메뉴 건너뛰기




Volumn 11, Issue 4, 2006, Pages 219-225

Advances in the diagnosis and management of von Willebrand disease

Author keywords

Bleeding; Diagnosis; von Willebrand disease; von Willebrand factor

Indexed keywords

ANTIFIBRINOLYTIC AGENT; BLOOD CLOTTING FACTOR 8; DESMOPRESSIN; HEMATOLOGIC AGENT; PLASMA DERIVED BLOOD CLOTTING FACTOR 8 CONCENTRATE VON WILLEBRAND FACTOR CONCENTRAT; RECOMBINANT BLOOD CLOTTING FACTOR 7A; RECOMBINANT BLOOD CLOTTING FACTOR 8; VON WILLEBRAND FACTOR;

EID: 33845705369     PISSN: 10245332     EISSN: 16078454     Source Type: Journal    
DOI: 10.1080/10245330600841311     Document Type: Review
Times cited : (8)

References (50)
  • 1
    • 12244272130 scopus 로고    scopus 로고
    • von Willebrand's disease in the year 2003: Towards the complete identification of gene defects for correct diagnosis and treatment
    • Castaman, G and Federici, AB and Rodeghiero, F and Mannucci, PM. (2003) von Willebrand's disease in the year 2003: Towards the complete identification of gene defects for correct diagnosis and treatment Haematologica, 88, pp. 94-108.
    • (2003) Haematologica , vol.88 , pp. 94-108
    • Castaman, G.1    Federici, A.B.2    Rodeghiero, F.3    Mannucci, P.M.4
  • 2
    • 0023164845 scopus 로고
    • Epidemiological investigation of the prevalence of von Willebrand's disease
    • Rodeghiero, F and Castaman, G and Dini, E. (1987) Epidemiological investigation of the prevalence of von Willebrand's disease Blood, 69, pp. 454-459.
    • (1987) Blood , vol.69 , pp. 454-459
    • Rodeghiero, F.1    Castaman, G.2    Dini, E.3
  • 3
    • 0036733501 scopus 로고    scopus 로고
    • Italian Association of Hemophilia Centers (AICE). Guidelines for the diagnosis and management of von Willebrand disease in Italy
    • Federici, AB and Castaman, G and Mannucci, PM. (2002) Italian Association of Hemophilia Centers (AICE). Guidelines for the diagnosis and management of von Willebrand disease in Italy Haemophilia, 8, pp. 607-621.
    • (2002) Haemophilia , vol.8 , pp. 607-621
    • Federici, A.B.1    Castaman, G.2    Mannucci, P.M.3
  • 4
    • 0028201807 scopus 로고
    • A revised classification of von Willebrand disease
    • Sadler, JE. (1994) A revised classification of von Willebrand disease Thromb Haemost, 71, pp. 520-525.
    • (1994) Thromb Haemost , vol.71 , pp. 520-525
    • Sadler, J.E.1
  • 5
    • 11044235267 scopus 로고    scopus 로고
    • Clinical diagnosis of von Willebrand disease
    • Federici, AB. (2004) Clinical diagnosis of von Willebrand disease Haemophilia, 10(Suppl. 4), pp. 169-176.
    • (2004) Haemophilia , vol.10 , Issue.SUPPL. 4 , pp. 169-176
    • Federici, A.B.1
  • 6
    • 0018779080 scopus 로고
    • Genetics of classic von Willebrand's disease. I. Phenotypic variation within families
    • Miller, CH and Graham, JB and Goldin, LR and Elston, RC. (1979) Genetics of classic von Willebrand's disease. I. Phenotypic variation within families Blood, 54, pp. 117-136.
    • (1979) Blood , vol.54 , pp. 117-136
    • Miller, C.H.1    Graham, J.B.2    Goldin, L.R.3    Elston, R.C.4
  • 7
    • 0020699959 scopus 로고
    • Heterogeneous abnormalities in the multimeric structure, antigenic properties, and plasma-platelet content of factor VIII/von Willebrand factor insubtypes of classic (type I) and variant (IIA) von Willebrand's disease
    • Weiss, HJ and Pietu, G and Rabinowitz, R and Girma, JP and Rogers, J and Meyer, D. (1983) Heterogeneous abnormalities in the multimeric structure, antigenic properties, and plasma-platelet content of factor VIII/von Willebrand factor insubtypes of classic (type I) and variant (IIA) von Willebrand's disease J Lab Clin Med, 101, pp. 411-425.
