-
1
-
-
70350279315
-
Atypical hemolytic-uremic syndrome
-
Noris M, Remuzzi G. Atypical hemolytic-uremic syndrome. N Engl J Med (2009) 361:1676-87. doi: 10.1056/NEJMra0902814
-
(2009)
N Engl J Med
, vol.361
, pp. 1676-1687
-
-
Noris, M.1
Remuzzi, G.2
-
2
-
-
84898645797
-
Update on hemolytic uremic syndrome: diagnostic and therapeutic recommendations
-
Salvadori M, Bertoni E. Update on hemolytic uremic syndrome: diagnostic and therapeutic recommendations. World J Nephrol (2013) 2:56-76. doi:10.5527/wjn.v2.i3.56
-
(2013)
World J Nephrol
, vol.2
, pp. 56-76
-
-
Salvadori, M.1
Bertoni, E.2
-
3
-
-
0020662906
-
Escherichia coli O157:H7 strains associated with haemorrhagic colitis in the United States produce a Shigella dysenteriae 1 (SHIGA) like cytotoxin
-
O'Brien AO, Lively TA, Chen ME, Rothman SW, Formal SB. Escherichia coli O157:H7 strains associated with haemorrhagic colitis in the United States produce a Shigella dysenteriae 1 (SHIGA) like cytotoxin. Lancet (1983) 1(8326 Pt 1):702. doi:10.1016/S0140-6736(83)91987-6
-
(1983)
Lancet
, vol.1
, Issue.8326
, pp. 702
-
-
O'Brien, A.O.1
Lively, T.A.2
Chen, M.E.3
Rothman, S.W.4
Formal, S.B.5
-
4
-
-
84878608990
-
Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome
-
Lemaire M, Frémeaux-Bacchi V, Schaefer F, Choi M, Tang WH, Le Quintrec M, et al. Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome. Nat Genet (2013) 45:531-6. doi:10.1038/ng.2590
-
(2013)
Nat Genet
, vol.45
, pp. 531-536
-
-
Lemaire, M.1
Frémeaux-Bacchi, V.2
Schaefer, F.3
Choi, M.4
Tang, W.H.5
Le Quintrec, M.6
-
5
-
-
84884821706
-
Targeted strategies in the prevention and management of atypical HUS recurrence after kidney transplantation
-
Zuber J, Le Quintrec M, Morris H, Frémeaux-Bacchi V, Loirat C, Legendre C. Targeted strategies in the prevention and management of atypical HUS recurrence after kidney transplantation. Transplant Rev (Orlando) (2013) 27:117-25. doi:10.1016/j.trre.2013.07.003
-
(2013)
Transplant Rev (Orlando)
, vol.27
, pp. 117-125
-
-
Zuber, J.1
Le Quintrec, M.2
Morris, H.3
Frémeaux-Bacchi, V.4
Loirat, C.5
Legendre, C.6
-
6
-
-
0015937612
-
Letter: plasma-C3 in haemolytic-uraemic syndrome and thrombotic thrombocytopenic purpura
-
Cameron JS, Vick R. Letter: plasma-C3 in haemolytic-uraemic syndrome and thrombotic thrombocytopenic purpura. Lancet (1973) 2:975. doi:10.1016/S0140-6736(73)92645-7
-
(1973)
Lancet
, vol.2
, pp. 975
-
-
Cameron, J.S.1
Vick, R.2
-
7
-
-
78650517945
-
New insights into postrenal transplant hemolytic uremic syndrome
-
Zuber J, Le Quintrec M, Sberro-Soussan R, Loirat C, Frémeaux-Bacchi V, Legendre C. New insights into postrenal transplant hemolytic uremic syndrome. Nat Rev Nephrol (2011) 7:23-35. doi:10.1038/nrneph.2010.155
-
(2011)
Nat Rev Nephrol
, vol.7
, pp. 23-35
-
-
Zuber, J.1
Le Quintrec, M.2
Sberro-Soussan, R.3
Loirat, C.4
Frémeaux-Bacchi, V.5
Legendre, C.6
-
9
-
-
84875382274
-
Complement disorders and hemolytic uremic syndrome
-
