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Famularo G, Minisola G, Nicotra GC, et al. 
Mesenteric and portal vein thrombosis associated with hyperhomocysteinemia and heterozygosity for factor V Leiden mutation. [Case Reports, Letter]
World J Gastroenterol 2005 Dec 28; 11(48):7700-1.
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Koshy A, Jeyakumari M 
Factor V Leiden is not commonly associated with idiopathic portal vein thrombosis in southern India. [Journal Article]
Indian J Gastroenterol 2006 May-Jun; 25(3):140-2.
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Piñar A, Saenz R, Rebollo J, et al. 
Portal and mesenteric vein thrombosis in a patient heterozygous for a mutation (Arg506-->Gln) in the factor V gen (factor V Leiden). [Case Reports, Journal Article]
J Clin Gastroenterol 1998 Dec; 27(4):361-3.
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Otrock ZK, Soweid AM, Salem ZM, et al. 
Portal, splenic and mesenteric vein thrombosis in a patient with factor V Leiden mutation and antithrombin III deficiency. [Journal Article]
Ann Hematol 2006 Jun; 85(6):413-4.
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Hertzberg MS, Underwood T, Favaloro EJ 
Mesenteric vein thrombosis secondary to combined protein C deficiency and double heterozygosity for factor V Leiden and prothrombin G20210A. [Case Reports, Letter]
Am J Hematol 1999 Nov; 62(3):199-200.
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Sönmezer M, Aytaç R, Demirel LC, et al. 
Mesenteric vein thrombosis in a pregnant patient heterozygous for the factor V (1691 G --> A) Leiden mutation. [Case Reports, Journal Article]
Eur J Obstet Gynecol Reprod Biol 2004 Jun 15; 114(2):234-5.
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Elhajj II, Salem ZM, Birjawi GA, et al. 
Heterozygous prothrombin 20210G/A mutation, associated with hyperhomocysteinemia, and homozygous methylenetetrahydrofolate reductase 677C/T mutation, in a patient with portal and mesenteric venous thrombosis. [Case Reports, Journal Article]
Hematol J 2004; 5(6):540-2.
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Oger E, Lacut K, Le Gal G, et al. 
Interrelation of hyperhomocysteinemia and inherited risk factors for venous thromboembolism. Results from the E.D.I.TH. study: A hospital-based case-control study. [JOURNAL ARTICLE]
Thromb Res 2006 Nov 24.
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Shah SR, Gupta AD, Sharma A, et al. 
Acute superior mesenteric vein thrombosis associated with factor V 'Leiden' gene mutation. [Case Reports, Journal Article]
J Assoc Physicians India 2003 Jun.:611-3.
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