247 related articles for article (PubMed ID: 12637218)
1. Thrombophilia in infancy: factor V Leiden and MTHFR or factor II double heterozygocity as a risk factor.
Koren A; Levin C; Hujirat Y; El-Hasid R; Kutai M; Lanir N; Shalev S; Brenner B
Pediatr Hematol Oncol; 2003; 20(3):219-27. PubMed ID: 12637218
[TBL] [Abstract][Full Text] [Related]
2. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians.
Eid SS; Rihani G
Clin Lab Sci; 2004; 17(4):200-2. PubMed ID: 15559724
[TBL] [Abstract][Full Text] [Related]
3. MTHFR C677T mutation, factor II G20210A mutation and factor V Leiden as risks factor for youth retinal vein occlusion.
Cruciani F; Moramarco A; Curto T; Labate A; Recupero V; Conti L; Gandolfo GM; Balacco Gabrieli C
Clin Ter; 2003; 154(5):299-303. PubMed ID: 14994919
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Thrombophilic mutations in Iranian patients with infertility and recurrent spontaneous abortion.
Behjati R; Modarressi MH; Jeddi-Tehrani M; Dokoohaki P; Ghasemi J; Zarnani AH; Aarabi M; Memariani T; Ghaffari M; Akhondi MA
Ann Hematol; 2006 Apr; 85(4):268-71. PubMed ID: 16450127
[TBL] [Abstract][Full Text] [Related]
6. Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients.
Dölek B; Eraslan S; Eroğlu S; Kesim BE; Ulutin T; Yalçiner A; Laleli YR; Gözükirmizi N
Clin Appl Thromb Hemost; 2007 Oct; 13(4):435-8. PubMed ID: 17911197
[TBL] [Abstract][Full Text] [Related]
7. The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population.
Said JM; Brennecke SP; Moses EK; Walker SP; Monagle PT; Campbell J; Bryant VJ; Borg AJ; Higgins JR
Aust N Z J Obstet Gynaecol; 2008 Dec; 48(6):536-41. PubMed ID: 19133039
[TBL] [Abstract][Full Text] [Related]
8. [Genetic thrombophilic defects (Factor V Leiden, prothrombin G20210A, MTHFR C677T) in women with recurrent fetal loss].
Kovacheva K; Ivanov P; Konova E; Simeonova M; Komsa-Penkova R
Akush Ginekol (Sofiia); 2007; 46(7):10-6. PubMed ID: 18333414
[TBL] [Abstract][Full Text] [Related]
9. AB0 blood group and risk of venous or arterial thrombosis in carriers of factor V Leiden or prothrombin G20210A polymorphisms.
Miñano A; Ordóñez A; España F; González-Porras JR; Lecumberri R; Fontcuberta J; Llamas P; Marín F; Estellés A; Alberca I; Vicente V; Corral J
Haematologica; 2008 May; 93(5):729-34. PubMed ID: 18387978
[TBL] [Abstract][Full Text] [Related]
10. The prevalence of methylenetetrahydrofolate reductase 677 C-T, factor V 1691 G-A, and prothrombin 20210 G-A mutations in healthy populations in Setif, Algeria.
Bourouba R; Houcher B; Djabi F; Egin Y; Akar N
Clin Appl Thromb Hemost; 2009 Oct; 15(5):529-34. PubMed ID: 18840629
[TBL] [Abstract][Full Text] [Related]
11. Inherited thrombophilia: a possible cause of in utero vascular thrombosis in children with intestinal atresia.
Johnson SM; Meyers RL
J Pediatr Surg; 2001 Aug; 36(8):1146-9. PubMed ID: 11479844
[TBL] [Abstract][Full Text] [Related]
12. Thrombophilia-related genetic variations in patients with pulmonary embolism in the main teaching hospital in Jordan.
Obeidat NM; Awidi A; Sulaiman NA; Abu-Khader IB
Saudi Med J; 2009 Jul; 30(7):921-5. PubMed ID: 19618008
[TBL] [Abstract][Full Text] [Related]
13. Thrombophilia testing in patients with venous thrombosis.
Caprini JA; Goldshteyn S; Glase CJ; Hathaway K
Eur J Vasc Endovasc Surg; 2005 Nov; 30(5):550-5. PubMed ID: 16055356
[TBL] [Abstract][Full Text] [Related]
14. The role of point mutations in the genes, predisposing inherited thrombophilia in the pathogeneses of proximal and distal deep vein thrombosis in Georgian population.
Pirtskhelani N; Kochiashvili N; Makhaldiani L; Pargalava N; Gaprindashvili E; Kartvelishvili K
Georgian Med News; 2014 Feb; (227):98-102. PubMed ID: 24632657
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Factor V Leiden, prothrombin G20210A and MTHFR gene mutations in inflammatory bowel disease.
Törüner M; Erkan O; Soykan I; Bozdayi M; Cetinkaya H; Yurdaydin C; Uzunalimoğlu O; Ozden A
Turk J Gastroenterol; 2004 Dec; 15(4):250-2. PubMed ID: 16249980
[TBL] [Abstract][Full Text] [Related]
17. Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage.
Coulam CB; Jeyendran RS; Fishel LA; Roussev R
Am J Reprod Immunol; 2006 May; 55(5):360-8. PubMed ID: 16635210
[TBL] [Abstract][Full Text] [Related]
18. Evaluation of factor V Leiden, prothrombin and methylenetetrahydrofolate reductase gene mutations in patients with severe pregnancy complications in northern Finland.
Jarvenpaa J; Pakkila M; Savolainen ER; Perheentupa A; Jarvela I; Ryynanen M
Gynecol Obstet Invest; 2006; 62(1):28-32. PubMed ID: 16514238
[TBL] [Abstract][Full Text] [Related]
19. Genetic thrombophilic mutations among couples with recurrent miscarriage.
Jivraj S; Rai R; Underwood J; Regan L
Hum Reprod; 2006 May; 21(5):1161-5. PubMed ID: 16431900
[TBL] [Abstract][Full Text] [Related]
20. Impact of inherited thrombophilia on the risk of recurrent venous thromboembolism onset in Georgian population.
Pirtskhelani N; Kochiashvili N; Makhaldiani L; Pargalava N; Gaprindashvili E; Kartvelishvili K
Georgian Med News; 2014 Feb; (227):93-7. PubMed ID: 24632656
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
