, Manotti C, D'Angelo A, Palareti G, De Stefano V, Berrettini M, Barbui T. Finazzi G, et al. Among authors: de stefano v. Am J Med. 1996 May;100(5):530-6. doi: 10.1016/s0002-9343(96)00060-5. Am J Med. 1996. PMID: 8644765

5

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.

6

Additional genetic risk factors for venous thromboembolism in carriers of the factor V Leiden mutation.

Tosetto A, Rodeghiero F, Martinelli I, De Stefano V, Missiaglia E, Chiusolo P, Mannucci PM. Tosetto A, et al. Among authors: de stefano v. Br J Haematol. 1998 Dec;103(3):871-6. doi: 10.1046/j.1365-2141.1998.01028.x. Br J Haematol. 1998. PMID: 9858248 Free article.

7

Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden).

Faioni EM, Franchi F, Bucciarelli P, Margaglione M, De Stefano V, Castaman G, Finazzi G, Mannucci PM. Faioni EM, et al. Among authors: de stefano v. Blood. 1999 Nov 1;94(9):3062-6. Blood. 1999. PMID: 10556190 Free article.

8

Interaction between hyperhomocysteinemia and inherited thrombophilic factors in venous thromboembolism.

De Stefano V, Casorelli I, Rossi E, Zappacosta B, Leone G. De Stefano V, et al. Semin Thromb Hemost. 2000;26(3):305-11. doi: 10.1055/s-2000-8473. Semin Thromb Hemost. 2000. PMID: 11011848 Review.

9

The expression pattern of c-mpl in megakaryocytes correlates with thrombotic risk in essential thrombocythemia.

Teofili L, Pierconti F, Di Febo A, Maggiano N, Vianelli N, Ascani S, Rossi E, Pileri S, Leone G, Larocca LM, De Stefano V. Teofili L, et al. Among authors: de stefano v. Blood. 2002 Jul 15;100(2):714-7. doi: 10.1182/blood.v100.2.714. Blood. 2002. PMID: 12091373 Free article.

10

Screening for inherited thrombophilia: indications and therapeutic implications.

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

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