Joseph C, Gattineni J. Complement disorders and hemolytic uremic syndrome. Curr Opin Pediatr (2013) 25:209-15. doi:10.1097/MOP.0b013e32835df48a
-
(2013)
Curr Opin Pediatr
, vol.25
, pp. 209-215
-
-
Joseph, C.1
Gattineni, J.2
-
10
-
-
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) 104:240-5. doi:10.1073/pnas.0603420103
-
(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
Carreras, L.4
Arranz, E.A.5
Garrido, C.A.6
-
11
-
-
54049137505
-
Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome
-
Frémeaux-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) 112:4948-52. doi:10.1182/blood-2008-01-133702
-
(2008)
Blood
, vol.112
, pp. 4948-4952
-
-
Frémeaux-Bacchi, V.1
Miller, E.C.2
Liszewski, M.K.3
Strain, L.4
Blouin, J.5
Brown, A.L.6
-
12
-
-
67651166873
-
Thrombomodulin mutations in atypical hemolytic-uremic syndrome
-
Delvaeye M, Noris M, De Vriese A, Esmon CT, Esmon NL, Ferrell G, et al. Thrombomodulin mutations in atypical hemolytic-uremic syndrome. N Engl J Med (2009) 361:345-57. doi:10.1056/NEJMoa0810739
-
(2009)
N Engl J Med
, vol.361
, pp. 345-357
-
-
Delvaeye, M.1
Noris, M.2
De Vriese, A.3
Esmon, C.T.4
Esmon, N.L.5
Ferrell, G.6
-
13
-
-
17744376183
-
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, Carreras Berges L, López-Trascasa M, Sánchez-Corral P, 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) 14:703-12. doi:10.1093/hmg/ddi099
-
(2005)
Hum Mol Genet
, vol.14
, pp. 703-712
-
-
Esparza-Gordillo, J.1
Goicoechea de Jorge, E.2
Buil, A.3
Carreras Berges, L.4
López-Trascasa, M.5
Sánchez-Corral, P.6
-
14
-
-
33644964155
-
Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree
-
Esparza-Gordillo J, Jorge EG, Garrido CA, Carreras L, López-Trascasa M, Sánchez-Corral P, et al. Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree. Mol Immunol (2006) 43:1769-75. doi:10.1016/j.molimm.2005.11.008
-
(2006)
Mol Immunol
, vol.43
, pp. 1769-1775
-
-
Esparza-Gordillo, J.1
Jorge, E.G.2
Garrido, C.A.3
Carreras, L.4
López-Trascasa, M.5
Sánchez-Corral, P.6
-
15
-
-
26944480588
-
The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts
-
Fremeaux-Bacchi V, Kemp EJ, Goodship JA, Dragon-Durey MA, Strain L, Loirat C, et al. The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts. J Med Genet (2005) 42:852-6. doi:10.1136/jmg.2005.030783
-
(2005)
J Med Genet
, vol.42
, pp. 852-856
-
-
Fremeaux-Bacchi, V.1
Kemp, E.J.2
Goodship, J.A.3
Dragon-Durey, M.A.4
Strain, L.5
Loirat, C.6
-
16
-
-
84949117415
-
New functional and structural insights from updated mutational databases for complement factor H, factor I, membrane cofactor protein and C3
-
Rodriguez E, Rallapalli PM, Osborne AJ, Perkins SJ. New functional and structural insights from updated mutational databases for complement factor H, factor I, membrane cofactor protein and C3. Biosci Rep (2014) 34(5):e00146. doi:10.1042/BSR20140117
-
(2014)
Biosci Rep
, vol.34
, Issue.5
-
-
Rodriguez, E.1
Rallapalli, P.M.2
Osborne, A.J.3
Perkins, S.J.4
-
17
-
-
