-
1
-
-
0023278579
-
HUS and TTP: Variable expression of a single entity
-
Remuzzi G. HUS and TTP: variable expression of a single entity. Kidney Int 1987; 32: 292-308
-
(1987)
Kidney Int
, vol.32
, pp. 292-308
-
-
Remuzzi, G.1
-
2
-
-
0032569884
-
Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolyticuremic syndrome
-
Furlan M, Robles R, Galbusera M et al. von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolyticuremic syndrome. N Engl J Med 1998; 339: 1578-1584
-
(1998)
N Engl J Med
, vol.339
, pp. 1578-1584
-
-
Furlan, M.1
Robles, R.2
Galbusera, M.3
-
3
-
-
0001478161
-
Hemolytic-uremic syndrome: Bilateral necrosis of the renal cortex in acute acquired hemolytic anemia
-
Gasser C, Gautier E, Steck A et al. Hemolytic-uremic syndrome: bilateral necrosis of the renal cortex in acute acquired hemolytic anemia. Schweiz MedWochenschr 1955; 85: 905-909
-
(1955)
Schweiz MedWochenschr
, vol.85
, pp. 905-909
-
-
Gasser, C.1
Gautier, E.2
Steck, A.3
-
4
-
-
0016804113
-
Recurrent hemolytic-uremic syndrome: A case report
-
Drukker A, Winterborn M, Bennett B et al. Recurrent hemolytic-uremic syndrome: a case report. Clin Nephrol 1975; 4: 68-72
-
(1975)
Clin Nephrol
, vol.4
, pp. 68-72
-
-
Drukker, A.1
Winterborn, M.2
Bennett, B.3
-
5
-
-
0017736408
-
Recurrent hemolytic-uremic syndrome. A report of two cases
-
Spirer Z, Knobel B, Earon J et al. Recurrent hemolytic-uremic syndrome. A report of two cases. Helv Paediatr Acta 1977; 32: 165-172
-
(1977)
Helv Paediatr Acta
, vol.32
, pp. 165-172
-
-
Spirer, Z.1
Knobel, B.2
Earon, J.3
-
6
-
-
0017737237
-
Hemolytic uremic syndrome with hypocomplementemia, serum C3NeF, and glomerular deposits of C3
-
Barre P, Kaplan BS, de Chadarevian JP et al. Hemolytic uremic syndrome with hypocomplementemia, serum C3NeF, and glomerular deposits of C3. Arch Pathol Lab Med 1977; 101: 357-361
-
(1977)
Arch Pathol Lab Med
, vol.101
, pp. 357-361
-
-
Barre, P.1
Kaplan, B.S.2
De Chadarevian, J.P.3
-
7
-
-
0019387503
-
Hypocomplementaemia due to a genetic deficiency of beta 1H globulin
-
Thompson RA, Winterborn MH. Hypocomplementaemia due to a genetic deficiency of beta 1H globulin. Clin Exp Immunol 1981; 46: 110-119
-
(1981)
Clin Exp Immunol
, vol.46
, pp. 110-119
-
-
Thompson, R.A.1
Winterborn, M.H.2
-
8
-
-
59449088846
-
Eculizumab for congenital atypical hemolyticuremic syndrome
-
Gruppo RA, Rother RP. Eculizumab for congenital atypical hemolyticuremic syndrome. N Engl J Med 2009; 360: 544-546
-
(2009)
N Engl J Med
, vol.360
, pp. 544-546
-
-
Gruppo, R.A.1
Rother, R.P.2
-
9
-
-
59449107473
-
Eculizumab for atypical hemolytic-uremic syndrome
-
Nurnberger J, Philipp T, Witzke O et al. Eculizumab for atypical hemolytic-uremic syndrome. N Engl J Med 2009; 360: 542-544
-
(2009)
N Engl J Med
, vol.360
, pp. 542-544
-
-
Nurnberger, J.1
Philipp, T.2
Witzke, O.3
-
10
-
-
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
-
11
-
-
84860141031
-
A new era in the diagnosis and treatment of atypical haemolytic uraemic syndrome
-
Westra D, Wetzels JF, Volokhina EB et al. A new era in the diagnosis and treatment of atypical haemolytic uraemic syndrome. Neth J Med 2012; 70: 121-129
-
(2012)
Neth J Med
, vol.70
, pp. 121-129
-
-
Westra, D.1
Wetzels, J.F.2
Volokhina, E.B.3
-
12
-
-
84860246424
-
Need for long-term follow-up in enterohemorrhagic Escherichia coli-associated hemolytic uremic syndrome due to late-emerging sequelae
-
Rosales A, Hofer J, Zimmerhackl LB et al. Need for long-term follow-up in enterohemorrhagic Escherichia coli-associated hemolytic uremic syndrome due to late-emerging sequelae. Clin Infect Dis 2012; 54: 1413-1421
-
(2012)
