-
1
-
-
84906077328
-
Syndromes of thrombotic microangiopathy
-
COI: 1:CAS:528:DC%2BC2cXhs1equ7bE, PID: 25119611
-
George JN, Nester CM (2014) Syndromes of thrombotic microangiopathy. N Engl J Med 371:654–666
-
(2014)
N Engl J Med
, vol.371
, pp. 654-666
-
-
George, J.N.1
Nester, C.M.2
-
2
-
-
0029925856
-
Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis
-
COI: 1:CAS:528:DyaK28XivFGhtb4%3D, PID: 8639781
-
Furlan M, Robles R, Lammle B (1996) 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)
Blood
, vol.87
, pp. 4223-4234
-
-
Furlan, M.1
Robles, R.2
Lammle, B.3
-
3
-
-
0029878123
-
Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion
-
COI: 1:CAS:528:DyaK28XivFGhtb8%3D, PID: 8639782
-
Tsai HM (1996) Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion. Blood 87:4235–4244
-
(1996)
Blood
, vol.87
, pp. 4235-4244
-
-
Tsai, H.M.1
-
4
-
-
0030973267
-
Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura
-
COI: 1:CAS:528:DyaK2sXivVOntro%3D, PID: 9129011
-
Furlan M, Robles R, Solenthaler M, Wassmer M, Sandoz P, Lammle B (1997) Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura. Blood 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
-
5
-
-
0035798582
-
Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura
-
COI: 1:CAS:528:DC%2BD3MXosVKgsLw%3D, PID: 11557746
-
Zheng X, Chung D, Takayama TK, Majerus EM, Sadler JE, Fujikawa K (2001) Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura. J Biol Chem 276:41059–41063
-
(2001)
J Biol Chem
, vol.276
, pp. 41059-41063
-
-
Zheng, X.1
Chung, D.2
Takayama, T.K.3
Majerus, E.M.4
Sadler, J.E.5
Fujikawa, K.6
-
6
-
-
0020428664
-
Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura
-
COI: 1:STN:280:DyaL3s%2Fjs1yksA%3D%3D, PID: 6813740
-
Moake JL, Rudy CK, Troll JH, Weinstein MJ, Colannino NM, Azocar J, Seder RH, Hong SL, Deykin D (1982) Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura. N Engl J Med 307:1432–1435
-
(1982)
N Engl J Med
, vol.307
, pp. 1432-1435
-
-
Moake, J.L.1
Rudy, C.K.2
Troll, J.H.3
Weinstein, M.J.4
Colannino, N.M.5
Azocar, J.6
Seder, R.H.7
Hong, S.L.8
Deykin, D.9
-
7
-
-
0035807348
-
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
-
COI: 1:CAS:528:DC%2BD3MXnsFyit70%3D, PID: 11586351
-
Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V, Stabler SP, Sabio H, Bouhassira EE, Upshaw JD Jr, Ginsburg D, Tsai HM (2001) Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature 413:488–494
-
(2001)
Nature
, vol.413
, pp. 488-494
-
-
Levy, G.G.1
Nichols, W.C.2
Lian, E.C.3
Foroud, T.4
McClintick, J.N.5
McGee, B.M.6
Yang, A.Y.7
Siemieniak, D.R.8
Stark, K.R.9
Gruppo, R.10
Sarode, R.11
Shurin, S.B.12
Chandrasekaran, V.13
Stabler, S.P.14
Sabio, H.15
Bouhassira, E.E.16
Upshaw, J.D.17
Ginsburg, D.18
Tsai, H.M.19
-
8
-
-
0032569840
-
Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura
-
COI: 1:STN:280:DyaK1M%2Fjt1Sgsw%3D%3D, PID: 9828246
-
Tsai HM, Lian EC (1998) Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura. N Engl J Med 339:1585–1594
