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Volumn 20, Issue 2, 2009, Pages 89-100

Von Willebrand factor/factor VIII concentrates in the treatment of von Willebrand disease

Author keywords

Factor replacement; FVIII.C; High molecular weight multimers; Thromboprophylaxis; Von Willebrand disease; Von Willebrand factor; VWF:RCo

Indexed keywords

BIOSTATE; BLOOD CLOTTING FACTOR; BLOOD CLOTTING FACTOR 7; BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 8 CONCENTRATE; DESMOPRESSIN; EMOCLOT; FACTANE; FACTOR 8Y; FANHDI; GREENEIGHT; HAEMOSOLVATE FACTOR VIII; HEMORAAS SD PLUS H; INNOBRAND; KOATE P; LOW MOLECULAR WEIGHT HEPARIN; OCTANATE; OPTIVATE; RECOMBINANT BLOOD CLOTTING FACTOR 7A; RISTOCETIN COFACTOR; THROMBOCYTE CONCENTRATE; UNCLASSIFIED DRUG; VON WILLEBRAND FACTOR; VON WILLEBRAND FACTOR CONCENTRATE; WILATE; WILFACTIN;

EID: 62349135194     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/MBC.0b013e3283254570     Document Type: Review
Times cited : (37)

References (55)
  • 1
    • 3943048700 scopus 로고    scopus 로고
    • Treatment of von Willebrand disease
    • Mannucci PM. Treatment of von Willebrand disease. N Engl J Med 2004; 351:683-694.
    • (2004) N Engl J Med , vol.351 , pp. 683-694
    • Mannucci, P.M.1
  • 2
    • 0036733501 scopus 로고    scopus 로고
    • Guidelines for the diagnosis and management of von Willebrand disease in Italy. Italian Association of Hemophilia Center (AICE)
    • Federici AB, Castaman G, Mannucci PM. Guidelines for the diagnosis and management of von Willebrand disease in Italy. Italian Association of Hemophilia Center (AICE). Haemophilia 2002; 8:607-621.
    • (2002) Haemophilia , vol.8 , pp. 607-621
    • Federici, A.B.1    Castaman, G.2    Mannucci, P.M.3
  • 4
    • 12244272130 scopus 로고    scopus 로고
    • Von Willebrand disease in the year 2003: Towards the complete identification of gene defects for correct diagnosis and treatment
    • Castaman G, Federici AB, Rodeghiero F, Mannucci PM. Von Willebrand disease in the year 2003: towards the complete identification of gene defects for correct diagnosis and treatment. Haematologica 2003; 88:94-108.
    • (2003) Haematologica , vol.88 , pp. 94-108
    • Castaman, G.1    Federici, A.B.2    Rodeghiero, F.3    Mannucci, P.M.4
  • 5
    • 0014123936 scopus 로고
    • Correction of the hemostatic defects in von Willebrand disease
    • Perkins HA. Correction of the hemostatic defects in von Willebrand disease. Blood 1967; 30:375-380.
    • (1967) Blood , vol.30 , pp. 375-380
    • Perkins, H.A.1
  • 6
    • 83055187115 scopus 로고    scopus 로고
    • von Willebrand disease (VWD): Evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA)
    • Nichols WL, Hultin MB, James AH, Manco-Johnson MJ, Montgomery RR, Ortel TL, et al. von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA). Haemophilia 2008; 14:171-232.
    • (2008) Haemophilia , vol.14 , pp. 171-232
    • Nichols, W.L.1    Hultin, M.B.2    James, A.H.3    Manco-Johnson, M.J.4    Montgomery, R.R.5    Ortel, T.L.6
  • 8
    • 2342591992 scopus 로고    scopus 로고
    • A comparative in vitro evaluation of six von Willebrand factor concentrates
    • Lethagen S, Carlson M, Hillarp A. A comparative in vitro evaluation of six von Willebrand factor concentrates. Haemophilia 2004; 10:243-249.
    • (2004) Haemophilia , vol.10 , pp. 243-249
    • Lethagen, S.1    Carlson, M.2    Hillarp, A.3
  • 9
    • 10744220312 scopus 로고    scopus 로고
    • Humate-P Study Group. Successful treatment for patients with von Willebrand disease undergoing urgent surgery using factor VIII/VWF concentrates (Humate-P)
    • Thompson AR, Gill JC, Ewenstein BM, Mueller-Velten G, Schwartz BA, Humate-P Study Group. Successful treatment for patients with von Willebrand disease undergoing urgent surgery using factor VIII/VWF concentrates (Humate-P). Haemophilia 2004; 10:42-51.