Clin Infect Dis
, vol.54
, pp. 1413-1421
-
-
Rosales, A.1
Hofer, J.2
Zimmerhackl, L.B.3
-
13
-
-
84867997580
-
STEC-HUS, atypical HUS and TTP are all diseases of complement activation
-
Noris M, Mescia F, Remuzzi G. STEC-HUS, atypical HUS and TTP are all diseases of complement activation. Nat Rev Nephrol 2012; 8: 622-633
-
(2012)
Nat Rev Nephrol
, vol.8
, pp. 622-633
-
-
Noris, M.1
Mescia, F.2
Remuzzi, G.3
-
14
-
-
84863985862
-
Atypical hemolytic uremic syndrome in children: Complement mutations and clinical characteristics
-
Geerdink LM, Westra D, van Wijk JA et al. Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics. Pediatr Nephrol 2012; 27: 1283-1291
-
(2012)
Pediatr Nephrol
, vol.27
, pp. 1283-1291
-
-
Geerdink, L.M.1
Westra, D.2
Van Wijk, J.A.3
-
15
-
-
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
-
16
-
-
84867993202
-
Renal and neurological involvement in typical Shiga toxin-associated HUS
-
Trachtman H, Austin C, Lewinski M et al. Renal and neurological involvement in typical Shiga toxin-associated HUS. Nat Rev Nephrol 2012; 8: 658-669
-
(2012)
Nat Rev Nephrol
, vol.8
, pp. 658-669
-
-
Trachtman, H.1
Austin, C.2
Lewinski, M.3
-
17
-
-
5744228953
-
CT and MRI in haemolytic uraemic syndrome with central nervous system involvement: Distribution of lesions and prognostic value of imaging findings
-
Steinborn M, Leiz S, Rudisser K et al. CT and MRI in haemolytic uraemic syndrome with central nervous system involvement: distribution of lesions and prognostic value of imaging findings. Pediatr Radiol 2004; 34: 805-810
-
(2004)
Pediatr Radiol
, vol.34
, pp. 805-810
-
-
Steinborn, M.1
Leiz, S.2
Rudisser, K.3
-
18
-
-
34547633064
-
Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome
-
Sellier-Leclerc AL, Fremeaux-Bacchi V, Dragon-Durey MA et al. Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome. J Am Soc Nephrol 2007; 18: 2392-2400
-
(2007)
J Am Soc Nephrol
, vol.18
, pp. 2392-2400
-
-
Sellier-Leclerc, A.L.1
Fremeaux-Bacchi, V.2
Dragon-Durey, M.A.3
-
19
-
-
84896970663
-
Complement and its receptors: New insights into human disease
-
Holers VM. Complement and its receptors: new insights into human disease. Annu Rev Immunol 2014; 32: 433-459
-
(2014)
Annu Rev Immunol
, vol.32
, pp. 433-459
-
-
Holers, V.M.1
-
20
-
-
67651166873
-
Thrombomodulin mutations in atypical hemolytic-uremic syndrome
-
Delvaeye M, Noris M, De Vriese A et al. Thrombomodulin mutations in atypical hemolytic-uremic syndrome. N Engl J Med 2009; 361: 345-357
-
(2009)
N Engl J Med
, vol.361
, pp. 345-357
-
-
Delvaeye, M.1
Noris, M.2
De Vriese, A.3
-
21
-
-
0031970553
-
Genetic studies into inherited and sporadic hemolytic uremic syndrome
-
Warwicker P, Goodship TH, Donne RL et al. Genetic studies into inherited and sporadic hemolytic uremic syndrome. Kidney Int 1998; 53: 836-844
-
(1998)
Kidney Int
, vol.53
, pp. 836-844
-
-
Warwicker, P.1
Goodship, T.H.2
Donne, R.L.3
-
22
-
-
0242331610
-
Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome
-
Richards A, Kemp EJ, Liszewski MK 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 2003; 100: 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
-
23
-
-
19444369542
-
Complement factor I: A susceptibility gene for atypical haemolytic uraemic syndrome
-
Fremeaux-Bacchi V, Dragon-Durey MA, Blouin J et al. Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome. J Med Genet 2004; 41: e84
-
(2004)
J Med Genet
, vol.41
, pp. e84
-
-
Fremeaux-Bacchi, V.1
Dragon-Durey, M.A.2
Blouin, J.3
-
24
-
-
33846094404
-
Gain-offunction mutations in complement factor B are associated with atypical hemolytic uremic syndrome
-
