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Journal Abstract Search

516 related items for PubMed ID: 3487353

  • 1. A new von Willebrand variant (type I, New York): increased ristocetin-induced platelet aggregation and plasma von Willebrand factor containing the full range of multimers.
    Weiss HJ, Sussman II.
    Blood; 1986 Jul; 68(1):149-56. PubMed ID: 3487353
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  • 2. A probable double heterozygous type II von Willebrand's disease with increased ristocetin induced platelet aggregation.
    Kinoshita S, Yoshioka K, Kasahara M, Takamiya O.
    Am J Hematol; 1992 Jul; 40(3):192-8. PubMed ID: 1609773
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  • 3. Von Willebrand's disease with spontaneous platelet aggregation induced by an abnormal plasma von Willebrand factor.
    Grainick HR, Williams SB, McKeown LP, Rick ME, Maisonneuve P, Jenneau C, Sultan Y.
    J Clin Invest; 1985 Oct; 76(4):1522-9. PubMed ID: 2932469
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  • 11. Differentiation of patients with subtype IIb-like von Willebrand's disease by means of perfusion experiments with reconstituted blood.
    Sakariassen KS, Nieuwenhuis HK, Sixma JJ.
    Br J Haematol; 1985 Mar; 59(3):459-70. PubMed ID: 3918560
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  • 13. Distinct abnormalities in the interaction of purified types IIA and IIB von Willebrand factor with the two platelet binding sites, glycoprotein complexes Ib-IX and IIb-IIIa.
    De Marco L, Mazzucato M, De Roia D, Casonato A, Federici AB, Girolami A, Ruggeri ZM.
    J Clin Invest; 1990 Sep; 86(3):785-92. PubMed ID: 2394830
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  • 14. An atypical von Willebrand's disease with hyperreactivity of platelet aggregation.
    Niiya K, Kubonishi I, Taguchi H, Miyoshi I.
    Acta Haematol; 1984 Sep; 71(3):158-64. PubMed ID: 6424380
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  • 15. Pseudo-von Willebrand's disease. An intrinsic platelet defect with aggregation by unmodified human factor VIII/von Willebrand factor and enhanced adsorption of its high-molecular-weight multimers.
    Weiss HJ, Meyer D, Rabinowitz R, Pietu G, Girma JP, Vicic WJ, Rogers J.
    N Engl J Med; 1982 Feb 11; 306(6):326-33. PubMed ID: 6798442
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  • 16. Platelet activation and aggregation induced by recombinant von Willebrand factors reproducing four type 2B von Willebrand disease missense mutations.
    de Romeuf C, Hilbert L, Mazurier C.
    Thromb Haemost; 1998 Jan 11; 79(1):211-6. PubMed ID: 9459349
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  • 17. A novel von Willebrand factor mutation (I1372S) associated with type 2B-like von Willebrand disease: an elusive phenotype and a difficult diagnosis.
    Casonato A, Sartorello F, Pontara E, Gallinaro L, Bertomoro A, Grazia Cattini M, Daidone V, Szukowska M, Pagnan A.
    Thromb Haemost; 2007 Dec 11; 98(6):1182-7. PubMed ID: 18064311
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  • 18. von Willebrand's disease characterized by increased ristocetin sensitivity and the presence of all von Willebrand factor multimers in plasma.
    Holmberg L, Berntorp E, Donnér M, Nilsson IM.
    Blood; 1986 Sep 11; 68(3):668-72. PubMed ID: 3488775
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  • 19. Agglutination of formalin-fixed, platelet-type von Willebrand's disease platelets by human von Willebrand factor.
    Takahashi H, Shibata A.
    Thromb Haemost; 1984 Dec 29; 52(3):267-70. PubMed ID: 6241752
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  • 20. Type 2M von Willebrand disease variant characterized by abnormal von willebrand factor multimerization.
    Casonato A, Pontara E, Sartorello F, Bertomoro A, Durante C, Girolami A.
    J Lab Clin Med; 2001 Jan 29; 137(1):70-6. PubMed ID: 11150026
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