    • (2004) Haemophilia , vol.10 , pp. 42-51
    • Thompson, A.R.1    Gill, J.C.2    Ewenstein, B.M.3    Mueller-Velten, G.4    Schwartz, B.A.5
  • 10
    • 10744230522 scopus 로고    scopus 로고
    • Humate-P Study Group. Successful treatment of urgent bleeding in von Willebrand disease with factor VIII/VWF concentrate (Humate-P): Use of the ristocetin cofactor assay (VWF:RCo) to measure potency and to guide therapy
    • Gill JC, Ewenstein BM, Thompson AR, Mueller-Velten G, Schwartz BA, Humate-P Study Group. Successful treatment of urgent bleeding in von Willebrand disease with factor VIII/VWF concentrate (Humate-P): use of the ristocetin cofactor assay (VWF:RCo) to measure potency and to guide therapy. Haemophilia 2003; 9:688-695.
    • (2003) Haemophilia , vol.9 , pp. 688-695
    • Gill, J.C.1    Ewenstein, B.M.2    Thompson, A.R.3    Mueller-Velten, G.4    Schwartz, B.A.5
  • 11
    • 0344823956 scopus 로고    scopus 로고
    • Efficacy and safety of factor VIII/von Willebrand factor concentrate (Haemate-P) in preventing bleeding during surgery or invasive procedures in patients with von Willebrand disease
    • Franchini M, Rossetti G, Tagliaferri A, Pattacini C, Pozzoli D, Lippi G, et al. Efficacy and safety of factor VIII/von Willebrand factor concentrate (Haemate-P) in preventing bleeding during surgery or invasive procedures in patients with von Willebrand disease. Haematologica 2003; 88:1279-1283.
    • (2003) Haematologica , vol.88 , pp. 1279-1283
    • Franchini, M.1    Rossetti, G.2    Tagliaferri, A.3    Pattacini, C.4    Pozzoli, D.5    Lippi, G.6
  • 12
    • 0027746293 scopus 로고
    • Biological effects of a S/D-treated, very high purity, von Willebrand factor concentrate in five patients with severe von Willebrand disease
    • Meriane F, Zerhouni L, Djeha N, Meriane F, Zerhouni L, Djeha N. Biological effects of a S/D-treated, very high purity, von Willebrand factor concentrate in five patients with severe von Willebrand disease. Blood Coagul Fibrinolysis 1993; 4:1023-1029.
    • (1993) Blood Coagul Fibrinolysis , vol.4 , pp. 1023-1029
    • Meriane, F.1    Zerhouni, L.2    Djeha, N.3    Meriane, F.4    Zerhouni, L.5    Djeha, N.6
  • 13
    • 0024348884 scopus 로고
    • Use of a high-purity factor VIII concentrate (Humate-P) in von Willebrand disease
    • Berntorp E, Nilsson IM. Use of a high-purity factor VIII concentrate (Humate-P) in von Willebrand disease. Vox Sang 1989; 56:212-217.
    • (1989) Vox Sang , vol.56 , pp. 212-217
    • Berntorp, E.1    Nilsson, I.M.2
  • 14
    • 0028010958 scopus 로고
    • The use of intermediate and high purity factor VIII products in the treatment of von Willebrand disease
    • Hanna WT, Bona RD, Zimmerman CE, Carta CA, Hebert GZ, Rickles FR, et al. The use of intermediate and high purity factor VIII products in the treatment of von Willebrand disease. Thromb Haemost 1994; 71:173-179.
    • (1994) Thromb Haemost , vol.71 , pp. 173-179
    • Hanna, W.T.1    Bona, R.D.2    Zimmerman, C.E.3    Carta, C.A.4    Hebert, G.Z.5    Rickles, F.R.6
  • 16
    • 0037079717 scopus 로고    scopus 로고
    • Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: A prospective, multicenter study
    • Mannucci PM, Chediak J, Hanna W, Byrnes J, Ledford M, Ewenstein BM, et al. Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: a prospective, multicenter study. Blood 2002; 99:450-456.
