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    Results: 1 to 20 of 385

    1.

    The influence of thrombophilic risk factors on vascular access survival in chronic dialysis patients in a retrospective evaluation.

    Klamroth R, Orlovic M, Fritsche I, Seibt S, Seibt F, Wegscheider K, Landgraf H.

    Vasa. 2013 Jan;42(1):32-9. doi: 10.1024/0301-1526/a000245.

    PMID:
    23385224
    [PubMed - indexed for MEDLINE]
    2.

    Venous thrombosis in athletes.

    Grabowski G, Whiteside WK, Kanwisher M.

    J Am Acad Orthop Surg. 2013 Feb;21(2):108-17. doi: 10.5435/JAAOS-21-02-108. Review.

    PMID:
    23378374
    [PubMed - indexed for MEDLINE]
    3.

    Inherited thrombophilia with recurrent pregnancy loss in Turkish women--a real phenomenon?

    Yildiz G, Yavuzcan A, Yildiz P, Süer N, Tandoğan N.

    Ginekol Pol. 2012 Aug;83(8):598-603.

    PMID:
    23342883
    [PubMed - indexed for MEDLINE]
    4.
    5.

    Thrombophilic molecular markers in young patients (<40 years) with coronary artery disease.

    Sherpa M, Sharma S, Avasthi R.

    Indian J Pathol Microbiol. 2012 Jul-Sep;55(3):343-6. doi: 10.4103/0377-4929.101741.

    PMID:
    23032828
    [PubMed - indexed for MEDLINE]
    Free Article
    6.

    Necessity and risks of arterial blood sampling in healthy volunteer studies.

    Oertel BG, Vermehren J, Zimmermann M, Huynh TT, Doehring A, Ferreiros N, Senzel S, Schmitz-Rixen T, Erbe M, Geisslinger G, Harder S, Angst MS, Lötsch J.

    Clin Pharmacokinet. 2012 Oct 1;51(10):629-38.

    PMID:
    23018527
    [PubMed - indexed for MEDLINE]
    7.

    Thrombophilia and venous thromboembolism: RIETE experience.

    Monreal M, Campo RD, Papadakis E.

    Best Pract Res Clin Haematol. 2012 Sep;25(3):285-94. doi: 10.1016/j.beha.2012.07.007. Epub 2012 Aug 17. Review.

    PMID:
    22959545
    [PubMed - indexed for MEDLINE]
    8.

    MTHFR polymorphic variant C677T is associated to vascular complications in sickle-cell disease.

    Hatzlhofer BL, Bezerra MA, Santos MN, Albuquerque DM, Freitas EM, Costa FF, Araújo AS, Muniz MT.

    Genet Test Mol Biomarkers. 2012 Sep;16(9):1038-43. doi: 10.1089/gtmb.2011.0361. Epub 2012 Aug 27.

    PMID:
    22924497
    [PubMed - indexed for MEDLINE]
    9.

    Quality in molecular biology testing for inherited thrombophilia disorders.

    Cooper PC, Goodeve AC, Beauchamp NJ.

    Semin Thromb Hemost. 2012 Sep;38(6):600-12. doi: 10.1055/s-0032-1321491. Epub 2012 Aug 20. Review.

    PMID:
    22907670
    [PubMed - indexed for MEDLINE]
    10.

    Testing for heritable thrombophilia in children at Starship Children's Hospital: an audit of requests between 2004 and 2009.

    Bradbeer P, Teague L, Cole N.

    J Paediatr Child Health. 2012 Oct;48(10):921-5. doi: 10.1111/j.1440-1754.2012.02517.x. Epub 2012 Aug 19.

    PMID:
    22900528
    [PubMed - indexed for MEDLINE]
    11.

    Therapeutic correction of thrombin generation in dilution-induced coagulopathy: computational analysis based on a data set of healthy subjects.

    Mitrophanov AY, Rosendaal FR, Reifman J.

    J Trauma Acute Care Surg. 2012 Aug;73(2 Suppl 1):S95-S102. doi: 10.1097/TA.0b013e3182609bca.

    PMID:
    22847103
    [PubMed - indexed for MEDLINE]
    12.

    Inherited thrombophilia in pediatric ischemic stroke: an Egyptian study.