    • (1983) J Lab Clin Med , vol.101 , pp. 411-425
    • Weiss, H.J.1    Pietu, G.2    Rabinowitz, R.3    Girma, J.P.4    Rogers, J.5    Meyer, D.6
  • 8
    • 0021955653 scopus 로고
    • Heterogeneity of type I von Willebrand disease: Evidence for a subgroup with an abnormal von Willebrand factor
    • Mannucci, PM and Lombardi, R and Bader, R and (1985) Heterogeneity of type I von Willebrand disease: Evidence for a subgroup with an abnormal von Willebrand factor Blood, 66, pp. 796-802.
    • (1985) Blood , vol.66 , pp. 796-802
    • Mannucci, P.M.1    Lombardi, R.2    Bader, R.3
  • 9
    • 19944374427 scopus 로고    scopus 로고
    • von Willebrand disease: Laboratory aspects of diagnosis and treatment
    • Favaloro, EJ and Lillicrap, D and Lazzari, MA and (2004) von Willebrand disease: Laboratory aspects of diagnosis and treatment Haemophilia, 10(Suppl. 4), pp. 164-168.
    • (2004) Haemophilia , vol.10 , Issue.SUPPL. 4 , pp. 164-168
    • Favaloro, E.J.1    Lillicrap, D.2    Lazzari, M.A.3
  • 10
    • 2342656365 scopus 로고    scopus 로고
    • The diagnosis of von Willebrand disease: A guideline from the UK Haemophilia Centre Doctors' Organization
    • Laffan, M and Brown, SA and Collins, PW and (2004) The diagnosis of von Willebrand disease: A guideline from the UK Haemophilia Centre Doctors' Organization Haemophilia, 10, pp. 199-217.
    • (2004) Haemophilia , vol.10 , pp. 199-217
    • Laffan, M.1    Brown, S.A.2    Collins, P.W.3
  • 11
    • 0020068005 scopus 로고
    • 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 and Meyer, D and Rabinowitz, R and (1982) 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 N Engl J Med, 306, pp. 326-333.
    • (1982) N Engl J Med , vol.306 , pp. 326-333
    • Weiss, H.J.1    Meyer, D.2    Rabinowitz, R.3
  • 12
    • 0019998246 scopus 로고
    • Platelet-type von Willebrand's disease: Characterization of a new bleeding disorder
    • Miller, JL and Castella, A. (1982) Platelet-type von Willebrand's disease: Characterization of a new bleeding disorder Blood, 60, pp. 790-794.
    • (1982) Blood , vol.60 , pp. 790-794
    • Miller, J.L.1    Castella, A.2
  • 13
    • 0024425034 scopus 로고
    • New variant of von Willebrand disease with defective binding to factor VIII
    • Nishino, M and Girma, JP and Rothschild, C and Fressinaud, E and Meyer, D. (1989) New variant of von Willebrand disease with defective binding to factor VIII Blood, 74, pp. 1591-1599.
    • (1989) Blood , vol.74 , pp. 1591-1599
    • Nishino, M.1    Girma, J.P.2    Rothschild, C.3    Fressinaud, E.4    Meyer, D.5
  • 14
    • 0025012865 scopus 로고
    • A new von Willebrand factor (vWF) defect in a patient with factor VIII (FVIII) deficiency but with normal levels and multimeric patterns of both plasma and platelet vWF. Characterization of abnormal vWF/FVIII interaction
    • Mazurier, C and Dieval, J and Jorieux, S and Delobel, J and Goudemand, M. (1990) A new von Willebrand factor (vWF) defect in a patient with factor VIII (FVIII) deficiency but with normal levels and multimeric patterns of both plasma and platelet vWF. Characterization of abnormal vWF/FVIII interaction Blood, 75, pp. 20-26.
    • (1990) Blood , vol.75 , pp. 20-26
    • Mazurier, C.1    Dieval, J.2    Jorieux, S.3    Delobel, J.4    Goudemand, M.5
  • 15
    • 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 and Veyradier, A and Trichaud, F and (1998) Screening for von Willebrand disease with a new analyzer using high shear stress: A study of 60 cases Blood, 91, pp. 1325-1331.