    • (2002) Blood , vol.99 , pp. 450-456
    • Mannucci, P.M.1    Chediak, J.2    Hanna, W.3    Byrnes, J.4    Ledford, M.5    Ewenstein, B.M.6
  • 17
    • 0026650784 scopus 로고
    • Comparison of four virus-inactivated plasma concentrates for treatment of severe von Willebrand disease: A cross-over randomized trial
    • Mannucci PM, Tenconi PM, Castaman G, Rodeghiero F. Comparison of four virus-inactivated plasma concentrates for treatment of severe von Willebrand disease: a cross-over randomized trial. Blood 1992; 79:3130-3137.
    • (1992) Blood , vol.79 , pp. 3130-3137
    • Mannucci, P.M.1    Tenconi, P.M.2    Castaman, G.3    Rodeghiero, F.4
  • 18
    • 0031774616 scopus 로고    scopus 로고
    • Clinical management of patients with von Willebrand disease with a VHP VWF concentrate: The French experience
    • Goudemand J, Negrier C, Ounnoughene N, Sultan Y. Clinical management of patients with von Willebrand disease with a VHP VWF concentrate: the French experience. Haemophilia 1998; 4 (suppl 3):48-52.
    • (1998) Haemophilia , vol.4 , Issue.SUPPL. 3 , pp. 48-52
    • Goudemand, J.1    Negrier, C.2    Ounnoughene, N.3    Sultan, Y.4
  • 19
    • 0031797825 scopus 로고    scopus 로고
    • Pharmacokinetics, efficacy and safety of Humate-P in von Willebrand disease
    • Dobrkovska A, Krzensk U, Chediak JR. Pharmacokinetics, efficacy and safety of Humate-P in von Willebrand disease. Haemophilia 1998; 4 (suppl 3):33-39.
    • (1998) Haemophilia , vol.4 , Issue.SUPPL. 3 , pp. 33-39
    • Dobrkovska, A.1    Krzensk, U.2    Chediak, J.R.3
  • 20
    • 0036166457 scopus 로고    scopus 로고
    • Efficacy and safety of the factor VIII/von Willebrand factor concentrate, Haemate-P/Humate-P: Ristocetin cofactor unit dosing in patients with von Willebrand disease
    • Lillicrap D, Poon MC, Walker I, Xie F, Schwartz BA. Efficacy and safety of the factor VIII/von Willebrand factor concentrate, Haemate-P/Humate-P: ristocetin cofactor unit dosing in patients with von Willebrand disease. Thromb Haemost 2002; 87:224-230.
    • (2002) Thromb Haemost , vol.87 , pp. 224-230
    • Lillicrap, D.1    Poon, M.C.2    Walker, I.3    Xie, F.4    Schwartz, B.A.5
  • 21
    • 0000068529 scopus 로고
    • In vitro and in vivo characterization of a high-purity, solvent/detergent treated factor VIII concentrate: Evidence for its therapeutic efficacy in von Willebrand's disease
    • Mazurier C, De Romeuf C, Parquet-Gernez A, Goudemand M. In vitro and in vivo characterization of a high-purity, solvent/detergent treated factor VIII concentrate: evidence for its therapeutic efficacy in von Willebrand's disease. Eur J Haematol 1990; 75:228-233.
    • (1990) Eur J Haematol , vol.75 , pp. 228-233
    • Mazurier, C.1    De Romeuf, C.2    Parquet-Gernez, A.3    Goudemand, M.4
  • 22
    • 0025281796 scopus 로고
    • Clinical and laboratory evaluation of the treatment of von Willebrand disease patients with heat treated factor VIII concentrate (BPL 8Y)
    • Pasi KJ, Williams MD, Enayat MS, Hill FGH. Clinical and laboratory evaluation of the treatment of von Willebrand disease patients with heat treated factor VIII concentrate (BPL 8Y). Br J Haematol 1990; 75:228-233.
    • (1990) Br J Haematol , vol.75 , pp. 228-233
    • Pasi, K.J.1    Williams, M.D.2    Enayat, M.S.3    Hill, F.G.H.4
  • 23
    • 0027079911 scopus 로고
    • Pharmacokinetics and hemostatic effect of different factor VIII/von Willebrand factor concentrates in von Willebrand disease type III
    • Lethagen S, Berntorp E, Nilsson IM. Pharmacokinetics and hemostatic effect of different factor VIII/von Willebrand factor concentrates in von Willebrand disease type III. Ann Hematol 1992; 65:253-259.
