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Volumn 37, Issue 5, 2011, Pages 495-502

Nordic Haemophilia Council's practical guidelines on diagnosis and management of von Willebrand Disease

Author keywords

Guidelines; Nordic Haemophilia Council; von Willebrand disease

Indexed keywords

BLOOD CLOTTING FACTOR 8 CONCENTRATE; BLOOD CLOTTING FACTOR 8 PLUS VON WILLEBRAND FACTOR; C REACTIVE PROTEIN; DESMOPRESSIN; ORAL CONTRACEPTIVE AGENT; TRANEXAMIC ACID; VON WILLEBRAND FACTOR;

EID: 81755171930     PISSN: 00946176     EISSN: 10989064     Source Type: Journal    
DOI: 10.1055/s-0031-1281034     Document Type: Article
Times cited : (26)

References (33)
  • 3
    • 33644977050 scopus 로고    scopus 로고
    • A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: Results from a multicenter European study (MCMDM-1 VWD)
    • Tosetto A, Rodeghiero F, Castaman G et al. A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD). J Thromb Haemost 2006 4 4 766-773
    • (2006) J Thromb Haemost , vol.4 , Issue.4 , pp. 766-773
    • Tosetto, A.1    Rodeghiero, F.2    Castaman, G.3
  • 4
    • 56749160315 scopus 로고    scopus 로고
    • Generation and validation of the condensed MCMDM-1VWD bleeding questionnaire for von Willebrand disease
    • Bowman M, Mundell G, Grabell J et al. Generation and validation of the condensed MCMDM-1VWD bleeding questionnaire for von Willebrand disease. J Thromb Haemost 2008 6 12 2062-2066
    • (2008) J Thromb Haemost , vol.6 , Issue.12 , pp. 2062-2066
    • Bowman, M.1    Mundell, G.2    Grabell, J.3
  • 5
    • 0033926486 scopus 로고    scopus 로고
    • Desmopressin (DDAVP) in the treatment of bleeding disorders: The first twenty years
    • DOI 10.1046/j.1365-2516.2000.00059.x
    • Mannucci PM. Desmopressin (DDAVP) in the treatment of bleeding disorders: the first twenty years. Haemophilia 2000 6 Suppl 1 60-67 (Pubitemid 30468295)
    • (2000) Haemophilia , vol.6 , Issue.SUPPL. 1 , pp. 60-67
    • Mannucci, P.M.1
  • 6
    • 34748846640 scopus 로고    scopus 로고
    • Prevalence of von Willebrand disease in the Nordic region
    • Berntorp E, Önundarson PT. Prevalence of von Willebrand disease in the Nordic region. Haematologica Rep 2005 1 4-6
    • (2005) Haematologica Rep , vol.1 , pp. 4-6
    • Berntorp, E.1    Önundarson, P.T.2
  • 7
    • 38549157588 scopus 로고    scopus 로고
    • An update on the von Willebrand factor collagen binding assay: 21 Years of age and beyond adolescence but not yet a mature adult
    • DOI 10.1055/s-2007-1000364
    • Favaloro EJ. An update on the von Willebrand factor collagen binding assay: 21 years of age and beyond adolescence but not yet a mature adult. Semin Thromb Hemost 2007 33 8 727-744 (Pubitemid 351158442)
    • (2007) Seminars in Thrombosis and Hemostasis , vol.33 , Issue.8 , pp. 727-744
    • Favaloro, E.J.1
  • 10
    • 44949188303 scopus 로고    scopus 로고
    • Distribution of von Willebrand factor levels in young women with and without bleeding symptoms. Influence of ABO blood group and promoter haplotypes
    • DOI 10.1160/TH07-06-0419
    • Lethagen S, Hillarp A, Ekholm C, Mattson E, Halldén C, Friberg B. Distribution of von Willebrand factor levels in young women with and without bleeding symptoms: influence of ABO blood group and promoter haplotypes. Thromb Haemost 2008 99 6 1013-1018 (Pubitemid 351810482)
    • (2008) Thrombosis and Haemostasis , vol.99 , Issue.6 , pp. 1013-1018
    • Lethagen, S.1    Hillarp, A.2    Ekholm, C.3    Mattson, E.4    Hallden, C.5    Friberg, B.6
  • 12
