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Volumn 11, Issue 6, 2000, Pages 462-467

Systemic disorders associated with retinal vascular occlusion

Author keywords

[No Author keywords available]

Indexed keywords

FIBRIN;

EID: 0033669060     PISSN: 10408738     EISSN: None     Source Type: Journal    
DOI: 10.1097/00055735-200012000-00013     Document Type: Article
Times cited : (90)

References (44)
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    • Risk factors for central retinal vein occlusion
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    • Risk factors for branch retinal vein occlusion
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    • A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
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    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3
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    • The prothrombin gene G20210A mutation and the platelet glycoprotein Ilia polymorphism PIA2 in patients with central retinal vein occlusion
    • (1999) Thromb Res , vol.96 , pp. 323-327
    • Larsson, J.1    Hillarp, A.2
  • 42
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    • Hyperhomocysteinemia: A risk factor for central retinal vein occlusion
    • (2000) Am J Ophthalmol , vol.129 , pp. 640-644
    • Vine, A.K.1
  • 43
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    • Rapid HPLC determination of total homocysteine and other thiols in serum and plasma: Sex differences and correlation with cobalamin and folate concentrations in healthy subjects
    • (1994) Clin Chem , vol.40 , pp. 873-881
    • Jacobsen, D.W.1    Gatautis, V.J.2    Green, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.