Goicoechea de Jorge E, Harris CL, Esparza-Gordillo J et al. Gain-offunction mutations in complement factor B are associated with atypical hemolytic uremic syndrome. Proc Natl Acad Sci U S A 2007; 104: 240-245
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 240-245
-
-
Goicoechea De Jorge, E.1
Harris, C.L.2
Esparza-Gordillo, J.3
-
25
-
-
54049137505
-
Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome
-
Fremeaux-Bacchi V, Miller EC, Liszewski MK et al. Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome. Blood 2008; 112: 4948-4952
-
(2008)
Blood
, vol.112
, pp. 4948-4952
-
-
Fremeaux-Bacchi, V.1
Miller, E.C.2
Liszewski, M.K.3
-
26
-
-
84886949690
-
Post-transplant recurrence of atypical hemolytic uremic syndrome in a patient with thrombomodulin mutation
-
Sinibaldi S, Guzzo I, Piras R et al. Post-transplant recurrence of atypical hemolytic uremic syndrome in a patient with thrombomodulin mutation. Pediatr Transplant 2013; 17: E177-E181
-
(2013)
Pediatr Transplant
, vol.17
, pp. E177-E181
-
-
Sinibaldi, S.1
Guzzo, I.2
Piras, R.3
-
27
-
-
84878608990
-
Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome
-
Lemaire M, Fremeaux-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
Fremeaux-Bacchi, V.2
Schaefer, F.3
-
28
-
-
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
-
30
-
-
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 et al. Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome. Blood 2006; 108: 1267-1279
-
(2006)
Blood
, vol.108
, pp. 1267-1279
-
-
Caprioli, J.1
Noris, M.2
Brioschi, S.3
-
31
-
-
84874610717
-
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype
-
Bresin E, Rurali E, Caprioli J et al. Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype. J Am Soc Nephrol 2013; 24: 475-486
-
(2013)
J Am Soc Nephrol
, vol.24
, pp. 475-486
-
-
Bresin, E.1
Rurali, E.2
Caprioli, J.3
-
32
-
-
80052302283
-
Optimizing treatment strategies in paediatric atypical hemolytic uremic syndrome
-
Waters A. Optimizing treatment strategies in paediatric atypical hemolytic uremic syndrome. Pediatr Nephrol 2011; 26: 1917-1918
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 1917-1918
-
-
Waters, A.1
-
33
-
-
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 2010; 25: 2195-2202
-
(2010)
Nephrol Dial Transplant
, vol.25
, pp. 2195-2202
-
-
Westra, D.1
Volokhina, E.2
Van Der Heijden, E.3
-
34
-
-
84880767415
-
Complement factor H related proteins (CFHRs)
-
Skerka C, Chen Q, Fremeaux-Bacchi V et al. Complement factor H related proteins (CFHRs). Mol Immunol 2013; 56: 170-180
-
(2013)
Mol Immunol
, vol.56
, pp. 170-180
-
-
Skerka, C.1
Chen, Q.2
Fremeaux-Bacchi, V.3
-
35
-
-
33746655453
-
De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome
-
Heinen S, Sanchez-Corral P, Jackson MS et al. De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome. Hum Mutat 2006; 27: 292-293
-
(2006)
Hum Mutat
, vol.27
, pp. 292-293
-
-
Heinen, S.1
Sanchez-Corral, P.2
Jackson, M.S.3
-
36
-
-
38949155911
-
Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency
-
Jozsi 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
-
-
Jozsi, M.1
Licht, C.2
Strobel, S.3
-
37
-
-
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
-
38
-
-
84875029270
-
Complement factor H-related protein 1 deficiency and factor H antibodies in pediatric patients with atypical hemolytic uremic syndrome
-
Hofer J, Janecke AR, Zimmerhackl LB et al. Complement factor H-related protein 1 deficiency and factor H antibodies in pediatric patients with atypical hemolytic uremic syndrome. Clin J Am Soc Nephrol 2013; 8: 407-415
-
(2013)
Clin J Am Soc Nephrol
, vol.8
, pp. 407-415
-
