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335 related items for PubMed ID: 11246543

  • 1. Interaction of heritable and estrogen-induced thrombophilia: possible etiologies for ischemic optic neuropathy and ischemic stroke.
    Glueck CJ, Fontaine RN, Wang P.
    Thromb Haemost; 2001 Feb; 85(2):256-9. PubMed ID: 11246543
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 3. The 4G/4G polymorphism of the hypofibrinolytic plasminogen activator inhibitor type 1 gene: an independent risk factor for serious pregnancy complications.
    Glueck CJ, Phillips H, Cameron D, Wang P, Fontaine RN, Moore SK, Sieve-Smith L, Tracy T.
    Metabolism; 2000 Jul; 49(7):845-52. PubMed ID: 10909993
    [Abstract] [Full Text] [Related]

  • 4. Nonarteritic anterior ischemic optic neuropathy: associations with homozygosity for the C677T methylenetetrahydrofolate reductase mutation.
    Glueck CJ, Wang P, Bell H, Rangaraj V, Goldenberg N.
    J Lab Clin Med; 2004 Mar; 143(3):184-92. PubMed ID: 15007309
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  • 7. Spectrum and prevalence of prothrombotic single nucleotide polymorphism profiles in the Greek Cypriot population.
    Xenophontos SL, Hadjivassiliou M, Ayrton N, Karagrigoriou A, Pantzaris M, Nicolaides AN, Cariolou MA.
    Int Angiol; 2002 Dec; 21(4):322-9. PubMed ID: 12518110
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  • 9. 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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  • 10. [Genetics of blood coagulation in young stroke patients].
    Pongrácz E, Tordai A, Csornai M, Nagy Z.
    Ideggyogy Sz; 2002 Mar 20; 55(3-4):111-7. PubMed ID: 12122980
    [Abstract] [Full Text] [Related]

  • 11. Contraception-related deep venous thrombosis and pulmonary embolism in a 17-Year-old girl heterozygous for factor V leiden, prothrombin G20210A mutation, MTHFR C677T and homozygous for PAI-1 mutation: report of a family with multiple genetic risk factors and review of the literature.
    Lenicek Krleza J, Jakovljevic G, Bronic A, Coen Herak D, Bonevski A, Stepan-Giljevic J, Roic G.
    Pathophysiol Haemost Thromb; 2010 Mar 20; 37(1):24-9. PubMed ID: 20664190
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  • 12. 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 20; 85(11):1230-2. PubMed ID: 11064483
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  • 13. Comparison of thrombophilic gene mutations among patients experiencing recurrent miscarriage and deep vein thrombosis.
    Coulam CB, Wallis D, Weinstein J, DasGupta DS, Jeyendran RS.
    Am J Reprod Immunol; 2008 Nov 20; 60(5):426-31. PubMed ID: 18803625
    [Abstract] [Full Text] [Related]

  • 14. [C677T mutation in methylentetrahydrofolatereductase gene in patients with venous thromboses from the central region of Russia correlates with a high risk of pulmonary artery thromboembolism].
    Avdonin PV, Kirienko AI, Kozhevnikova LM, Shostak NA, Babadaeva NM, Leont'ev SG, Petukhov EB, Kubatiev AA, Savel'ev VS.
    Ter Arkh; 2006 Nov 20; 78(6):70-6. PubMed ID: 16881367
    [Abstract] [Full Text] [Related]

  • 15. Large volume donor plasmapheresis in inherited thrombophilia implicated in arterial thrombosis.
    Ovali E, Ratip S, Ozmenoglu M, Karti SS, Uçar F, Ukinç K, Yilmaz M, Koşucu P.
    Transfus Apher Sci; 2003 Jun 20; 28(3):201-6. PubMed ID: 12725943
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  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. [The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans].
    Guo C, Guo Q, Gong Y, Chen B, Liu Q, Li J, Gao G, Zhou H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug 22; 19(4):295-7. PubMed ID: 12170465
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  • 18. Amaurosis fugax: associations with heritable thrombophilia.
    Glueck CJ, Goldenberg N, Bell H, Golnik K, Wang P.
    Clin Appl Thromb Hemost; 2005 Jul 22; 11(3):235-41. PubMed ID: 16015408
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  • 19. Prediction of ischemic stroke in young Indians: is thrombophilia profiling a way out?
    Chatterjee T, Gupta N, Choudhry VP, Behari M, Saxena R, Ashraf MZ.
    Blood Coagul Fibrinolysis; 2013 Jun 22; 24(4):449-53. PubMed ID: 23337710
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  • 20. Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family.
    Zawadzki C, Gaveriaux V, Trillot N, Bauters A, Watel A, Alhenc-Gelas M, Preudhomme C, Jude B.
    Thromb Haemost; 1998 Dec 22; 80(6):1027-8. PubMed ID: 9869179
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