De Stefano V - Search Results

1

Obstetric complications and pregnancy-related venous thromboembolism: the effect of low-molecular-weight heparin on their prevention in carriers of factor V Leiden or prothrombin G20210A mutation.

Tormene D, Grandone E, De Stefano V, Tosetto A, Palareti G, Margaglione M, Castaman G, Rossi E, Ciminello A, Valdrè L, Legnani C, Tiscia GL, Bafunno V, Carraro S, Rodeghiero F, Simioni P. Tormene D, et al. Among authors: de stefano v. Thromb Haemost. 2012 Mar;107(3):477-84. doi: 10.1160/TH11-07-0470. Epub 2012 Jan 25. Thromb Haemost. 2012. PMID: 22273731

2

Markers of procoagulant imbalance in patients with inherited thrombophilic syndromes.

Mannucci PM, Tripodi A, Bottasso B, Baudo F, Finazzi G, De Stefano V, Palareti G, Manotti C, Mazzucconi MG, Castaman G. Mannucci PM, et al. Among authors: de stefano v. Thromb Haemost. 1992 Feb 3;67(2):200-2. Thromb Haemost. 1992. PMID: 1535736

3

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

4

Thrombosis during pregnancy and surgery in 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 Jun;71(6):799-800. Thromb Haemost. 1994. PMID: 7974352 No abstract available.

5

Prevalence of the 677C to T mutation in the methylenetetrahydrofolate reductase gene in Italian patients with venous thrombotic disease.

De Stefano V, Chiusolo P, Paciaroni K, Serra FG, Voso MT, Casorelli I, Rossi E, Leone G. De Stefano V, et al. Thromb Haemost. 1998 Mar;79(3):686-7. Thromb Haemost. 1998. PMID: 9531064 No abstract available.

6

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.

7

Prevalence of the factor II G20210A mutation in symptomatic patients with inherited thrombophilia.

De Stefano V, Chiusolo P, Paciaroni K, Casorelli I, Di Mario A, Rossi E, Leone G. De Stefano V, et al. Thromb Haemost. 1998 Aug;80(2):342-3. Thromb Haemost. 1998. PMID: 9716164 No abstract available.

8

Epidemiology of factor V Leiden: clinical implications.

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

9

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.

10

Risk of venous thromboembolism and clinical manifestations in carriers of antithrombin, protein C, protein S deficiency, or activated protein C resistance: a multicenter collaborative family study.

Bucciarelli P, Rosendaal FR, Tripodi A, Mannucci PM, De Stefano V, Palareti G, Finazzi G, Baudo F, Quintavalla R. Bucciarelli P, et al. Among authors: de stefano v. Arterioscler Thromb Vasc Biol. 1999 Apr;19(4):1026-33. doi: 10.1161/01.atv.19.4.1026. Arterioscler Thromb Vasc Biol. 1999. PMID: 10195932

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