-
1
-
-
32944456736
-
Current concepts in thrombotic thrombocytopenic purpura
-
Tsai HM. Current concepts in thrombotic thrombocytopenic purpura. Annu Rev Med 2006;57:419-436
-
(2006)
Annu Rev Med
, vol.57
, pp. 419-436
-
-
Tsai, H.M.1
-
2
-
-
33744523004
-
Advances in the pathogenesis, diagnosis and treatment of thrombotic thrombocytopenic purpura and hemolytic uremic syndrome
-
Franchini M, Zaffanello M, Veneri D. Advances in the pathogenesis, diagnosis and treatment of thrombotic thrombocytopenic purpura and hemolytic uremic syndrome. Thromb Res 2006;118:177-184
-
(2006)
Thromb Res
, vol.118
, pp. 177-184
-
-
Franchini, M.1
Zaffanello, M.2
Veneri, D.3
-
3
-
-
0037158606
-
Thrombotic microangiopathies
-
Moake JL. Thrombotic microangiopathies. N Engl J Med 2002;347:589-600
-
(2002)
N Engl J Med
, vol.347
, pp. 589-600
-
-
Moake, J.L.1
-
5
-
-
15244357262
-
The "cutting" edge: Von Willebrand factor-cleaving protease activity in thrombotic microangiopathies
-
Haspel RL, Jarolim P. The "cutting" edge: von Willebrand factor-cleaving protease activity in thrombotic microangiopathies. Transits Apher Sci 2005;32:177-184
-
(2005)
Transits Apher Sci
, vol.32
, pp. 177-184
-
-
Haspel, R.L.1
Jarolim, P.2
-
6
-
-
33646360865
-
Thrombotic thrombocytopenic purpura
-
George JN. Thrombotic thrombocytopenic purpura. N Engl J Med 2006;354:1927-1935
-
(2006)
N Engl J Med
, vol.354
, pp. 1927-1935
-
-
George, J.N.1
-
7
-
-
0037160539
-
Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains
-
Cal S, Obaya AJ, Llamazares M, Garabaya C, Quesada V, Lopez-Otin C. Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains. Gene 2002;283:49-62
-
(2002)
Gene
, vol.283
, pp. 49-62
-
-
Cal, S.1
Obaya, A.J.2
Llamazares, M.3
Garabaya, C.4
Quesada, V.5
Lopez-Otin, C.6
-
8
-
-
0035798582
-
Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura
-
Zheng X, Chung D, Takayama TK, Majerus EM, Sadler JE, Fujikawa K. Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura. J Biol Chem 2001;276:41059-4063
-
(2001)
J Biol Chem
, vol.276
, pp. 41059-44063
-
-
Zheng, X.1
Chung, D.2
Takayama, T.K.3
Majerus, E.M.4
Sadler, J.E.5
Fujikawa, K.6
-
9
-
-
0035885962
-
Partial amino acid sequence of purified von Willebrand factor-cleaving protease
-
Gerritsen HE, Robles R, Lammle B, Furlan M. Partial amino acid sequence of purified von Willebrand factor-cleaving protease. Blood 2001;98:1654-1661
-
(2001)
Blood
, vol.98
, pp. 1654-1661
-
-
Gerritsen, H.E.1
Robles, R.2
Lammle, B.3
Furlan, M.4
-
10
-
-
0037111571
-
Cloning, expression, and functional characterization of the von Willebrand factor-cleaving protease (ADAMTS13)
-
Plaimauer B, Zimmermann K, Volkel D, et al. Cloning, expression, and functional characterization of the von Willebrand factor-cleaving protease (ADAMTS13). Blood 2002;100:3626-3632
-
(2002)
Blood
, vol.100
, pp. 3626-3632
-
-
Plaimauer, B.1
Zimmermann, K.2
Volkel, D.3
-
11
-
-
0023058313
-
-
Ruoslahti E, Pierschbacher MD. Arg-Gly-Asp: a versatile cell recognition signal. Cell 1986;44:517-518
-
Ruoslahti E, Pierschbacher MD. Arg-Gly-Asp: a versatile cell recognition signal. Cell 1986;44:517-518
-
-
-
-
12
-
-
28344435221
-
Cleavage of ultra-large von Willebrand factor by ADAMTS-13 under flow conditions
-
Dong JF. Cleavage of ultra-large von Willebrand factor by ADAMTS-13 under flow conditions. J Thromb Haemost 2005;3:1710-1716
-
(2005)
J Thromb Haemost
, vol.3
, pp. 1710-1716
-
-
Dong, J.F.1
-
13
-
-
0034759807
-
A novel human metalloprotease synthesized in the liver and secreted into the blood: Possibly, the von Willebrand factor-cleaving protease?
-
Soejima K, Mimura N, Hirashima M, et al. A novel human metalloprotease synthesized in the liver and secreted into the blood: possibly, the von Willebrand factor-cleaving protease? J Biochem (Tokyo) 2001;130:475-480
-
(2001)
J Biochem (Tokyo)
, vol.130
, pp. 475-480
-
-
Soejima, K.1
Mimura, N.2
Hirashima, M.3
-
14
-
-
0035807348
-
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
-
Levy GG, Nichols WC, Lian EC, et al. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature 2001;413:488-494
-
(2001)
Nature
, vol.413
, pp. 488-494
-
-
Levy, G.G.1
Nichols, W.C.2
Lian, E.C.3
-
15
-
-
33646756171
-
Human endothelial cells synthesize and release ADAMTS-13
-
Turner N, Nolasco L, Tao Z, Dong JF, Moake J. Human endothelial cells synthesize and release ADAMTS-13. J Thromb Haemost 2006;4:1396-1404
-
(2006)
J Thromb Haemost
, vol.4
, pp. 1396-1404
-
-
Turner, N.1
Nolasco, L.2
Tao, Z.3
Dong, J.F.4
Moake, J.5
-
16
-
-
0032918258
-
Recovery and half-life of von Willebrand factor-cleaving protease after plasma therapy in patients with thrombotic thrombocytopenic purpura
-
Furlan M, Robles R, Morselli B, Sandoz P, Lammle B. Recovery and half-life of von Willebrand factor-cleaving protease after plasma therapy in patients with thrombotic thrombocytopenic purpura. Thromb Haemost 1999;81:8-13
-
(1999)
Thromb Haemost
, vol.81
, pp. 8-13
-
-
Furlan, M.1
Robles, R.2
Morselli, B.3
Sandoz, P.4
Lammle, B.5
-
17
-
-
28444462885
-
Platelet-derived VWF-cleaving metalloprotease ADAMTS-13
-
Liu L, Choi H, Bernardo A, et al. Platelet-derived VWF-cleaving metalloprotease ADAMTS-13. J Thromb Haemost 2005;3:2536-2544
-
(2005)
J Thromb Haemost
, vol.3
, pp. 2536-2544
-
-
Liu, L.1
Choi, H.2
Bernardo, A.3
-
18
-
-
0036893186
-
ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions
-
Dong JF, Moake JL, Nolasco L, et al. ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions. Blood 2002;100:4033-4039
-
(2002)
Blood
, vol.100
, pp. 4033-4039
-
-
Dong, J.F.1
Moake, J.L.2
Nolasco, L.3
-
19
-
-
3042839778
-
Effects of inflammatory cytokines on the release and cleavage of the endothelial cell-derived ultralarge von Willebrand factor multimers under flow
-
Bernardo A, Ball C, Nolasco L, Moake JF, Dong JF. Effects of inflammatory cytokines on the release and cleavage of the endothelial cell-derived ultralarge von Willebrand factor multimers under flow. Blood 2004;104:100-106
-
(2004)
Blood
, vol.104
, pp. 100-106
-
-
Bernardo, A.1
Ball, C.2
Nolasco, L.3
Moake, J.F.4
Dong, J.F.5
-
20
-
-
33645090687
-
