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Thrombophilia: genetic polymorphisms and their association with retinal vascular occlusive disease.

Chak M, Wallace GR, Graham EM, Stanford MR.

Br J Ophthalmol. 2001 Jul;85(7):883-6. Review. No abstract available. PMID: 11423467 [PubMed - indexed for MEDLINE]Related articlesFree article

Heritable thrombophilia and hypofibrinolysis. Possible causes of retinal vein occlusion.

Glueck CJ, Bell H, Vadlamani L, Gupta A, Fontaine RN, Wang P, Stroop D, Gruppo R.

Arch Ophthalmol. 1999 Jan;117(1):43-9.PMID: 9930159 [PubMed - indexed for MEDLINE]Related articles

Prevalence of three prothrombotic polymorphisms. Factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase (MTHFR) C 677T in Argentina. On behalf of the Grupo Cooperativo Argentino de Hemostasia y Trombosis.

Genoud V, Castañon M, Annichino-Bizzacchi J, Korin J, Kordich L.

Thromb Res. 2000 Nov 1;100(3):127-31. No abstract available. PMID: 11108898 [PubMed - indexed for MEDLINE]Related articles

Hyperhomocysteinemia and BRVO.

Yanamandra K, Thurmon TF, Bocchini JA Jr, Kooragayala LM.

Ophthalmology. 2003 Oct;110(10):2069; author reply 2069. No abstract available. PMID: 14522804 [PubMed - indexed for MEDLINE]Related articles

Coexistence of thrombophilic gene polymorphisms among 559 unrelated consecutive patients with a history of thrombosis.

Madonna P, Piemontino U, De Stefano V, Albisinni R, Cerbone AM, Di Minno G.

Thromb Res. 2001 Feb 15;101(4):317-9. No abstract available. PMID: 11320983 [PubMed - indexed for MEDLINE]Related articles

Analysis of genetic polymorphisms related to thrombosis and other risk factors in patients with retinal vein occlusion.

Salomon O, Moisseiev J, Rosenberg N, Vidne O, Yassur I, Zivelin A, Treister G, Steinberg DM, Seligsohn U.

Blood Coagul Fibrinolysis. 1998 Oct;9(7):617-22.PMID: 9863710 [PubMed - indexed for MEDLINE]Related articles

Thrombophilic risk factors in patients with central retinal vein occlusion.

Marcucci R, Bertini L, Giusti B, Brunelli T, Fedi S, Cellai AP, Poli D, Pepe G, Abbate R, Prisco D.

Thromb Haemost. 2001 Sep;86(3):772-6.PMID: 11583306 [PubMed - indexed for MEDLINE]Related articles

Analysis of three genetic polymorphisms as risk factors for thrombosis.

Giordano P, Micelli M, Coppola B, Trerotoli P, De Lucia D, Iolascon A.

Int J Clin Lab Res. 1999;29(4):174-5. No abstract available. PMID: 10784380 [PubMed - indexed for MEDLINE]Related articles

Absence of association of thrombophilia polymorphisms with intrauterine growth restriction.

Infante-Rivard C, Rivard GE, Yotov WV, Génin E, Guiguet M, Weinberg C, Gauthier R, Feoli-Fonseca JC.

N Engl J Med. 2002 Jul 4;347(1):19-25.PMID: 12097536 [PubMed - indexed for MEDLINE]Related articlesFree article

Prothrombotic and vascular risk factors in NAION.

Egan R.

Ophthalmology. 2000 Dec;107(12):2116-7. No abstract available. PMID: 11097559 [PubMed - indexed for MEDLINE]Related articles

Retinal vein occlusion: a form of venous thrombosis or a complication of atherosclerosis? A meta-analysis of thrombophilic factors.

Janssen MC, den Heijer M, Cruysberg JR, Wollersheim H, Bredie SJ.

Thromb Haemost. 2005 Jun;93(6):1021-6. Review.PMID: 15968383 [PubMed - indexed for MEDLINE]Related articles

Thrombophilic mutations and risk of retinal vein occlusion.

Biancardi AL, Gadelha T, Borges WI, Vieira de Moraes H Jr, Spector N.

Arq Bras Oftalmol. 2007 Nov-Dec;70(6):971-4.PMID: 18235909 [PubMed - indexed for MEDLINE]Related articlesFree article

Interaction between hyperhomocysteinemia, mutated methylenetetrahydrofolatereductase (MTHFR) and inherited thrombophilic factors in recurrent venous thrombosis.

Keijzer MB, den Heijer M, Blom HJ, Bos GM, Willems HP, Gerrits WB, Rosendaal FR.

Thromb Haemost. 2002 Nov;88(5):723-8.PMID: 12428084 [PubMed - indexed for MEDLINE]Related articles

Mutations C677T and A1298C of the 5,10-methylenetetrahydrofolate reductase gene and fasting plasma homocysteine levels are not associated with the increased risk of venous thromboembolic disease.

Domagala TB, Adamek L, Nizankowska E, Sanak M, Szczeklik A.

Blood Coagul Fibrinolysis. 2002 Jul;13(5):423-31.PMID: 12138370 [PubMed - indexed for MEDLINE]Related articles

Genetic determinants of fasting and post-methionine hyperhomocysteinemia in patients with retinal vein occlusion.

Marcucci R, Giusti B, Betti I, Evangelisti L, Fedi S, Sodi A, Cappelli S, Menchini U, Abbate R, Prisco D.

Thromb Res. 2003 Apr 15;110(1):7-12.PMID: 12877902 [PubMed - indexed for MEDLINE]Related articles

Application of the TaqMan-PCR for genotyping of the prothrombin G20210A mutation and of the thermolabile methylenetetrahydrofolate reductase mutation.

Happich D, Madlener K, Schwaab R, Hanfland P, Pötzsch B.

Thromb Haemost. 2000 Jul;84(1):144-5. No abstract available. PMID: 10928490 [PubMed - indexed for MEDLINE]Related articles

Primary thrombophilia in Mexico. II. Factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase C677T polymorphism in thrombophilic Mexican mestizos.

Ruiz-Argüelles GJ, Garcés-Eisele J, Reyes-Núñez V, Ramírez-Cisneros FJ.

Am J Hematol. 2001 Jan;66(1):28-31.PMID: 11426488 [PubMed - indexed for MEDLINE]Related articles

Thrombophilic mutations impart a high risk of pregnancy-related venous thrombosis.

Press RD.

Mol Diagn. 2000 Jun;5(2):158. No abstract available. PMID: 11066018 [PubMed - indexed for MEDLINE]Related articles

A boy with venous thrombosis, homozygous for factor V Leiden, prothrombin G20210A and MTHFR C667t mutations, but belonging to an asymptomatic family.

Soria JM, Quintana R, Vallvé C, Iruin G, Cortés C, Fontcuberta J.

Haematologica. 2000 Nov;85(11):1230-2. No abstract available. PMID: 11064483 [PubMed - indexed for MEDLINE]Related articlesFree article

A homozygosity state for 20210A prothrombin variant in a young woman as cause of a deep venous thrombosis during pregnancy.

Acquila M, Bicocchi MP, Mori PG, Odino S, Valetto A, Bottini F.

Eur J Haematol. 2000 Jul;65(1):80-1. No abstract available. PMID: 10914946 [PubMed - indexed for MEDLINE]Related articles