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Journal Abstract Search

149 related items for PubMed ID: 22098125

  • 21. Evaluation of Factor V Leiden, Prothrombin G20210A, MTHFR C677T and MTHFR A1298C gene polymorphisms in retinopathy of prematurity in a Turkish cohort.
    Aydin H, Gunay M, Celik G, Gunay BO, Aydin UT, Karaman A.
    Ophthalmic Genet; 2016 Dec; 37(4):415-418. PubMed ID: 27018927
    [Abstract] [Full Text] [Related]

  • 22. Inherited thrombophilia: a possible cause of in utero vascular thrombosis in children with intestinal atresia.
    Johnson SM, Meyers RL.
    J Pediatr Surg; 2001 Aug; 36(8):1146-9. PubMed ID: 11479844
    [Abstract] [Full Text] [Related]

  • 23. Role of thrombophilic risk factors in children with non-stroke cerebral palsy.
    Fattal-Valevski A, Kenet G, Kupferminc MJ, Mesterman R, Leitner Y, Rimon E, Harel S, Hassner A.
    Thromb Res; 2005 Aug; 116(2):133-7. PubMed ID: 15907528
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  • 24. COL4A1 mutation in two preterm siblings with antenatal onset of parenchymal hemorrhage.
    de Vries LS, Koopman C, Groenendaal F, Van Schooneveld M, Verheijen FW, Verbeek E, Witkamp TD, van der Worp HB, Mancini G.
    Ann Neurol; 2009 Jan; 65(1):12-8. PubMed ID: 19194877
    [Abstract] [Full Text] [Related]

  • 25. Genetic polymorphisms of hemostasis genes and primary outcome of very low birth weight infants.
    Härtel C, König I, Köster S, Kattner E, Kuhls E, Küster H, Möller J, Müller D, Kribs A, Segerer H, Wieg C, Herting E, Göpel W.
    Pediatrics; 2006 Aug; 118(2):683-9. PubMed ID: 16882823
    [Abstract] [Full Text] [Related]

  • 26. Prevalence of thrombophilia in women with severe ovarian hyperstimulation syndrome and cost-effectiveness of screening.
    Fábregues F, Tàssies D, Reverter JC, Carmona F, Ordinas A, Balasch J.
    Fertil Steril; 2004 Apr; 81(4):989-95. PubMed ID: 15066453
    [Abstract] [Full Text] [Related]

  • 27. Association between factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations and events of the arterial circulatory system: a meta-analysis of published studies.
    Kim RJ, Becker RC.
    Am Heart J; 2003 Dec; 146(6):948-57. PubMed ID: 14660985
    [Abstract] [Full Text] [Related]

  • 28. Relationship between polymorphisms in thrombophilic genes and preeclampsia in a Brazilian population.
    Dalmáz CA, Santos KG, Botton MR, Tedoldi CL, Roisenberg I.
    Blood Cells Mol Dis; 2006 Dec; 37(2):107-10. PubMed ID: 16963292
    [Abstract] [Full Text] [Related]

  • 29. Thrombophilia: a risk factor for cerebral palsy?
    Yehezkely-Schildkraut V, Kutai M, Hugeirat Y, Levin C, Shalev SA, Mazor G, Koren A.
    Isr Med Assoc J; 2005 Dec; 7(12):808-11. PubMed ID: 16382706
    [Abstract] [Full Text] [Related]

  • 30. Inherited thrombophilia in infertile women: implication in unexplained infertility.
    Casadei L, Puca F, Privitera L, Zamaro V, Emidi E.
    Fertil Steril; 2010 Jul; 94(2):755-7. PubMed ID: 19939360
    [Abstract] [Full Text] [Related]

  • 31. MTHFR C677T mutation, factor II G20210A mutation and factor V Leiden as risks factor for youth retinal vein occlusion.
    Cruciani F, Moramarco A, Curto T, Labate A, Recupero V, Conti L, Gandolfo GM, Balacco Gabrieli C.
    Clin Ter; 2003 Jul; 154(5):299-303. PubMed ID: 14994919
    [Abstract] [Full Text] [Related]

  • 32. Associations between inherited thrombophilias, gestational age, and cerebral palsy.
    Gibson CS, MacLennan AH, Hague WM, Haan EA, Priest K, Chan A, Dekker GA, South Australian Cerebral Palsy Research Group.
    Am J Obstet Gynecol; 2005 Oct; 193(4):1437. PubMed ID: 16202738
    [Abstract] [Full Text] [Related]

  • 33. The prevalence of factor V Leiden (G1691A), prothrombin G20210A and methylenetetrahydrofolate reductase C677T mutations in Jordanian patients with beta-thalassemia major.
    Al-Sweedan SA, Jaradat S, Iraqi M, Beshtawi M.
    Blood Coagul Fibrinolysis; 2009 Dec; 20(8):675-8. PubMed ID: 19710606
    [Abstract] [Full Text] [Related]

  • 34. Genetic thrombophilias and preeclampsia: a meta-analysis.
    Lin J, August P.
    Obstet Gynecol; 2005 Jan; 105(1):182-92. PubMed ID: 15625161
    [Abstract] [Full Text] [Related]

  • 35. Risk of recurrent venous thrombosis in patients with G20210A mutation in the prothrombin gene or factor V Leiden mutation.
    González-Porras JR, García-Sanz R, Alberca I, López ML, Balanzategui A, Gutierrez O, Lozano F, San Miguel J.
    Blood Coagul Fibrinolysis; 2006 Jan; 17(1):23-8. PubMed ID: 16607075
    [Abstract] [Full Text] [Related]

  • 36. No association of factor V Leiden, prothrombin G20210A, and MTHFR C677T gene polymorphisms with kidney allograft survival: a multicenter study.
    Meyer M, Laux G, Scherer S, Tran TH, Opelz G, Mytilineos J.
    Transplantation; 2007 Apr 27; 83(8):1055-8. PubMed ID: 17452895
    [Abstract] [Full Text] [Related]

  • 37. Thrombophilia-related genetic variations in patients with pulmonary embolism in the main teaching hospital in Jordan.
    Obeidat NM, Awidi A, Sulaiman NA, Abu-Khader IB.
    Saudi Med J; 2009 Jul 27; 30(7):921-5. PubMed ID: 19618008
    [Abstract] [Full Text] [Related]

  • 38. Thrombophilia in young patients with acute myocardial infarction.
    Celik M, Altintas A, Celik Y, Karabulut A, Ayyildiz O.
    Saudi Med J; 2008 Jan 27; 29(1):48-54. PubMed ID: 18176672
    [Abstract] [Full Text] [Related]

  • 39. Combined thrombophilic mutations in women with unexplained recurrent miscarriage.
    Sotiriadis A, Vartholomatos G, Pavlou M, Kolaitis N, Dova L, Stefos T, Paraskevaidis E, Kalantaridou SN.
    Am J Reprod Immunol; 2007 Feb 27; 57(2):133-41. PubMed ID: 17217367
    [Abstract] [Full Text] [Related]

  • 40. Genetic and acquired prothrombotic risk factors and sudden hearing loss.
    Capaccio P, Ottaviani F, Cuccarini V, Bottero A, Schindler A, Cesana BM, Censuales S, Pignataro L.
    Laryngoscope; 2007 Mar 27; 117(3):547-51. PubMed ID: 17334320
    [Abstract] [Full Text] [Related]

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