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    Results: 1 to 20 of 180

    1.

    von Willebrand disease and cardiopulmonary bypass: a case report.

    Teppone-Martin OL, Zhao M, Norris TE.

    AANA J. 2013 Feb;81(1):60-4.

    PMID:
    23513326
    [PubMed - indexed for MEDLINE]
    2.

    Conservative management of massive hematoperitoneum caused by ovulation in a patient with severe form of von Willebrand disease--a case report.

    Terzic M, Likic I, Pilic I, Bila J, Knezevic N.

    Clin Exp Obstet Gynecol. 2012;39(4):537-40.

    PMID:
    23444764
    [PubMed - indexed for MEDLINE]
    3.

    VWF propeptide and ratios between VWF, VWF propeptide, and FVIII in the characterization of type 1 von Willebrand disease.

    Eikenboom J, Federici AB, Dirven RJ, Castaman G, Rodeghiero F, Budde U, Schneppenheim R, Batlle J, Canciani MT, Goudemand J, Peake I, Goodeve A; MCMDM-1VWD Study Group.

    Blood. 2013 Mar 21;121(12):2336-9. doi: 10.1182/blood-2012-09-455089. Epub 2013 Jan 24.

    PMID:
    23349392
    [PubMed - indexed for MEDLINE]
    4.

    Collagen binding provides a sensitive screen for variant von Willebrand disease.

    Flood VH, Gill JC, Friedman KD, Christopherson PA, Jacobi PM, Hoffmann RG, Montgomery RR, Haberichter SL; Zimmerman Program Investigators.

    Clin Chem. 2013 Apr;59(4):684-91. doi: 10.1373/clinchem.2012.199000. Epub 2013 Jan 22.

    PMID:
    23340442
    [PubMed - indexed for MEDLINE]
    5.

    Mechanisms by which von Willebrand disease mutations destabilize the A2 domain.

    Xu AJ, Springer TA.

    J Biol Chem. 2013 Mar 1;288(9):6317-24. doi: 10.1074/jbc.M112.422618. Epub 2013 Jan 15.

    PMID:
    23322777
    [PubMed - indexed for MEDLINE]
    6.
    7.

    Severe transfuse related acute lung injury (TRALI) syndrome in a 14 years old girl with a history of type I von Willebrand disease.

    Arghir OC, Ionescu FC, Apostol A.

    Pneumologia. 2012 Jul-Sep;61(3):175-7.

    PMID:
    23173380
    [PubMed - indexed for MEDLINE]
    8.

    Structural basis of type 2A von Willebrand disease investigated by molecular dynamics simulations and experiments.

    Interlandi G, Ling M, Tu AY, Chung DW, Thomas WE.

    PLoS One. 2012;7(10):e45207. doi: 10.1371/journal.pone.0045207. Epub 2012 Oct 23.

    PMID:
    23110044
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    9.

    Von Willebrand disease.

    Berntorp E.

    Pediatr Blood Cancer. 2013;60 Suppl 1:S34-6. doi: 10.1002/pbc.24337. Epub 2012 Oct 25. Review.

    PMID:
    23109385
    [PubMed - indexed for MEDLINE]
    10.

    Living with von Willebrand disease.

    Musick LP.

    Am J Nurs. 2012 Nov;112(11):12. doi: 10.1097/01.NAJ.0000422233.94813.46. No abstract available.

    PMID:
    23099568
    [PubMed - indexed for MEDLINE]
    11.

    A novel D235Y mutation in the GP1BA gene enhances platelet interaction with von Willebrand factor in an Iranian family with platelet-type von Willebrand disease.

    Enayat S, Ravanbod S, Rassoulzadegan M, Jazebi M, Tarighat S, Ala F, Emsley J, Othman M.

    Thromb Haemost. 2012 Nov;108(5):946-54. doi: 10.1160/TH12-04-0189. Epub 2012 Sep 26.

    PMID:
    23014764
    [PubMed - indexed for MEDLINE]
    12.

    Hemophilic arthropathy in patients with von Willebrand disease.

    van Galen KP, Mauser-Bunschoten EP, Leebeek FW.