    • (1992) Ann Hematol , vol.65 , pp. 253-259
    • Lethagen, S.1    Berntorp, E.2    Nilsson, I.M.3
  • 24
    • 34250691461 scopus 로고    scopus 로고
    • Surgical Study Group. von Willebrand factor/factor VIII concentrate (Haemate P) dosing based on pharmacokinetics: A prospective multicenter trial in elective surgery
    • Lethagen S, Kyrle PA, Castaman G, Haertel S, Mannucci PM, HAEMATE P Surgical Study Group. von Willebrand factor/factor VIII concentrate (Haemate P) dosing based on pharmacokinetics: a prospective multicenter trial in elective surgery. J Thromb Haemost 2007; 5:1420-1430.
    • (2007) J Thromb Haemost , vol.5 , pp. 1420-1430
    • Lethagen, S.1    Kyrle, P.A.2    Castaman, G.3    Haertel, S.4    Mannucci, P.M.5    HAEMATE, P.6
  • 26
    • 0031774614 scopus 로고    scopus 로고
    • Summary of a workshop on potency and dosage of von Willebrand factor concentrates
    • Chang AC, Rick ME, Ross Pierce L, Weinstein MJ. Summary of a workshop on potency and dosage of von Willebrand factor concentrates. Haemophilia 1998; 4 (suppl 3):1-6.
    • (1998) Haemophilia , vol.4 , Issue.SUPPL. 3 , pp. 1-6
    • Chang, A.C.1    Rick, M.E.2    Ross Pierce, L.3    Weinstein, M.J.4
  • 27
    • 0036120805 scopus 로고    scopus 로고
    • A comparative multilaboratory assessment of three factor VIII/von Willebrand factor concentrates
    • Favaloro EJ, Bukuya M, Martinelli T, Tzouroutis J, Duncan E, Welldon K, et al. A comparative multilaboratory assessment of three factor VIII/von Willebrand factor concentrates. Thromb Haemost 2002; 87:466-476.
    • (2002) Thromb Haemost , vol.87 , pp. 466-476
    • Favaloro, E.J.1    Bukuya, M.2    Martinelli, T.3    Tzouroutis, J.4    Duncan, E.5    Welldon, K.6
  • 28
    • 33746595318 scopus 로고    scopus 로고
    • Composition, quality control, and labeling of plasma-derived products for the treatment of von Willebrand disease
    • Mazurier C. Composition, quality control, and labeling of plasma-derived products for the treatment of von Willebrand disease. Semin Thromb Hemost 2006; 32:529-536.
    • (2006) Semin Thromb Hemost , vol.32 , pp. 529-536
    • Mazurier, C.1
  • 29
    • 33749011946 scopus 로고    scopus 로고
    • Comparative analysis and classification of von Willebrand factor/factor VIII concentrates: Impact on treatment of patients with von Willebrand disease
    • Budde U, Metzner HJ, Müller HG. Comparative analysis and classification of von Willebrand factor/factor VIII concentrates: impact on treatment of patients with von Willebrand disease. Semin Thromb Hemost 2006; 32:626-635.
    • (2006) Semin Thromb Hemost , vol.32 , pp. 626-635
    • Budde, U.1    Metzner, H.J.2    Müller, H.G.3
  • 30
    • 1842524080 scopus 로고    scopus 로고
    • In vitro study of a triple-secured von Willebrand factor concentrate
    • Mazurier C, Poulle M, Samor B, Hilbert L, Chtourou S. In vitro study of a triple-secured von Willebrand factor concentrate. Vox Sang 2004; 86:100-104.
    • (2004) Vox Sang , vol.86 , pp. 100-104
    • Mazurier, C.1    Poulle, M.2    Samor, B.3    Hilbert, L.4    Chtourou, S.5
  • 31
    • 0023091143 scopus 로고
    • Assessment of multimeric structure and ristocetin-induced binding to platelets of von Willebrand factor present in cryoprecipitate and different factor VIII concentrates
    • Lopez-Fernandez MF, Lopez-Berges C, Corral M, Garcia-Talavera JR, Lopez Borrasca A, Batlle J. Assessment of multimeric structure and ristocetin-induced binding to platelets of von Willebrand factor present in cryoprecipitate and different factor VIII concentrates. Vox Sang 1987; 52:15-19.