Systemic antithrombotic effects of ADAMTS13
-
Chauhan AK, Motto DG, Lamb CB, et al. Systemic antithrombotic effects of ADAMTS13. J Exp Med 2006;203:767-776
-
(2006)
J Exp Med
, vol.203
, pp. 767-776
-
-
Chauhan, A.K.1
Motto, D.G.2
Lamb, C.B.3
-
21
-
-
0029907370
-
Willebrand factor: Molecular size and functional activity
-
Furlan M. Von Willebrand factor: molecular size and functional activity. Ann Hematol 1996;72:341-348
-
(1996)
Ann Hematol
, vol.72
, pp. 341-348
-
-
Von, F.M.1
-
22
-
-
0030973267
-
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 1997;89:3097-3103
-
(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
-
23
-
-
0026069774
-
Heterogeneity of plasma von Willebrand factor multimers resulting from proteolysis of the constituent subunit
-
Dent JA, Galbusera M, Ruggeri ZM. Heterogeneity of plasma von Willebrand factor multimers resulting from proteolysis of the constituent subunit. J Clin Invest 1991;88:774-782
-
(1991)
J Clin Invest
, vol.88
, pp. 774-782
-
-
Dent, J.A.1
Galbusera, M.2
Ruggeri, Z.M.3
-
24
-
-
0037125931
-
Processing of von Willebrand factor by ADAMTS-13
-
Chung DW, Fujikawa K. Processing of von Willebrand factor by ADAMTS-13. Biochemistry 2002;41:11065-11070
-
(2002)
Biochemistry
, vol.41
, pp. 11065-11070
-
-
Chung, D.W.1
Fujikawa, K.2
-
25
-
-
33846592202
-
Conformational stability and domain unfolding of the von Willebrand factor A domains
-
Auton M, Cruz MA, Moake J. Conformational stability and domain unfolding of the von Willebrand factor A domains. J Mol Biol 2007;366:986-1000
-
(2007)
J Mol Biol
, vol.366
, pp. 986-1000
-
-
Auton, M.1
Cruz, M.A.2
Moake, J.3
-
26
-
-
34247887680
-
Further characterization of ADAMTS-13 inactivation by thrombin
-
Lam JK, Chion CK, Zanardelli S, Lane DA, Crawley JT. Further characterization of ADAMTS-13 inactivation by thrombin. J Thromb Haemost 2007;5:1010-1018
-
(2007)
J Thromb Haemost
, vol.5
, pp. 1010-1018
-
-
Lam, J.K.1
Chion, C.K.2
Zanardelli, S.3
Lane, D.A.4
Crawley, J.T.5
-
27
-
-
12844270458
-
Proteolytic inactivation of ADAMTS13 by thrombin and plasmin
-
Crawley JT, Lam JK, Ranee JB, Mollica LR, O'Donnell JS, Lane DA. Proteolytic inactivation of ADAMTS13 by thrombin and plasmin. Blood 2005;105:1085-1093
-
(2005)
Blood
, vol.105
, pp. 1085-1093
-
-
Crawley, J.T.1
Lam, J.K.2
Ranee, J.B.3
Mollica, L.R.4
O'Donnell, J.S.5
Lane, D.A.6
-
28
-
-
0037305592
-
Changes in von Willebrand factor-cleaving protease (ADAMTS13) activity after infusion of desmopressin
-
Reiter RA, Knöbl P, Varadi K, Turecek PL. Changes in von Willebrand factor-cleaving protease (ADAMTS13) activity after infusion of desmopressin. Blood 2002;101:946-948
-
(2002)
Blood
, vol.101
, pp. 946-948
-
-
Reiter, R.A.1
Knöbl, P.2
Varadi, K.3
Turecek, P.L.4
-
29
-
-
11244281582
-
Fatal congenital thrombotic thrombocytopenic purpura with apparent ADAMTS-13 inhibitor: In vitro inhibition of ADAMTS-13 activity by hemoglobin
-
Studt J-D, Hovinga JAK, Antoine G, et al. Fatal congenital thrombotic thrombocytopenic purpura with apparent ADAMTS-13 inhibitor: in vitro inhibition of ADAMTS-13 activity by hemoglobin. Blood 2005;105:542-544
-
(2005)
Blood
, vol.105
, pp. 542-544
-
-
Studt, J.-D.1
Hovinga, J.A.K.2
Antoine, G.3
-
30
-
-
0035525768
-
Changes in health and disease of the metalloprotease that cleaves von Willebrand factor
-
Mannucci PM, Canciani MT, Forza I, Lussana F, Lattuada A, Rossi E. Changes in health and disease of the metalloprotease that cleaves von Willebrand factor. Blood 2001;98:2730-2735
-
(2001)
Blood
, vol.98
, pp. 2730-2735
-
-
Mannucci, P.M.1
Canciani, M.T.2
Forza, I.3
Lussana, F.4
Lattuada, A.5
Rossi, E.6
-
31
-
-
1242322066
-
Thrombotic thrombocytopenic purpura-hemolytic uremic syndrome following allogeneic HPC transplantation: A diagnostic dilemma
-
George JN, Li X, McMinn JR, Terrell DR, Vesely SK, Selby GB. Thrombotic thrombocytopenic purpura-hemolytic uremic syndrome following allogeneic HPC transplantation: a diagnostic dilemma. Transfusion 2004;44:294-304
-
(2004)
Transfusion
, vol.44
, pp. 294-304
-
-
George, J.N.1
Li, X.2
McMinn, J.R.3
Terrell, D.R.4
Vesely, S.K.5
Selby, G.B.6
-
32
-
-
0035003931
-
The clinical features, risk factors and outcome of thrombotic thrombocytopenic purpura occurring after bone marrow transplantation
-
Fuge R, Bird JM, Fraser A, et al. The clinical features, risk factors and outcome of thrombotic thrombocytopenic purpura occurring after bone marrow transplantation. Br J Haematol 2001;113:58-64
-
(2001)
Br J Haematol
, vol.113
, pp. 58-64
-
-
Fuge, R.1
Bird, J.M.2
Fraser, A.3
-
33
-
-
0029656155
-
Hemolytic uremic syndrome in solid-organ transplant recipients
-
Singh N, Gayowski T, Marino IR. Hemolytic uremic syndrome in solid-organ transplant recipients. Transpl Int 1996;9:68-75
-
(1996)
Transpl Int
, vol.9
, pp. 68-75
-
-
Singh, N.1
Gayowski, T.2
Marino, I.R.3
-
34
-
-
33846828701
-
Thrombotic microangiopathy following allogeneic hematopoietic stem cell transplantation
-
Kojouri K, George JN. Thrombotic microangiopathy following allogeneic hematopoietic stem cell transplantation. Curr Opin Oncol 2007;19:148-154
-
(2007)
Curr Opin Oncol
, vol.19
, pp. 148-154
-
-
Kojouri, K.1
George, J.N.2
-
35
-
-
10744228488
-
Posttransplantation thrombotic thrombocytopenic purpura: A single-center experience and a contemporary review
-
Elliott MA, Nichols WL Jr, Plumhoff EA, et al. Posttransplantation thrombotic thrombocytopenic purpura: a single-center experience and a contemporary review. Mayo Clin Proc 2003;78:421-430
-
(2003)
Mayo Clin Proc
, vol.78
, pp. 421-430
-
-
Elliott, M.A.1
Nichols Jr, W.L.2
Plumhoff, E.A.3
-
36
-
-
0033151555
-
von Willebrand factor proteolysis is deficient in classic, but not in bone marrow transplantation-associated, thrombotic thrombocytopenic purpura
-
van der Plas RM, Schiphorst ME, Huizinga EG, et al. von Willebrand factor proteolysis is deficient in classic, but not in bone marrow transplantation-associated, thrombotic thrombocytopenic purpura. Blood 1999;93:3798-3802
-
(1999)
Blood
, vol.93
, pp. 3798-3802
-
-
van der Plas, R.M.1
Schiphorst, M.E.2
Huizinga, E.G.3
-
37
-
-
0034775082
-
