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Journal Abstract Search

174 related items for PubMed ID: 7831648

  • 1. Characterization of partial gene deletions in type III von Willebrand disease with alloantibody inhibitors.
    Mancuso DJ, Tuley EA, Castillo R, de Bosch N, Mannucci PM, Sadler JE.
    Thromb Haemost; 1994 Aug; 72(2):180-5. PubMed ID: 7831648
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  • 2. Gene deletions correlate with the development of alloantibodies in von Willebrand disease.
    Shelton-Inloes BB, Chehab FF, Mannucci PM, Federici AB, Sadler JE.
    J Clin Invest; 1987 May; 79(5):1459-65. PubMed ID: 3033024
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  • 5. Laboratory diagnosis of von Willebrand disease type 1/2E (2A subtype IIE), type 1 Vicenza and mild type 1 caused by mutations in the D3, D4, B1-B3 and C1-C2 domains of the von Willebrand factor gene. Role of von Willebrand factor multimers and the von Willebrand factor propeptide/antigen ratio.
    Gadisseur A, Berneman Z, Schroyens W, Michiels JJ.
    Acta Haematol; 2009 May; 121(2-3):128-38. PubMed ID: 19506359
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  • 6. Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin.
    Eikenboom JC, Castaman G, Vos HL, Bertina RM, Rodeghiero F.
    Thromb Haemost; 1998 Apr; 79(4):709-17. PubMed ID: 9569178
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  • 7. Three distinct candidate point mutations of the von Willebrand factor gene in four patients with type IIA von Willebrand disease.
    Sugiura I, Matsushita T, Tanimoto M, Takahashi I, Yamazaki T, Yamamoto K, Takamatsu J, Kamiya T, Saito H.
    Thromb Haemost; 1992 Jun 01; 67(6):612-7. PubMed ID: 1380739
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  • 9. The genetic defect of type I von Willebrand disease "Vicenza" is linked to the von Willebrand factor gene.
    Randi AM, Sacchi E, Castaman GC, Rodeghiero F, Mannucci PM.
    Thromb Haemost; 1993 Feb 01; 69(2):173-6. PubMed ID: 8456430
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  • 12. von Willebrand disease: a database of point mutations, insertions, and deletions. For the Consortium on von Willebrand Factor Mutations and Polymorphisms, and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.
    Ginsburg D, Sadler JE.
    Thromb Haemost; 1993 Feb 01; 69(2):177-84. PubMed ID: 8456431
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  • 13. Characterization of recessive severe type 1 and 3 von Willebrand Disease (VWD), asymptomatic heterozygous carriers versus bloodgroup O-related von Willebrand factor deficiency, and dominant type 1 VWD.
    Michiels JJ, Berneman Z, Gadisseur A, van der Planken M, Schroyens W, van de Velde A, van Vliet H.
    Clin Appl Thromb Hemost; 2006 Jul 01; 12(3):277-95. PubMed ID: 16959681
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  • 15. Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiological investigation.
    Castaman G, Eikenboom JC, Bertina RM, Rodeghiero F.
    Thromb Haemost; 1999 Sep 01; 82(3):1065-70. PubMed ID: 10494765
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  • 16. Genetic defects in von Willebrand disease type 3 in Indian and Greek patients.
    Gupta PK, Saxena R, Adamtziki E, Budde U, Oyen F, Obser T, Schneppenheim R.
    Blood Cells Mol Dis; 2008 Sep 01; 41(2):219-22. PubMed ID: 18485763
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  • 17. [Mutation (Ala737-->Glu) in type 2A von Willebrand disease].
    Wang Y, Zhang J, Wan H.
    Zhonghua Xue Ye Xue Za Zhi; 1999 Mar 01; 20(3):117-9. PubMed ID: 11601234
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  • 18. Identification of mutations in the canine von Willebrand factor gene associated with type III von Willebrand disease.
    Rieger M, Schwarz HP, Turecek PL, Dorner F, van Mourik JA, Mannhalter C.
    Thromb Haemost; 1998 Aug 01; 80(2):332-7. PubMed ID: 9716162
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  • 19. A common splice site mutation is shared by two families with different type 2N von Willebrand disease mutations.
    Nesbitt IM, Hampton KK, Preston FE, Peake IR, Goodeve AC.
    Thromb Haemost; 1999 Sep 01; 82(3):1061-4. PubMed ID: 10494764
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  • 20. Mutations in von Willebrand factor multimerization domains are not a common cause of classical type 1 von Willebrand disease.
    Keeney S, Cumming A, Hay C.
    Thromb Haemost; 1999 Nov 01; 82(5):1446-50. PubMed ID: 10595636
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