-
1
-
-
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 2010; 5: 1844-1859.
-
(2010)
Clin J Am Soc Nephrol
, vol.5
, pp. 1844-1859
-
-
Noris, M.1
Caprioli, J.2
Bresin, E.3
-
2
-
-
84876044818
-
Genetics and outcome of atypical hemolytic uremic syndrome: A nationwide French series comparing children and adults
-
Fremeaux-Bacchi V, Fakhouri F, Garnier A 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: 554-562.
-
(2013)
Clin J Am Soc Nephrol
, vol.8
, pp. 554-562
-
-
Fremeaux-Bacchi, V.1
Fakhouri, F.2
Garnier, A.3
-
3
-
-
20544437666
-
Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome
-
Dragon-Durey MA, Loirat C, Cloarec S et al. Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome. J Am Soc Nephrol 2005; 16: 555-563.
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 555-563
-
-
Dragon-Durey, M.A.1
Loirat, C.2
Cloarec, S.3
-
4
-
-
78649863686
-
Clinical features of anti-factor H autoantibody-associated hemolytic uremic syndrome
-
Dragon-Durey MA, Sethi SK, Bagga A et al. Clinical features of anti-factor H autoantibody-associated hemolytic uremic syndrome. J Am Soc Nephrol 2010; 21: 2180-2187.
-
(2010)
J Am Soc Nephrol
, vol.21
, pp. 2180-2187
-
-
Dragon-Durey, M.A.1
Sethi, S.K.2
Bagga, A.3
-
5
-
-
84878608990
-
Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome
-
Lemaire M, Frémeaux-Bacchi V, Schaefer F et al. Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome. Nat Genet 2013; 45: 531-536.
-
(2013)
Nat Genet
, vol.45
, pp. 531-536
-
-
Lemaire, M.1
Frémeaux-Bacchi, V.2
Schaefer, F.3
-
6
-
-
75649133611
-
Association of factor h autoantibodies with deletions of cfhr1, cfhr3, cfhr4, and with mutations in cfh, cfi, cd46, and c3 in patients with atypical hemolytic uremic syndrome
-
Moore I, Strain L, Pappworth I et al. Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome. Blood 2010; 115: 379-387.
-
(2010)
Blood
, vol.115
, pp. 379-387
-
-
Moore, I.1
Strain, L.2
Pappworth, I.3
-
7
-
-
38949155911
-
Factor h autoantibodies in atypical hemolytic uremic syndrome correlate with cfhr1/cfhr3 deficiency
-
Jó zsi M, Licht C, Strobel S et al. Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency. Blood 2008; 111: 1512-1514.
-
(2008)
Blood
, vol.111
, pp. 1512-1514
-
-
Jó Zsi, M.1
Licht, C.2
Strobel, S.3
-
8
-
-
67650508077
-
The high frequency of complement factor h related cfhr1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome
-
Dragon-Durey MA, Blanc C, Marliot F et al. The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome. J Med Genet 2009; 46: 447-450.
-
(2009)
J Med Genet
, vol.46
, pp. 447-450
-
-
Dragon-Durey, M.A.1
Blanc, C.2
Marliot, F.3
-
9
-
-
84876170850
-
Determining the population frequency of the cfhr3/cfhr1 deletion at 1q32
-
Holmes LV, Strain L, Staniforth SJ et al. Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32. PLoS One [online] 2013; 8: e60352.
-
(2013)
PLoS One [Online
, vol.8
-
-
Holmes, L.V.1
Strain, L.2
Staniforth, S.J.3
-
10
-
-
84866556872
-
Overall neutralization of complement factor h by autoantibodies in the acute phase of the autoimmune form of atypical hemolytic uremic syndrome
-
Blanc C, Roumenina LT, Ashraf Y et al. Overall neutralization of complement factor H by autoantibodies in the acute phase of the autoimmune form of atypical hemolytic uremic syndrome. J Immunol 2012; 189: 3528-3537.
-
(2012)
J Immunol
, vol.189
, pp. 3528-3537
-
-
Blanc, C.1
Roumenina, L.T.2
Ashraf, Y.3
-
11
-
-
84899769165
-
Prompt plasma exchanges and immunosuppressive treatment improves the outcomes of anti-factor H autoantibody-associated hemolytic uremic syndrome in children
-
Sinha A, Gulati A, Saini S et al. Prompt plasma exchanges and immunosuppressive treatment improves the outcomes of anti-factor H autoantibody-associated hemolytic uremic syndrome in children. Kidney Int 2014; 85: 1151-1160.
-
(2014)
Kidney Int
, vol.85
, pp. 1151-1160
-
-
Sinha, A.1
Gulati, A.2
Saini, S.3
-
12
-
-
78049291873
-
Escherichia coli O157
-
Pennington H. Escherichia coli O157. Lancet 2010; 376: 1428-1435.
-
(2010)
Lancet
, vol.376
, pp. 1428-1435
-
-
Pennington, H.1
-
13
-
-
84888048107
-
Standardisation of the factor H autoantibody assay
-
Watson R, Lindner S, Bordereau P et al. Standardisation of the factor H autoantibody assay. Immunobiology 2013; 219: 9-16.
-
(2013)
Immunobiology
, vol.219
, pp. 9-16
-
-
Watson, R.1
Lindner, S.2
Bordereau, P.3
-
14
-
-
84890548424
-
Long-term remission of atypical HUS with anti-factor H antibodies after cyclophosphamide pulses
-
Sana G, Dragon-Durey MA, Charbit M et al. Long-term remission of atypical HUS with anti-factor H antibodies after cyclophosphamide pulses. Pediatr Nephrol 2013; 29: 75-83.
-
(2013)
Pediatr Nephrol
, vol.29
, pp. 75-83
-
-
Sana, G.1
Dragon-Durey, M.A.2
Charbit, M.3
-
15
-
-
84878589219
-
Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome
-
Legendre CM, Licht C, Muus P et al. Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome. N Engl J Med 2013; 368: 2169-2181
-
(2013)
N Engl J Med
, vol.368
, pp. 2169-2181
-
-
Legendre, C.M.1
Licht, C.2
Muus, P.3
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