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) 108:1267-79. doi:10.1182/blood-2005-10-007252
-
(2006)
Blood
, vol.108
, pp. 1267-1279
-
-
Caprioli, J.1
Noris, M.2
Brioschi, S.3
Pianetti, G.4
Castelletti, F.5
Bettinaglio, P.6
-
18
-
-
0035143299
-
The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20
-
Caprioli J, Bettinaglio P, Zipfel PF, Amadei B, Daina E, Gamba S, et al. The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20. J Am Soc Nephrol (2001) 12:297-307
-
(2001)
J Am Soc Nephrol
, vol.12
, pp. 297-307
-
-
Caprioli, J.1
Bettinaglio, P.2
Zipfel, P.F.3
Amadei, B.4
Daina, E.5
Gamba, S.6
-
19
-
-
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) 5:1844-59. doi:10.2215/CJN.02210310
-
(2010)
Clin J Am Soc Nephrol
, vol.5
, pp. 1844-1859
-
-
Noris, M.1
Caprioli, J.2
Bresin, E.3
Mossali, C.4
Pianetti, G.5
Gamba, S.6
-
20
-
-
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) 16:2150-5. doi:10.1681/ASN.2005010103
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 2150-2155
-
-
Kavanagh, D.1
Kemp, E.J.2
Mayland, E.3
Winney, R.J.4
Duffield, J.S.5
Warwick, G.6
-
21
-
-
34548309310
-
Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome
-
Kavanagh D, Richards A, Noris M, Hauhart R, Liszewski MK, Karpman D, et al. Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome. Mol Immunol (2008) 45:95-105. doi:10.1016/j.molimm.2007.05.004
-
(2008)
Mol Immunol
, vol.45
, pp. 95-105
-
-
Kavanagh, D.1
Richards, A.2
Noris, M.3
Hauhart, R.4
Liszewski, M.K.5
Karpman, D.6
-
22
-
-
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, Kavanagh D, Barlow PN, Herbert AP, 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) 115:379-87. doi:10.1182/blood-2009-05-221549
-
(2010)
Blood
, vol.115
, pp. 379-387
-
-
Moore, I.1
Strain, L.2
Pappworth, I.3
Kavanagh, D.4
Barlow, P.N.5
Herbert, A.P.6
-
23
-
-
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, Riedl M, Rosales A, Giner T, 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) 8:407-15. doi:10.2215/CJN.01260212
-
(2013)
Clin J Am Soc Nephrol
, vol.8
, pp. 407-415
-
-
Hofer, J.1
Janecke, A.R.2
Zimmerhackl, L.B.3
Riedl, M.4
Rosales, A.5
Giner, T.6
-
24
-
-
34547633064
-
Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome
-
Sellier-Leclerc AL, Fremeaux-Bacchi V, Dragon-Durey MA, Macher MA, Niaudet P, Guest G, et al. Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome. J Am Soc Nephrol (2007) 18:2392-400. doi:10.1681/ASN.2006080811
-
(2007)
J Am Soc Nephrol
, vol.18
, pp. 2392-2400
-
-
Sellier-Leclerc, A.L.1
Fremeaux-Bacchi, V.2
Dragon-Durey, M.A.3
Macher, M.A.4
Niaudet, P.5
Guest, G.6
-
25
-
-
0242331610
-
Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome
-
Richards A, Kemp EJ, Liszewski MK, Goodship JA, Lampe AK, Decorte R, 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) 100:12966-71. doi:10.1073/pnas.2135497100
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 12966-12971
-
-
Richards, A.1
Kemp, E.J.2
Liszewski, M.K.3
Goodship, J.A.4
Lampe, A.K.5
Decorte, R.6
-
26
-
-
75749153964