    • (1998) Blood , vol.91 , pp. 1325-1331
    • Fressinaud, E.1    Veyradier, A.2    Trichaud, F.3
  • 16
    • 23844511270 scopus 로고    scopus 로고
    • The platelet function analyzer (PFA-100): An update on its clinical use
    • Franchini, M. (2005) The platelet function analyzer (PFA-100): An update on its clinical use Clin Lab, 51, pp. 367-372.
    • (2005) Clin Lab , vol.51 , pp. 367-372
    • Franchini, M.1
  • 17
    • 0034537373 scopus 로고    scopus 로고
    • Ristocetin cofactor and collagen binding activities normalized to antigen levels for a rapid diagnosis of type 2 von Willebrand disease - Single center comparison of four different assays
    • Federici, AB and Canciani, MT and Forza, I and Cozzi, G. (2000) Ristocetin cofactor and collagen binding activities normalized to antigen levels for a rapid diagnosis of type 2 von Willebrand disease - single center comparison of four different assays Thromb Haemost, 84, pp. 1127-1128.
    • (2000) Thromb Haemost , vol.84 , pp. 1127-1128
    • Federici, A.B.1    Canciani, M.T.2    Forza, I.3    Cozzi, G.4
  • 18
    • 0027465930 scopus 로고
    • Type I von Willebrand disease, subtype "platelet low": Decreased platelet adhesion can be explained by low synthesis of von Willebrand factor in endothelial cells
    • Federici, AB and de Groot, PG and Moia, M and Ijsseldijk, MJ and Sixma, JJ and Mannucci, PM. (1993) Type I von Willebrand disease, subtype "platelet low": Decreased platelet adhesion can be explained by low synthesis of von Willebrand factor in endothelial cells Br J Haematol, 83, pp. 88-93.
    • (1993) Br J Haematol , vol.83 , pp. 88-93
    • Federici, A.B.1    de Groot, P.G.2    Moia, M.3    Ijsseldijk, M.J.4    Sixma, J.J.5    Mannucci, P.M.6
  • 19
    • 0030836531 scopus 로고    scopus 로고
    • Gene defects in 150 unrelated French cases with type 2 von Willebrand disease: From the patient to the gene. INSERM network on molecular abnormalities in von Willebrand disease
    • Meyer, D and Fressinaud, E and Gaucher, C and Lavergne, JM and Hilbert, L and Ribba, AS and Jorieux, S and Mazurier, C. (1997) Gene defects in 150 unrelated French cases with type 2 von Willebrand disease: From the patient to the gene. INSERM network on molecular abnormalities in von Willebrand disease Thromb Haemost, 78, pp. 451-456.
    • (1997) Thromb Haemost , vol.78 , pp. 451-456
    • Meyer, D.1    Fressinaud, E.2    Gaucher, C.3    Lavergne, J.M.4    Hilbert, L.5    Ribba, A.S.6    Jorieux, S.7    Mazurier, C.8
  • 20
    • 0026630044 scopus 로고
    • Impaired intracellular transport produced by a subset of type IIA von Willebrand disease mutations
    • Lyons, SE and Bruck, ME and Bowie, EJ and Ginsburg, D. (1992) Impaired intracellular transport produced by a subset of type IIA von Willebrand disease mutations J Biol Chem, 267, pp. 4424-4430.
    • (1992) J Biol Chem , vol.267 , pp. 4424-4430
    • Lyons, S.E.1    Bruck, M.E.2    Bowie, E.J.3    Ginsburg, D.4
  • 21
    • 0034912146 scopus 로고    scopus 로고
    • A molecular approach to the classification of von Willebrand disease
    • Schneppenheim, R and Budde, U and Ruggeri, ZM. (2001) A molecular approach to the classification of von Willebrand disease Best Pract Res Clin Haematol, 14, pp. 281-298.
    • (2001) Best Pract Res Clin Haematol , vol.14 , pp. 281-298
    • Schneppenheim, R.1    Budde, U.2    Ruggeri, Z.M.3
  • 22
    • 14544302314 scopus 로고    scopus 로고
    • New concepts in von Willebrand disease
    • Sadler, JE. (2005) New concepts in von Willebrand disease Annu Rev Med, 56, pp. 173-1791.
    • (2005) Annu Rev Med , vol.56 , pp. 173-1791
    • Sadler, J.E.1
  • 23
    • 4444278190 scopus 로고    scopus 로고
    • Type IIB von Willebrand disease: A paradox explains how von Willebrand factor works
    • Ruggeri, ZM. (2004) Type IIB von Willebrand disease: A paradox explains how von Willebrand factor works J Thromb Haemost, 2, pp. 2-6.