Von Willebrand factor-cleaving protease activity and proteolysis of von Willebrand factor in bone marrow transplant-associated thrombotic microangiopathy
-
Arai S, Allan C, Streiff M, Hutchins GM, Vogelsang GB, Tsai HM. Von Willebrand factor-cleaving protease activity and proteolysis of von Willebrand factor in bone marrow transplant-associated thrombotic microangiopathy. Hematol J 2001;2:292-299
-
(2001)
Hematol J
, vol.2
, pp. 292-299
-
-
Arai, S.1
Allan, C.2
Streiff, M.3
Hutchins, G.M.4
Vogelsang, G.B.5
Tsai, H.M.6
-
38
-
-
33745123633
-
Prospective study on the behaviour of the metalloprotease ADAMTS13 and of von Willebrand factor after bone marrow transplantation
-
Peyvandi F, Siboni SM, Lambertenghi Deliliers D, et al. Prospective study on the behaviour of the metalloprotease ADAMTS13 and of von Willebrand factor after bone marrow transplantation. Br J Haematol 2006;134:187-195
-
(2006)
Br J Haematol
, vol.134
, pp. 187-195
-
-
Peyvandi, F.1
Siboni, S.M.2
Lambertenghi Deliliers, D.3
-
39
-
-
0037968640
-
ADAMTS13 activity in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: Relation to presenting features and clinical outcomes in a prospective cohort of 142 patients
-
Vesely SK, George JN, Lammle B, et al. ADAMTS13 activity in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: relation to presenting features and clinical outcomes in a prospective cohort of 142 patients. Blood 2003;102:60-68
-
(2003)
Blood
, vol.102
, pp. 60-68
-
-
Vesely, S.K.1
George, J.N.2
Lammle, B.3
-
40
-
-
33745435227
-
Thrombotic microangiopathy with acquired deficiency in ADAMTS 13 activity in lung transplant recipients
-
Mal H, Veyradier A, Brugiere O, et al. Thrombotic microangiopathy with acquired deficiency in ADAMTS 13 activity in lung transplant recipients. Transplantation 2006;81:1628-1632
-
(2006)
Transplantation
, vol.81
, pp. 1628-1632
-
-
Mal, H.1
Veyradier, A.2
Brugiere, O.3
-
41
-
-
0037184329
-
Inhibitors of ADAMTS13: A potential factor in the cause of thrombotic microangiopathy in a renal allograft recipient
-
Pham PT, Danovitch GM, Wilkinson AH, et al. Inhibitors of ADAMTS13: a potential factor in the cause of thrombotic microangiopathy in a renal allograft recipient. Transplantation 2002;74:1077-1080
-
(2002)
Transplantation
, vol.74
, pp. 1077-1080
-
-
Pham, P.T.1
Danovitch, G.M.2
Wilkinson, A.H.3
-
42
-
-
33751026965
-
High titer of ADAMTS13 inhibitor associated with thrombotic microangiopathy of the gut and skeletal muscle after allogeneic hematopoietic stem cell transplantation
-
Adachi T, Matsushita T, Ichihashi R, et al. High titer of ADAMTS13 inhibitor associated with thrombotic microangiopathy of the gut and skeletal muscle after allogeneic hematopoietic stem cell transplantation. Int J Hematol 2006;83:415-419
-
(2006)
Int J Hematol
, vol.83
, pp. 415-419
-
-
Adachi, T.1
Matsushita, T.2
Ichihashi, R.3
-
43
-
-
0036275582
-
Impaired activity of plasma von Willebrand factor-cleaving protease may predict the occurrence of hepatic veno-occlusive disease after stem cell transplantation
-
Park YD, Yoshioka A, Kawa K, et al. Impaired activity of plasma von Willebrand factor-cleaving protease may predict the occurrence of hepatic veno-occlusive disease after stem cell transplantation. Bone Marrow Transplant 2002;29:789-794
-
(2002)
Bone Marrow Transplant
, vol.29
, pp. 789-794
-
-
Park, Y.D.1
Yoshioka, A.2
Kawa, K.3
-
44
-
-
33646455016
-
Plasma ADAMTS13 activity may predict early adverse events in living donor liver transplantation: Observations in 3 cases
-
Ko S, Okano E, Kanehiro H, et al. Plasma ADAMTS13 activity may predict early adverse events in living donor liver transplantation: observations in 3 cases. Liver Transpl 2006;12:859-869
-
(2006)
Liver Transpl
, vol.12
, pp. 859-869
-
-
Ko, S.1
Okano, E.2
Kanehiro, H.3
-
45
-
-
33751164665
-
From humoral rejection to generalized thrombotic microangiopathy - role of acquired ADAMTS13 deficiency in a renal allograft recipient
-
Ulinski T, Charpentier A, Colombat M, et al. From humoral rejection to generalized thrombotic microangiopathy - role of acquired ADAMTS13 deficiency in a renal allograft recipient. Am J Transplant 2006;6:3030-3036
-
(2006)
Am J Transplant
, vol.6
, pp. 3030-3036
-
-
Ulinski, T.1
Charpentier, A.2
Colombat, M.3
-
46
-
-
0033135056
-
Deficient activity of von Willebrand's factor-cleaving protease in patients with disseminated malignancies
-
Oleksowicz L, Bhagwati N, DeLeon-Fernandez M. Deficient activity of von Willebrand's factor-cleaving protease in patients with disseminated malignancies. Cancer Res 1999;59:2244-2250
-
(1999)
Cancer Res
, vol.59
, pp. 2244-2250
-
-
Oleksowicz, L.1
Bhagwati, N.2
DeLeon-Fernandez, M.3
-
47
-
-
0038712157
-
Patients with localized and disseminated tumors have reduced but measurable levels of ADAMTS-13 (von Willebrand factor cleaving protease)
-
Mannucci PM, Karimi M, Mosalaei A, Canciani MT, Peyvandi F. Patients with localized and disseminated tumors have reduced but measurable levels of ADAMTS-13 (von Willebrand factor cleaving protease). Haematologica 2003;88:454-458
-
(2003)
Haematologica
, vol.88
, pp. 454-458
-
-
Mannucci, P.M.1
Karimi, M.2
Mosalaei, A.3
Canciani, M.T.4
Peyvandi, F.5
-
48
-
-
0037085694
-
Deficiency of von Willebrand factor-cleaving protease activity in the plasma of malignant patients
-
Koo BH, Oh D, Chung SY, et al. Deficiency of von Willebrand factor-cleaving protease activity in the plasma of malignant patients. Thromb Res 2002;105:471-476
-
(2002)
Thromb Res
, vol.105
, pp. 471-476
-
-
Koo, B.H.1
Oh, D.2
Chung, S.Y.3
-
49
-
-
0037089066
-
Cancer-related thrombotic microangiopathy secondary to von Willebrand factor-cleaving protease deficiency
-
Blot E, Decaudin D, Veyradier A, Bardier A, Zagame OL, Pouillart P. Cancer-related thrombotic microangiopathy secondary to von Willebrand factor-cleaving protease deficiency. Thromb Res 2002;106:127-130
-
(2002)
Thromb Res
, vol.106
, pp. 127-130
-
-
Blot, E.1
Decaudin, D.2
Veyradier, A.3
Bardier, A.4
Zagame, O.L.5
Pouillart, P.6
-
50
-
-
0035003933
-