-
(1998)
N Engl J Med
, vol.339
, pp. 1585-1594
-
-
Tsai, H.M.1
Lian, E.C.2
-
9
-
-
84862498528
-
Unexpected frequency of Upshaw-Schulman syndrome in pregnancy-onset thrombotic thrombocytopenic purpura
-
COI: 1:CAS:528:DC%2BC38XhtVGns73P, PID: 22547583
-
Moatti-Cohen M, Garrec C, Wolf M, Boisseau P, Galicier L, Azoulay E, Stepanian A, Delmas Y, Rondeau E, Bezieau S, Coppo P, Veyradier A (2012) Unexpected frequency of Upshaw-Schulman syndrome in pregnancy-onset thrombotic thrombocytopenic purpura. Blood 119:5888–5897
-
(2012)
Blood
, vol.119
, pp. 5888-5897
-
-
Moatti-Cohen, M.1
Garrec, C.2
Wolf, M.3
Boisseau, P.4
Galicier, L.5
Azoulay, E.6
Stepanian, A.7
Delmas, Y.8
Rondeau, E.9
Bezieau, S.10
Coppo, P.11
Veyradier, A.12
-
10
-
-
84904095940
-
Thrombotic thrombocytopenic purpura and pregnancy: presentation, management, and subsequent pregnancy outcomes
-
COI: 1:CAS:528:DC%2BC2cXht1WktbrP, PID: 24859360
-
Scully M, Thomas M, Underwood M, Watson H, Langley K, Camilleri RS, Clark A, Creagh D, Rayment R, Mcdonald V, Roy A, Evans G, McGuckin S, Ni AF, Maclean R, Lester W, Nash M, Scott R, Brien O (2014) Thrombotic thrombocytopenic purpura and pregnancy: presentation, management, and subsequent pregnancy outcomes. Blood 124:211–219
-
(2014)
Blood
, vol.124
, pp. 211-219
-
-
Scully, M.1
Thomas, M.2
Underwood, M.3
Watson, H.4
Langley, K.5
Camilleri, R.S.6
Clark, A.7
Creagh, D.8
Rayment, R.9
Mcdonald, V.10
Roy, A.11
Evans, G.12
McGuckin, S.13
Ni, A.F.14
Maclean, R.15
Lester, W.16
Nash, M.17
Scott, R.18
Brien, O.19
-
11
-
-
84864041240
-
Residual plasmatic activity of ADAMTS13 is correlated with phenotype severity in congenital thrombotic thrombocytopenic purpura
-
COI: 1:CAS:528:DC%2BC38XhtFCktL%2FF, PID: 22529288
-
Lotta LA, Wu HM, Mackie IJ, Noris M, Veyradier A, Scully MA, Remuzzi G, Coppo P, Liesner R, Donadelli R, Loirat C, Gibbs RA, Horne A, Yang S, Garagiola I, Musallam KM, Peyvandi F (2012) Residual plasmatic activity of ADAMTS13 is correlated with phenotype severity in congenital thrombotic thrombocytopenic purpura. Blood 120:440–448
-
(2012)
Blood
, vol.120
, pp. 440-448
-
-
Lotta, L.A.1
Wu, H.M.2
Mackie, I.J.3
Noris, M.4
Veyradier, A.5
Scully, M.A.6
Remuzzi, G.7
Coppo, P.8
Liesner, R.9
Donadelli, R.10
Loirat, C.11
Gibbs, R.A.12
Horne, A.13
Yang, S.14
Garagiola, I.15
Musallam, K.M.16
Peyvandi, F.17
-
12
-
-
23744486523
-
ADAMTS13 autoantibodies in patients with thrombotic microangiopathies and other immunomediated diseases
-
COI: 1:CAS:528:DC%2BD2MXosVejtrw%3D, PID: 15890682
-
Rieger M, Mannucci PM, Kremer Hovinga JA, Herzog A, Gerstenbauer G, Konetschny C, Zimmermann K, Scharrer I, Peyvandi F, Galbusera M, Remuzzi G, Bohm M, Plaimauer B, Lammle B, Scheiflinger F (2005) ADAMTS13 autoantibodies in patients with thrombotic microangiopathies and other immunomediated diseases. Blood 106:1262–1267
-
(2005)
Blood
, vol.106
, pp. 1262-1267
-
-
Rieger, M.1
Mannucci, P.M.2
Kremer Hovinga, J.A.3
Herzog, A.4