    Blood Rev. 2012 Nov;26(6):261-6. doi: 10.1016/j.blre.2012.09.002. Epub 2012 Sep 23. Review.

    PMID:
    23010260
    [PubMed - indexed for MEDLINE]
    13.

    Efficacy and safety during formulation switch of a pasteurized VWF/FVIII concentrate: results from an Italian prospective observational study in patients with von Willebrand disease.

    Castaman G, Coppola A, Zanon E, Boeri E, Musso M, Siragusa S, Federici AB, Mancuso G, Barillari G, Biasoli C, Feola G, Franchini M, Moratelli S, Gamba G, Schinco P, Valdrè L, Dragani A, Mazzucconi G, Tagliaferri A, Morfini M.

    Haemophilia. 2013 Jan;19(1):82-8. doi: 10.1111/hae.12005. Epub 2012 Sep 7.

    PMID:
    22957493
    [PubMed - indexed for MEDLINE]
    14.

    Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand disease.

    de Wee EM, Sanders YV, Mauser-Bunschoten EP, van der Bom JG, Degenaar-Dujardin ME, Eikenboom J, de Goede-Bolder A, Laros-van Gorkom BA, Meijer K, Hamulyák K, Nijziel MR, Fijnvandraat K, Leebeek FW; WiN study group.

    Thromb Haemost. 2012 Oct;108(4):683-92. Epub 2012 Aug 23.

    PMID:
    22918553
    [PubMed - indexed for MEDLINE]
    15.

    von Willebrand disease biology.

    Blombäck M, Eikenboom J, Lane D, Denis C, Lillicrap D.

    Haemophilia. 2012 Jul;18 Suppl 4:141-7. doi: 10.1111/j.1365-2516.2012.02840.x. No abstract available.

    PMID:
    22726098
    [PubMed - indexed for MEDLINE]
    16.

    Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients.

    Yadegari H, Driesen J, Pavlova A, Biswas A, Hertfelder HJ, Oldenburg J.

    Thromb Haemost. 2012 Oct;108(4):662-71. Epub 2012 Aug 7.

    PMID:
    22871923
    [PubMed - indexed for MEDLINE]
    17.

    Management of delivery with FVIII/VWF concentrates in a pregnant woman with type 3 von Willebrand disease and alloantibodies.

    Martín-Salces M, Jiménez-Yuste V, Álvarez-Román MT, Rivas-Pollmar I, Rodríguez de la Rúa A.

    Thromb Haemost. 2012 Oct;108(4):796-8. Epub 2012 Jul 26. No abstract available.

    PMID:
    22836221
    [PubMed - indexed for MEDLINE]
    18.

    Prophylaxis in severe forms of von Willebrand's disease: results from the von Willebrand Disease Prophylaxis Network (VWD PN).

    Abshire TC, Federici AB, Alvárez MT, Bowen J, Carcao MD, Cox Gill J, Key NS, Kouides PA, Kurnik K, Lail AE, Leebeek FW, Makris M, Mannucci PM, Winikoff R, Berntorp E; VWD PN.

    Haemophilia. 2013 Jan;19(1):76-81. doi: 10.1111/j.1365-2516.2012.02916.x. Epub 2012 Jul 23.

    PMID:
    22823000
    [PubMed - indexed for MEDLINE]
    19.

    Methodological concerns regarding 'Assessment of von Willebrand disease as a risk factor for primary postpartum haemorrhage'.

    Modi R, McGwin G Jr.

    Haemophilia. 2012 Sep;18(5):e379. doi: 10.1111/j.1365-2516.2012.02910.x. Epub 2012 Jul 23. No abstract available.

    PMID:
    22816615
    [PubMed - indexed for MEDLINE]
    20.

    Effect of genetic variation in STXBP5 and STX2 on von Willebrand factor and bleeding phenotype in type 1 von Willebrand disease patients.

    van Loon JE, Sanders YV, de Wee EM, Kruip MJ, de Maat MP, Leebeek FW.

    PLoS One. 2012;7(7):e40624. doi: 10.1371/journal.pone.0040624. Epub 2012 Jul 6.

    PMID:
    22792389
    [PubMed - indexed for MEDLINE]
    Free PMC Article

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