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324 related items for PubMed ID: 9930159

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Prothrombin polymorphism A19911G, factor V HR2 haplotype A4070G, and plasminogen activator-inhibitor-1 polymorphism 4G/5G and the risk of retinal vein occlusion.
    Kuhli-Hattenbach C, Hellstern P, Nägler DK, Kohnen T, Hattenbach LO.
    Ophthalmic Genet; 2017 Jan; 38(5):413-417. PubMed ID: 28085526
    [Abstract] [Full Text] [Related]

  • 3. The plasminogen activator inhibitor-1 gene, hypofibrinolysis, and osteonecrosis.
    Glueck CJ, Fontaine RN, Gruppo R, Stroop D, Sieve-Smith L, Tracy T, Wang P.
    Clin Orthop Relat Res; 1999 Sep; (366):133-46. PubMed ID: 10627727
    [Abstract] [Full Text] [Related]

  • 4. Ocular vascular thrombotic events: central retinal vein and central retinal artery occlusions.
    Glueck CJ, Ping Wang, Hutchins R, Petersen MR, Golnik K.
    Clin Appl Thromb Hemost; 2008 Jul; 14(3):286-94. PubMed ID: 18160589
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

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  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Thrombophilic mutations as risk factor for retinal vein occlusion: a case-control study.
    Russo PD, Damante G, Pasca S, Turello M, Barillari G.
    Clin Appl Thromb Hemost; 2015 May; 21(4):373-7. PubMed ID: 24569626
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 4G/5G polymorphism of PAI-1 gene promoter and fibrinolytic capacity in patients with deep vein thrombosis.
    Sartori MT, Wiman B, Vettore S, Dazzi F, Girolami A, Patrassi GM.
    Thromb Haemost; 1998 Dec; 80(6):956-60. PubMed ID: 9869167
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. The plasminogen activator inhibitor (PAI)-1 promoter 4G/4G genotype is not associated with ischemic stroke in a population of German children. Childhood Stroke Study Group.
    Nowak-Göttl U, Sträter R, Kosch A, von Eckardstein A, Schobess R, Luigs P, Nabel P, Vielhaber H, Kurnik K, Junker R.
    Eur J Haematol; 2001 Jan; 66(1):57-62. PubMed ID: 11168509
    [Abstract] [Full Text] [Related]

  • 13. [Prevalence of thrombophilic mutations of FV Leiden, prothrombin G20210A and PAl-1 4G/5G and their combinations in a group of 1450 healthy middle-aged individuals in the Prague and Central Bohemian regions (results of FRET real-time PCR assay)].
    Kvasnicka J, Hájková J, Bobcíková P, Kvasnicka T, Dusková D, Poletínová S, Kieferová V.
    Cas Lek Cesk; 2012 Jan; 151(2):76-82. PubMed ID: 22515013
    [Abstract] [Full Text] [Related]

  • 14. The association of factor V G1961A (factor V Leiden), prothrombin G20210A, MTHFR C677T and PAI-1 4G/5G polymorphisms with recurrent pregnancy loss in Bosnian women.
    Jusić A, Balić D, Avdić A, Pođanin M, Balić A.
    Med Glas (Zenica); 2018 Aug 01; 15(2):158-163. PubMed ID: 29703881
    [Abstract] [Full Text] [Related]

  • 15. Plasminogen activator inhibitor-1 4G/5G polymorphism, factor V Leiden, prothrombin mutations and the risk of VTE recurrence.
    Sundquist K, Wang X, Svensson PJ, Sundquist J, Hedelius A, Larsson Lönn S, Zöller B, Memon AA.
    Thromb Haemost; 2015 Nov 25; 114(6):1156-64. PubMed ID: 26245493
    [Abstract] [Full Text] [Related]

  • 16. CENTRAL RETINAL VEIN OCCLUSION IN OTHERWISE HEALTHY CHILDREN AND ADOLESCENTS: Association With Multigenetic Variants of Thrombophilia.
    Bremond-Gignac D, Daruich A, Gallet M, Menoud PA, Nowomiejska K, Rejdak R, Behar-Cohen F, Benkhalifa M, Copin H.
    Retina; 2020 Jul 25; 40(7):1339-1343. PubMed ID: 31095065
    [Abstract] [Full Text] [Related]

  • 17. The factor V Leiden mutation, high factor VIII, and high plasminogen activator inhibitor activity: etiologies for sporadic miscarriage.
    Glueck CJ, Pranikoff J, Aregawi D, Haque M, Zhu B, Tracy T, Wang P.
    Metabolism; 2005 Oct 25; 54(10):1345-9. PubMed ID: 16154434
    [Abstract] [Full Text] [Related]

  • 18. Polycystic ovary syndrome, the G1691A factor V Leiden mutation, and plasminogen activator inhibitor activity: associations with recurrent pregnancy loss.
    Glueck CJ, Wang P, Bornovali S, Goldenberg N, Sieve L.
    Metabolism; 2003 Dec 25; 52(12):1627-32. PubMed ID: 14669168
    [Abstract] [Full Text] [Related]

  • 19. Hypofibrinolysis, thrombophilia, osteonecrosis.
    Glueck CJ, Freiberg RA, Fontaine RN, Tracy T, Wang P.
    Clin Orthop Relat Res; 2001 May 25; (386):19-33. PubMed ID: 11347834
    [Abstract] [Full Text] [Related]

  • 20. Prevalence of genetic risk factors related with thrombophilia and hypofibrinolysis in patients with osteonecrosis of the femoral head in Poland.
    Gagala J, Buraczynska M, Mazurkiewicz T, Ksiazek A.
    BMC Musculoskelet Disord; 2013 Sep 11; 14():264. PubMed ID: 24025446
    [Abstract] [Full Text] [Related]

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