    • 23044515558 scopus 로고    scopus 로고
    • Provisional criteria for the diagnosis of VWD type 1
    • DOI 10.1111/j.1538-7836.2005.01245.x
    • Sadler JE, Rodeghiero F, ISTH SSC Subcommittee on von Willebrand Factor. Provisional criteria for the diagnosis of VWD type 1. J Thromb Haemost 2005 3 4 775-777 (Pubitemid 41647892)
    • (2005) Journal of Thrombosis and Haemostasis , vol.3 , Issue.4 , pp. 775-777
    • Sadler, J.E.1    Rodeghiero, F.2
  • 13
    • 33846433760 scopus 로고    scopus 로고
    • Risk of excessive bleeding associated with marginally low von Willebrand factor and mild platelet dysfunction
    • DOI 10.1111/j.1538-7836.2007.02326.x
    • Gudmundsdottir BR, Marder VJ, Onundarson PT. Risk of excessive bleeding associated with marginally low von Willebrand factor and mild platelet dysfunction. J Thromb Haemost 2007 5 2 274-281 (Pubitemid 46139451)
    • (2007) Journal of Thrombosis and Haemostasis , vol.5 , Issue.2 , pp. 274-281
    • Gudmundsdottir, B.R.1    Marder, V.J.2    Onundarson, P.T.3
  • 14
    • 33644979514 scopus 로고    scopus 로고
    • Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD
    • Eikenboom J, Van Marion V, Putter H et al. Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD. J Thromb Haemost 2006 4 4 774-782
    • (2006) J Thromb Haemost , vol.4 , Issue.4 , pp. 774-782
    • Eikenboom, J.1    Van Marion, V.2    Putter, H.3
  • 15
    • 77949445945 scopus 로고    scopus 로고
    • Low von Willebrand factor: Sometimes a risk factor and sometimes a disease
    • Sadler JE. Low von Willebrand factor: sometimes a risk factor and sometimes a disease. Hematology Am Soc Hematol Educ Program 2009 106-112
    • (2009) Hematology Am Soc Hematol Educ Program , pp. 106-112
    • Sadler, J.E.1
  • 16
    • 63149116476 scopus 로고    scopus 로고
    • Toward a new paradigm for the identification and functional characterization of von Willebrand disease
    • Favaloro EJ. 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
  • 17
  • 21
    • 0034912198 scopus 로고    scopus 로고
    • Congenital von Willebrand disease type 3: Clinical manifestations, pathophysiology and molecular biology
    • DOI 10.1053/beha.2001.0139
    • Eikenboom JC. Congenital von Willebrand disease type 3: clinical manifestations, pathophysiology and molecular biology. Best Pract Res Clin Haematol 2001 14 2 365-379 (Pubitemid 32677085)
    • (2001) Best Practice and Research in Clinical Haematology , vol.14 , Issue.2 , pp. 365-379
    • Eikenboom, J.C.J.1
  • 23
    • 35748955202 scopus 로고    scopus 로고
    • Differential identification of a rare form of platelet-type (pseudo-) von Willebrand disease (VWD) from Type 2B VWD using a simplified ristocetin-induced-platelet-agglutination mixing assay and confirmed by genetic analysis [3]
    • DOI 10.1111/j.1365-2141.2007.06850.x
    • Favaloro EJ, Patterson D, Denholm A et al. Differential identification of a rare form of platelet-type (pseudo-) von Willebrand disease (VWD) from type 2B VWD using a simplified ristocetin-induced-platelet-agglutination mixing assay and confirmed by genetic analysis. Br J Haematol 2007 139 4 623-626 (Pubitemid 350043816)
    • (2007) British Journal of Haematology , vol.139 , Issue.4 , pp. 623-626
    • Favaloro, E.J.1    Patterson, D.2    Denholm, A.3    Mead, S.4    Gilbert, A.5    Collins, A.6    Estell, J.7    George, P.M.8    Smith, M.P.9
  • 24
    • 34247543029 scopus 로고    scopus 로고
    • Acquired von Willebrand syndrome: An update
    • DOI 10.1002/ajh.20830
