메뉴 건너뛰기




Volumn 10, Issue 6, 1999, Pages 1234-1241

Unrecognized pattern of von Willebrand factor abnormalities in hemolytic uremic syndrome and thrombotic thrombocytopenic purpura

Author keywords

[No Author keywords available]

Indexed keywords

VON WILLEBRAND FACTOR;

EID: 0033061320     PISSN: 10466673     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (27)

References (34)
  • 1
    • 0001898520 scopus 로고
    • Thrombotic microangiopathy
    • edited by Tischer CC, Brenner BM, Philadelphia, Lippincott
    • Remuzzi G, Ruggenenti P, Bertani T: Thrombotic microangiopathy. In: Renal Pathology, edited by Tischer CC, Brenner BM, Philadelphia, Lippincott, 1994, pp 1154-1184
    • (1994) Renal Pathology , pp. 1154-1184
    • Remuzzi, G.1    Ruggenenti, P.2    Bertani, T.3
  • 2
    • 0017588199 scopus 로고
    • Treatment of thrombotic thrombocytopenic purpura with plasma
    • Byrnes JJ, Khurana M: Treatment of thrombotic thrombocytopenic purpura with plasma. N Engl J Med 297: 1386-1389, 1977
    • (1977) N Engl J Med , vol.297 , pp. 1386-1389
    • Byrnes, J.J.1    Khurana, M.2
  • 3
    • 0027418266 scopus 로고
    • Thrombotic thrombocytopenic purpura: Evidence that infusion rather than removal of plasma induces remission of the disease
    • Ruggenenti P, Galbusera M, Plata Cornejo RP, Bellavita P, Remuzzi G: Thrombotic thrombocytopenic purpura: Evidence that infusion rather than removal of plasma induces remission of the disease. Am J Kidney Dis 21: 314-318, 1993
    • (1993) Am J Kidney Dis , vol.21 , pp. 314-318
    • Ruggenenti, P.1    Galbusera, M.2    Plata Cornejo, R.P.3    Bellavita, P.4    Remuzzi, G.5
  • 4
    • 0026048114 scopus 로고
    • Comparison of plasma exchange with plasma infusion in the treatment of thrombotic thrombocytopenic purpura. Canadian Apheresis Study Group
    • Rock GA, Shumak KH, Buskard NA, Blanchette VS, Kelton JG, Nair RC, Spasoff RA: Comparison of plasma exchange with plasma infusion in the treatment of thrombotic thrombocytopenic purpura. Canadian Apheresis Study Group. N Engl J Med 325: 393-397, 1991
    • (1991) N Engl J Med , vol.325 , pp. 393-397
    • Rock, G.A.1    Shumak, K.H.2    Buskard, N.A.3    Blanchette, V.S.4    Kelton, J.G.5    Nair, R.C.6    Spasoff, R.A.7
  • 5
    • 0028233149 scopus 로고
    • Solvent/ detergent-treated plasma suppresses shear-induced platelet aggregation and prevents episodes of thrombotic thrombocytopenic purpura
    • Moake J, Chintagumpala M, Turner N, McPherson P, Nolasco L, Steuber C, Santiago-Borrero P, Horowitz M, Pehta J: Solvent/ detergent-treated plasma suppresses shear-induced platelet aggregation and prevents episodes of thrombotic thrombocytopenic purpura. Blood 84: 490-497, 1994
    • (1994) Blood , vol.84 , pp. 490-497
    • Moake, J.1    Chintagumpala, M.2    Turner, N.3    McPherson, P.4    Nolasco, L.5    Steuber, C.6    Santiago-Borrero, P.7    Horowitz, M.8    Pehta, J.9
  • 6
    • 0021858462 scopus 로고
    • Immunohistochemistry of vascular lesion in thrombotic thrombocytopenic purpura, with special reference to factor VIII related antigen
