-
2
-
-
84880799517
-
Complement therapy in atypical haemolytic uraemic syndrome (aHUS)
-
Wong EK, Goodship TH, Kavanagh D. Complement therapy in atypical haemolytic uraemic syndrome (aHUS). Mol Immunol. 2013;56(3):199-212.
-
(2013)
Mol Immunol
, vol.56
, Issue.3
, pp. 199-212
-
-
Wong, E.K.1
Goodship, T.H.2
Kavanagh, D.3
-
3
-
-
84878589219
-
Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome
-
Legendre CM, Licht C, Muus P, Greenbaum LA, Babu S, Bedrosian C, et al. Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome. N Engl J Med. 2013;368(23):2169-81.
-
(2013)
N Engl J Med
, vol.368
, Issue.23
, pp. 2169-2181
-
-
Legendre, C.M.1
Licht, C.2
Muus, P.3
Greenbaum, L.A.4
Babu, S.5
Bedrosian, C.6
-
4
-
-
0031970553
-
Genetic studies into inherited and sporadic hemolytic uremic syndrome
-
Warwicker P, Goodship TH, Donne RL, Pirson Y, Nicholls A, Ward RM, et al. Genetic studies into inherited and sporadic hemolytic uremic syndrome. Kidney Int. 1998;53(4):836-44.
-
(1998)
Kidney Int
, vol.53
, Issue.4
, pp. 836-844
-
-
Warwicker, P.1
Goodship, T.H.2
Donne, R.L.3
Pirson, Y.4
Nicholls, A.5
Ward, R.M.6
-
5
-
-
27744452766
-
Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome
-
Kavanagh D, Kemp EJ, Mayland E, Winney RJ, Duffield JS, Warwick G, et al. Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome. J Am Soc Nephrol. 2005;16(7):2150-5.
-
(2005)
J Am Soc Nephrol
, vol.16
, Issue.7
, pp. 2150-2155
-
-
Kavanagh, D.1
Kemp, E.J.2
Mayland, E.3
Winney, R.J.4
Duffield, J.S.5
Warwick, G.6
-
6
-
-
33747159590
-
Genetics of HUS: The impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome
-
Caprioli J, Noris M, Brioschi S, Pianetti G, Castelletti F, Bettinaglio P, et al. Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome. Blood. 2006;108(4):1267-79.
-
(2006)
Blood
, vol.108
, Issue.4
, pp. 1267-1279
-
-
Caprioli, J.1
Noris, M.2
Brioschi, S.3
Pianetti, G.4
Castelletti, F.5
Bettinaglio, P.6
-
7
-
-
54049137505
-
Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome
-
Fremeaux-Bacchi V, Miller EC, Liszewski MK, Strain L, Blouin J, Brown AL, et al. Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome. Blood. 2008;112(13):4948-52.
-
(2008)
Blood
, vol.112
, Issue.13
, pp. 4948-4952
-
-
Fremeaux-Bacchi, V.1
Miller, E.C.2
Liszewski, M.K.3
Strain, L.4
Blouin, J.5
Brown, A.L.6
-
8
-
-
33846094404
-
Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome
-
Goicoechea De Jorge E, Harris CL, Esparza-Gordillo J, Carreras L, Arranz EA, Garrido CA, et al. Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome. Proc Natl Acad Sci U S A. 2007;104(1):240-5.
-
(2007)
Proc Natl Acad Sci U S A.
, vol.104
, Issue.1
, pp. 240-245
-
-
Goicoechea De Jorge, E.1
Harris, C.L.2
Esparza-Gordillo, J.3
Carreras, L.4
Arranz, E.A.5
Garrido, C.A.6
-
9
-
-
67449119124
-
The binding of factor H to a complex of physiological polyanions and C3b on cells is impaired in atypical hemolytic uremic syndrome
-
Ferreira VP, Herbert AP, Cortes C, McKee KA, Blaum BS, Esswein ST, et al. The binding of factor H to a complex of physiological polyanions and C3b on cells is impaired in atypical hemolytic uremic syndrome. J Immunol. 2009;182(11):7009-18.
-
(2009)
J Immunol
, vol.182
, Issue.11
, pp. 7009-7018
-
-
Ferreira, V.P.1
Herbert, A.P.2
Cortes, C.3
McKee, K.A.4
Blaum, B.S.5
Esswein, S.T.6
-
10
-
-
84876044818
-
Genetics and outcome of atypical hemolytic uremic syndrome: A nationwide French series comparing children and adults
-
Fremeaux-Bacchi V, Fakhouri F, Garnier A, Bienaime F, Dragon-Durey MA, Ngo S, et al. Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults. Clin J Am Soc Nephrol. 2013;8(4):554-62.