-
Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome
-
Bienaime F, Dragon-Durey MA, Regnier CH, Nilsson SC, Kwan WH, Blouin J, et al. Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome. Kidney Int (2010) 77:339-49. doi:10.1038/ki.2009.472
-
(2010)
Kidney Int
, vol.77
, pp. 339-349
-
-
Bienaime, F.1
Dragon-Durey, M.A.2
Regnier, C.H.3
Nilsson, S.C.4
Kwan, W.H.5
Blouin, J.6
-
27
-
-
85061974325
-
-
In: Pagon RA, Adam MP, Ardinger HH, Bird TD, Dolan CR, Fong C-T, et al. editors. GeneReviews® [Internet]. Seattle, WA: University of Washington; 1993-2014
-
Noris M, Bresin E, Mele C, Remuzzi G. Atypical hemolytic-uremic syndrome. In: Pagon RA, Adam MP, Ardinger HH, Bird TD, Dolan CR, Fong C-T, et al. editors. GeneReviews® [Internet]. Seattle, WA: University of Washington; 1993-2014 (2013). p. 9-26
-
(2013)
Atypical hemolytic-uremic syndrome
, pp. 9-26
-
-
Noris, M.1
Bresin, E.2
Mele, C.3
Remuzzi, G.4
-
28
-
-
74249114451
-
Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I
-
Nilsson SC, Kalchishkova N, Trouw LA, Fremeaux-Bacchi V, Villoutreix BO, Blom AM. Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I. Eur J Immunol (2010) 40:172-85. doi:10.1002/eji.200939280
-
(2010)
Eur J Immunol
, vol.40
, pp. 172-185
-
-
Nilsson, S.C.1
Kalchishkova, N.2
Trouw, L.A.3
Fremeaux-Bacchi, V.4
Villoutreix, B.O.5
Blom, A.M.6
-
29
-
-
84886949690
-
Post-transplant recurrence of atypical hemolytic uremic syndrome in a patient with thrombomodulin mutation
-
Sinibaldi S, Guzzo I, Piras R, Bresin E, Emma F, Dello Strologo L. Post-transplant recurrence of atypical hemolytic uremic syndrome in a patient with thrombomodulin mutation. Pediatr Transplant (2013) 17:E177-81. doi:10.1111/petr.12151
-
(2013)
Pediatr Transplant
, vol.17
, pp. E177-E181
-
-
Sinibaldi, S.1
Guzzo, I.2
Piras, R.3
Bresin, E.4
Emma, F.5
Dello Strologo, L.6
-
30
-
-
77951257162
-
A novel mutation in the complement factor B gene (CFB) and atypical hemolytic uremic syndrome
-
Tawadrous H, Maga T, Sharma J, Kupferman J, Smith RJ, Schoeneman M. A novel mutation in the complement factor B gene (CFB) and atypical hemolytic uremic syndrome. Pediatr Nephrol (2010) 25:947-51. doi:10.1007/s00467-009-1415-3
-
(2010)
Pediatr Nephrol
, vol.25
, pp. 947-951
-
-
Tawadrous, H.1
Maga, T.2
Sharma, J.3
Kupferman, J.4
Smith, R.J.5
Schoeneman, M.6
-
32
-
-
53749084348
-
Complement and the atypical hemolytic uremic syndrome in children
-
Loirat C, Noris M, Fremeaux-Bacchi V. Complement and the atypical hemolytic uremic syndrome in children. Pediatr Nephrol (2008) 23:1957-72. doi:10.1007/s00467-008-0872-4
-
(2008)
Pediatr Nephrol
, vol.23
, pp. 1957-1972
-
-
Loirat, C.1
Noris, M.2
Fremeaux-Bacchi, V.3
-
33
-
-
77952682366
-
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome
-
Maga TK, Nishimura CJ, Weaver AE, Frees KL, Smith RJ. Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. Hum Mutat (2010) 31:E1445-60. doi:10.1002/humu.21256
-
(2010)
Hum Mutat
, vol.31
, pp. E1445-E1460
-
-
Maga, T.K.1