    • Asada Y, Sumiyoshi A, Hayashi T, Suzumiya J, Kaketani K: Immunohistochemistry of vascular lesion in thrombotic thrombocytopenic purpura, with special reference to factor VIII related antigen. Thromb Res 38: 469-479, 1985
    • (1985) Thromb Res , vol.38 , pp. 469-479
    • Asada, Y.1    Sumiyoshi, A.2    Hayashi, T.3    Suzumiya, J.4    Kaketani, K.5
  • 7
    • 0025243601 scopus 로고
    • Cell biology of von Willebrand factor
    • Wagner DD: Cell biology of von Willebrand factor. Annu Rev Cell Biol 6: 217-246, 1990
    • (1990) Annu Rev Cell Biol , vol.6 , pp. 217-246
    • Wagner, D.D.1
  • 8
    • 0023612519 scopus 로고
    • von Willebrand factor and von Willebrand disease
    • Ruggeri ZM, Zimmerman TS: von Willebrand factor and von Willebrand disease. Blood 70: 895-904, 1987
    • (1987) Blood , vol.70 , pp. 895-904
    • Ruggeri, Z.M.1    Zimmerman, T.S.2
  • 9
    • 0029925856 scopus 로고    scopus 로고
    • Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis
    • Furlan M, Robles R, Lammle B: Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis. Blood 87: 4223-4234, 1996
    • (1996) Blood , vol.87 , pp. 4223-4234
    • Furlan, M.1    Robles, R.2    Lammle, B.3
  • 10
    • 0022852282 scopus 로고
    • Involvement of large plasma von Willebrand factor (vWF) multimers and unusually large vWF forms derived from endothelial cells in shear stress-induced platelet aggregation
    • Moake JL, Turner NA, Stathopoulos NA, Nolasco LH, Hellums JD: Involvement of large plasma von Willebrand factor (vWF) multimers and unusually large vWF forms derived from endothelial cells in shear stress-induced platelet aggregation. J Clin Invest 78: 1456-1461, 1986
    • (1986) J Clin Invest , vol.78 , pp. 1456-1461
    • Moake, J.L.1    Turner, N.A.2    Stathopoulos, N.A.3    Nolasco, L.H.4    Hellums, J.D.5
  • 11
    • 0028103748 scopus 로고
    • Haemolytic-uraemic syndrome: Basic science
    • Moake JL: Haemolytic-uraemic syndrome: Basic science. Lancet 343: 393-397, 1994
    • (1994) Lancet , vol.343 , pp. 393-397
    • Moake, J.L.1
  • 12
    • 0024734977 scopus 로고
    • Abnormalities of von Willebrand factor multimers in thrombotic thombocytopenic purpura and the hemolytic-uremic syndrome
    • Moake JL, McPherson PD: Abnormalities of von Willebrand factor multimers in thrombotic thombocytopenic purpura and the hemolytic-uremic syndrome. Am J Med 87: 9N-15N, 1989
    • (1989) Am J Med , vol.87
    • Moake, J.L.1    McPherson, P.D.2
  • 13
    • 0024395146 scopus 로고
    • Enhanced proteolysis of plasma von Willebrand factor in thrombotic thrombocytopenic purpura and the hemolytic uremic syndrome
    • Mannucci PM, Lombardi R, Lattuada A, Ruggenenti P, Viganò GL, Barbui T, Remuzzi G: Enhanced proteolysis of plasma von Willebrand factor in thrombotic thrombocytopenic purpura and the hemolytic uremic syndrome. Blood 74: 978-983, 1989
    • (1989) Blood , vol.74 , pp. 978-983
    • Mannucci, P.M.1    Lombardi, R.2    Lattuada, A.3    Ruggenenti, P.4    Viganò, G.L.5    Barbui, T.6    Remuzzi, G.7
  • 14
    • 0029024101 scopus 로고
    • The hemolytic uremic syndrome
    • Remuzzi G, Ruggenenti P: The hemolytic uremic syndrome. Kidney Int 48: 2-19, 1995
