-
1
-
-
42649105187
-
Renal thrombotic microangiopathies induced by severe hypertension
-
Zhang, B., Xing, C., Yu, X., et al. Renal thrombotic microangiopathies induced by severe hypertension. Hypertens Res 31 (2008), 479–483.
-
(2008)
Hypertens Res
, vol.31
, pp. 479-483
-
-
Zhang, B.1
Xing, C.2
Yu, X.3
-
2
-
-
78651410434
-
The development of atypical hemolytic uremic syndrome depends on complement C5
-
de Jorge, E.G., Macor, P., Paixao-Cavalcante, D., et al. The development of atypical hemolytic uremic syndrome depends on complement C5. J Am Soc Nephrol 22 (2011), 137–145.
-
(2011)
J Am Soc Nephrol
, vol.22
, pp. 137-145
-
-
de Jorge, E.G.1
Macor, P.2
Paixao-Cavalcante, D.3
-
3
-
-
84908611206
-
Dynamics of complement activation in aHUS and how to monitor eculizumab therapy
-
Noris, M., Galbusera, M., Gastoldi, S., et al. Dynamics of complement activation in aHUS and how to monitor eculizumab therapy. Blood 124 (2014), 1715–1726.
-
(2014)
Blood
, vol.124
, pp. 1715-1726
-
-
Noris, M.1
Galbusera, M.2
Gastoldi, S.3
-
4
-
-
77958587405
-
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype
-
Noris, M., Caprioli, J., Bresin, E., et al. Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype. Clin J Am Soc Nephrol 5 (2010), 1844–1859.
-
(2010)
Clin J Am Soc Nephrol
, vol.5
, pp. 1844-1859
-
-
Noris, M.1
Caprioli, J.2
Bresin, E.3
-
5
-
-
77952682366
-
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome
-
Maga, T.K., Nishimura, C.J., Weaver, A.E., et al. Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. Hum Mutat 31 (2010), E1445–E1460.
-
(2010)
Hum Mutat
, vol.31
, pp. E1445-E1460
-
-
Maga, T.K.1
Nishimura, C.J.2
Weaver, A.E.3
-
6
-
-
80053572803
-
Age-related penetrance of hereditary atypical hemolytic uremic syndrome
-
Sullivan, M., Rybicki, L.A., Winter, A., et al. Age-related penetrance of hereditary atypical hemolytic uremic syndrome. Ann Hum Genet 75 (2011), 639–647.
-
(2011)
Ann Hum Genet
, vol.75
, pp. 639-647
-
-
Sullivan, M.1
Rybicki, L.A.2
Winter, A.3
-
7
-
-
34548400755
-
Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background
-
Bresin, E., Daina, E., Noris, M., et al., for the International Registry of Recurrent and Familial HUS/TTP. Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background. Clin J Am Soc Nephrol 1 (2006), 88–99.
-
(2006)
Clin J Am Soc Nephrol
, vol.1
, pp. 88-99
-
-
Bresin, E.1
Daina, E.2
Noris, M.3
-
8
-
-
84878589219
-
Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome
-
Legendre, C.M., Licht, C., Muus, P., et al. Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome. N Engl J Med 368 (2013), 2169–2181.
-
(2013)
N Engl J Med
, vol.368
, pp. 2169-2181
-
-
Legendre, C.M.1
Licht, C.2
Muus, P.3
-
9
-
-
84929128976
-
Efficacy and safety of eculizumab in atypical hemolytic uremic syndrome from 2-year extensions of phase 2 studies
-
Licht, C., Greenbaum, L.A., Muus, P., et al. Efficacy and safety of eculizumab in atypical hemolytic uremic syndrome from 2-year extensions of phase 2 studies. Kidney Int 87 (2015), 1061–1073.