Nishimura, C.J.2
Weaver, A.E.3
Frees, K.L.4
Smith, R.J.5
-
34
-
-
40449085427
-
The complement factor H R1210C mutation is associated with atypical hemolytic uremic syndrome
-
Martinez-Barricarte R, Pianetti G, Gautard R, Misselwitz J, Strain L, Fremeaux-Bacchi V, et al. The complement factor H R1210C mutation is associated with atypical hemolytic uremic syndrome. J Am Soc Nephrol (2008) 19:639-46. doi:10.1681/ASN.2007080923
-
(2008)
J Am Soc Nephrol
, vol.19
, pp. 639-646
-
-
Martinez-Barricarte, R.1
Pianetti, G.2
Gautard, R.3
Misselwitz, J.4
Strain, L.5
Fremeaux-Bacchi, V.6
-
35
-
-
76949087440
-
Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome
-
Abarrategui-Garrido C, Martínez-Barricarte R, López-Trascasa M, de Córdoba SR, Sánchez-Corral P. Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome. Blood (2009) 114:4261-71. doi:10.1182/blood-2009-05-223834
-
(2009)
Blood
, vol.114
, pp. 4261-4271
-
-
Abarrategui-Garrido, C.1
Martínez-Barricarte, R.2
López-Trascasa, M.3
de Córdoba, S.R.4
Sánchez-Corral, P.5
-
36
-
-
57649230771
-
Complement factor H related proteins in immune diseases
-
Skerka C, Zipfel PF. Complement factor H related proteins in immune diseases. Vaccine (2008) 26(Suppl 8):I9-14. doi:10.1016/j.vaccine.2008.11.021
-
(2008)
Vaccine
, vol.26
, pp. I9-I14
-
-
Skerka, C.1
Zipfel, P.F.2
-
37
-
-
33750855444
-
Atypical haemolytic uraemic syndrome associated with a hybrid complement gene
-
Venables JP, Strain L, Routledge D, Bourn D, Powell HM, Warwicker P, et al. Atypical haemolytic uraemic syndrome associated with a hybrid complement gene. PLoS Med (2006) 3:e431. doi:10.1371/journal.pmed.0030431
-
(2006)
PLoS Med
, vol.3
-
-
Venables, J.P.1
Strain, L.2
Routledge, D.3
Bourn, D.4
Powell, H.M.5
Warwicker, P.6
-
38
-
-
84855862414
-
A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome
-
Francis NJ, McNicholas B, Awan A, Waldron M, Reddan D, Sadlier D, et al. A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome. Blood (2012) 119:591-601. doi:10.1182/blood-2011-03-339903
-
(2012)
Blood
, vol.119
, pp. 591-601
-
-
Francis, N.J.1
McNicholas, B.2
Awan, A.3
Waldron, M.4
Reddan, D.5
Sadlier, D.6
-
39
-
-
38949155911
-
Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency
-
Józsi M, Licht C, Strobel S, Zipfel SL, Richter H, Heinen S, et al. Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency. Blood (2008) 111:1512-4. doi:10.1182/blood-2007-09-109876
-
(2008)
Blood
, vol.111
, pp. 1512-1514
-
-
Józsi, M.1
Licht, C.2
Strobel, S.3
Zipfel, S.L.4
Richter, H.5
Heinen, S.6
-
40
-
-
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, Loirat C, Blouin J, Sautes-Fridman C, 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) 46:447-50. doi:10.1136/jmg.2008.064766
-
(2009)
J Med Genet
, vol.46
, pp. 447-450
-
-
Dragon-Durey, M.A.1
Blanc, C.2
Marliot, F.3
Loirat, C.4
Blouin, J.5
Sautes-Fridman, C.6
-
41
-
-
77956231486
-
DEAP-HUS: deficiency of CFHR plasma proteins and autoantibody-positive form of hemolytic uremic syndrome