    Shatla HM, Tomoum HY, Elsayed SM, Aly RH, Shatla RH, Ismail MA, El-Ghany NA, Fakhry AI, Abd Allah NA, Yonca E, Nejat AM.

    Pediatr Neurol. 2012 Aug;47(2):114-8. doi: 10.1016/j.pediatrneurol.2012.05.008.

    PMID:
    22759687
    [PubMed - indexed for MEDLINE]
    13.

    Influence of hereditary or acquired thrombophilias on the treatment of venous thromboembolism.

    Kearon C.

    Curr Opin Hematol. 2012 Sep;19(5):363-70. doi: 10.1097/MOH.0b013e328356745b. Review.

    PMID:
    22759630
    [PubMed - indexed for MEDLINE]
    14.

    Flow-simulated thrombin generation profiles as a predictor of thrombotic risk among pre-menopausal women.

    Jordan SW, Corriere MA, Vossen CY, Rosendaal FR, Chaikof EL.

    Thromb Haemost. 2012 Aug;108(2):258-65. doi: 10.1160/TH12-02-0098. Epub 2012 Jun 12.

    PMID:
    22688389
    [PubMed - indexed for MEDLINE]
    15.

    Evaluation of the presence of hereditary and acquired thrombophilias in Brazilian children and adolescents with diagnoses of portal vein thrombosis.

    Ferri PM, Rodrigues Ferreira A, Fagundes ED, Xavier SG, Dias Ribeiro D, Fernandes AP, Borges KB, Liu SM, de Melo Mdo C, Roquete ML, Penna FJ.

    J Pediatr Gastroenterol Nutr. 2012 Nov;55(5):599-604. doi: 10.1097/MPG.0b013e318261814d.

    PMID:
    22684349
    [PubMed - indexed for MEDLINE]
    16.

    Prevalence of inherited thrombophilia in patients with documented stent thrombosis.

    Zavalloni D, Presbitero P, Lodigiani C, Mango R, Cogliati T, Quaglia I, Corrada E, Mendolicchio GL, Gasparini GL, Rossi ML, Ferrazzi P, Belli G, Pagnotta P, Rota LL.

    Circ J. 2012;76(8):1874-9. Epub 2012 May 26.

    PMID:
    22665071
    [PubMed - indexed for MEDLINE]
    Free Article
    17.

    Frequency of thrombophilic genetic polymorphisms among Saudi subjects compared with other populations.

    Settin AA, Alghasham A, Ali A, Dowaidar M, Ismail H.

    Hematology. 2012 May;17(3):176-82. doi: 10.1179/102453312X13376952196575.

    PMID:
    22664118
    [PubMed - indexed for MEDLINE]
    18.

    Management of patients undergoing rhinoplasty while receiving anticoagulant therapy.

    Bracaglia R, Tambasco D, D'ettorre M, Gentileschi S.

    Aesthetic Plast Surg. 2012 Oct;36(5):1087-9. doi: 10.1007/s00266-012-9922-1. Epub 2012 Jun 3.

    PMID:
    22660949
    [PubMed - indexed for MEDLINE]
    19.

    Inherited thrombophilia may be a causative factor for osteonecrosis of femoral head in male patients with developmental dysplasia of the hip: a case series.

    Ömeroğlu H, Inan U.

    Arch Orthop Trauma Surg. 2012 Sep;132(9):1281-5. doi: 10.1007/s00402-012-1554-z. Epub 2012 May 27.

    PMID:
    22643805
    [PubMed - indexed for MEDLINE]
    20.

    Risk of placenta-mediated pregnancy complications or pregnancy-related VTE in VTE-asymptomatic families of probands with VTE and heterozygosity for factor V Leiden or G20210 prothrombin mutation.

    Cordoba I, Pegenaute C, González-López TJ, Chillon C, Sarasquete ME, Martin-Herrero F, Guerrero C, Cabrero M, Garcia Sanchez MH, Pabon P, Lozano FS, Gonzalez M, Alberca I, González-Porras JR.

    Eur J Haematol. 2012 Sep;89(3):250-5. doi: 10.1111/j.1600-0609.2012.01809.x. Epub 2012 Jun 29.

    PMID:
    22642978
    [PubMed - indexed for MEDLINE]

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