메뉴 건너뛰기




Volumn 13, Issue 10, 2015, Pages 1806-1814

Evaluation of an heterogeneous group of patients with von Willebrand disease using an assay alternative to ristocetin induced platelet agglutination

Author keywords

GPIbalpha protein, human; Ristocetin; Von Willebrand disease, type 2; Von Willebrand diseases; Von Willebrand factor

Indexed keywords

GLYCOPROTEIN IB; RISTOCETIN; VON WILLEBRAND FACTOR; ADHESION RECEPTOR; BIOLOGICAL MARKER; THROMBIN RECEPTOR;

EID: 84942984350     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/jth.13062     Document Type: Article
Times cited : (11)

References (37)
  • 1
    • 0023164845 scopus 로고
    • Epidemiological investigation of the prevalence of von Willebrand's disease
    • Rodeghiero F, Castaman G, Dini E. Epidemiological investigation of the prevalence of von Willebrand's disease. Blood 1987; 69: 454-9.
    • (1987) Blood , vol.69 , pp. 454-459
    • Rodeghiero, F.1    Castaman, G.2    Dini, E.3
  • 3
    • 0033502512 scopus 로고    scopus 로고
    • Laboratory assessment as a critical component of the appropriate diagnosis and sub-classification of von Willebrand's disease
    • Favaloro EJ. Laboratory assessment as a critical component of the appropriate diagnosis and sub-classification of von Willebrand's disease. Blood Rev 1999; 13: 185-204.
    • (1999) Blood Rev , vol.13 , pp. 185-204
    • Favaloro, E.J.1
  • 4
    • 3943048700 scopus 로고    scopus 로고
    • Treatment of von Willebrand's disease
    • Mannucci PM. Treatment of von Willebrand's disease. N Engl J Med 2004; 351: 683-94.
    • (2004) N Engl J Med , vol.351 , pp. 683-694
    • Mannucci, P.M.1
  • 6
    • 57149107591 scopus 로고    scopus 로고
    • The role of molecular genetics in diagnosing von Willebrand disease
    • James P, Lillicrap D. The role of molecular genetics in diagnosing von Willebrand disease. Semin Thromb Hemost 2008; 34: 502-8.
    • (2008) Semin Thromb Hemost , vol.34 , pp. 502-508
    • James, P.1    Lillicrap, D.2
  • 8
    • 3242676770 scopus 로고    scopus 로고
    • Binding of platelet glycoprotein Ibα to von Willebrand factor domain A1 stimulates the cleavage of the adjacent domain A2 by ADAMTS13
    • Nishio K, Anderson PJ, Zheng XL, Sadler JE. Binding of platelet glycoprotein Ibα to von Willebrand factor domain A1 stimulates the cleavage of the adjacent domain A2 by ADAMTS13. Proc Natl Acad Sci USA 2004; 101: 10578-83.
    • (2004) Proc Natl Acad Sci USA , vol.101 , pp. 10578-10583
    • Nishio, K.1    Anderson, P.J.2    Zheng, X.L.3    Sadler, J.E.4
  • 10
    • 0018871618 scopus 로고
    • Heightened interaction between platelets and factor VIII/von Willebrand factor in a new subtype of von Willebrand's disease
    • Ruggeri ZM, Pareti FI, Mannucci PM, Ciavarella N, Zimmerman TS. Heightened interaction between platelets and factor VIII/von Willebrand factor in a new subtype of von Willebrand's disease. N Engl J Med 1980; 302: 1047-51.
    • (1980) N Engl J Med , vol.302 , pp. 1047-1051
    • Ruggeri, Z.M.1    Pareti, F.I.2    Mannucci, P.M.3    Ciavarella, N.4    Zimmerman, T.S.5
  • 11
    • 0026323814 scopus 로고
    • The rapid differentiation of type IIb von Willebrand's disease from platelet-type (pseudo-) von Willebrand's disease by the "neutral" monoclonal antibody binding assay
    • Scott JP, Montgomery RR. The rapid differentiation of type IIb von Willebrand's disease from platelet-type (pseudo-) von Willebrand's disease by the "neutral" monoclonal antibody binding assay. Am J Clin Pathol 1991; 96: 723-8.
    • (1991) Am J Clin Pathol , vol.96 , pp. 723-728
    • Scott, J.P.1    Montgomery, R.R.2
  • 12
    • 33646679113 scopus 로고    scopus 로고
    • Measurement of von Willebrand factor binding to a recombinant fragment of glycoprotein Ibalpha in an enzyme-linked immunosorbent assay-based method: performances in patients with type 2B von Willebrand disease
    • Caron C, Hilbert L, Vanhoorelbeke K, Deckmyn H, Goudemand J, Mazurier C. Measurement of von Willebrand factor binding to a recombinant fragment of glycoprotein Ibalpha in an enzyme-linked immunosorbent assay-based method: performances in patients with type 2B von Willebrand disease. Br J Haematol 2006; 133: 655-63.