-
Zipfel PF, Mache C, Müller D, Licht C, Wigger M, Skerka C, et al. DEAP-HUS: deficiency of CFHR plasma proteins and autoantibody-positive form of hemolytic uremic syndrome. Pediatr Nephrol (2010) 25:2009-19. doi:10.1007/s00467-010-1446-9
-
(2010)
Pediatr Nephrol
, vol.25
, pp. 2009-2019
-
-
Zipfel, P.F.1
Mache, C.2
Müller, D.3
Licht, C.4
Wigger, M.5
Skerka, C.6
-
42
-
-
84860141031
-
A new era in the diagnosis and treatment of atypical haemolytic uraemic syndrome
-
Westra D, Wetzels JF, Volokhina EB, van den Heuvel LP, van de Kar NC. A new era in the diagnosis and treatment of atypical haemolytic uraemic syndrome. Neth J Med (2012) 70:121-9
-
(2012)
Neth J Med
, vol.70
, pp. 121-129
-
-
Westra, D.1
Wetzels, J.F.2
Volokhina, E.B.3
van den Heuvel, L.P.4
van de Kar, N.C.5
-
43
-
-
0242694369
-
The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children
-
Loirat C, Niaudet P. The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children. Pediatr Nephrol (2003) 18:1095-101. doi:10.1007/s00467-003-1289-8
-
(2003)
Pediatr Nephrol
, vol.18
, pp. 1095-1101
-
-
Loirat, C.1
Niaudet, P.2
-
44
-
-
0026073049
-
Post-transplantation outcome of patients with hemolytic-uremic syndrome: update
-
Hébert D, Kim EM, Sibley RK, Mauer MS. Post-transplantation outcome of patients with hemolytic-uremic syndrome: update. Pediatr Nephrol (1991) 5:162-7. doi:10.1007/BF00852876
-
(1991)
Pediatr Nephrol
, vol.5
, pp. 162-167
-
-
Hébert, D.1
Kim, E.M.2
Sibley, R.K.3
Mauer, M.S.4
-
45
-
-
0022621084
-
Recurrence of hemolytic uremic syndrome in renal transplant recipients
-
Hebert D, Sibley RK, Mauer SM. Recurrence of hemolytic uremic syndrome in renal transplant recipients. Kidney Int Suppl (1986) 19:S51-8
-
(1986)
Kidney Int Suppl
, vol.19
, pp. S51-S58
-
-
Hebert, D.1
Sibley, R.K.2
Mauer, S.M.3
-
46
-
-
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, Monnens LA, Wetzels JF. Renal transplantation in patients with hemolytic uremic syndrome: high rate of recurrence and increased incidence of acute rejections. Transplantation (2003) 76:821-6. doi:10.1097/01.TP.0000085083.74065.1B
-
(2003)
Transplantation
, vol.76
, pp. 821-826
-
-
Artz, M.A.1
Steenbergen, E.J.2
Hoitsma, A.J.3
Monnens, L.A.4
Wetzels, J.F.5
-
47
-
-
0034034718
-
Hemolytic uremic syndrome Recurrence after renal transplantation. Groupe Cooperatif de l'Ile-de-France (GCIF)
-
Lahlou A, Lang P, Charpentier B, Barrou B, Glotz D, Baron C, et al. Hemolytic uremic syndrome. Recurrence after renal transplantation. Groupe Cooperatif de l'Ile-de-France (GCIF). Medicine (Baltimore) (2000) 79:90-102. doi:10.1097/00005792-200003000-00003
-
(2000)
Medicine (Baltimore)
, vol.79
, pp. 90-102
-
-
Lahlou, A.1
Lang, P.2
Charpentier, B.3
Barrou, B.4
Glotz, D.5
Baron, C.6
-
48
-
-
0035959420
-
Recurrence of hemolytic uremic syndrome after renal transplantation in children: a report of the North American Pediatric Renal Transplant Cooperative Study
-
