De Stefano V - Search Results

1

Prevalence of factor V Leiden and the G20210A prothrombin-gene mutation in inflammatory bowel disease.

Papa A, De Stefano V, Gasbarrini A, Chiusolo P, Cianci R, Casorelli I, Paciaroni K, Cammarota G, Leone G, Gasbarrini G. Papa A, et al. Among authors: de stefano v. Blood Coagul Fibrinolysis. 2000 Jul;11(5):499-503. doi: 10.1097/00001721-200007000-00013. Blood Coagul Fibrinolysis. 2000. PMID: 10937811

2

Thrombosis in antithrombin-III deficiency.

De Stefano V, Leone G. De Stefano V, et al. Ann Intern Med. 1992 Nov 15;117(10):875. doi: 10.7326/0003-4819-117-10-875_1. Ann Intern Med. 1992. PMID: 1416567 No abstract available.

3

Hematological causes of venous thrombosis in young people: high incidence of myeloproliferative disorder as underlying disease in patients with splanchnic venous thrombosis.

Teofili L, De Stefano V, Leone G, Micalizzi P, Iovino MS, Alfano G, Bizzi B. Teofili L, et al. Among authors: de stefano v. Thromb Haemost. 1992 Mar 2;67(3):297-301. Thromb Haemost. 1992. PMID: 1641818

4

Hepatocarcinoma in cirrhosis. Is antithrombin III a neoplastic marker?

Grieco A, De Stefano V, Cassano A, Ciabattoni A, Garufi C, Astone A, Leone G, Barone C. Grieco A, et al. Among authors: de stefano v. Dig Dis Sci. 1991 Jul;36(7):990-2. doi: 10.1007/BF01297153. Dig Dis Sci. 1991. PMID: 1649042

5

Mortality related to thrombosis in congenital antithrombin III deficiency.

De Stefano V, Leone G. De Stefano V, et al. Lancet. 1991 Apr 6;337(8745):847-8. doi: 10.1016/0140-6736(91)92549-h. Lancet. 1991. PMID: 1672929 Free article. No abstract available.

6

[Essential thrombocythemia: pregnancy].

Leone G, De Stefano V, D'Addosio A. Leone G, et al. Among authors: de stefano v. Haematologica. 1991 Jun;76 Suppl 3:365-7. Haematologica. 1991. PMID: 1752533 Review. Italian. No abstract available.

7

Arterial thrombosis as clinical manifestation of congenital protein C deficiency.

De Stefano V, Leone G, Micalizzi P, Teofili L, Falappa PG, Pollari G, Bizzi B. De Stefano V, et al. Ann Hematol. 1991 May;62(5):180-3. doi: 10.1007/BF01703145. Ann Hematol. 1991. PMID: 2049465

8

Association of Graves' disease and prekallikrein congenital deficiency in a patient belonging to the first CRM+ prekallikrein-deficient Italian family.

De Stefano V, Leone G, Teofili L, De Marinis L, Micalizzi P, Fiumara C, Bizzi B. De Stefano V, et al. Among authors: de marinis l. Thromb Res. 1990 Dec 1;60(5):397-404. doi: 10.1016/0049-3848(90)90222-x. Thromb Res. 1990. PMID: 2084960

9

Mesenteric vein thrombosis in protein S congenital deficiency.

De Stefano V, Leone G, Teofili L, Micalizzi P, Netri G, Bizzi B. De Stefano V, et al. Thromb Res. 1990 Mar 15;57(6):935-44. doi: 10.1016/0049-3848(90)90160-e. Thromb Res. 1990. PMID: 2143322

10

Antithrombin III congenital defects: revising classification system.

De Stefano V, Leone G. De Stefano V, et al. Thromb Haemost. 1989 Sep 29;62(2):820-1. Thromb Haemost. 1989. PMID: 2604796 No abstract available.

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