-
(2015)
Kidney Int
, vol.87
, pp. 1061-1073
-
-
Licht, C.1
Greenbaum, L.A.2
Muus, P.3
-
10
-
-
84975266700
-
Terminal complement inhibitor eculizumab in adult patients with atypical hemolytic uremic syndrome: a single-arm, open-label trial
-
Fakhouri, F., Hourmant, M., Campistol, J.M., et al. Terminal complement inhibitor eculizumab in adult patients with atypical hemolytic uremic syndrome: a single-arm, open-label trial. Am J Kidney Dis 68 (2016), 84–93.
-
(2016)
Am J Kidney Dis
, vol.68
, pp. 84-93
-
-
Fakhouri, F.1
Hourmant, M.2
Campistol, J.M.3
-
11
-
-
0242601270
-
Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease
-
Caprioli, J., Castelletti, F., Bucchioni, S., et al., for the International Registry of Recurrent and Familial HUS/TTP. Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease. Hum Mol Genet 12 (2003), 3385–3395.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 3385-3395
-
-
Caprioli, J.1
Castelletti, F.2
Bucchioni, S.3
-
12
-
-
84874610717
-
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype
-
Bresin, E., Rurali, E., Caprioli, J., et al., for the European Working Party on Complement Genetics in Renal Diseases. Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype. J Am Soc Nephrol 24 (2013), 475–486.
-
(2013)
J Am Soc Nephrol
, vol.24
, pp. 475-486
-
-
Bresin, E.1
Rurali, E.2
Caprioli, J.3
-
13
-
-
0142250921
-
Thrombotic microangiopathy after renal transplantation in the United States
-
Reynolds, J.C., Agodoa, L.Y., Yuan, C.M., Abbott, K.C., Thrombotic microangiopathy after renal transplantation in the United States. Am J Kidney Dis 42 (2003), 1058–1068.
-
(2003)
Am J Kidney Dis
, vol.42
, pp. 1058-1068
-
-
Reynolds, J.C.1
Agodoa, L.Y.2
Yuan, C.M.3
Abbott, K.C.4
-
14
-
-
75749153964
-
Mutations in components of complement influence the outcome of factor I-associated atypical hemolytic uremic syndrome
-
Bienaime, F., Dragon-Durey, M.A., Regnier, C.H., et al. Mutations in components of complement influence the outcome of factor I-associated atypical hemolytic uremic syndrome. Kidney Int 77 (2010), 339–349.
-
(2010)
Kidney Int
, vol.77
, pp. 339-349
-
-
Bienaime, F.1
Dragon-Durey, M.A.2
Regnier, C.H.3
-
15
-
-
0242331610
-
Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome
-
Richards, A., Kemp, E.J., Liszewski, M.K., et al. Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome. Proc Natl Acad Sci U S A 100 (2003), 12966–12971.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 12966-12971
-
-
Richards, A.1
Kemp, E.J.2
Liszewski, M.K.3
-
16
-
-
77957575143
-
Variant-specific quantification of factor H in plasma identifies null alleles associated with atypical hemolytic uremic syndrome
-
Hakobyan, S., Tortajada, A., Harris, C.L., et al. Variant-specific quantification of factor H in plasma identifies null alleles associated with atypical hemolytic uremic syndrome. Kidney Int 78 (2010), 782–788.
-
(2010)
Kidney Int
, vol.78
, pp. 782-788
-
-
Hakobyan, S.1
Tortajada, A.2
Harris, C.L.3
-
17
-
-
84923573522
-
Functional characterization of two novel non-synonymous alterations in CD46 and a Q950H change in factor H found in atypical hemolytic uremic syndrome patients
-
Mohlin, F.C., Nilsson, S.C., Levart, T.K., et al. Functional characterization of two novel non-synonymous alterations in CD46 and a Q950H change in factor H found in atypical hemolytic uremic syndrome patients. Mol Immunol 65 (2015), 367–376.
-
(2015)
Mol Immunol
, vol.65
, pp. 367-376
-
-
Mohlin, F.C.1
Nilsson, S.C.2
Levart, T.K.3
-
18
-
-
84860711841
-
A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function
-
Roumenina, L.T., Frimat, M., Miller, E.C., et al. A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function. Blood 119 (2012), 4182–4191.