Quan A, Sullivan EK, Alexander SR. Recurrence of hemolytic uremic syndrome after renal transplantation in children: a report of the North American Pediatric Renal Transplant Cooperative Study. Transplantation (2001) 72:742-5. doi:10.1097/00007890-200108270-00033
-
(2001)
Transplantation
, vol.72
, pp. 742-745
-
-
Quan, A.1
Sullivan, E.K.2
Alexander, S.R.3
-
49
-
-
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, Castelletti F, Stefanov R, Hill P, et al. Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background. Clin J Am Soc Nephrol (2006) 1:88-99. doi:10.2215/CJN.00050505
-
(2006)
Clin J Am Soc Nephrol
, vol.1
, pp. 88-99
-
-
Bresin, E.1
Daina, E.2
Noris, M.3
Castelletti, F.4
Stefanov, R.5
Hill, P.6
-
50
-
-
49349112382
-
Hemolytic uremic syndrome recurrence after renal transplantation
-
Loirat C, Fremeaux-Bacchi V. Hemolytic uremic syndrome recurrence after renal transplantation. Pediatr Transplant (2008) 12:619-29. doi:10.1111/j.1399-3046.2008.00910.x
-
(2008)
Pediatr Transplant
, vol.12
, pp. 619-629
-
-
Loirat, C.1
Fremeaux-Bacchi, V.2
-
51
-
-
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, Kamar N, Jablonski M, Lionet A, 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) 13:663-75. doi:10.1111/ajt.12077
-
(2013)
Am J Transplant
, vol.13
, pp. 663-675
-
-
Le Quintrec, M.1
Zuber, J.2
Moulin, B.3
Kamar, N.4
Jablonski, M.5
Lionet, A.6
-
52
-
-
44449165673
-
Successful pre-transplant management of a patient with anti-factor H autoantibodies-associated haemolytic uraemic syndrome
-
Kwon T, Dragon-Durey MA, Macher MA, Baudouin V, Maisin A, Peuchmaur M, et al. Successful pre-transplant management of a patient with anti-factor H autoantibodies-associated haemolytic uraemic syndrome. Nephrol Dial Transplant (2008) 23:2088-90. doi:10.1093/ndt/gfn063
-
(2008)
Nephrol Dial Transplant
, vol.23
, pp. 2088-2090
-
-
Kwon, T.1
Dragon-Durey, M.A.2
Macher, M.A.3
Baudouin, V.4
Maisin, A.5
Peuchmaur, M.6
-
53
-
-
65249156546
-
Anti-Factor H autoantibodies in a fifth renal transplant recipient with atypical hemolytic and uremic syndrome
-
Le Quintrec M, Zuber J, Noel LH, Thervet E, Frémeaux-Bacchi V, Niaudet P, et al. Anti-Factor H autoantibodies in a fifth renal transplant recipient with atypical hemolytic and uremic syndrome. Am J Transplant (2009) 9:1223-9. doi:10.1111/j.1600-6143.2009.02586.x
-
(2009)
Am J Transplant
, vol.9
, pp. 1223-1229
-
-
Le Quintrec, M.1
Zuber, J.2
Noel, L.H.3
Thervet, E.4
Frémeaux-Bacchi, V.5
Niaudet, P.6
-
54
-
-
72549110489
-
Successful renal transplantation in factor H autoantibody associated HUS with CFHR1 and 3 deficiency and CFH variant G2850T
-
Waters AM, Pappworth I, Marchbank K, Bockenhauer D, Tullus K, Pickering MC, et al. Successful renal transplantation in factor H autoantibody associated HUS with CFHR1 and 3 deficiency and CFH variant G2850T. Am J Transplant (2010) 10:168-72. doi:10.1111/j.1600-6143.2009.02870.x
-
(2010)
Am J Transplant
, vol.10
, pp. 168-172
-
-
Waters, A.M.1
Pappworth, I.2
Marchbank, K.3