Microangiopathic haemolytic anaemia in metastasizing malignant tumours is not associated with a severe deficiency of the von Willebrand factor-cleaving protease
-
Fontana S, Gerritsen HE, Kremer Hovinga J, Furlan M, Lammle B. Microangiopathic haemolytic anaemia in metastasizing malignant tumours is not associated with a severe deficiency of the von Willebrand factor-cleaving protease. Br J Haematol 2001;113:100-102
-
(2001)
Br J Haematol
, vol.113
, pp. 100-102
-
-
Fontana, S.1
Gerritsen, H.E.2
Kremer Hovinga, J.3
Furlan, M.4
Lammle, B.5
-
51
-
-
0037272731
-
Presence of ADAMTS13 activity in a patient with metastatic cancer and thrombotic microangiopathy
-
Forman RB, Benkel SA, Novik Y, Tsai HM. Presence of ADAMTS13 activity in a patient with metastatic cancer and thrombotic microangiopathy. Acta Haematol 2003;109:150-152
-
(2003)
Acta Haematol
, vol.109
, pp. 150-152
-
-
Forman, R.B.1
Benkel, S.A.2
Novik, Y.3
Tsai, H.M.4
-
52
-
-
0345303929
-
ADAMTS-13 activity in patients with brain and prostate tumors is mildly reduced, but not correlated to stage of malignancy and metastasis
-
Böhm M, Gerlach R, Beecken WD, Scheuer T, Stier-Bruck I, Scharrer I. ADAMTS-13 activity in patients with brain and prostate tumors is mildly reduced, but not correlated to stage of malignancy and metastasis. Thromb Res 2003;111:33-37
-
(2003)
Thromb Res
, vol.111
, pp. 33-37
-
-
Böhm, M.1
Gerlach, R.2
Beecken, W.D.3
Scheuer, T.4
Stier-Bruck, I.5
Scharrer, I.6
-
53
-
-
0030957526
-
Human immunodeficiency virus infection and thrombotic microangiopathy
-
Hymes KB, Karpatkin S. Human immunodeficiency virus infection and thrombotic microangiopathy. Semin Hematol 1997;34:117-125
-
(1997)
Semin Hematol
, vol.34
, pp. 117-125
-
-
Hymes, K.B.1
Karpatkin, S.2
-
54
-
-
84866781580
-
The pathogenesis of HIV-related thrombotic thrombocytopenic purpura - is it different? ISBT
-
Series 2006;
-
Gunther K, Garizio D, Dhlamini B. The pathogenesis of HIV-related thrombotic thrombocytopenic purpura - is it different? ISBT Science Series 2006;1:246-250
-
Science
, vol.1
, pp. 246-250
-
-
Gunther, K.1
Garizio, D.2
Dhlamini, B.3
-
55
-
-
23944499570
-
Thrombotic thrombocytopenic purpura in HIV infected patients
-
Miller RF, Scully M, Cohen H, et al. Thrombotic thrombocytopenic purpura in HIV infected patients. Int J STD AIDS 2005;16:538-542
-
(2005)
Int J STD AIDS
, vol.16
, pp. 538-542
-
-
Miller, R.F.1
Scully, M.2
Cohen, H.3
-
56
-
-
0036125205
-
Willebrand factor-cleaving protease inhibitor in a patient with human immunodeficiency syndrome-associated thrombotic thrombocytopenic purpura
-
Sahud MA, Claster S, Liu L, Ero M, Harris K, von Furlan M. Willebrand factor-cleaving protease inhibitor in a patient with human immunodeficiency syndrome-associated thrombotic thrombocytopenic purpura. Br J Haematol 2002;116:909-911
-
(2002)
Br J Haematol
, vol.116
, pp. 909-911
-
-
Sahud, M.A.1
Claster, S.2
Liu, L.3
Ero, M.4
Harris, K.5
von Furlan, M.6
-
57
-
-
34548135253
-
ADAMTS13 activity and the presence of acquired inhibitors in human immunodeficiency virus-related thrombotic thrombocytopenic purpura
-
Gunther K, Garizio D, Nesara P. ADAMTS13 activity and the presence of acquired inhibitors in human immunodeficiency virus-related thrombotic thrombocytopenic purpura. Transfusion 2007;47:1710-1716
-
(2007)
Transfusion
, vol.47
, pp. 1710-1716
-
-
Gunther, K.1
Garizio, D.2
Nesara, P.3
-
58
-
-
0035885927
-
Specific von Willebrand factor-cleaving protease in thrombotic microangiopathy: A study of 111 cases
-
Veyradier A, Obert B, Houllier A, Meyer D, Girma JP. Specific von Willebrand factor-cleaving protease in thrombotic microangiopathy: a study of 111 cases. Blood 2001;98:1765-1772
-
(2001)
Blood
, vol.98
, pp. 1765-1772
-
-
Veyradier, A.1
Obert, B.2
Houllier, A.3
Meyer, D.4
Girma, J.P.5
-
59
-
-
0035035397
-
von Willebrand factor and von Willebrand factor-cleaving metalloprotease activity in Escherichia coli O157:H7-associated hemolytic uremic syndrome
-
Tsai HM, Chandler WL, Sarode R, et al. von Willebrand factor and von Willebrand factor-cleaving metalloprotease activity in Escherichia coli O157:H7-associated hemolytic uremic syndrome. Pediatr Res 2001;49:653-659
-
(2001)
Pediatr Res
, vol.49
, pp. 653-659
-
-
Tsai, H.M.1
Chandler, W.L.2
Sarode, R.3
-
60
-
-
33744814937
-
Hemolytic uremic syndrome: An overview
-
Amirlak I, Amirlak B. Hemolytic uremic syndrome: an overview. Nephrologie 2006;11:213-218
-
(2006)
Nephrologie
, vol.11
, pp. 213-218
-
-
Amirlak, I.1
Amirlak, B.2
-
61
-
-
0037339175
-
Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome
-
Veyradier A, Obert B, Haddad E, et al. Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome. J Pediatr 2003;142:310-317
-
(2003)
J Pediatr
, vol.142
, pp. 310-317
-
-
Veyradier, A.1
Obert, B.2
Haddad, E.3
-
62
-
-
34248187207
-
Overlapping features of thrombotic thrombocytopenic purpura and systemic lupus erythematosus
-
George JN, Vesely SK, James JA. Overlapping features of thrombotic thrombocytopenic purpura and systemic lupus erythematosus. South Med J 2007;100:512-514
-
(2007)
South Med J
, vol.100
, pp. 512-514
-
-
George, J.N.1
Vesely, S.K.2
James, J.A.3
-
63
-
-
0034861756
-
Acquired deficiency of von Willebrand factor-cleaving protease in a patient suffering from acute systemic lupus erythematosus
-
Gungor R, Furlan M, Lammle B, Kuhn F, Seger RA. Acquired deficiency of von Willebrand factor-cleaving protease in a patient suffering from acute systemic lupus erythematosus. Rheumatology 2001;40:940-942
-
(2001)
Rheumatology
, vol.40
, pp. 940-942
-
-
Gungor, R.1
Furlan, M.2
Lammle, B.3
Kuhn, F.4
Seger, R.A.5
-
64
-
-
0036024145
-
Occurrence of thrombotic thrombocytopenic purpura in a systemic lupus erythematosus patient with antiphospholipid antibodies in association with a decreased activity of von Willebrand factor-cleaving protease
-
Matsuda J, Sanaka T, Gohchi K, et al. Occurrence of thrombotic thrombocytopenic purpura in a systemic lupus erythematosus patient with antiphospholipid antibodies in association with a decreased activity of von Willebrand factor-cleaving protease. Lupus 2002;11:463-464
-
(2002)
Lupus
, vol.11
, pp. 463-464
-
-
Matsuda, J.1