-
Hofer, J.1
Janecke, A.R.2
Zimmerhackl, L.B.3
-
39
-
-
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
-
40
-
-
14644424005
-
Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32
-
Esparza-Gordillo J, Goicoechea de Jorge E, Buil A et al. Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32. Hum Mol Genet 2005; 14: 703-712
-
(2005)
Hum Mol Genet
, vol.14
, pp. 703-712
-
-
Esparza-Gordillo, J.1
Goicoechea De Jorge, E.2
Buil, A.3
-
42
-
-
70350279315
-
Atypical hemolytic-uremic syndrome
-
Noris M, Remuzzi G. Atypical hemolytic-uremic syndrome. N Engl J Med 2009; 361: 1676-1687
-
(2009)
N Engl J Med
, vol.361
, pp. 1676-1687
-
-
Noris, M.1
Remuzzi, G.2
-
43
-
-
84885717017
-
Abnormalities in the alternative pathway of complement in children with hematopoietic stem cell transplant-associated thrombotic microangiopathy
-
Jodele S, Licht C, Goebel J et al. Abnormalities in the alternative pathway of complement in children with hematopoietic stem cell transplant-associated thrombotic microangiopathy. Blood 2013; 122: 2003-2007
-
(2013)
Blood
, vol.122
, pp. 2003-2007
-
-
Jodele, S.1
Licht, C.2
Goebel, J.3
-
44
-
-
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 2010; 21: 859-867
-
(2010)
J Am Soc Nephrol
, vol.21
, pp. 859-867
-
-
Fakhouri, F.1
Roumenina, L.2
Provot, F.3
-
45
-
-
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 2013; 22: 704-712
-
(2013)
Curr Opin Nephrol Hypertens
, vol.22
, pp. 704-712
-
-
Noris, M.1
Remuzzi, G.2
-
46
-
-
84883552294
-
The endothelial glycocalyx as a potential modifier of the hemolytic uremic syndrome
-
Boels MG, Lee DH, van den Berg BM et al. The endothelial glycocalyx as a potential modifier of the hemolytic uremic syndrome. Eur J Intern Med 2013; 24: 503-509
-
(2013)
Eur J Intern Med
, vol.24
, pp. 503-509
-
-
Boels, M.G.1
Lee, D.H.2
Van Den Berg, B.M.3
-
47
-
-
0344624868
-
The pathogenesis and treatment of hemolytic uremic syndrome
-
Kaplan BS, Meyers KE, Schulman SL. The pathogenesis and treatment of hemolytic uremic syndrome. J Am Soc Nephrol 1998; 9: 1126-1133
-
(1998)
J Am Soc Nephrol
, vol.9
, pp. 1126-1133
-
-
Kaplan, B.S.1
Meyers, K.E.2
Schulman, S.L.3
-
49
-
-
79151471122
-
AHUS caused by complement dysregulation: New therapies on the horizon
-
Waters AM, Licht C. aHUS caused by complement dysregulation: new therapies on the horizon. Pediatr Nephrol 2011; 26: 41-57
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 41-57
-
-
Waters, A.M.1
Licht, C.2
-
50
-
-
0018610481
-
Treatment of the hemolytic uremic syndrome with plasma
-
Remuzzi G, Misiani R, Marchesi D et al. Treatment of the hemolytic uremic syndrome with plasma. Clin Nephrol 1979; 12: 279-284
-
(1979)
Clin Nephrol
, vol.12
, pp. 279-284
-
-
Remuzzi, G.1
Misiani, R.2
Marchesi, D.3
-
52
-
-
77956135186
-
Genetics and genetic testing in hemolytic uremic syndrome/thrombotic thrombocytopenic purpura
-
Noris M, Remuzzi G. Genetics and genetic testing in hemolytic uremic syndrome/thrombotic thrombocytopenic purpura. Semin Nephrol 2010; 30: 395-408
-
(2010)
Semin Nephrol
, vol.30
, pp. 395-408
-
-
Noris, M.1
Remuzzi, G.2
-
53
-
-
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
-
54
-
-
61549117207
-
Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome
-
Ariceta G, Besbas N, Johnson S et al. Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome. Pediatr Nephrol 2009; 24: 687-696
-
(2009)
Pediatr Nephrol
, vol.24
, pp. 687-696
-
-
Ariceta, G.1
Besbas, N.2
Johnson, S.3
-
55
-
-
84906556500
-
Cardiovascular complications in atypical haemolytic uraemic syndrome
-
Noris M, Remuzzi G. Cardiovascular complications in atypical haemolytic uraemic syndrome. Nat Rev Nephrol 2014; 10: 174-180
