138 related articles for article (PubMed ID: 10544935)
1. Budd-Chiari syndrome in a patient heterozygous for both factor V Leiden and the G20210A mutation on the prothrombin gene.
Oner AF; Arslan S; Caksen H; Ceylan A
Thromb Haemost; 1999 Oct; 82(4):1366-7. PubMed ID: 10544935
[No Abstract] [Full Text] [Related]
2. Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome.
Sipahi T; Duru F; Yarah N; Akar N
Eur J Pediatr; 2001 Mar; 160(3):198. PubMed ID: 11277387
[No Abstract] [Full Text] [Related]
3. Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene.
Bucciarelli P; Franchi F; Alatri A; Bettini P; Moia M
Thromb Haemost; 1998 Feb; 79(2):445-6. PubMed ID: 9493607
[No Abstract] [Full Text] [Related]
4. 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
Thromb Res; 2000 Dec; 100(6):567-8. PubMed ID: 11197916
[No Abstract] [Full Text] [Related]
5. Budd-Chiari syndrome related to factor V Leiden mutation.
Delarive J; Gonvers JJ
Am J Gastroenterol; 1998 Apr; 93(4):651-2. PubMed ID: 9576466
[TBL] [Abstract][Full Text] [Related]
6. Associations of coagulation factor V Leiden and prothrombin G20210A mutations with Budd-Chiari syndrome and portal vein thrombosis: a systematic review and meta-analysis.
Qi X; Ren W; De Stefano V; Fan D
Clin Gastroenterol Hepatol; 2014 Nov; 12(11):1801-12.e7. PubMed ID: 24793031
[TBL] [Abstract][Full Text] [Related]
7. Inherited prothrombotic defects in Budd-Chiari syndrome and portal vein thrombosis: a study from North India.
Bhattacharyya M; Makharia G; Kannan M; Ahmed RP; Gupta PK; Saxena R
Am J Clin Pathol; 2004 Jun; 121(6):844-7. PubMed ID: 15198356
[TBL] [Abstract][Full Text] [Related]
8. Multiple thrombophilic factors in a patient with Budd-Chiari syndrome.
Brancaccio V; Iannaccone L; Margaglione M; Guardascione MA; Amitrano L
Clin Lab Haematol; 2002 Feb; 24(1):61-3. PubMed ID: 11843901
[TBL] [Abstract][Full Text] [Related]
9. JAK2V617F and prothrombin G20210A gene mutations in a patient with Budd-Chiari syndrome and essential thrombocythemia.
Musallam KM; Aoun EG; Mahfouz RA; Khalife M; Taher AT
Clin Appl Thromb Hemost; 2010 Aug; 16(4):472-4. PubMed ID: 19223280
[TBL] [Abstract][Full Text] [Related]
10. Budd-Chiari syndrome associated with factor V leiden mutation: a report of 6 patients.
Hoffman R; Nimer A; Lanir N; Brenner B; Baruch Y
Liver Transpl Surg; 1999 Mar; 5(2):96-100. PubMed ID: 10071347
[TBL] [Abstract][Full Text] [Related]
11. Hyperhomocysteinaemia and factor V Leiden mutation are associated with Budd-Chiari syndrome.
Colak Y; Karasu Z; Oruc N; Can C; Balým Z; Akarca U; Gunsar F; Ersoz G; Tokat Y; Batur Y
Eur J Gastroenterol Hepatol; 2006 Aug; 18(8):917-20. PubMed ID: 16825912
[TBL] [Abstract][Full Text] [Related]
12. Risk of recurrent venous thrombosis in patients with G20210A mutation in the prothrombin gene or factor V Leiden mutation.
González-Porras JR; García-Sanz R; Alberca I; López ML; Balanzategui A; Gutierrez O; Lozano F; San Miguel J
Blood Coagul Fibrinolysis; 2006 Jan; 17(1):23-8. PubMed ID: 16607075
[TBL] [Abstract][Full Text] [Related]
13. Acute Budd-Chiari syndrome treated by liver transplantation in a woman homozygous for factor V Leiden.
Blanshard C; Pasi J; Rolles K; Davidson B; Jain S; Burroughs A
Eur J Gastroenterol Hepatol; 1996 Sep; 8(9):925-7. PubMed ID: 8889463
[TBL] [Abstract][Full Text] [Related]
14. Third trimester nonrecurrent fetal loss is associated with factor V Leiden and prothrombin gene mutations.
Karateke A; Haliloglu B; Gurbuz A
J Matern Fetal Neonatal Med; 2005 Nov; 18(5):299-304. PubMed ID: 16390788
[TBL] [Abstract][Full Text] [Related]
15. Risk of Budd-Chiari syndrome associated with factor V Leiden and G20210A prothrombin mutation: a meta-analysis.
Zhang P; Zhang J; Sun G; Gao X; Wang H; Yan W; Xu H; Zu M; Ma H; Wang W; Lu Z
PLoS One; 2014; 9(4):e95719. PubMed ID: 24755609
[TBL] [Abstract][Full Text] [Related]
16. Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients.
Yasa MH; Bolaman Z; Yukselen V; Kadikoylu G; Karaoglul AO; Batun S
Hepatogastroenterology; 2007; 54(77):1438-42. PubMed ID: 17708272
[TBL] [Abstract][Full Text] [Related]
17. Spontaneous superficial vein thrombosis in a young patient double heterozygous for factor V Leiden and the prothrombin G20210A mutation: a case report.
Vayá A; Llopis I; Trenor R; Mira Y; Estellés A; Aznar J
Haematologica; 2000; 85(E-letters):E11. PubMed ID: 11114826
[No Abstract] [Full Text] [Related]
18. Relations of Budd-Chiari syndrome to prothrombin gene mutation.
Lin GL; Xu PQ; Qi H; Lian JH; Zheng H; Dang XW
Hepatobiliary Pancreat Dis Int; 2004 May; 3(2):214-8. PubMed ID: 15138112
[TBL] [Abstract][Full Text] [Related]
19. The G1691A mutation of the factor V gene (factor V Leiden) and the G20210A mutation of the prothrombin gene as risk factors in thrombotic microangiopathies.
Sucker C; Kurschat C; Hetzel GR; Grabensee B; Maruhn-Debowski B; Loncar R; Ostojic L; Scharf RE; Zotz RB
Clin Appl Thromb Hemost; 2009; 15(3):360-3. PubMed ID: 19448164
[TBL] [Abstract][Full Text] [Related]
20. Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism--pooled analysis of 8 case-control studies including 2310 cases and 3204 controls. Study Group for Pooled-Analysis in Venous Thromboembolism.
Emmerich J; Rosendaal FR; Cattaneo M; Margaglione M; De Stefano V; Cumming T; Arruda V; Hillarp A; Reny JL
Thromb Haemost; 2001 Sep; 86(3):809-16. PubMed ID: 11583312
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