    • (2004) J Thromb Haemost , vol.2 , pp. 2-6
    • Ruggeri, Z.M.1
  • 24
    • 13344295095 scopus 로고    scopus 로고
    • Initiation of platelet adhesion by arrest onto fibrinogen or translocation on von Willebrand factor
    • Savage, B and Saldivar, E and Ruggeri, ZM. (1996) Initiation of platelet adhesion by arrest onto fibrinogen or translocation on von Willebrand factor Cell, 84, pp. 289-297.
    • (1996) Cell , vol.84 , pp. 289-297
    • Savage, B.1    Saldivar, E.2    Ruggeri, Z.M.3
  • 25
    • 0034677986 scopus 로고    scopus 로고
    • Interaction of von Willebrand factor domain A1 with platelet glycoprotein Ibalpha-(1-289). Slow intrinsic binding kinetics mediate rapid platelet adhesion
    • Miura, S and Li, CQ and Cao, Z and Wang, H and Wardell, MR and Sadler, JE. (2000) Interaction of von Willebrand factor domain A1 with platelet glycoprotein Ibalpha-(1-289). Slow intrinsic binding kinetics mediate rapid platelet adhesion J Biol Chem, 275, pp. 7539-7546.
    • (2000) J Biol Chem , vol.275 , pp. 7539-7546
    • Miura, S.1    Li, C.Q.2    Cao, Z.3    Wang, H.4    Wardell, M.R.5    Sadler, J.E.6
  • 26
    • 0029796142 scopus 로고    scopus 로고
    • Type 2M: Milwaukee-1 von Willebrand disease: An in-frame deletion in the Cys509-Cys695 loop of the von Willebrand factor A1 domain causes deficient binding of von Willebrand factor to platelets
    • Mancuso, DJ and Kroner, PA and Christopherson, PA and Vokac, EA and Gill, JC and Montgomery, RR. (1996) Type 2M: Milwaukee-1 von Willebrand disease: An in-frame deletion in the Cys509-Cys695 loop of the von Willebrand factor A1 domain causes deficient binding of von Willebrand factor to platelets Blood, 88, pp. 2259-2568.
    • (1996) Blood , vol.88 , pp. 2259-2568
    • Mancuso, D.J.1    Kroner, P.A.2    Christopherson, P.A.3    Vokac, E.A.4    Gill, J.C.5    Montgomery, R.R.6
  • 27
    • 0032032301 scopus 로고    scopus 로고
    • Type 2M von Willebrand disease: F606I and I662F mutations in the glycoprotein Ib binding domain selectively impair ristocetin- but not botrocetin-mediated binding of von Willebrand factor to platelets
    • Hillery, CA and Mancuso, DJ and Sadler, JE and (1998) Type 2M von Willebrand disease: F606I and I662F mutations in the glycoprotein Ib binding domain selectively impair ristocetin- but not botrocetin-mediated binding of von Willebrand factor to platelets Blood, 91, pp. 1572-1581.
    • (1998) Blood , vol.91 , pp. 1572-1581
    • Hillery, C.A.1    Mancuso, D.J.2    Sadler, J.E.3
  • 28
    • 0023852791 scopus 로고
    • von Willebrand disease "Vicenza" with larger-than-normal (supranormal) von Willebrand factor multimers
    • Mannucci, PM and Lombardi, R and Castaman, G and (1988) von Willebrand disease "Vicenza" with larger-than-normal (supranormal) von Willebrand factor multimers Blood, 71, pp. 65-70.
    • (1988) Blood , vol.71 , pp. 65-70
    • Mannucci, P.M.1    Lombardi, R.2    Castaman, G.3
  • 29
    • 0033971892 scopus 로고    scopus 로고
    • Von Willebrand disease type 2M "Vicenza" in Italian and German patients: Identification of the first candidate mutation (G3864A; R1205H) in 8 families
    • Schneppenheim, R and Federici, AB and Budde, U and (2000) Von Willebrand disease type 2M "Vicenza" in Italian and German patients: Identification of the first candidate mutation (G3864A; R1205H) in 8 families Thromb Haemost, 82, pp. 136-140.