    • (1987) Vox Sang , vol.52 , pp. 15-19
    • Lopez-Fernandez, M.F.1    Lopez-Berges, C.2    Corral, M.3    Garcia-Talavera, J.R.4    Lopez Borrasca, A.5    Batlle, J.6
  • 32
    • 0028314508 scopus 로고
    • Proteolysis of von Willebrand factor in therapeutic plasma concentrates
    • Mannucci PM, Lattuada A, Ruggeri ZM. Proteolysis of von Willebrand factor in therapeutic plasma concentrates. Blood 1994; 83:3018-3027.
    • (1994) Blood , vol.83 , pp. 3018-3027
    • Mannucci, P.M.1    Lattuada, A.2    Ruggeri, Z.M.3
  • 33
    • 0031773567 scopus 로고    scopus 로고
    • Characterization of factor VIII/von Willebrand factor concentrates using a modified method of von Willebrand factor multimer analysis
    • Metzner HJ, Hermentin P, Cuesta-Linker T, Langner S, Muller HG, Friedebold J. Characterization of factor VIII/von Willebrand factor concentrates using a modified method of von Willebrand factor multimer analysis. Haemophilia 1998; 4 (suppl 3):25-32.
    • (1998) Haemophilia , vol.4 , Issue.SUPPL. 3 , pp. 25-32
    • Metzner, H.J.1    Hermentin, P.2    Cuesta-Linker, T.3    Langner, S.4    Muller, H.G.5    Friedebold, J.6
  • 35
    • 0027308088 scopus 로고
    • Pharmacokinetics of monoclonally-purified and recombinant factor VIII in patients with severe von Willebrand disease
    • Morfini M, Mannucci PM, Tenconi PM, Longo G, Mazzucconi MG, Rodeghiero F, et al. Pharmacokinetics of monoclonally-purified and recombinant factor VIII in patients with severe von Willebrand disease. Thromb Haemost 1993; 70:270-272.
    • (1993) Thromb Haemost , vol.70 , pp. 270-272
    • Morfini, M.1    Mannucci, P.M.2    Tenconi, P.M.3    Longo, G.4    Mazzucconi, M.G.5    Rodeghiero, F.6
  • 36
    • 0030748121 scopus 로고    scopus 로고
    • New treatments of von Willebrand disease: Plasma derived von Willebrand factor concentrates
    • Menache D, Aronson DL. New treatments of von Willebrand disease: plasma derived von Willebrand factor concentrates. Thromb Haemost 1997; 78:566-570.
    • (1997) Thromb Haemost , vol.78 , pp. 566-570
    • Menache, D.1    Aronson, D.L.2
  • 37
    • 0026562062 scopus 로고
    • Further evidence for recessive inheritance of von Willebrand disease with abnormal binding of von Willebrand factor to factor VIII
    • Lopez-Fernandez MF, Blanco-Lopez MJ, Castineira MP, Batlle J. Further evidence for recessive inheritance of von Willebrand disease with abnormal binding of von Willebrand factor to factor VIII. Am J Hematol 1992; 40:20-27.
    • (1992) Am J Hematol , vol.40 , pp. 20-27
    • Lopez-Fernandez, M.F.1    Blanco-Lopez, M.J.2    Castineira, M.P.3    Batlle, J.4
  • 38
    • 34250626034 scopus 로고    scopus 로고
    • Comparison of the pharmacokinetics of two von Willebrand factor concentrates [Biostate and AHF (High Purity)] in people with von Willebrand disorder. A randomised cross-over, multicentre study
    • Favaloro EJ, Lloyd J, Rowell J, Baker R, Rickard K, Kershaw G, et al. Comparison of the pharmacokinetics of two von Willebrand factor concentrates [Biostate and AHF (High Purity)] in people with von Willebrand disorder. A randomised cross-over, multicentre study. Thromb Haemost 2007; 97:922-930.
    • (2007) Thromb Haemost , vol.97 , pp. 922-930
    • Favaloro, E.J.1    Lloyd, J.2    Rowell, J.3    Baker, R.4    Rickard, K.5    Kershaw, G.6
  • 39
    • 38549152286 scopus 로고    scopus 로고
    • Time to think outside the box? Proposals for a new approach to future pharmacokinetic studies of von Willebrand factor concentrates in people with von Willebrand disease
    • Favaloro FJ, Kershaw G, McLachlan AJ, Lloyd J. Time to think outside the box? Proposals for a new approach to future pharmacokinetic studies of von Willebrand factor concentrates in people with von Willebrand disease. Semin Thromb Hemost 2007; 33:745-758.