-
(2014)
Nat Rev Nephrol
, vol.10
, pp. 174-180
-
-
Noris, M.1
Remuzzi, G.2
-
56
-
-
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 2013; 13: 663-675
-
(2013)
Am J Transplant
, vol.13
, pp. 663-675
-
-
Le Quintrec, M.1
Zuber, J.2
Moulin, B.3
-
57
-
-
0141590417
-
Renal transplantation in patients with hemolytic uremic syndrome: High rate of recurrence and increased incidence of acute rejections
-
Artz MA, Steenbergen EJ, Hoitsma AJ et al. Renal transplantation in patients with hemolytic uremic syndrome: high rate of recurrence and increased incidence of acute rejections. Transplantation 2003; 76: 821-826
-
(2003)
Transplantation
, vol.76
, pp. 821-826
-
-
Artz, M.A.1
Steenbergen, E.J.2
Hoitsma, A.J.3
-
58
-
-
33748904355
-
The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria
-
Hillmen P, Young NS, Schubert J et al. The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria. N Engl J Med 2006; 355: 1233-1243
-
(2006)
N Engl J Med
, vol.355
, pp. 1233-1243
-
-
Hillmen, P.1
Young, N.S.2
Schubert, J.3
-
60
-
-
70350130833
-
Safety and long-term efficacy of eculizumab in a renal transplant patient with recurrent atypical hemolytic-uremic syndrome
-
Chatelet V, Fremeaux-Bacchi V, Lobbedez T et al. Safety and long-term efficacy of eculizumab in a renal transplant patient with recurrent atypical hemolytic-uremic syndrome. Am J Transplant 2009; 9: 2644-2645
-
(2009)
Am J Transplant
, vol.9
, pp. 2644-2645
-
-
Chatelet, V.1
Fremeaux-Bacchi, V.2
Lobbedez, T.3
-
61
-
-
77949570344
-
Maintenance of kidney function following treatment with eculizumab and discontinuation of plasma exchange after a third kidney transplant for atypical hemolytic uremic syndrome associated with a CFH mutation
-
Davin JC, Gracchi V, Bouts A et al. Maintenance of kidney function following treatment with eculizumab and discontinuation of plasma exchange after a third kidney transplant for atypical hemolytic uremic syndrome associated with a CFH mutation. Am J Kidney Dis 2010; 55: 708-711
-
(2010)
Am J Kidney Dis
, vol.55
, pp. 708-711
-
-
Davin, J.C.1
Gracchi, V.2
Bouts, A.3
-
62
-
-
84884971310
-
Eculizumab in atypical hemolytic-uremic syndrome
-
Legendre CM, Licht C, Loirat C. Eculizumab in atypical hemolytic-uremic syndrome. N Engl J Med 2013; 369: 1379-1380
-
(2013)
N Engl J Med
, vol.369
, pp. 1379-1380
-
-
Legendre, C.M.1
Licht, C.2
Loirat, C.3
-
63
-
-
84888127097
-
A systematic review of eculizumab for atypical haemolytic uraemic syndrome (aHUS)
-
Rathbone J, Kaltenthaler E, Richards A et al. A systematic review of eculizumab for atypical haemolytic uraemic syndrome (aHUS). BMJ Open 2013; 3: e003573
-
(2013)
BMJ Open
, vol.3
-
-
Rathbone, J.1
Kaltenthaler, E.2
Richards, A.3
-
64
-
-
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
-
65
-
-
84870534251
-
Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation
-
Zuber J, Le Quintrec M, Krid S et al. Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation. Am J Transplant 2012; 12: 3337-3354
-
(2012)
Am J Transplant
, vol.12
, pp. 3337-3354
-
-
Zuber, J.1
Le Quintrec, M.2
Krid, S.3
-
66
-
-
84867993256
-
Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies
-
Zuber J, Fakhouri F, Roumenina LT et al. French Study Group for a HCG. Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies. Nat Rev Nephrol 2012; 8: 643-657
-
(2012)
Nat Rev Nephrol
, vol.8
, pp. 643-657
-
-
Zuber, J.1
Fakhouri, F.2
Roumenina, L.T.3
-
67
-
-
84887807231
-
A multicomponent serogroup B meningococcal vaccine is licensed for use in Europe: What do we know, and what are we yet to learn?