Sanaka, T.2
Gohchi, K.3
-
65
-
-
0141649437
-
Von Willebrand factor cleaving protease (ADAMTS-13) in 123 patients with connective tissue diseases (systemic lupus erythematosus and systemic sclerosis)
-
Mannucci PM, Vanoli M, Forza I, Canciani MT, Scorza R. Von Willebrand factor cleaving protease (ADAMTS-13) in 123 patients with connective tissue diseases (systemic lupus erythematosus and systemic sclerosis). Haematologica 2003;88:914-918
-
(2003)
Haematologica
, vol.88
, pp. 914-918
-
-
Mannucci, P.M.1
Vanoli, M.2
Forza, I.3
Canciani, M.T.4
Scorza, R.5
-
66
-
-
8844286829
-
von Willebrand factor cleaving protease (ADAMTS-13) and ADAMTS-13 neutralizing autoantibodies in 100 patients with thrombotic thrombocytopenic purpura
-
Peyvandi F, Ferrari S, Lavoretano S, Canciani MT, Mannucci PM. von Willebrand factor cleaving protease (ADAMTS-13) and ADAMTS-13 neutralizing autoantibodies in 100 patients with thrombotic thrombocytopenic purpura. Br J Haematol 2004;127:433-439
-
(2004)
Br J Haematol
, vol.127
, pp. 433-439
-
-
Peyvandi, F.1
Ferrari, S.2
Lavoretano, S.3
Canciani, M.T.4
Mannucci, P.M.5
-
67
-
-
0742305180
-
Clinical usefulness of a functional assay for the von Willebrand factor cleaving protease (ADAMTS 13) and its inhibitor in a patient with thrombotic thrombocytopenic purpura
-
Rick ME, Austin H, Leitman SF, Krizek DM, Aronson DL. Clinical usefulness of a functional assay for the von Willebrand factor cleaving protease (ADAMTS 13) and its inhibitor in a patient with thrombotic thrombocytopenic purpura. Am J Hematol 2004;75:96-100
-
(2004)
Am J Hematol
, vol.75
, pp. 96-100
-
-
Rick, M.E.1
Austin, H.2
Leitman, S.F.3
Krizek, D.M.4
Aronson, D.L.5
-
68
-
-
26844502395
-
Acquired thrombotic thrombocytopenic purpura as the presenting symptom of systemic lupus erythematosus. Successful treatment with plasma exchange and immunosuppression-report of two cases
-
Starck M, Abedinpour F, Dendorfer U, et al. Acquired thrombotic thrombocytopenic purpura as the presenting symptom of systemic lupus erythematosus. Successful treatment with plasma exchange and immunosuppression-report of two cases. Eur J Haematol 2005;75:436-440
-
(2005)
Eur J Haematol
, vol.75
, pp. 436-440
-
-
Starck, M.1
Abedinpour, F.2
Dendorfer, U.3
-
69
-
-
34547880378
-
Successful treatment of refractory thrombotic thrombocytopenic purpura with cyclosporin and corticosteroids in a patient with systemic lupus erythematosus and antibodies to ADAMTS13
-
Enami T, Suzuki T, Ito S, et al. Successful treatment of refractory thrombotic thrombocytopenic purpura with cyclosporin and corticosteroids in a patient with systemic lupus erythematosus and antibodies to ADAMTS13. Intern Med 2007;46:1033-1037
-
(2007)
Intern Med
, vol.46
, pp. 1033-1037
-
-
Enami, T.1
Suzuki, T.2
Ito, S.3
-
70
-
-
23744486523
-
ADAMTS13 autoantibodies in patients with thrombotic microangiopathies and other immunomediated diseases
-
Rieger M, Mannucci PM, Kremer Hovinga JA, et al. ADAMTS13 autoantibodies in patients with thrombotic microangiopathies and other immunomediated diseases. Blood 2005;106:1262-1267
-
(2005)
Blood
, vol.106
, pp. 1262-1267
-
-
Rieger, M.1
Mannucci, P.M.2
Kremer Hovinga, J.A.3
-
71
-
-
33846406399
-
Decreased ADAMTS13 activity in plasma from patients with thrombotic thrombocytopenic purpura
-
Kobayashi T, Wada H, Kamikura Y, et al. Decreased ADAMTS13 activity in plasma from patients with thrombotic thrombocytopenic purpura. Thromb Res 2007;119:447-452
-
(2007)
Thromb Res
, vol.119
, pp. 447-452
-
-
Kobayashi, T.1
Wada, H.2
Kamikura, Y.3
-
72
-
-
5644272713
-
Thrombotic thrombocytopenic purpura with severe ADAMTS-13 deficiency in two patients with primary antiphospholipid syndrome
-
Amoura Z, Costedoat-Chalumeau N, Veyradier A, et al. Thrombotic thrombocytopenic purpura with severe ADAMTS-13 deficiency in two patients with primary antiphospholipid syndrome. Arthritis Rheum 2004;50:3260-3264
-
(2004)
Arthritis Rheum
, vol.50
, pp. 3260-3264
-
-
Amoura, Z.1
Costedoat-Chalumeau, N.2
Veyradier, A.3
-
73
-
-
33747835305
-
Deficient activity of von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura in the setting of adult-onset Still's disease
-
Hirata S, Okamoto H, Ohta S, et al. Deficient activity of von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura in the setting of adult-onset Still's disease. Rheumatology 2006;45:1046-1047
-
(2006)
Rheumatology
, vol.45
, pp. 1046-1047
-
-
Hirata, S.1
Okamoto, H.2
Ohta, S.3
-
74
-
-
33748552315
-
Analyses of ADAMTS13 activity and its inhibitor in patients with thrombotic thrombocytopenic purpura secondary to connective tissue diseases: Observations in a single hospital
-
Sato T, Hanaoka R, Ohshima M, et al. Analyses of ADAMTS13 activity and its inhibitor in patients with thrombotic thrombocytopenic purpura secondary to connective tissue diseases: observations in a single hospital. Clin Exp Rheumatol 2006;24:454-455
-
(2006)
Clin Exp Rheumatol
, vol.24
, pp. 454-455
-
-
Sato, T.1
Hanaoka, R.2
Ohshima, M.3
-
75
-
-
33645732493
-
Alteration of ADAMTS13 antigen levels in patients with idiopathic thrombotic thrombocytopenic purpura, idiopathic thrombocytopenic purpura and systemic lupus erythematosus
-
Liu F, Feys HB, Dong N, Zhao Y, Ruan C. Alteration of ADAMTS13 antigen levels in patients with idiopathic thrombotic thrombocytopenic purpura, idiopathic thrombocytopenic purpura and systemic lupus erythematosus. Thromb Haemost 2006;95:749-750
-
(2006)
Thromb Haemost
, vol.95
, pp. 749-750
-
-
Liu, F.1
Feys, H.B.2
Dong, N.3
Zhao, Y.4
Ruan, C.5
-
76
-
-
3242705780
-
Reseau d'Etude des Microangiopathies Thrombotiques de l'Adulte. Severe ADAMTS13 deficiency in adult idiopathic thrombotic microangiopathies defines a subset of patients characterized by various autoimmune manifestations, lower platelet count, and mild renal involvement
-
Coppo P, Bengoufa D, Veyradier A, et al. Reseau d'Etude des Microangiopathies Thrombotiques de l'Adulte. Severe ADAMTS13 deficiency in adult idiopathic thrombotic microangiopathies defines a subset of patients characterized by various autoimmune manifestations, lower platelet count, and mild renal involvement. Medicine (Baltimore) 2004;83:233-244