-
(2012)
Blood
, vol.119
, pp. 4182-4191
-
-
Roumenina, L.T.1
Frimat, M.2
Miller, E.C.3
-
19
-
-
44549083235
-
Regulated complement deposition on the surface of human endothelial cells: effect of tobacco smoke and shear stress
-
Yin, W., Ghebrehiwet, B., Weksler, B., Peerschke, E.I., Regulated complement deposition on the surface of human endothelial cells: effect of tobacco smoke and shear stress. Thromb Res 122 (2008), 221–228.
-
(2008)
Thromb Res
, vol.122
, pp. 221-228
-
-
Yin, W.1
Ghebrehiwet, B.2
Weksler, B.3
Peerschke, E.I.4
-
20
-
-
84902589905
-
Biomarkers of terminal complement activation confirm the diagnosis of aHUS and differentiate aHUS from TTP
-
Cataland, S.R., Holers, V.M., Geyer, S., et al. Biomarkers of terminal complement activation confirm the diagnosis of aHUS and differentiate aHUS from TTP. Blood 123 (2014), 3733–3738.
-
(2014)
Blood
, vol.123
, pp. 3733-3738
-
-
Cataland, S.R.1
Holers, V.M.2
Geyer, S.3
-
21
-
-
84947930096
-
Complement activation patterns in atypical haemolytic uraemic syndrome during acute phase and in remission
-
Volokhina, E.B., Westra, D., van der Velden, T.J., et al. Complement activation patterns in atypical haemolytic uraemic syndrome during acute phase and in remission. Clin Exp Immunol 181 (2015), 306–313.
-
(2015)
Clin Exp Immunol
, vol.181
, pp. 306-313
-
-
Volokhina, E.B.1
Westra, D.2
van der Velden, T.J.3
-
22
-
-
84929518595
-
Complement factor C4d is a common denominator in thrombotic microangiopathy
-
Chua, J.S., Baelde, H.J., Zandbergen, M., et al. Complement factor C4d is a common denominator in thrombotic microangiopathy. J Am Soc Nephrol 26 (2015), 2239–2247.
-
(2015)
J Am Soc Nephrol
, vol.26
, pp. 2239-2247
-
-
Chua, J.S.1
Baelde, H.J.2
Zandbergen, M.3
-
23
-
-
84874417661
-
Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome
-
Le Quintrec, M., Zuber, J., Moulin, B., et al. Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome. Am J Transplant 13 (2013), 663–675.
-
(2013)
Am J Transplant
, vol.13
, pp. 663-675
-
-
Le Quintrec, M.1
Zuber, J.2
Moulin, B.3
-
24
-
-
84887024143
-
Managing and preventing atypical hemolytic uremic syndrome recurrence after kidney transplantation
-
Noris, M., Remuzzi, G., Managing and preventing atypical hemolytic uremic syndrome recurrence after kidney transplantation. Curr Opin Nephrol Hypertens 22 (2013), 704–712.
-
(2013)
Curr Opin Nephrol Hypertens
, vol.22
, pp. 704-712
-
-
Noris, M.1
Remuzzi, G.2
-
25
-
-
84871942008
-
Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome
-
Sallee, M., Ismail, K., Fakhouri, F., et al. Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome. BMC Nephrol, 14, 2013, 3.
-
(2013)
BMC Nephrol
, vol.14
, pp. 3
-
-
Sallee, M.1
Ismail, K.2
Fakhouri, F.3
-
26
-
-
77952556624
-
Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations
-
Fakhouri, F., Roumenina, L., Provot, F., et al. Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations. J Am Soc Nephrol 21 (2010), 859–867.
-
(2010)
J Am Soc Nephrol
, vol.21
, pp. 859-867
-
-
Fakhouri, F.1
Roumenina, L.2
Provot, F.3
-
27
-
-
0347423198
-
Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure
-
Chobanian, A.V., Bakris, G.L., Black, H.R., et al. Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertension 42 (2003), 1206–1252.
