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Journal Abstract Search

224 related items for PubMed ID: 6982283

  • 41. Pregnancy and delivery in women with von Willebrand's disease and different von Willebrand factor mutations.
    Castaman G, Tosetto A, Rodeghiero F.
    Haematologica; 2010 Jun; 95(6):963-9. PubMed ID: 19951969
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  • 42. 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
    [Abstract] [Full Text] [Related]

  • 43. [Diagnosis of von Willebrand's disease subtypes by the analysis of multimeric composition of plasma von Willebrand factor].
    Quiroga T, Pérez M, Pereira J, Mezzano D.
    Rev Med Chil; 1993 Sep; 121(9):987-93. PubMed ID: 8191164
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  • 44. An Arg545----Cys545 substitution mutation of the von Willebrand factor in type IIB von Willebrand's disease.
    Donnér M, Andersson AM, Kristoffersson AC, Nilsson IM, Dahlbäck B, Holmberg L.
    Eur J Haematol; 1991 Nov; 47(5):342-5. PubMed ID: 1761120
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  • 45. Multimeric pattern discrepancy between platelet and plasma von Willebrand factor in type IIC von Willebrand disease.
    Batlle J, López Fernández MF, Fernández Villamor A, López Berges C, Zimmerman TS.
    Am J Hematol; 1986 May; 22(1):87-8. PubMed ID: 3485375
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  • 46. Type I Padua: a new variant of von Willebrand's disease.
    Casonato A, Pontara E, Dannhauser D, Bertomoro A, Sartori MT, Girolami A.
    Br J Haematol; 1992 Aug; 81(4):615-6. PubMed ID: 1390253
    [No Abstract] [Full Text] [Related]

  • 47. von Willebrand's factor and von Willebrand's disease.
    Matsushita T, Dong Z, Sadler JE.
    Curr Opin Hematol; 1994 Sep; 1(5):362-8. PubMed ID: 9371306
    [Abstract] [Full Text] [Related]

  • 48. A novel candidate mutation (Arg611-->His) in type I 'platelet discordant' von Willebrand's disease with desmopressin-induced thrombocytopenia.
    Castaman G, Eikenboom JC, Rodeghiero F, Briët E, Reitsma PH.
    Br J Haematol; 1995 Mar; 89(3):656-8. PubMed ID: 7734373
    [Abstract] [Full Text] [Related]

  • 49. 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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  • 53. Molecular defects in haemophilia A and von Willebrand's disease.
    Gralnick HR, Coller BS.
    Lancet; 1976 Apr 17; 1(7964):837-8. PubMed ID: 56653
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  • 54. Von Willebrand's disease: combined qualitative and quantitative abnormalities.
    Gralnick HR, Sultan Y, Coller BS.
    N Engl J Med; 1977 May 05; 296(18):1024-30. PubMed ID: 300468
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  • 55. Structure - function relationship of factor VIII/von Willebrand factor. Application to the study of variant von Willebrand's disease and cryosupernatant prepared from normal plasma.
    Pietu G, Obert B, Larrieu MJ, Meyer D.
    Thromb Res; 1977 May 05; 19(4-5):671-85. PubMed ID: 6777898
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  • 57. Type IIB von Willebrand's disease with probable autosomal recessive inheritance and presenting as thrombocytopenia in infancy.
    Donnér M, Holmberg L, Nilsson IM.
    Br J Haematol; 1987 Jul 05; 66(3):349-54. PubMed ID: 3497666
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  • 59. Multicenter comparison of von Willebrand factor multimer sizing techniques. Report of the Factor VIII and von Willebrand Factor Subcommittee.
    Mannucci PM, Abildgaard CF, Gralnick HR, Hill FG, Hoyer LW, Lombardi R, Nilsson IM, Tuddenham E, Meyer D.
    Thromb Haemost; 1985 Dec 17; 54(4):873-6. PubMed ID: 3879020
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  • 60. Ins405AsnPro mutation in the von Willebrand factor propeptide in recessive type 2A (IIC) von Willebrand's disease.
    Holmberg L, Karpman D, Isaksson C, Kristoffersson AC, Lethagen S, Schneppenheim R.
    Thromb Haemost; 1998 Apr 17; 79(4):718-22. PubMed ID: 9569179
    [Abstract] [Full Text] [Related]

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