-
(2004)
Medicine (Baltimore)
, vol.83
, pp. 233-244
-
-
Coppo, P.1
Bengoufa, D.2
Veyradier, A.3
-
77
-
-
30344470197
-
Drug-induced thrombotic microangiopathy
-
Zakarija A, Bennet C. Drug-induced thrombotic microangiopathy. Semin Thromb Hemost 2005;31:681-690
-
(2005)
Semin Thromb Hemost
, vol.31
, pp. 681-690
-
-
Zakarija, A.1
Bennet, C.2
-
78
-
-
2542490269
-
Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura
-
Zheng XL, Kaufman RM, Goodnough LT, Sadler JE. Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura. Blood 2004;103:4043-4049
-
(2004)
Blood
, vol.103
, pp. 4043-4049
-
-
Zheng, X.L.1
Kaufman, R.M.2
Goodnough, L.T.3
Sadler, J.E.4
-
79
-
-
10744222930
-
Von Willebrand factor-cleaving protease activity in thrombotic microangiopathy after living donor liver transplantation: A case report
-
Nakazawa Y, Hashikura Y, Urata K, et al. Von Willebrand factor-cleaving protease activity in thrombotic microangiopathy after living donor liver transplantation: a case report. Liver Transpl 2003;9:1328-1333
-
(2003)
Liver Transpl
, vol.9
, pp. 1328-1333
-
-
Nakazawa, Y.1
Hashikura, Y.2
Urata, K.3
-
80
-
-
0034660472
-
Thrombotic thrombocytopenic purpura associated with clopidogrel
-
Bennett CL, Connors JM, Carwile JM, et al. Thrombotic thrombocytopenic purpura associated with clopidogrel. N Engl J Med 2000;342:1773-1777
-
(2000)
N Engl J Med
, vol.342
, pp. 1773-1777
-
-
Bennett, C.L.1
Connors, J.M.2
Carwile, J.M.3
-
81
-
-
10744224391
-
Clopidogrelassociated TTP: An update of pharmacovigilance efforts conducted by independent researchers, pharmaceutical suppliers, and the Food and Drug Administration
-
Zakarija A, Bandarenko N, Pandey DK, et al. Clopidogrelassociated TTP: an update of pharmacovigilance efforts conducted by independent researchers, pharmaceutical suppliers, and the Food and Drug Administration. Stroke 2004;35:533-537
-
(2004)
Stroke
, vol.35
, pp. 533-537
-
-
Zakarija, A.1
Bandarenko, N.2
Pandey, D.K.3
-
82
-
-
0034674030
-
Antibody inhibitors to von Willebrand factor metalloproteinase and increased binding of von Willebrand factor to platelets in ticlopidine-associated thrombotic thrombocytopenic purpura
-
Tsai HM, Rice L, Sarode R, Chow TW, Moake JL. Antibody inhibitors to von Willebrand factor metalloproteinase and increased binding of von Willebrand factor to platelets in ticlopidine-associated thrombotic thrombocytopenic purpura. Ann Intern Med 2000;132:794-799
-
(2000)
Ann Intern Med
, vol.132
, pp. 794-799
-
-
Tsai, H.M.1
Rice, L.2
Sarode, R.3
Chow, T.W.4
Moake, J.L.5
-
83
-
-
0032055447
-
Thrombotic thrombocytopenic purpura associated with ticlopidine. A review of 60 cases
-
Bennett CL, Weinberg PD, Rozenberg-Ben-Dror K, Yarnold PR, Kwaan HC, Green D. Thrombotic thrombocytopenic purpura associated with ticlopidine. A review of 60 cases. Ann Intern Med 1998;128:541-544
-
(1998)
Ann Intern Med
, vol.128
, pp. 541-544
-
-
Bennett, C.L.1
Weinberg, P.D.2
Rozenberg-Ben-Dror, K.3
Yarnold, P.R.4
Kwaan, H.C.5
Green, D.6
-
84
-
-
0035491909
-
Ticlopidine-associated thrombotic thrombocytopenic purpura with an IgG-type inhibitor to von Willebrand factor-cleaving protease activity
-
Sugio Y, Okamura T, Shimoda K, et al. Ticlopidine-associated thrombotic thrombocytopenic purpura with an IgG-type inhibitor to von Willebrand factor-cleaving protease activity. Int J Hematol 2001;74:347-351
-
(2001)
Int J Hematol
, vol.74
, pp. 347-351
-
-
Sugio, Y.1
Okamura, T.2
Shimoda, K.3
-
85
-
-
34548542028
-
-
Bennett CL, Kim B, Zakarija Aet alSERF-TTP Research Group. Two mechanistic pathways for thienopyridine-associated thrombotic thrombocytopenic purpura: a report from the SERF-TTP Research Group and the RADAR Project. J Am Coll Cardiol 2007;50:1138-1143
-
Bennett CL, Kim B, Zakarija Aet alSERF-TTP Research Group. Two mechanistic pathways for thienopyridine-associated thrombotic thrombocytopenic purpura: a report from the SERF-TTP Research Group and the RADAR Project. J Am Coll Cardiol 2007;50:1138-1143
-
-
-
-
86
-
-
0024391413
-
Cancer-associated hemolytic-uremic syndrome: Analysis of 85 cases from a national registry
-
Lesesne JB, Rothschild N, Erickson B, et al. Cancer-associated hemolytic-uremic syndrome: analysis of 85 cases from a national registry. J Clin Oncol 1989;7:781-789
-
(1989)
J Clin Oncol
, vol.7
, pp. 781-789
-
-
Lesesne, J.B.1
Rothschild, N.2
Erickson, B.3
-
87
-
-
0021907561
-
Carcinoma-associated hemolytic-uremic syndrome: A complication of mitomycin C chemotherapy
-
Cantrell JE, Phillips TM, Schein PS. Carcinoma-associated hemolytic-uremic syndrome: a complication of mitomycin C chemotherapy. J Clin Oncol 1985;3:723-734
-
(1985)
J Clin Oncol
, vol.3
, pp. 723-734
-
-
Cantrell, J.E.1
Phillips, T.M.2
Schein, P.S.3
-
88
-
-
0029563176
-
Hemostatic abnormalities and increased vascular endothelial cell markers in patients with red cell fragmentation syndrome induced by mitomycin C
-
Nagaya S, Wada H, Oka K, et al. Hemostatic abnormalities and increased vascular endothelial cell markers in patients with red cell fragmentation syndrome induced by mitomycin C. Am J Hematol 1995;50:237-243
-
(1995)
Am J Hematol
, vol.50
, pp. 237-243
-
-
Nagaya, S.1
Wada, H.2
Oka, K.3
-
89
-
-
0033134916
-
A review of hemolytic uremic syndrome in patients treated with gemcitabine therapy
-
Fung MC, Storniolo AM, Nguyen B, Anting M, Brookfield W, Vigil J. A review of hemolytic uremic syndrome in patients treated with gemcitabine therapy. Cancer 1999;85:2023-2032
-
(1999)
Cancer
, vol.85
, pp. 2023-2032
-
-
Fung, M.C.1
Storniolo, A.M.2
Nguyen, B.3
Anting, M.4
Brookfield, W.5
Vigil, J.6
-
90
-
-
2642566772
-
Gemcitabine-associated thrombotic microangiopathy
-
Humphreys BD, Sharman JP, Henderson JM, et al. Gemcitabine-associated thrombotic microangiopathy. Cancer 2004;100:2664-2670
-
(2004)
Cancer
, vol.100
, pp. 2664-2670
-
-
Humphreys, B.D.1
Sharman, J.P.2
Henderson, J.M.3
-
91
-
-
0033564449
-
Thrombotic microangiopathy associated with interferon therapy for patients with chronic myelogenous leukemia: Coincidence or true side effect?