-
(2003)
Hypertension
, vol.42
, pp. 1206-1252
-
-
Chobanian, A.V.1
Bakris, G.L.2
Black, H.R.3
-
28
-
-
42049119459
-
Association between thrombotic microangiopathy and reduced ADAMTS13 activity in malignant hypertension
-
van den Born, B.J., van der Hoeven, N.V., Groot, E., et al. Association between thrombotic microangiopathy and reduced ADAMTS13 activity in malignant hypertension. Hypertension 51 (2008), 862–866.
-
(2008)
Hypertension
, vol.51
, pp. 862-866
-
-
van den Born, B.J.1
van der Hoeven, N.V.2
Groot, E.3
-
29
-
-
4344685290
-
Signs and symptoms of thin basement membrane nephropathy: a prospective regional study on primary glomerular disease—The Limburg Renal Registry
-
van Paassen, P., van Breda Vriesman, P.J., van Rie, H., Tervaert, J.W., Signs and symptoms of thin basement membrane nephropathy: a prospective regional study on primary glomerular disease—The Limburg Renal Registry. Kidney Int 66 (2004), 909–913.
-
(2004)
Kidney Int
, vol.66
, pp. 909-913
-
-
van Paassen, P.1
van Breda Vriesman, P.J.2
van Rie, H.3
Tervaert, J.W.4
-
30
-
-
77954328285
-
Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS)
-
Westra, D., Volokhina, E., van der Heijden, E., et al. Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS). Nephrol Dial Transplant 25 (2010), 2195–2202.
-
(2010)
Nephrol Dial Transplant
, vol.25
, pp. 2195-2202
-
-
Westra, D.1
Volokhina, E.2
van der Heijden, E.3
-
31
-
-
84864419719
-
Novel C3 mutation p.Lys65Gln in aHUS affects complement factor H binding
-
Volokhina, E., Westra, D., Xue, X., et al. Novel C3 mutation p.Lys65Gln in aHUS affects complement factor H binding. Pediatr Nephrol 27 (2012), 1519–1524.
-
(2012)
Pediatr Nephrol
, vol.27
, pp. 1519-1524
-
-
Volokhina, E.1
Westra, D.2
Xue, X.3
-
32
-
-
79551489573
-
A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome
-
Maga, T.K., Meyer, N.C., Belsha, C., et al. A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome. Nephrol Dial Transplant 26 (2011), 739–741.
-
(2011)
Nephrol Dial Transplant
, vol.26
, pp. 739-741
-
-
Maga, T.K.1
Meyer, N.C.2
Belsha, C.3
-
33
-
-
20544437666
-
Anti-factor H autoantibodies associated with atypical hemolytic uremic syndrome
-
Dragon-Durey, M.A., Loirat, C., Cloarec, S., et al. Anti-factor H autoantibodies associated with atypical hemolytic uremic syndrome. J Am Soc Nephrol 16 (2005), 555–563.
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 555-563
-
-
Dragon-Durey, M.A.1
Loirat, C.2
Cloarec, S.3
-
34
-
-
84930322599
-
Effect of blood sampling, processing, and storage on the measurement of complement activation biomarkers
-
Yang, S., McGookey, M., Wang, Y., et al. Effect of blood sampling, processing, and storage on the measurement of complement activation biomarkers. Am J Clin Pathol 143 (2015), 558–565.
-
(2015)
Am J Clin Pathol
, vol.143
, pp. 558-565
-
-
Yang, S.1
McGookey, M.2
Wang, Y.3
-
35
-
-
19944430192
-
Functional analysis of the classical, alternative, and MBL pathways of the complement system: standardization and validation of a simple ELISA
-
Seelen, M.A., Roos, A., Wieslander, J., et al. Functional analysis of the classical, alternative, and MBL pathways of the complement system: standardization and validation of a simple ELISA. J Immunol Methods 296 (2005), 187–198.
-
(2005)
J Immunol Methods
, vol.296
, pp. 187-198
-
-
Seelen, M.A.1
Roos, A.2
Wieslander, J.3
|