    • (2000) Thromb Haemost , vol.82 , pp. 136-140
    • Schneppenheim, R.1    Federici, A.B.2    Budde, U.3
  • 30
    • 0034912338 scopus 로고    scopus 로고
    • Type 2N von Willebrand disease: Clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology
    • Mazurier, C and Goudemand, J and Hilbert, L and Caron, C and Fressinaud, E and Meyer, D. (2001) Type 2N von Willebrand disease: Clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology Best Pract Res Clin Haematol, 14, pp. 337-347.
    • (2001) Best Pract Res Clin Haematol , vol.14 , pp. 337-347
    • Mazurier, C.1    Goudemand, J.2    Hilbert, L.3    Caron, C.4    Fressinaud, E.5    Meyer, D.6
  • 32
    • 0019349927 scopus 로고
    • Precipitating antibodies to factor VIII/von Willebrand factor in von Willebrand's disease: Effects on replacement therapy
    • Mannucci, PM and Ruggeri, ZM and Ciavarella, N and Kazatchkine, MD and Mowbray, JF. (1981) Precipitating antibodies to factor VIII/von Willebrand factor in von Willebrand's disease: Effects on replacement therapy Blood, 57, pp. 25-31.
    • (1981) Blood , vol.57 , pp. 25-31
    • Mannucci, P.M.1    Ruggeri, Z.M.2    Ciavarella, N.3    Kazatchkine, M.D.4    Mowbray, J.F.5
  • 33
    • 2342625955 scopus 로고    scopus 로고
    • Management of von Willebrand disease: A guideline from the UK Haemophilia Centre Doctors' Organization
    • Pasi, KJ and Collins, PW and Keeling, DM and (2004) Management of von Willebrand disease: A guideline from the UK Haemophilia Centre Doctors' Organization Haemophilia, 10, pp. 218-231.
    • (2004) Haemophilia , vol.10 , pp. 218-231
    • Pasi, K.J.1    Collins, P.W.2    Keeling, D.M.3
  • 34
    • 3943048700 scopus 로고    scopus 로고
    • Treatment of von Willebrand's disease
    • Mannucci, PM. (2004) Treatment of von Willebrand's disease N Engl J Med, 351, pp. 683-694.
    • (2004) N Engl J Med , vol.351 , pp. 683-694
    • Mannucci, P.M.1
  • 35
    • 0032560732 scopus 로고    scopus 로고
    • Hemostatic drugs
    • Mannucci, PM. (1998) Hemostatic drugs N Engl J Med, 339, pp. 245-253.
    • (1998) N Engl J Med , vol.339 , pp. 245-253
    • Mannucci, P.M.1
  • 36
    • 0035093753 scopus 로고    scopus 로고
    • Retrospective review of the management of elective surgery with desmopressin and clotting factor concentrates in patients with von Willebrand disease
    • Nitu-Whalley, IC and Griffioen, A and Harrington, C and Lee, CA. (2001) Retrospective review of the management of elective surgery with desmopressin and clotting factor concentrates in patients with von Willebrand disease Am J Hematol, 66, pp. 280-284.
    • (2001) Am J Hematol , vol.66 , pp. 280-284
    • Nitu-Whalley, I.C.1    Griffioen, A.2    Harrington, C.3    Lee, C.A.4
  • 37
    • 12144289138 scopus 로고    scopus 로고
    • Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: Results of a multicenter European study
    • Federici, AB and Mazurier, C and Berntorp, E and (2004) Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: Results of a multicenter European study Blood, 103, pp. 2032-2038.
    • (2004) Blood , vol.103 , pp. 2032-2038
    • Federici, A.B.1    Mazurier, C.2    Berntorp, E.3
  • 39
    • 0025772810 scopus 로고
    • Clinical indications for desmopressin (DDAVP) in congenital and acquired von Willebrand disease
    • Rodeghiero, F and Castaman, G and Mannucci, PM. (1991) Clinical indications for desmopressin (DDAVP) in congenital and acquired von Willebrand disease Blood Rev, 5, pp. 155-161.
    • (1991) Blood Rev , vol.5 , pp. 155-161
    • Rodeghiero, F.1    Castaman, G.2    Mannucci, P.M.3
  • 40
    • 0024410234 scopus 로고
    • Hyponatremia and seizures in young children given DDAVP
    • Smith, TJ and Gill, JC and Ambruso, DR and Hathaway, WE. (1989) Hyponatremia and seizures in young children given DDAVP Am J Hematol, 31, pp. 199-202.