-
Ravandi-Kashani F, Cortes J, Talpaz M, Kantarjian HM. Thrombotic microangiopathy associated with interferon therapy for patients with chronic myelogenous leukemia: coincidence or true side effect? Cancer 1999;85:2583-2588
-
(1999)
Cancer
, vol.85
, pp. 2583-2588
-
-
Ravandi-Kashani, F.1
Cortes, J.2
Talpaz, M.3
Kantarjian, H.M.4
-
92
-
-
0037346638
-
Vascular events associated with alpha interferon therapy
-
Al-Zahrani H, Gupta V, Minden MD, Messner HA, Lipton JH. Vascular events associated with alpha interferon therapy. Leuk Lymphoma 2003;44:471-475
-
(2003)
Leuk Lymphoma
, vol.44
, pp. 471-475
-
-
Al-Zahrani, H.1
Gupta, V.2
Minden, M.D.3
Messner, H.A.4
Lipton, J.H.5
-
93
-
-
0035909844
-
Quinine-associated thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: Frequency, clinical features, and long-term outcomes
-
Kojouri K, Vesely SK, George JN. Quinine-associated thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: frequency, clinical features, and long-term outcomes. Ann Intern Med 2001;135:1047-1051
-
(2001)
Ann Intern Med
, vol.135
, pp. 1047-1051
-
-
Kojouri, K.1
Vesely, S.K.2
George, J.N.3
-
94
-
-
0346122960
-
Quinine induced HUS-TTP: An unusual presentation
-
Baliga RS, Wingo CS. Quinine induced HUS-TTP: an unusual presentation. Am J Med Sci 2003;326:378-380
-
(2003)
Am J Med Sci
, vol.326
, pp. 378-380
-
-
Baliga, R.S.1
Wingo, C.S.2
-
95
-
-
0026100473
-
Quinine-induced immune thrombocytopenia associated with hemolytic uremic syndrome: A new clinical entity
-
Gottschall JL, Elliot W, Lianos E, McFarland JG, Wolfmeyer K, Aster RH. Quinine-induced immune thrombocytopenia associated with hemolytic uremic syndrome: a new clinical entity. Blood 1991;77:306-310
-
(1991)
Blood
, vol.77
, pp. 306-310
-
-
Gottschall, J.L.1
Elliot, W.2
Lianos, E.3
McFarland, J.G.4
Wolfmeyer, K.5
Aster, R.H.6
-
96
-
-
0028131634
-
Quinine-induced immune thrombocytopenia with hemolytic uremic syndrome: Clinical and serological findings in nine patients and review of literature
-
Gottschall JL, Neahring B, McFarland JG, Wu GG, Weitekamp LA, Aster RH. Quinine-induced immune thrombocytopenia with hemolytic uremic syndrome: clinical and serological findings in nine patients and review of literature. Am J Hematol 1994;47:283-289
-
(1994)
Am J Hematol
, vol.47
, pp. 283-289
-
-
Gottschall, J.L.1
Neahring, B.2
McFarland, J.G.3
Wu, G.G.4
Weitekamp, L.A.5
Aster, R.H.6
-
97
-
-
1642539974
-
Thienopyridine-linked thrombotic microangiopathy association with endothelial cell apoptosis and activation of MAP kinase signalling cascades
-
Mauro M, Zlatopolskiy A, Raife TJ, Laurence J. Thienopyridine-linked thrombotic microangiopathy association with endothelial cell apoptosis and activation of MAP kinase signalling cascades. Br J Haematol 2004;124:200-210
-
(2004)
Br J Haematol
, vol.124
, pp. 200-210
-
-
Mauro, M.1
Zlatopolskiy, A.2
Raife, T.J.3
Laurence, J.4
-
98
-
-
0034824687
-
Drug-associated thrombotic thrombocytopenic purpura-hemolytic uremic syndrome
-
Medina PJ, Sipols JM, George JN. Drug-associated thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Curr Opin Hematol 2001;8:286-293
-
(2001)
Curr Opin Hematol
, vol.8
, pp. 286-293
-
-
Medina, P.J.1
Sipols, J.M.2
George, J.N.3
-
99
-
-
0042703238
-
The association of pregnancy with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome
-
George JN. The association of pregnancy with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Curr Opin Hematol 2003;10:339-344
-
(2003)
Curr Opin Hematol
, vol.10
, pp. 339-344
-
-
George, J.N.1
-
100
-
-
33750994949
-
Acute activation of the endothelium results in increased levels of active von Willebrand factor in hemolysis, elevated liver enzymes and low platelets (HELLP) syndrome
-
Hulstein JJ, van Runnard Heimel PJ, Franx A, et al. Acute activation of the endothelium results in increased levels of active von Willebrand factor in hemolysis, elevated liver enzymes and low platelets (HELLP) syndrome. J Thromb Haemost 2006;4:2569-2575
-
(2006)
J Thromb Haemost
, vol.4
, pp. 2569-2575
-
-
Hulstein, J.J.1
van Runnard Heimel, P.J.2
Franx, A.3
-
101
-
-
0141813562
-
Mild to moderate reduction of a von Willebrand factor cleaving protease (ADAMTS-13) in pregnant women with HELLP microangiopathic syndrome
-
Lattuada A, Rossi E, Calzarossa C, Candolfi R, Mannucci PM. Mild to moderate reduction of a von Willebrand factor cleaving protease (ADAMTS-13) in pregnant women with HELLP microangiopathic syndrome. Haematologica 2003;88:1029-1034
-
(2003)
Haematologica
, vol.88
, pp. 1029-1034
-
-
Lattuada, A.1
Rossi, E.2
Calzarossa, C.3
Candolfi, R.4
Mannucci, P.M.5
-
103
-
-
0035048637
-
Low activity of von Willebrand factor-cleaving protease is not restricted to patients suffering from thrombotic thrombocytopenic purpura
-
Loof AH, van Vliet HH, Kappers-Klunne MC. Low activity of von Willebrand factor-cleaving protease is not restricted to patients suffering from thrombotic thrombocytopenic purpura. Br J Haematol 2001;112:1087-1088
-
(2001)
Br J Haematol
, vol.112
, pp. 1087-1088
-
-
Loof, A.H.1
van Vliet, H.H.2
Kappers-Klunne, M.C.3
-
104
-
-
0037100531
-
Von Willebrand factor-cleaving protease (ADAMTS13) in thrombocytopenic disorders: A severely deficient activity is specific for thrombotic thrombocytopenic purpura
-
Bianchi V, Robles R, Alberio L, Furlan M, Lammle B. Von Willebrand factor-cleaving protease (ADAMTS13) in thrombocytopenic disorders: a severely deficient activity is specific for thrombotic thrombocytopenic purpura. Blood 2002;100:710-713
-
(2002)
Blood
, vol.100
, pp. 710-713
-
-
Bianchi, V.1
Robles, R.2
Alberio, L.3
Furlan, M.4
Lammle, B.5
-
105
-
-
0035885931
-
Decreased von Willebrand factor protease activity associated with thrombocytopenic disorders
-
Moore JC, Hayward CP, Warkentin TE, Kelton JG. Decreased von Willebrand factor protease activity associated with thrombocytopenic disorders. Blood 2001;98:1842-1846
-
(2001)
Blood
, vol.98
, pp. 1842-1846
-
-
Moore, J.C.1
Hayward, C.P.2
Warkentin, T.E.3
Kelton, J.G.4
-
106
-
-
34247144637
-
Activation of endothelial cells, coagulation and fibrinolysis in children with Dengue virus infection
-
Sosothikul D, Seksarn P, Pongsewalak S, Thisyakorn U, Lusher J. Activation of endothelial cells, coagulation and fibrinolysis in children with Dengue virus infection. Thromb Haemost 2007;97:627-634
-
(2007)
Thromb Haemost
, vol.97
, pp. 627-634
-
-
Sosothikul, D.1
Seksarn, P.2
Pongsewalak, S.3
Thisyakorn, U.4
Lusher, J.5
-
107
-
-
33846291847
-
Increased von Willebrand factor over decreased ADAMTS13 activity may contribute to the development of liver disturbance and multiorgan failure in patients with alcoholic hepatitis
-
Matsuyama T, Uemura M, Ishikawa M, et al. Increased von Willebrand factor over decreased ADAMTS13 activity may contribute to the development of liver disturbance and multiorgan failure in patients with alcoholic hepatitis. Alcohol Clin Exp Res 2007;31(Suppl 1):S27-35
-
(2007)
Alcohol Clin Exp Res
, vol.31
, Issue.SUPPL. 1
-
-
Matsuyama, T.1
Uemura, M.2
Ishikawa, M.3
-
108
-
-
34447309717
-
ADAMTS13 activity to antigen ratio in physiological and pathological conditions associated with an increased risk of thrombosis
-