Gerstenbauer, G.5
Konetschny, C.6
Zimmermann, K.7
Scharrer, I.8
Peyvandi, F.9
Galbusera, M.10
Remuzzi, G.11
Bohm, M.12
Plaimauer, B.13
Lammle, B.14
Scheiflinger, F.15
-
13
-
-
0026048114
-
Comparison of plasma exchange with plasma infusion in the treatment of thrombotic thrombocytopenic purpura. Canadian Apheresis Study Group
-
COI: 1:STN:280:DyaK3M3oslOnug%3D%3D, PID: 2062330
-
Rock GA, Shumak KH, Buskard NA, Blanchette VS, Kelton JG, Nair RC, Spasoff RA (1991) 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)
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
-
14
-
-
84899053379
-
How I treat: the clinical differentiation and initial treatment of adult patients with atypical hemolytic uremic syndrome
-
COI: 1:CAS:528:DC%2BC2cXntVejt7c%3D, PID: 24599547
-
Cataland SR, Wu HM (2014) How I treat: the clinical differentiation and initial treatment of adult patients with atypical hemolytic uremic syndrome. Blood 123:2478–2484
-
(2014)
Blood
, vol.123
, pp. 2478-2484
-
-
Cataland, S.R.1
Wu, H.M.2
-
15
-
-
33748342133
-
The use of intermediate purity factor VIII concentrate BPL 8Y as prophylaxis and treatment in congenital thrombotic thrombocytopenic purpura
-
PID: 16925793
-
Scully M, Gattens M, Khair K, Liesner R (2006) The use of intermediate purity factor VIII concentrate BPL 8Y as prophylaxis and treatment in congenital thrombotic thrombocytopenic purpura. Br J Haematol 135:101–104
-
(2006)
Br J Haematol
, vol.135
, pp. 101-104
-
-
Scully, M.1
Gattens, M.2
Khair, K.3
Liesner, R.4
-
16
-
-
84904127650
-
Preemptive rituximab infusions after remission efficiently prevent relapses in acquired thrombotic thrombocytopenic purpura
-
COI: 1:CAS:528:DC%2BC2cXht1WktbrO, PID: 24869941
-
Hie M, Gay J, Galicier L, Provot F, Presne C, Poullin P, Bonmarchand G, Wynckel A, Benhamou Y, Vanhille P, Servais A, Bordessoule D, Coindre JP, Hamidou M, Vernant JP, Veyradier A, Coppo P (2014) Preemptive rituximab infusions after remission efficiently prevent relapses in acquired thrombotic thrombocytopenic purpura. Blood 124:204–210
-
(2014)
Blood
, vol.124
, pp. 204-210
-
-
Hie, M.1
Gay, J.2
Galicier, L.3
Provot, F.4
Presne, C.5
Poullin, P.6
Bonmarchand, G.7
Wynckel, A.8
Benhamou, Y.9
Vanhille, P.10
Servais, A.11
Bordessoule, D.12
Coindre, J.P.13
Hamidou, M.14
Vernant, J.P.15
Veyradier, A.16
Coppo, P.17
-
17
-
-
84940002418
-
Caplacizumab, anti-VWF nanobody potentially changing the treatment paradigm in thrombotic thrombocytopenic purpura: results of the TITAN trial. In: Abstracts of the 56th ASH annual meeting and exposition, San Francisco, 6–9 December 2014, abstract no
-
Peyvandi F for the TITAN Investigators, Duby C
-
Peyvandi F for the TITAN Investigators, Duby C (2014) Caplacizumab, anti-VWF nanobody potentially changing the treatment paradigm in thrombotic thrombocytopenic purpura: results of the TITAN trial. In: Abstracts of the 56th ASH annual meeting and exposition, San Francisco, 6–9 December 2014, abstract no. 229
-
(2014)
-
-
|