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Volumn 37, Issue 5, 2011, Pages 535-541

Diagnosis and management of adult patients with von Willebrand disease in South Australia

Author keywords

mutations; severity; subtypes; type 2M; von Willebrand disorder

Indexed keywords

BLOOD CLOTTING FACTOR 8 CONCENTRATE; DESMOPRESSIN; RECOMBINANT BLOOD CLOTTING FACTOR 8; RISTOCETIN; TRANEXAMIC ACID;

EID: 80053594111     PISSN: 00946176     EISSN: 10989064     Source Type: Journal    
DOI: 10.1055/s-0031-1281040     Document Type: Article
Times cited : (14)

References (22)
  • 2
    • 0031828438 scopus 로고    scopus 로고
    • Diagnosis of von Willebrand disease
    • Federici A B. Diagnosis of von Willebrand disease. Haemophilia 1998 4 4 654-660 (Pubitemid 28351901)
    • (1998) Haemophilia , vol.4 , Issue.4 , pp. 654-660
    • Federici, A.B.1
  • 3
    • 11044235267 scopus 로고    scopus 로고
    • Clinical diagnosis of von Willebrand disease
    • Federici A B. Clinical diagnosis of von Willebrand disease. Haemophilia 2004 10 Suppl 4 169-176 (Pubitemid 40045438)
    • (2004) Haemophilia, Supplement , vol.10 , Issue.4 , pp. 169-176
    • Federici, A.B.1
  • 4
    • 63149116476 scopus 로고    scopus 로고
    • Toward a new paradigm for the identification and functional characterization of von Willebrand disease
    • Favaloro E J. Toward a new paradigm for the identification and functional characterization of von Willebrand disease. Semin Thromb Hemost 2009 35 1 60-75
    • (2009) Semin Thromb Hemost , vol.35 , Issue.1 , pp. 60-75
    • Favaloro, E.J.1
  • 6
    • 0027185973 scopus 로고
    • Von Willebrand's disease: Laboratory investigation using an improved functional assay for von Willebrand factor
    • Favaloro E J., Grispo L, Dinale A, Berndt M, Koutts J. von Willebrand's disease: laboratory investigation using an improved functional assay for von Willebrand factor. Pathology 1993 25 2 152-158 (Pubitemid 23232673)
    • (1993) Pathology , vol.25 , Issue.2 , pp. 152-158
    • Favaloro, E.J.1    Grispo, L.2    Dinale, A.3    Berndt, M.4    Koutts, J.5
  • 7
    • 0028022060 scopus 로고
    • Familial discrepancy between the one-stage and two-stage factor VIII methods in a subgroup of patients with haemophilia A
    • Duncan E M., Duncan B M., Tunbridge L J., Lloyd J V. Familial discrepancy between the one-stage and two-stage factor VIII methods in a subgroup of patients with haemophilia A. Br J Haematol 1994 87 4 846-848 (Pubitemid 24264662)
    • (1994) British Journal of Haematology , vol.87 , Issue.4 , pp. 846-848
    • Duncan, E.M.1    Duncan, B.M.2    Tunbridge, L.J.3    Lloyd, J.V.4
  • 8
    • 61349120111 scopus 로고    scopus 로고
    • Evaluation of three automated chromogenic FVIII kits for the diagnosis of mild discrepant haemophilia A
    • Rodgers S E., Duncan E M., Sobieraj-Teague M, Lloyd J V. Evaluation of three automated chromogenic FVIII kits for the diagnosis of mild discrepant haemophilia A. Int J Lab Hematol 2009 31 2 180-188
    • (2009) Int J Lab Hematol , vol.31 , Issue.2 , pp. 180-188
    • Rodgers, S.E.1    Duncan, E.M.2    Sobieraj-Teague, M.3    Lloyd, J.V.4
  • 9
    • 0030040896 scopus 로고    scopus 로고
    • The defective interaction between von Willebrand factor and factor VIII in a patient with type 1 von Willebrand disease is caused by substitution of Arg19 and His54 in mature von Willebrand factor
    • Kroner P A., Foster P A., Fahs S A., Montgomery R R. The defective interaction between von Willebrand factor and factor VIII in a patient with type 1 von Willebrand disease is caused by substitution of Arg19 and His54 in mature von Willebrand factor. Blood 1996 87 3 1013-1021 (Pubitemid 26043530)
    • (1996) Blood , vol.87 , Issue.3 , pp. 1013-1021
    • Kroner, P.A.1    Foster, P.A.2    Fahs, S.A.3    Montgomery, R.R.4
  • 17
    • 0036162077 scopus 로고    scopus 로고
    • Use of the collagen-binding assay for von Willebrand factor in the analysis of type 2M von Willebrand disease: A comparison with the ristocetin cofactor assay
    • DOI 10.1046/j.1365-2141.2002.03199.x
    • Riddell A F., Jenkins P V., Nitu-Whalley I C., McCraw A H., Lee C A., Brown S A. Use of the collagen-binding assay for von Willebrand factor in the analysis of type 2M von Willebrand disease: a comparison with the ristocetin cofactor assay. Br J Haematol 2002 116 1 187-192 (Pubitemid 34122080)
    • (2002) British Journal of Haematology , vol.116 , Issue.1 , pp. 187-192
    • Riddell, A.F.1    Jenkins, P.V.2    Nitu-Whalley, I.C.3    McCraw, A.H.4    Lee, C.A.5    Brown, S.A.6
  • 19
    • 84871592508 scopus 로고    scopus 로고
    • Available at
    • ISTH-SSC VWF online database. Available at: www.vwf.group.shef.ac.uk Accessed November 29, 2010
    • (2010) ISTH-SSC VWF Online Database
  • 20
    • 60249092963 scopus 로고    scopus 로고
    • Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: A cohort study of 67 patients
    • Federici A B., Mannucci P M., Castaman G et al. Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients. Blood 2009 113 3 526-534
    • (2009) Blood , vol.113 , Issue.3 , pp. 526-534
    • Federici, A.B.1    Mannucci, P.M.2    Castaman, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.