    • (2007) Semin Thromb Hemost , vol.33 , pp. 745-758
    • Favaloro, F.J.1    Kershaw, G.2    McLachlan, A.J.3    Lloyd, J.4
  • 40
    • 34250169072 scopus 로고    scopus 로고
    • Treatment of severe von Willebrand disease with a high-purity von Willebrand factor concentrate (Wilfactin): A prospective study of 50 patients
    • Borel-Derlon A, Federici AB, Roussel-Robert V, Goudemand J, Lee CA, Scharrer I, et al. Treatment of severe von Willebrand disease with a high-purity von Willebrand factor concentrate (Wilfactin): a prospective study of 50 patients. J Thromb Haemost 2007; 5:1115-1124.
    • (2007) J Thromb Haemost , vol.5 , pp. 1115-1124
    • Borel-Derlon, A.1    Federici, A.B.2    Roussel-Robert, V.3    Goudemand, J.4    Lee, C.A.5    Scharrer, I.6
  • 41
    • 2942557314 scopus 로고    scopus 로고
    • Bleeding prophylaxis for major surgery in patients with type 2 von Willebrand disease with an intermediate purity factor VIII - von Willebrand factor concentrate (Haemate P)
    • Michiels JJ, Berneman ZN, van der Planken M, Schroyens W, Budde U, van Vliet HH. Bleeding prophylaxis for major surgery in patients with type 2 von Willebrand disease with an intermediate purity factor VIII - von Willebrand factor concentrate (Haemate P). Blood Coagul Fibrinolysis 2004; 15:323-330.
    • (2004) Blood Coagul Fibrinolysis , vol.15 , pp. 323-330
    • Michiels, J.J.1    Berneman, Z.N.2    van der Planken, M.3    Schroyens, W.4    Budde, U.5    van Vliet, H.H.6
  • 42
    • 0033985083 scopus 로고    scopus 로고
    • Collagen binding assay for von Willebrand factor (VWF:CBA): Detection of von Willebrand disease (VWD), and discrimination of VWD subtypes, depends on collagen source
    • Favaloro EJ. Collagen binding assay for von Willebrand factor (VWF:CBA): detection of von Willebrand disease (VWD), and discrimination of VWD subtypes, depends on collagen source. Thromb Haemost 2000; 83:127-135.
    • (2000) Thromb Haemost , vol.83 , pp. 127-135
    • Favaloro, E.J.1
  • 43
    • 0032519496 scopus 로고    scopus 로고
    • Screening for von Willebrand disease with a new analyzer using high shear stress: A study of 60 cases
    • Fressinaud E, Veyradier A, Truchaud F, Martin I, Boyer-Neumann C, Trossaert M, et al. Screening for von Willebrand disease with a new analyzer using high shear stress: a study of 60 cases. Blood 1998; 91:1325-1331.
    • (1998) Blood , vol.91 , pp. 1325-1331
    • Fressinaud, E.1    Veyradier, A.2    Truchaud, F.3    Martin, I.4    Boyer-Neumann, C.5    Trossaert, M.6
  • 44
    • 0032773694 scopus 로고    scopus 로고
    • Evaluation of the PFA-100 system in the diagnosis and therapeutic monitoring of patients with von Willebrand disease
    • Cattaneo M, Federici AB, Lecchi A, Agati B, Lombardi R, Stabile F, et al. Evaluation of the PFA-100 system in the diagnosis and therapeutic monitoring of patients with von Willebrand disease. Thromb Haemost 1999; 82:35-39.
    • (1999) Thromb Haemost , vol.82 , pp. 35-39
    • Cattaneo, M.1    Federici, A.B.2    Lecchi, A.3    Agati, B.4    Lombardi, R.5    Stabile, F.6
  • 45
    • 51349134516 scopus 로고    scopus 로고
    • PFA-100 monitoring of von Willebrand factor (VWF) responses to DDAVP and FVIII/VWF concentrate substitution in von Willebrand disease type 1 and 2
    • van Vliet HH, Kappers-Klunne MC, Leebeek FW, Michiels JJ. PFA-100 monitoring of von Willebrand factor (VWF) responses to DDAVP and FVIII/VWF concentrate substitution in von Willebrand disease type 1 and 2. Thromb Haemost 2008; 100:462-468.
