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Journal Abstract Search

229 related items for PubMed ID: 16015408

  • 1. Amaurosis fugax: associations with heritable thrombophilia.
    Glueck CJ, Goldenberg N, Bell H, Golnik K, Wang P.
    Clin Appl Thromb Hemost; 2005 Jul; 11(3):235-41. PubMed ID: 16015408
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  • 2. Ocular vascular thrombotic events: a diagnostic window to familial thrombophilia (compound factor V Leiden and prothrombin gene heterozygosity) and thrombosis.
    Glueck CJ, Wang P.
    Clin Appl Thromb Hemost; 2009 Feb; 15(1):12-8. PubMed ID: 18796459
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  • 3. Idiopathic intracranial hypertension: associations with thrombophilia and hypofibrinolysis in men.
    Glueck CJ, Goldenberg N, Golnik K, Sieve L, Wang P.
    Clin Appl Thromb Hemost; 2005 Oct; 11(4):441-8. PubMed ID: 16244770
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  • 4. 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. PubMed ID: 9930159
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  • 5. Amaurosis fugax caused by heritable thrombophilia-hypofibrinolysis in cases without carotid atherosclerosis: thromboprophylaxis prevents subsequent transient monocular partial blindness.
    Glueck CJ, Golnik K, Ping Wang.
    Clin Appl Thromb Hemost; 2007 Apr; 13(2):124-9. PubMed ID: 17456620
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  • 7. Associations of thrombophilia, hypofibrinolysis, and retinal vein occlusion.
    Glueck CJ, Wang P, Bell H, Rangaraj V, Goldenberg N.
    Clin Appl Thromb Hemost; 2005 Oct; 11(4):375-89. PubMed ID: 16244763
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  • 10. Thrombotic events after starting exogenous testosterone in men with previously undiagnosed familial thrombophilia.
    Glueck CJ, Goldenberg N, Budhani S, Lotner D, Abuchaibe C, Gowda M, Nayar T, Khan N, Wang P.
    Transl Res; 2011 Oct; 158(4):225-34. PubMed ID: 21925119
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  • 11. Risk Factors of Thrombophilia-Related Mutations for Early and Late Pregnancy Loss.
    Borsi E, Potre O, Ionita I, Samfireag M, Secosan C, Potre C.
    Medicina (Kaunas); 2024 Mar 22; 60(4):. PubMed ID: 38674167
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  • 12. Ramifications of four concurrent thrombophilic mutations and one hypofibrinolytic mutation.
    Glueck CJ, Goldenberg N, Wang P, Aregawi D.
    Clin Appl Thromb Hemost; 2004 Oct 22; 10(4):365-71. PubMed ID: 15497023
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  • 14. Analysis of thrombophilic genetic mutations in patients with Sheehan's syndrome: is thrombophilia responsible for the pathogenesis of Sheehan's syndrome?
    Gokalp D, Tuzcu A, Bahceci M, Ayyildiz O, Yurt M, Celik Y, Alpagat G.
    Pituitary; 2011 Jun 22; 14(2):168-73. PubMed ID: 21107737
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  • 16. Hypofibrinolysis, thrombophilia, osteonecrosis.
    Glueck CJ, Freiberg RA, Fontaine RN, Tracy T, Wang P.
    Clin Orthop Relat Res; 2001 May 22; (386):19-33. PubMed ID: 11347834
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  • 18. Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations.
    Ozdemir O, Yenicesu GI, Silan F, Köksal B, Atik S, Ozen F, Göl M, Cetin A.
    Genet Test Mol Biomarkers; 2012 Apr 22; 16(4):279-86. PubMed ID: 22047507
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  • 19. Combined germline variations of thrombophilic genes promote genesis of lung cancer.
    Ozen F, Polat F, Arslan S, Ozdemir O.
    Asian Pac J Cancer Prev; 2013 Apr 22; 14(9):5449-54. PubMed ID: 24175756
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  • 20. Thrombophilia as a cause for central and branch retinal artery occlusion in patients without an apparent embolic source.
    Salomon O, Huna-Baron R, Moisseiev J, Rosenberg N, Rubovitz A, Steinberg DM, Davidson J, Sela BA, Seligsohn U.
    Eye (Lond); 2001 Aug 22; 15(Pt 4):511-4. PubMed ID: 11767028
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