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229 related items for PubMed ID: 25103891

  • 1. Storage and secretion of naturally occurring von Willebrand factor A domain variants.
    Groeneveld DJ, Wang JW, Mourik MJ, Dirven RJ, Valentijn KM, Voorberg J, Reitsma PH, Eikenboom J.
    Br J Haematol; 2014 Nov; 167(4):529-40. PubMed ID: 25103891
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  • 2. Von Willebrand disease and Weibel-Palade bodies.
    Wang JW, Eikenboom J.
    Hamostaseologie; 2010 Aug; 30(3):150-5. PubMed ID: 20680229
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  • 3. Biogenesis of Weibel-Palade bodies in von Willebrand's disease variants with impaired von Willebrand factor intrachain or interchain disulfide bond formation.
    Wang JW, Groeneveld DJ, Cosemans G, Dirven RJ, Valentijn KM, Voorberg J, Reitsma PH, Eikenboom J.
    Haematologica; 2012 Jun; 97(6):859-66. PubMed ID: 22207689
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  • 6. 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 Jun; 121(2-3):128-38. PubMed ID: 19506359
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  • 8. Laboratory diagnosis and molecular classification of von Willebrand disease.
    Gadisseur A, Hermans C, Berneman Z, Schroyens W, Deckmyn H, Michiels JJ.
    Acta Haematol; 2009 Jun; 121(2-3):71-84. PubMed ID: 19506352
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  • 12. Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease-causing variants of von Willebrand factor.
    Michaux G, Hewlett LJ, Messenger SL, Goodeve AC, Peake IR, Daly ME, Cutler DF.
    Blood; 2003 Oct 01; 102(7):2452-8. PubMed ID: 12791651
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  • 13. The dominant p.Thr274Pro mutation in the von Willebrand factor propeptide causes the von Willebrand disease type 1 phenotype in two unrelated patients.
    Pagliari MT, Baronciani L, Cordiglieri C, Colpani P, Cozzi G, Siboni SM, Peyvandi F.
    Haemophilia; 2022 Mar 01; 28(2):292-300. PubMed ID: 35064738
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  • 19. Characterization, classification, and treatment of von Willebrand diseases: a critical appraisal of the literature and personal experiences.
    Michiels JJ, Gadisseur A, Budde U, Berneman Z, van der Planken M, Schroyens W, van de Velde A, van Vliet H.
    Semin Thromb Hemost; 2005 Nov 01; 31(5):577-601. PubMed ID: 16276467
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