    • (2008) Thromb Haemost , vol.100 , pp. 462-468
    • van Vliet, H.H.1    Kappers-Klunne, M.C.2    Leebeek, F.W.3    Michiels, J.J.4
  • 46
    • 51349090488 scopus 로고    scopus 로고
    • A better approach to monitoring of therapy in von Willebrand disease?
    • Favaloro EJ. A better approach to monitoring of therapy in von Willebrand disease? Thromb Haemost 2008; 100:371-373.
    • (2008) Thromb Haemost , vol.100 , pp. 371-373
    • Favaloro, E.J.1
  • 47
    • 0032916792 scopus 로고    scopus 로고
    • Inhibitors in German hemophilia A patients treated with a double virus inactivated factor VIII concentrate bind to the C2 domain of FVIII light chain
    • Laub R, Di Giambattista M, Fondu P, Brackmann HH, Lenk H, Saenko EL, et al. Inhibitors in German hemophilia A patients treated with a double virus inactivated factor VIII concentrate bind to the C2 domain of FVIII light chain. Thromb Haemost 1999; 81:39-44.
    • (1999) Thromb Haemost , vol.81 , pp. 39-44
    • Laub, R.1    Di Giambattista, M.2    Fondu, P.3    Brackmann, H.H.4    Lenk, H.5    Saenko, E.L.6
  • 48
    • 0028814316 scopus 로고
    • Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep-vein thrombosis
    • Koster T, Blann AD, Briet E, Vandenbroucke JP, Rosendaal FR. Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep-vein thrombosis. Lancet 1995; 345:152-155.
    • (1995) Lancet , vol.345 , pp. 152-155
    • Koster, T.1    Blann, A.D.2    Briet, E.3    Vandenbroucke, J.P.4    Rosendaal, F.R.5
  • 50
    • 0034680013 scopus 로고    scopus 로고
    • High plasma levels of factor VIII and the risk of recurrent venous thromboembolism
    • Kyrle PA, Minar E, Hirschl M, Bialonczyk C, Stain M, Schneider B, et al. High plasma levels of factor VIII and the risk of recurrent venous thromboembolism. N Engl J Med 2000; 343:457-462.
    • (2000) N Engl J Med , vol.343 , pp. 457-462
    • Kyrle, P.A.1    Minar, E.2    Hirschl, M.3    Bialonczyk, C.4    Stain, M.5    Schneider, B.6
  • 51
    • 0036712293 scopus 로고    scopus 로고
    • Venous thromboembolism in von Willebrand disease
    • Mannucci PM. Venous thromboembolism in von Willebrand disease. Thromb Haemost 2002; 88:378-379.
    • (2002) Thromb Haemost , vol.88 , pp. 378-379
    • Mannucci, P.M.1
  • 52
    • 0036713595 scopus 로고    scopus 로고
    • Venous thrombosis following the use of intermediate purity FVIII concentrate to treat patients with von Willebrand's disease
    • Makris M, Colvin B, Gupta V, Shields ML, Smith MP. Venous thrombosis following the use of intermediate purity FVIII concentrate to treat patients with von Willebrand's disease. Thromb Haemost 2002; 88:387-388.
    • (2002) Thromb Haemost , vol.88 , pp. 387-388
    • Makris, M.1    Colvin, B.2    Gupta, V.3    Shields, M.L.4    Smith, M.P.5
  • 53
    • 4444351161 scopus 로고    scopus 로고
    • Mountain States Regional Thrombophilia Group. Elevated plasma factor VIII and D-dimer levels as predictors of poor outcomes of thrombosis in children
    • Goldenberg NA, Knapp-Clevenger R, Manco-Johnson MJ, Mountain States Regional Thrombophilia Group. Elevated plasma factor VIII and D-dimer levels as predictors of poor outcomes of thrombosis in children. N Engl J Med 2004; 351:1081-1088.
    • (2004) N Engl J Med , vol.351 , pp. 1081-1088
    • Goldenberg, N.A.1    Knapp-Clevenger, R.2    Manco-Johnson, M.J.3
  • 54
    • 4444368246 scopus 로고    scopus 로고
    • Factor VIII, D-dimer, and thromboembolism in children
    • Nowak-Gottl U, Kosch A. Factor VIII, D-dimer, and thromboembolism in children. N Engl J Med 2004; 351:1051-1053.
    • (2004) N Engl J Med , vol.351 , pp. 1051-1053
    • Nowak-Gottl, U.1    Kosch, A.2


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