-
(2013)
Clin J Am Soc Nephrol
, vol.8
, Issue.4
, pp. 554-562
-
-
Fremeaux-Bacchi, V.1
Fakhouri, F.2
Garnier, A.3
Bienaime, F.4
Dragon-Durey, M.A.5
Ngo, S.6
-
11
-
-
77958587405
-
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype
-
Noris M, Caprioli J, Bresin E, Mossali C, Pianetti G, Gamba S, et al. Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype. Clin J Am Soc Nephrol. 2010;5(10):1844-59.
-
(2010)
Clin J Am Soc Nephrol
, vol.5
, Issue.10
, pp. 1844-1859
-
-
Noris, M.1
Caprioli, J.2
Bresin, E.3
Mossali, C.4
Pianetti, G.5
Gamba, S.6
-
12
-
-
77952556624
-
Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations
-
Fakhouri F, Roumenina L, Provot F, Sallee M, Caillard S, Couzi L, et al. Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations. J Am Soc Nephrol. 2010;21(5):859-67.
-
(2010)
J Am Soc Nephrol
, vol.21
, Issue.5
, pp. 859-867
-
-
Fakhouri, F.1
Roumenina, L.2
Provot, F.3
Sallee, M.4
Caillard, S.5
Couzi, L.6
-
13
-
-
79953691827
-
Mutations in complement regulatory proteins predispose to preeclampsia: A genetic analysis of the PROMISSE cohort
-
Salmon JE, Heuser C, Triebwasser M, Liszewski MK, Kavanagh D, Roumenina L, et al. Mutations in complement regulatory proteins predispose to preeclampsia: a genetic analysis of the PROMISSE cohort. PLoS Med. 2011;8(3), e1001013.
-
(2011)
PLoS Med
, vol.8
, Issue.3
-
-
Salmon, J.E.1
Heuser, C.2
Triebwasser, M.3
Liszewski, M.K.4
Kavanagh, D.5
Roumenina, L.6
-
14
-
-
0028951539
-
Ocular involvement in haemolytic uraemic syndrome-case report and review of the literature
-
Eberhard OK, Labjuhn SO, Olbricht CJ. Ocular involvement in haemolytic uraemic syndrome-case report and review of the literature. Nephrol Dial Transplant. 1995;10(2):266-9.
-
(1995)
Nephrol Dial Transplant
, vol.10
, Issue.2
, pp. 266-269
-
-
Eberhard, O.K.1
Labjuhn, S.O.2
Olbricht, C.J.3
-
15
-
-
42049119459
-
Association between thrombotic microangiopathy and reduced ADAMTS13 activity in malignant hypertension
-
van den Born BJ, van der Hoeven NV, Groot E, Lenting PJ, Meijers JC, Levi M, et al. Association between thrombotic microangiopathy and reduced ADAMTS13 activity in malignant hypertension. Hypertension. 2008;51(4):862-6.
-
(2008)
Hypertension
, vol.51
, Issue.4
, pp. 862-866
-
-
Van Den Born, B.J.1
Van Der Hoeven, N.V.2
Groot, E.3
Lenting, P.J.4
Meijers, J.C.5
Levi, M.6
-
16
-
-
77956532403
-
Predictive features of severe acquired ADAMTS13 deficiency in idiopathic thrombotic microangiopathies: The French TMA reference center experience
-
Coppo P, Schwarzinger M, Buffet M, Wynckel A, Clabault K, Presne C, et al. Predictive features of severe acquired ADAMTS13 deficiency in idiopathic thrombotic microangiopathies: the French TMA reference center experience. PLoS One. 2010;5(4), e10208.
-
(2010)
PLoS One
, vol.5
, Issue.4
, pp. e10208
-
-
Coppo, P.1
Schwarzinger, M.2
Buffet, M.3
Wynckel, A.4
Clabault, K.5
Presne, C.6
-
17
-
-
84909590646
-
Renal recovery with eculizumab in atypical hemolytic uremic syndrome following prolonged dialysis
-
Povey H, Vundru R, Junglee N, Jibani M. Renal recovery with eculizumab in atypical hemolytic uremic syndrome following prolonged dialysis. Clin Nephrol. 2014;82(5):326-31.
-
(2014)
Clin Nephrol
, vol.82
, Issue.5
, pp. 326-331
-
-
Povey, H.1
Vundru, R.2
Junglee, N.3
Jibani, M.4
-
18
-
-
84908098893
-
Discontinuation of eculizumab maintenance treatment for atypical hemolytic uremic syndrome: A report of 10 cases
-
Ardissino G, Testa S, Possenti I, Tel F, Paglialonga F, Salardi S, et al. Discontinuation of eculizumab maintenance treatment for atypical hemolytic uremic syndrome: a report of 10 cases. Am J Kidney Dis. 2014;64(4):633-7.
-
(2014)
Am J Kidney Dis
, vol.64
, Issue.4
, pp. 633-637
-
-
Ardissino, G.1
Testa, S.2
Possenti, I.3
Tel, F.4
Paglialonga, F.5
Salardi, S.6
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