    • (1989) Am J Hematol , vol.31 , pp. 199-202
    • Smith, T.J.1    Gill, J.C.2    Ambruso, D.R.3    Hathaway, W.E.4
  • 41
    • 0024433021 scopus 로고
    • Desmopressin and thrombosis
    • Mannucci, PM and Lusher, JM. (1989) Desmopressin and thrombosis Lancet, 2, pp. 675.
    • (1989) Lancet , vol.2 , pp. 675
    • Mannucci, P.M.1    Lusher, J.M.2
  • 42
    • 0035312982 scopus 로고    scopus 로고
    • How I treat patients with von Willebrand disease
    • Mannucci, PM. (2001) How I treat patients with von Willebrand disease Blood, 97, pp. 1915-1919.
    • (2001) Blood , vol.97 , pp. 1915-1919
    • Mannucci, P.M.1
  • 43
    • 0033926486 scopus 로고    scopus 로고
    • Desmopressin (DDAVP) in the treatment of bleeding disorders: The first twenty years
    • Mannucci, PM. (2000) Desmopressin (DDAVP) in the treatment of bleeding disorders: The first twenty years Haemophilia, 6(Suppl. 1), pp. 60-67.
    • (2000) Haemophilia , vol.6 , Issue.SUPPL. 1 , pp. 60-67
    • Mannucci, P.M.1
  • 44
    • 0037079717 scopus 로고    scopus 로고
    • Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: A prospective, multicenter study
    • and the Alphanate Study Group
    • Mannucci, PM and Chediak, J and Hanna, W and Byrnes, J and Marlies, L and Ewenstein, BM. (2002) Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: A prospective, multicenter study Blood, 99, pp. 450-456. and the Alphanate Study Group
    • (2002) Blood , vol.99 , pp. 450-456
    • Mannucci, P.M.1    Chediak, J.2    Hanna, W.3    Byrnes, J.4    Marlies, L.5    Ewenstein, B.M.6
  • 45
    • 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's disease
    • Franchini, M and Rossetti, G and Tagliaferri, A and Pattacini, C and Pozzoli, D and Lippi, G and Manzato, F and Bertuzzo, D and Gandini, G. (2003) 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's disease Haematologica, 88, pp. 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    Manzato, F.7    Bertuzzo, D.8    Gandini, G.9
  • 46
    • 0033965869 scopus 로고    scopus 로고
    • High levels of factor VIII and venous thrombosis
    • Rosendaal, FR. (2000) High levels of factor VIII and venous thrombosis Throm Haemost, 83, pp. 1-2.
    • (2000) Throm Haemost , vol.83 , pp. 1-2
    • Rosendaal, F.R.1
  • 47
    • 0036712293 scopus 로고    scopus 로고
    • Venous thromboembolism in von Willebrand disease
    • Mannucci, PM. (2002) Venous thromboembolism in von Willebrand disease Thromb Haemost, 88, pp. 378-379.
    • (2002) Thromb Haemost , vol.88 , pp. 378-379
    • Mannucci, P.M.1
  • 48
    • 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 and Colvin, B and Gupta, V and Shields, ML and Smith, MP. (2002) Venous thrombosis following the use of intermediate purity FVIII concentrate to treat patients with von Willebrand's disease Thromb Haemost, 88, pp. 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
  • 49
    • 12344275278 scopus 로고    scopus 로고
    • Treatment of von Willebrand disease
    • Rodeghiero, F and Castaman, G. (2005) Treatment of von Willebrand disease Semin Hematol, 42, pp. 29-35.
    • (2005) Semin Hematol , vol.42 , pp. 29-35
    • Rodeghiero, F.1    Castaman, G.2
  • 50
    • 0023469711 scopus 로고
    • Life-threatening reaction to factor VIII concentrate in a patient with severe von Willebrand disease and alloantibodies to von Willebrand factor
    • Mannucci, PM and Tamaro, G and Narchi, G and Candotti, G and Federici, A and Altieri, D and Tedesco, F. (1987) Life-threatening reaction to factor VIII concentrate in a patient with severe von Willebrand disease and alloantibodies to von Willebrand factor Eur J Haematol, 39, pp. 467-470.
    • (1987) Eur J Haematol , vol.39 , pp. 467-470
    • Mannucci, P.M.1    Tamaro, G.2    Narchi, G.3    Candotti, G.4    Federici, A.5    Altieri, D.6    Tedesco, F.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.