    • (1995) Kidney Int , vol.48 , pp. 2-19
    • Remuzzi, G.1    Ruggenenti, P.2
  • 15
    • 0030000015 scopus 로고    scopus 로고
    • The pathophysiology and management of thrombotic thrombocytopenic purpura
    • Ruggenenti P, Remuzzi G: The pathophysiology and management of thrombotic thrombocytopenic purpura. Eur J Haematol 56: 191-207, 1996
    • (1996) Eur J Haematol , vol.56 , pp. 191-207
    • Ruggenenti, P.1    Remuzzi, G.2
  • 16
    • 0028867871 scopus 로고
    • Treatment of thrombotic microangiopathy
    • Ruggenenti P, Remuzzi G: Treatment of thrombotic microangiopathy. J Nephrol 8: 255-272, 1995
    • (1995) J Nephrol , vol.8 , pp. 255-272
    • Ruggenenti, P.1    Remuzzi, G.2
  • 17
    • 0030049869 scopus 로고    scopus 로고
    • Bilateral nephrectomy stopped disease progression in plasma-resistant hemolytic uremic syndrome with neurological signs and coma
    • Remuzzi G, Galbusera M, Salvadori M, Rizzoni G, Paris S, Ruggenenti P: Bilateral nephrectomy stopped disease progression in plasma-resistant hemolytic uremic syndrome with neurological signs and coma. Kidney Int 49: 282-286, 1996
    • (1996) Kidney Int , vol.49 , pp. 282-286
    • Remuzzi, G.1    Galbusera, M.2    Salvadori, M.3    Rizzoni, G.4    Paris, S.5    Ruggenenti, P.6
  • 18
    • 0019442145 scopus 로고
    • The complex multimeric composition of factor VIII/von Willebrand factor
    • Ruggeri ZM, Zimmerman TS: The complex multimeric composition of factor VIII/von Willebrand factor. Blood 57: 1140-1143, 1981
    • (1981) Blood , vol.57 , pp. 1140-1143
    • Ruggeri, Z.M.1    Zimmerman, T.S.2
  • 19
    • 0022405292 scopus 로고
    • High-resolution analysis of von Willebrand factor multimeric composition defines a new variant of type I von Willebrand disease with aberrant structure but presence of all size multimers (type IC)
    • Ciavarella G, Ciavarella N, Antoncecchi S, De Mattia D, Ranieri P, Dent J, Zimmerman TS, Ruggeri ZM: High-resolution analysis of von Willebrand factor multimeric composition defines a new variant of type I von Willebrand disease with aberrant structure but presence of all size multimers (type IC). Blood 66: 1423-1429, 1985
    • (1985) Blood , vol.66 , pp. 1423-1429
    • Ciavarella, G.1    Ciavarella, N.2    Antoncecchi, S.3    De Mattia, D.4    Ranieri, P.5    Dent, J.6    Zimmerman, T.S.7    Ruggeri, Z.M.8
  • 20
    • 0028266474 scopus 로고
    • Shear stress enhances the proteolysis of von Willebrand factor in normal plasma
    • Tsai HM, Sussman II, Nagel RL: Shear stress enhances the proteolysis of von Willebrand factor in normal plasma. Blood 83: 2171-2179, 1994
    • (1994) Blood , vol.83 , pp. 2171-2179
    • Tsai, H.M.1    Sussman, I.I.2    Nagel, R.L.3
  • 21
    • 0025268599 scopus 로고
    • Calpain proteolysis of von Willebrand factor enhances its binding to platelet membrane glycoprotein IIb/IIIa: An explanation for platelet aggregation in thrombotic thrombocytopenic purpura
    • Moore JC, Murphy WG, Kelton JG: Calpain proteolysis of von Willebrand factor enhances its binding to platelet membrane glycoprotein IIb/IIIa: An explanation for platelet aggregation in thrombotic thrombocytopenic purpura. Br J Haematol 74: 457-464, 1990