    • Franchini M, Lippi G. Acquired von Willebrand syndrome: an update. Am J Hematol 2007 82 5 368-375 (Pubitemid 46651140)
    • (2007) American Journal of Hematology , vol.82 , Issue.5 , pp. 368-375
    • Franchini, M.1    Lippi, G.2
  • 25
    • 1242330853 scopus 로고    scopus 로고
    • Acquired von Willebrand syndrome 2004: International Registry. Diagnosis and management from online to bedside
    • Federici AB, Budde U, Rand JH. Acquired von Willebrand syndrome 2004: International Registrydiagnosis and management from online to bedside. Hamostaseologie 2004 24 1 50-55 (Pubitemid 38233047)
    • (2004) Hamostaseologie , vol.24 , Issue.1 , pp. 50-55
    • Federici, A.B.1    Budde, U.2    Rand, J.H.3
  • 26
    • 0023634567 scopus 로고
    • Intranasal and intravenous administration of desmopressin: Effect on F VIII/vWF, pharmacokinetics and reproducibility
    • Lethagen S, Harris AS, Sjörin E, Nilsson IM. Intranasal and intravenous administration of desmopressin: effect on F VIII/vWF, pharmacokinetics and reproducibility. Thromb Haemost 1987 58 4 1033-1036
    • (1987) Thromb Haemost , vol.58 , Issue.4 , pp. 1033-1036
    • Lethagen, S.1    Harris, A.S.2    Sjörin, E.3    Nilsson, I.M.4
  • 27
    • 0027158362 scopus 로고
    • Self-treatment with desmopressin intranasal spray in patients with bleeding disorders: Effect on bleeding symptoms and socioeconomic factors
    • Lethagen S, Ragnarson Tennvall G. Self-treatment with desmopressin intranasal spray in patients with bleeding disorders: effect on bleeding symptoms and socioeconomic factors. Ann Hematol 1993 66 5 257-260 (Pubitemid 23179050)
    • (1993) Annals of Hematology , vol.66 , Issue.5 , pp. 257-260
    • Lethagen, S.1    Tennvall, G.R.2
  • 28
    • 43549097149 scopus 로고    scopus 로고
    • Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): Results from the European Study MCMDM-1VWD
    • Castaman G, Lethagen S, Federici AB et al. Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD. Blood 2008 111 7 3531-3539
    • (2008) Blood , vol.111 , Issue.7 , pp. 3531-3539
    • Castaman, G.1    Lethagen, S.2    Federici, A.B.3
  • 31
    • 0142240329 scopus 로고    scopus 로고
    • Gastrointestinal Bleeding, Angiodysplasia, Cardiovascular Disease, and Acquired von Willebrand Syndrome
    • DOI 10.1016/S0887-7963(03)00037-3
    • Warkentin TE, Moore JC, Anand SS, Lonn EM, Morgan DG. Gastrointestinal bleeding, angiodysplasia, cardiovascular disease, and acquired von Willebrand syndrome. Transfus Med Rev 2003 17 4 272-286 (Pubitemid 37310934)
    • (2003) Transfusion Medicine Reviews , vol.17 , Issue.4 , pp. 272-286
    • Warkentin, T.E.1    Moore, J.C.2    Anand, S.S.3    Lonn, E.M.4    Morgan, D.G.5
  • 32
    • 19944364505 scopus 로고    scopus 로고
    • Long-term prophylaxis in von Willebrand disease
    • Berntorp E, Petrini P. Long-term prophylaxis in von Willebrand disease. Blood Coagul Fibrinolysis 2005 16 Suppl 1 S23-S26 (Pubitemid 40756405)
    • (2005) Blood Coagulation and Fibrinolysis , vol.16 , Issue.SUPPL. 1
    • Berntorp, E.1    Petrini, P.2
  • 33
    • 58449095384 scopus 로고    scopus 로고
    • Use of recombinant factor VIIa in inherited and acquired von Willebrand disease
    • Sucker C, Scharf RE, Zotz RB. Use of recombinant factor VIIa in inherited and acquired von Willebrand disease. Clin Appl Thromb Hemost 2009 15 1 27-31
    • (2009) Clin Appl Thromb Hemost , vol.15 , Issue.1 , pp. 27-31
    • Sucker, C.1    Scharf, R.E.2    Zotz, R.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.