    • (2006) Br J Haematol , vol.133 , pp. 655-663
    • Caron, C.1    Hilbert, L.2    Vanhoorelbeke, K.3    Deckmyn, H.4    Goudemand, J.5    Mazurier, C.6
  • 13
    • 0036733501 scopus 로고    scopus 로고
    • Guidelines for the diagnosis and management of von Willebrand disease in Italy
    • Federici AB, Castaman G, Mannucci PM. Guidelines for the diagnosis and management of von Willebrand disease in Italy. Haemophilia 2002; 8: 607-21.
    • (2002) Haemophilia , vol.8 , pp. 607-621
    • Federici, A.B.1    Castaman, G.2    Mannucci, P.M.3
  • 15
    • 84935687838 scopus 로고    scopus 로고
    • Platelet-dependent von Willebrand factor activity. Nomenclature and methodology: communication from the SSC of the ISTH
    • Bodo I, Eikenboom J, Montgomery R, Patzke J, Schneppenheim R, Di Paola J, Subcommittee on von Willebrand factor. Platelet-dependent von Willebrand factor activity. Nomenclature and methodology: communication from the SSC of the ISTH. J Thromb Haemost 2015; 13: 1345-50.
    • (2015) J Thromb Haemost , vol.13 , pp. 1345-1350
    • Bodo, I.1    Eikenboom, J.2    Montgomery, R.3    Patzke, J.4    Schneppenheim, R.5    Di Paola, J.6
  • 16
    • 0842307008 scopus 로고    scopus 로고
    • A sensitive ristocetin co-factor activity assay with recombinant glycoprotein Ibalpha for the diagnosis of patients with low von Willebrand factor levels
    • Federici AB, Canciani MT, Forza I, Mannucci PM, Marchese P, Ware J, Ruggeri ZM. A sensitive ristocetin co-factor activity assay with recombinant glycoprotein Ibalpha for the diagnosis of patients with low von Willebrand factor levels. Haematologica 2004; 89: 77-85.
    • (2004) Haematologica , vol.89 , pp. 77-85
    • Federici, A.B.1    Canciani, M.T.2    Forza, I.3    Mannucci, P.M.4    Marchese, P.5    Ware, J.6    Ruggeri, Z.M.7
  • 18
    • 0027227873 scopus 로고
    • Elevated platelet count as a cause of abnormal von Willebrand factor multimer distribution in plasma
    • Budde U, Scharf RE, Franke P, Hartmann-Budde K, Dent JA, Ruggeri ZM. Elevated platelet count as a cause of abnormal von Willebrand factor multimer distribution in plasma. Blood 1993; 82: 1749-57.
    • (1993) Blood , vol.82 , pp. 1749-1757
    • Budde, U.1    Scharf, R.E.2    Franke, P.3    Hartmann-Budde, K.4    Dent, J.A.5    Ruggeri, Z.M.6
  • 21
    • 78649998454 scopus 로고    scopus 로고
    • Development of a newfunctional assay for von Willebrand factor binding to platelet GpIba that does not require ristocetin
    • Schneppenheim R, Obser T, Budde U, Patzke J. Development of a newfunctional assay for von Willebrand factor binding to platelet GpIba that does not require ristocetin. Hamostaseologie 2010; 30: FC4-05.
    • (2010) Hamostaseologie , vol.30 , pp. FC4-F05
    • Schneppenheim, R.1    Obser, T.2    Budde, U.3    Patzke, J.4
  • 23
    • 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 AB, Mannucci PM, Castaman G, Baronciani L, Bucciarelli P, Canciani MT, Pecci A, Lenting PJ, de Groot PG. 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: 526-34.
    • (2009) Blood , vol.113 , pp. 526-534
    • Federici, A.B.1    Mannucci, P.M.2    Castaman, G.3    Baronciani, L.4    Bucciarelli, P.5    Canciani, M.T.6    Pecci, A.7    Lenting, P.J.8    de Groot, P.G.9
  • 24
    • 0022539610 scopus 로고
    • 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. 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. Blood 1986; 68: 149-56.
    • (1986) Blood , vol.68 , pp. 149-156
    • Weiss, H.J.1    Sussman, I.I.2
  • 25
    • 0022445253 scopus 로고
    • von Willebrand's disease characterized by increased ristocetin sensitivity and the presence of all von Willebrand factor multimers in plasma
    • Holmberg L, Berntorp E, Donner M, Nilsson IM. von Willebrand's disease characterized by increased ristocetin sensitivity and the presence of all von Willebrand factor multimers in plasma. Blood 1986; 68: 668-72.
    • (1986) Blood , vol.68 , pp. 668-672
    • Holmberg, L.1    Berntorp, E.2    Donner, M.3    Nilsson, I.M.4
  • 26
    • 29244469439 scopus 로고    scopus 로고