    • (1990) Br J Haematol , vol.74 , pp. 457-464
    • Moore, J.C.1    Murphy, W.G.2    Kelton, J.G.3
  • 26
    • 0025787417 scopus 로고
    • Prognostic markers in diarrhoea-associated haemolytic-uraemic syndrome: Initial neutrophil count, human neutrophil elastase and von Willebrand factor antigen
    • Milford DV, Staten J, MacGreggor I, Dawes J, Taylor CM, Hill FG: Prognostic markers in diarrhoea-associated haemolytic-uraemic syndrome: Initial neutrophil count, human neutrophil elastase and von Willebrand factor antigen. Nephrol Dial Transplant 6: 232-237, 1991
    • (1991) Nephrol Dial Transplant , vol.6 , pp. 232-237
    • Milford, D.V.1    Staten, J.2    MacGreggor, I.3    Dawes, J.4    Taylor, C.M.5    Hill, F.G.6
  • 29
    • 0026667389 scopus 로고
    • Interleukin-8 and polymorphoneutrophil leukocyte activation in hemolytic uremic syndrome of childhood
    • Fitzpatrick MM, Shah V, Trompeter RS, Dillon MJ, Barratt TM: Interleukin-8 and polymorphoneutrophil leukocyte activation in hemolytic uremic syndrome of childhood. Kidney Int 42: 951-956, 1992
    • (1992) Kidney Int , vol.42 , pp. 951-956
    • Fitzpatrick, M.M.1    Shah, V.2    Trompeter, R.S.3    Dillon, M.J.4    Barratt, T.M.5
  • 30
    • 0029125985 scopus 로고
    • Thrombotic thrombocytopenic purpura
    • Moake JL: Thrombotic thrombocytopenic purpura. Thromb Haemostasis 74: 240-245, 1995
    • (1995) Thromb Haemostasis , vol.74 , pp. 240-245
    • Moake, J.L.1
  • 31
    • 0030973267 scopus 로고    scopus 로고
    • Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura
    • Furlan M, Robles R, Solenthaler M, Wassmer M, Sandoz P, Lammle B: Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura. Blood 89: 3097-3103, 1997
    • (1997) Blood , vol.89 , pp. 3097-3103
    • Furlan, M.1    Robles, R.2    Solenthaler, M.3    Wassmer, M.4    Sandoz, P.5    Lammle, B.6
  • 32
    • 0032522952 scopus 로고    scopus 로고
    • Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura
    • Furlan M, Robles R, Solenthaler M, Lammle B: Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura. Blood 91: 2839-2846, 1998
    • (1998) Blood , vol.91 , pp. 2839-2846
    • Furlan, M.1    Robles, R.2    Solenthaler, M.3    Lammle, B.4
  • 33
    • 0023608525 scopus 로고
    • Calcium-dependent cysteine protease activity in the sera of patients with thrombotic thrombocytopenic purpura
    • Murphy WG, Moore JC, Kelton JG: Calcium-dependent cysteine protease activity in the sera of patients with thrombotic thrombocytopenic purpura. Blood 70: 1683-1687, 1987
    • (1987) Blood , vol.70 , pp. 1683-1687
    • Murphy, W.G.1    Moore, J.C.2    Kelton, J.G.3
  • 34
    • 0026002050 scopus 로고
    • A cathepsin-like cysteine proteinase proaggregating activity in thrombotic thrombocytopenic purpura
    • Falanga A, Consonni R, Ruggenenti P, Barbui T: A cathepsin-like cysteine proteinase proaggregating activity in thrombotic thrombocytopenic purpura. Br J Haematol 79: 474-480, 1991
    • (1991) Br J Haematol , vol.79 , pp. 474-480
    • Falanga, A.1    Consonni, R.2    Ruggenenti, P.3    Barbui, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.