-
Martin NG, Snape MD. A multicomponent serogroup B meningococcal vaccine is licensed for use in Europe: what do we know, and what are we yet to learn? Expert Rev Vaccines 2013; 12: 837-858
-
(2013)
Expert Rev Vaccines
, vol.12
, pp. 837-858
-
-
Martin, N.G.1
Snape, M.D.2
-
68
-
-
84874435634
-
Meningococcal sepsis complicating eculizumab treatment despite prior vaccination
-
Struijk GH, Bouts AH, Rijkers GT et al. Meningococcal sepsis complicating eculizumab treatment despite prior vaccination. Am J Transplant 2013; 13: 819-820
-
(2013)
Am J Transplant
, vol.13
, pp. 819-820
-
-
Struijk, G.H.1
Bouts, A.H.2
Rijkers, G.T.3
-
69
-
-
84868562798
-
Best supportive care and therapeutic plasma exchange with or without eculizumab in Shiga-toxin-producing E. Coli O104:H4 induced haemolytic-uraemic syndrome: An analysis of the German STEC-HUS registry
-
Kielstein JT, Beutel G, Fleig S et al. Best supportive care and therapeutic plasma exchange with or without eculizumab in Shiga-toxin-producing E. coli O104:H4 induced haemolytic-uraemic syndrome: an analysis of the German STEC-HUS registry. Nephrol Dial Transplant 2012; 27: 3807-3815
-
(2012)
Nephrol Dial Transplant
, vol.27
, pp. 3807-3815
-
-
Kielstein, J.T.1
Beutel, G.2
Fleig, S.3
-
70
-
-
84908098893
-
Discontinuation of eculizumab maintenance treatment for atypical hemolytic uremic syndrome: A report of 10 cases
-
[Epub ahead of print]
-
Ardissino G, Testa S, Possenti I et al. Discontinuation of eculizumab maintenance treatment for atypical hemolytic uremic syndrome: a report of 10 cases. Am J Kidney Dis 2014; doi: 10.1053/j.ajkd.2014.01.434. [Epub ahead of print]
-
(2014)
Am J Kidney Dis
-
-
Ardissino, G.1
Testa, S.2
Possenti, I.3
-
71
-
-
84884181358
-
Living kidney transplantation in adult patients with atypical haemolytic uraemic syndrome
-
Verhave JC, Westra D, van Hamersvelt HW et al. Living kidney transplantation in adult patients with atypical haemolytic uraemic syndrome. Neth J Med 2013; 71: 342-347
-
(2013)
Neth J Med
, vol.71
, pp. 342-347
-
-
Verhave, J.C.1
Westra, D.2
Van Hamersvelt, H.W.3
-
72
-
-
33644914494
-
Calcineurin inhibitor-free immunosuppression in renal allograft recipients with thrombotic microangiopathy/hemolytic uremic syndrome
-
Oyen O, Strom EH, Midtvedt K et al. Calcineurin inhibitor-free immunosuppression in renal allograft recipients with thrombotic microangiopathy/hemolytic uremic syndrome. Am J Transplant 2006; 6: 412-418
-
(2006)
Am J Transplant
, vol.6
, pp. 412-418
-
-
Oyen, O.1
Strom, E.H.2
Midtvedt, K.3
-
73
-
-
0034997865
-
Targeting complement in therapy
-
Kirschfink M. Targeting complement in therapy. Immunol Rev 2001; 180: 177-189
-
(2001)
Immunol Rev
, vol.180
, pp. 177-189
-
-
Kirschfink, M.1
-
74
-
-
84887096975
-
Soluble CR1 therapy improves complement regulation in C3 glomerulopathy
-
Zhang Y, Nester CM, Holanda DG et al. Soluble CR1 therapy improves complement regulation in C3 glomerulopathy. J Am Soc Nephrol 2013; 24: 1820-1829
-
(2013)
J Am Soc Nephrol
, vol.24
, pp. 1820-1829
-
-
Zhang, Y.1
Nester, C.M.2
Holanda, D.G.3
-
75
-
-
84934442096
-
CR2-mediated targeting of complement inhibitors: Bench-to-bedside using a novel strategy for site-specific complement modulation
-
Holers VM, Rohrer B, Tomlinson S. CR2-mediated targeting of complement inhibitors: bench-to-bedside using a novel strategy for site-specific complement modulation. Adv Exp Med Biol 2013; 735: 137-154
-
(2013)
Adv Exp Med Biol
, vol.735
, pp. 137-154
-
-
Holers, V.M.1
Rohrer, B.2
Tomlinson, S.3
|