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Journal Abstract Search

195 related items for PubMed ID: 14747183

  • 21. Portal vein thrombosis in children and adolescents: the low prevalence of hereditary thrombophilic disorders.
    Pinto RB, Silveira TR, Bandinelli E, Röhsig L.
    J Pediatr Surg; 2004 Sep; 39(9):1356-61. PubMed ID: 15359390
    [Abstract] [Full Text] [Related]

  • 22. Thrombophilia and immunological disorders in pregnancies as risk factors for small for gestational age infants.
    Verspyck E, Le Cam-Duchez V, Goffinet F, Tron F, Marpeau L, Borg JY.
    BJOG; 2002 Jan; 109(1):28-33. PubMed ID: 11843372
    [Abstract] [Full Text] [Related]

  • 23. A Study on Hereditary Thrombophilia and Stroke in a Cohort from Sri Lanka.
    Kalpage HA, Sumathipala DS, Goonasekara HW, Dissanayake VH.
    J Stroke Cerebrovasc Dis; 2016 Jan; 25(1):102-9. PubMed ID: 26522268
    [Abstract] [Full Text] [Related]

  • 24. [Genomic diagnosis of thrombophilia in women: clinical relevance].
    Luxembourg B, Lindhoff-Last E.
    Hamostaseologie; 2007 Feb; 27(1):22-31. PubMed ID: 17279273
    [Abstract] [Full Text] [Related]

  • 25. Cerebral venous and sinus thrombosis and thrombophilic mutations in Western Iran: association with factor V Leiden.
    Rahimi Z, Mozafari H, Bigvand AH, Doulabi RM, Vaisi-Raygani A, Afshari D, Razazian N, Rezaei M.
    Clin Appl Thromb Hemost; 2010 Aug; 16(4):430-4. PubMed ID: 19703820
    [Abstract] [Full Text] [Related]

  • 26. Prevalence of inherited thrombophilia in patients with severe ovarian hyperstimulation syndrome.
    Machac S, Lubusky M, Prochazka M, Streda R.
    Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2006 Nov; 150(2):289-92. PubMed ID: 17426795
    [Abstract] [Full Text] [Related]

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  • 28. Impact of inherited thrombophilia on the risk of recurrent venous thromboembolism onset in Georgian population.
    Pirtskhelani N, Kochiashvili N, Makhaldiani L, Pargalava N, Gaprindashvili E, Kartvelishvili K.
    Georgian Med News; 2014 Feb; (227):93-7. PubMed ID: 24632656
    [Abstract] [Full Text] [Related]

  • 29. Frequency of selected thrombophilias in women with placental abruption.
    Procházka M, Lubuský M, Slavík L, Hrachovec P, Zielina P, Kudela M, Lindqvist PG.
    Aust N Z J Obstet Gynaecol; 2007 Aug; 47(4):297-301. PubMed ID: 17627684
    [Abstract] [Full Text] [Related]

  • 30. 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]

  • 31. The role of point mutations in the genes, predisposing inherited thrombophilia in the pathogeneses of proximal and distal deep vein thrombosis in Georgian population.
    Pirtskhelani N, Kochiashvili N, Makhaldiani L, Pargalava N, Gaprindashvili E, Kartvelishvili K.
    Georgian Med News; 2014 Feb; (227):98-102. PubMed ID: 24632657
    [Abstract] [Full Text] [Related]

  • 32. 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; 24(4):449-53. PubMed ID: 23337710
    [Abstract] [Full Text] [Related]

  • 33. Thrombophilia in childhood: to test or not to test.
    Heleen van Ommen C, Middeldorp S.
    Semin Thromb Hemost; 2011 Oct; 37(7):794-801. PubMed ID: 22187402
    [Abstract] [Full Text] [Related]

  • 34. Thrombophilic mutations in Iranian patients with infertility and recurrent spontaneous abortion.
    Behjati R, Modarressi MH, Jeddi-Tehrani M, Dokoohaki P, Ghasemi J, Zarnani AH, Aarabi M, Memariani T, Ghaffari M, Akhondi MA.
    Ann Hematol; 2006 Apr; 85(4):268-71. PubMed ID: 16450127
    [Abstract] [Full Text] [Related]

  • 35. Association of common thrombophilias and antiphospholipid antibodies with success rate of in vitro fertilisation.
    Steinvil A, Raz R, Berliner S, Steinberg DM, Zeltser D, Levran D, Shimron O, Sella T, Chodick G, Shalev V, Salomon O.
    Thromb Haemost; 2012 Dec; 108(6):1192-7. PubMed ID: 23052827
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  • 37. Multiple thrombophilic single nucleotide polymorphisms lack a significant effect on outcomes in fresh IVF cycles: an analysis of 1717 patients.
    Patounakis G, Bergh E, Forman EJ, Tao X, Lonczak A, Franasiak JM, Treff N, Scott RT.
    J Assist Reprod Genet; 2016 Jan; 33(1):67-73. PubMed ID: 26545911
    [Abstract] [Full Text] [Related]

  • 38. Lack of association between inherited thrombophilic risk factors and idiopathic sudden sensorineural hearing loss in Italian patients.
    Cadoni G, Scipione S, Rocca B, Agostino S, La Greca C, Bonvissuto D, Paludetti G.
    Ann Otol Rhinol Laryngol; 2006 Mar; 115(3):195-200. PubMed ID: 16572609
    [Abstract] [Full Text] [Related]

  • 39. 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]

  • 40. Congenital prothrombotic disorders in children with peripheral venous and arterial thromboses.
    Albisetti M, Moeller A, Waldvogel K, Bernet-Buettiker V, Cannizzaro V, Anagnostopoulos A, Balmer C, Schmugge M.
    Acta Haematol; 2007 Aug 01; 117(3):149-55. PubMed ID: 17159337
    [Abstract] [Full Text] [Related]

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