Feys HB, Canciani MT, Peyvandi F, Deckmyn H, Vanhoorelbeke K, Mannucci PM. ADAMTS13 activity to antigen ratio in physiological and pathological conditions associated with an increased risk of thrombosis. Br J Haematol 2007;138:534-540
-
(2007)
Br J Haematol
, vol.138
, pp. 534-540
-
-
Feys, H.B.1
Canciani, M.T.2
Peyvandi, F.3
Deckmyn, H.4
Vanhoorelbeke, K.5
Mannucci, P.M.6
-
109
-
-
3242701302
-
Plasma levels of von Willebrand factor regulate ADAMTS-13, its major cleaving protease
-
Mannucci PM, Capoferri C, Canciani MT. Plasma levels of von Willebrand factor regulate ADAMTS-13, its major cleaving protease. Br J Haematol 2004;126:213-218
-
(2004)
Br J Haematol
, vol.126
, pp. 213-218
-
-
Mannucci, P.M.1
Capoferri, C.2
Canciani, M.T.3
-
110
-
-
30444461242
-
Severe secondary deficiency of von Willebrand factor-cleaving protease (ADAMTS13) in patients with sepsis-induced disseminated intravascular coagulation: Its correlation with development of renal failure
-
Ono T, Mimuro J, Madoiwa S, et al. Severe secondary deficiency of von Willebrand factor-cleaving protease (ADAMTS13) in patients with sepsis-induced disseminated intravascular coagulation: its correlation with development of renal failure. Blood 2006;107:528-534
-
(2006)
Blood
, vol.107
, pp. 528-534
-
-
Ono, T.1
Mimuro, J.2
Madoiwa, S.3
-
111
-
-
33846901167
-
Acquired ADAMTS-13 deficiency in pediatric patients with severe sepsis
-
Nguyen TC, Liu A, Liu L, et al. Acquired ADAMTS-13 deficiency in pediatric patients with severe sepsis. Haematologica 2007;92:121-124
-
(2007)
Haematologica
, vol.92
, pp. 121-124
-
-
Nguyen, T.C.1
Liu, A.2
Liu, L.3
-
112
-
-
35448943220
-
ADAMTS-13, von Willebrand factor and related parameters in severe sepsis and septic shock
-
In press
-
Kremer Hovinga JA, Zeerleder S, Kessler P, et al. ADAMTS-13, von Willebrand factor and related parameters in severe sepsis and septic shock. J Thromb Haemost 2007; In press
-
(2007)
J Thromb Haemost
-
-
Kremer Hovinga, J.A.1
Zeerleder, S.2
Kessler, P.3
-
113
-
-
34748855578
-
Decreased ADAMTS-13 (A disintegrin-like and metalloprotease with thrombospondin type 1 repeats) is associated with a poor prognosis in sepsis-induced organ failure
-
Martin K, Borgel D, Lerolle N, et al. Decreased ADAMTS-13 (A disintegrin-like and metalloprotease with thrombospondin type 1 repeats) is associated with a poor prognosis in sepsis-induced organ failure. Crit Care Med 2007;35:2375-2382
-
(2007)
Crit Care Med
, vol.35
, pp. 2375-2382
-
-
Martin, K.1
Borgel, D.2
Lerolle, N.3
-
114
-
-
0035425365
-
Are increased levels of von Willebrand factor in chronic coronary heart disease caused by decrease in von Willebrand factor cleaving protease activity? A study by an immunoassay with antibody against intact bond 842Tyr-843Met of the von Willebrand factor protein
-
He S, Cao H, Magnusson CG, et al. Are increased levels of von Willebrand factor in chronic coronary heart disease caused by decrease in von Willebrand factor cleaving protease activity? A study by an immunoassay with antibody against intact bond 842Tyr-843Met of the von Willebrand factor protein. Thromb Res 2001;103:241-248
-
(2001)
Thromb Res
, vol.103
, pp. 241-248
-
-
He, S.1
Cao, H.2
Magnusson, C.G.3
-
115
-
-
0344942587
-
Decreased levels of von Willebrand factor-cleaving protease in coronary heart disease and thrombotic thrombocytopenic purpura: Study of a simplified method for assaying the enzyme activity based on ristocetin-induced platelet aggregation
-
Yoo G, Blomback M, Schenck-Gustafsson K, He S. Decreased levels of von Willebrand factor-cleaving protease in coronary heart disease and thrombotic thrombocytopenic purpura: study of a simplified method for assaying the enzyme activity based on ristocetin-induced platelet aggregation. Br J Haematol 2003;121:123-129
-
(2003)
Br J Haematol
, vol.121
, pp. 123-129
-
-
Yoo, G.1
Blomback, M.2
Schenck-Gustafsson, K.3
He, S.4
-
116
-
-
33750058829
-
Reduced von Willebrand factor-cleaving protease (ADAMTS13) activity in acute myocardial infarction
-
Kaikita K, Soejima K, Matsukawa M, Nakagaki T, Ogawa H. Reduced von Willebrand factor-cleaving protease (ADAMTS13) activity in acute myocardial infarction. J Thromb Haemost 2006;4:2490-2493
-
(2006)
J Thromb Haemost
, vol.4
, pp. 2490-2493
-
-
Kaikita, K.1
Soejima, K.2
Matsukawa, M.3
Nakagaki, T.4
Ogawa, H.5
-
117
-
-
33847380326
-
ADAMTS13 and von Willebrand factor and the risk of myocardial infarction in men
-
Chion CK, Doggen CJ, Crawley JT, Lane DA, Rosendaal FR. ADAMTS13 and von Willebrand factor and the risk of myocardial infarction in men. Blood 2007;109:1998-2000
-
(2007)
Blood
, vol.109
, pp. 1998-2000
-
-
Chion, C.K.1
Doggen, C.J.2
Crawley, J.T.3
Lane, D.A.4
Rosendaal, F.R.5
-
118
-
-
34547931246
-
Serial changes in von Willebrand factor-cleaving protease (ADAMTS13) and prognosis after acute myocardial infarction
-
Matsukawa M, Kaikita K, Soejima K, et al. Serial changes in von Willebrand factor-cleaving protease (ADAMTS13) and prognosis after acute myocardial infarction. Am J Cardiol 2007;100:758-763
-
(2007)
Am J Cardiol
, vol.100
, pp. 758-763
-
-
Matsukawa, M.1
Kaikita, K.2
Soejima, K.3
-
119
-
-
3042538950
-
The frequency of P475S polymorphism in von Willebrand factor-cleaving protease in the Chinese population and its relevance to arterial thrombotic disorders
-
Ruan C, Dai L, Su J, Wang Z, Ruan C. The frequency of P475S polymorphism in von Willebrand factor-cleaving protease in the Chinese population and its relevance to arterial thrombotic disorders. Thromb Haemost 2004;91:1257-1258
-
(2004)
Thromb Haemost
, vol.91
, pp. 1257-1258
-
-
Ruan, C.1
Dai, L.2
Su, J.3
Wang, Z.4
Ruan, C.5
-
120
-
-
33750949797
-
High von Willebrand factor levels increase the risk of first ischemic stroke: Influence of ADAMTS13, inflammation, and genetic variability
-
Bongers TN, de Maat MP, van Goor ML, et al. High von Willebrand factor levels increase the risk of first ischemic stroke: influence of ADAMTS13, inflammation, and genetic variability. Stroke 2006;37:2672-2677
-
(2006)
Stroke
, vol.37
, pp. 2672-2677
-
-
Bongers, T.N.1
de Maat, M.P.2
van Goor, M.L.3
-
121
-
-
20844458787
-
Opposite changes of ADAMTS-13 and von Willebrand factor after cardiac surgery
-
Mannucci PM, Parolari A, Canciani MT, Alemanni F, Camera M. Opposite changes of ADAMTS-13 and von Willebrand factor after cardiac surgery. J Thromb Haemost 2005;3:397-399
-
(2005)
J Thromb Haemost
, vol.3
, pp. 397-399
-
-
Mannucci, P.M.1
Parolari, A.2
Canciani, M.T.3
Alemanni, F.4
Camera, M.5
-
122
-
-
33846946851
-
Relatively increased von Willebrand factor activity after off-pump coronary artery bypass graft surgery
-
Lo B, Nierich AP, Kalkman CJ, Fijnheer R. Relatively increased von Willebrand factor activity after off-pump coronary artery bypass graft surgery. Thromb Haemost 2007;97:21-26
-
(2007)
Thromb Haemost
, vol.97
, pp. 21-26
-
-
Lo, B.1
Nierich, A.P.2
Kalkman, C.J.3
Fijnheer, R.4
-
123
-
-
30344483206
-
Pathogenesis of thrombotic thrombocytopenic purpura: ADAMTS13 deficiency and beyond
-
Lian EC. Pathogenesis of thrombotic thrombocytopenic purpura: ADAMTS13 deficiency and beyond. Semin Thromb Hemost 2005;31:625-632
-
(2005)
Semin Thromb Hemost
, vol.31
, pp. 625-632
-
-
Lian, E.C.1
|