    • Expression studies on a novel type 2B variant of the von Willebrand factor gene (R1308L) characterized by defective collagen binding
    • Baronciani L, Federici AB, Beretta M, Cozzi G, Canciani MT, Mannucci PM. Expression studies on a novel type 2B variant of the von Willebrand factor gene (R1308L) characterized by defective collagen binding. J Thromb Haemost 2005; 3: 2689-94.
    • (2005) J Thromb Haemost , vol.3 , pp. 2689-2694
    • Baronciani, L.1    Federici, A.B.2    Beretta, M.3    Cozzi, G.4    Canciani, M.T.5    Mannucci, P.M.6
  • 27
    • 36949030473 scopus 로고    scopus 로고
    • 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 CM, Daidone V, Szukowska M, Pagnan A. A novel von Willebrand factor mutation (I1372S) associated with type 2B-like von Willebrand disease: an elusive phenotype and a difficult diagnosis. Thromb Haemost 2007; 98: 1182-7.
    • (2007) Thromb Haemost , vol.98 , pp. 1182-1187
    • Casonato, A.1    Sartorello, F.2    Pontara, E.3    Gallinaro, L.4    Bertomoro, A.5    Grazia, C.M.6    Daidone, V.7    Szukowska, M.8    Pagnan, A.9
  • 28
    • 0028345761 scopus 로고
    • Multiple substitutions in the von Willebrand factor gene that mimic the pseudogene sequence
    • Eikenboom JCJ, Vink T, Briët E, Sixma JJ, Reitsma PH. Multiple substitutions in the von Willebrand factor gene that mimic the pseudogene sequence. Proc Natl Acad Sci USA 1994; 91: 2221-4.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 2221-2224
    • Eikenboom, J.C.J.1    Vink, T.2    Briët, E.3    Sixma, J.J.4    Reitsma, P.H.5
  • 29
    • 27144461083 scopus 로고    scopus 로고
    • A novel nanobody that detects the gain-of-function phenotype of von Willebrand factor in ADAMTS13 deficiency and von Willebrand disease type 2B
    • Hulstein JJ, de Groot PG, Silence K, Veyradier A, Fijnheer R, Lenting PJ. A novel nanobody that detects the gain-of-function phenotype of von Willebrand factor in ADAMTS13 deficiency and von Willebrand disease type 2B. Blood 2005; 106: 3035-42.
    • (2005) Blood , vol.106 , pp. 3035-3042
    • Hulstein, J.J.1    de Groot, P.G.2    Silence, K.3    Veyradier, A.4    Fijnheer, R.5    Lenting, P.J.6
  • 30
    • 84937609814 scopus 로고    scopus 로고
    • Misfolding of vWF to pathologically disordered conformations impacts the severity of von Willebrand disease
    • Tischer A, Madde P, Moon-Tasson L, Auton M. Misfolding of vWF to pathologically disordered conformations impacts the severity of von Willebrand disease. Biophys J 2014; 107: 1185-95.
    • (2014) Biophys J , vol.107 , pp. 1185-1195
    • Tischer, A.1    Madde, P.2    Moon-Tasson, L.3    Auton, M.4
  • 32
    • 0030696578 scopus 로고    scopus 로고
    • Laboratory assays for von Willebrand factor: relative contribution to the dagnosis of von Willebrand's disease
    • Favaloro EJ, Koutts J. Laboratory assays for von Willebrand factor: relative contribution to the dagnosis of von Willebrand's disease. Pathology 1997; 29: 385-91.
    • (1997) Pathology , vol.29 , pp. 385-391
    • Favaloro, E.J.1    Koutts, J.2
  • 34
    • 84898678042 scopus 로고    scopus 로고
    • Evaluation of an automated method for measuring von Willebrand factor activity in clinical samples without ristocetin
    • Graf L, Moffat KA, Carlino SA, Chan AK, Iorio A, Giulivi A, Hayward CP. Evaluation of an automated method for measuring von Willebrand factor activity in clinical samples without ristocetin. Int J Lab Hematol 2014; 36: 341-51.
    • (2014) Int J Lab Hematol , vol.36 , pp. 341-351
    • Graf, L.1    Moffat, K.A.2    Carlino, S.A.3    Chan, A.K.4    Iorio, A.5    Giulivi, A.6    Hayward, C.P.7
  • 35
    • 84905119570 scopus 로고    scopus 로고
    • Comparison of von Willebrand factor (VWF) activity VWF:Ac with VWF ristocetin cofactor activity VWF:RCo
    • Geisen U, Zieger B, Nakamura L, Weis A, Heinz J, Michiels JJ, Heilmann C. Comparison of von Willebrand factor (VWF) activity VWF:Ac with VWF ristocetin cofactor activity VWF:RCo. Thromb Res 2014; 134: 246-50.
    • (2014) Thromb Res , vol.134 , pp. 246-250
    • Geisen, U.1    Zieger, B.2    Nakamura, L.3    Weis, A.4    Heinz, J.5    Michiels, J.J.6    Heilmann, C.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.