Bockenhauer, D.4
Tullus, K.5
Pickering, M.C.6
-
55
-
-
19444369542
-
Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome
-
Fremeaux-Bacchi V, Dragon-Durey MA, Blouin J, Vigneau C, Kuypers D, Boudailliez B, et al. Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome. J Med Genet (2004) 41:e84. doi:10.1136/jmg.2004.019083
-
(2004)
J Med Genet
, vol.41
-
-
Fremeaux-Bacchi, V.1
Dragon-Durey, M.A.2
Blouin, J.3
Vigneau, C.4
Kuypers, D.5
Boudailliez, B.6
-
56
-
-
58249107188
-
Recurrent atypical hemolytic uremic syndrome associated with factor I mutation in a living related renal transplant recipient
-
Chan MR, Thomas CP, Torrealba JR, Djamali A, Fernandez LA, Nishimura CJ, et al. Recurrent atypical hemolytic uremic syndrome associated with factor I mutation in a living related renal transplant recipient. Am J Kidney Dis (2009) 53:321-6. doi:10.1053/j.ajkd.2008.06.027
-
(2009)
Am J Kidney Dis
, vol.53
, pp. 321-326
-
-
Chan, M.R.1
Thomas, C.P.2
Torrealba, J.R.3
Djamali, A.4
Fernandez, L.A.5
Nishimura, C.J.6
-
57
-
-
34248664063
-
A missense mutation in factor I (IF) predisposes to atypical haemolytic uraemic syndrome
-
Geelen J, van den Dries K, Roos A, van de Kar N, de Kat Angelino C, Klasen I, et al. A missense mutation in factor I (IF) predisposes to atypical haemolytic uraemic syndrome. Pediatr Nephrol (2007) 22:371-5. doi:10.1007/s00467-006-0320-2
-
(2007)
Pediatr Nephrol
, vol.22
, pp. 371-375
-
-
Geelen, J.1
van den Dries, K.2
Roos, A.3
van de Kar, N.4
de Kat Angelino, C.5
Klasen, I.6
-
58
-
-
33751536085
-
A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation
-
Nilsson SC, Karpman D, Vaziri-Sani F, Kristoffersson AC, Salomon R, Provot F, et al. A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation. Mol Immunol (2007) 44:1835-44. doi:10.1016/j.molimm.2006.10.005
-
(2007)
Mol Immunol
, vol.44
, pp. 1835-1844
-
-
Nilsson, S.C.1
Karpman, D.2
Vaziri-Sani, F.3
Kristoffersson, A.C.4
Salomon, R.5
Provot, F.6
-
59
-
-
68449088805
-
Prophylactic plasma exchange in CD46-associated atypical haemolytic uremic syndrome
-
Davin JC, Buter N, Groothoff J, van Wijk J, Bouts A, Strain L, et al. Prophylactic plasma exchange in CD46-associated atypical haemolytic uremic syndrome. Pediatr Nephrol (2009) 24:1757-60. doi:10.1007/s00467-009-1188-8
-
(2009)
Pediatr Nephrol
, vol.24
, pp. 1757-1760
-
-
Davin, J.C.1
Buter, N.2
Groothoff, J.3
van Wijk, J.4
Bouts, A.5
Strain, L.6
-
60
-
-
33745812440
-
Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome
-
Fremeaux-Bacchi V, Moulton EA, Kavanagh D, Dragon-Durey MA, Blouin J, Caudy A, et al. Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome. J Am Soc Nephrol (2006) 17:2017-25. doi:10.1681/ASN.2005101051
-
(2006)
J Am Soc Nephrol
, vol.17
, pp. 2017-2025
-
-
Fremeaux-Bacchi, V.1
Moulton, E.A.2
Kavanagh, D.3
Dragon-Durey, M.A.4
Blouin, J.5
Caudy, A.6
-
61
-
-
84874610717
-
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype
-
Bresin E, Rurali E, Caprioli J, Sanchez-Corral P, Fremeaux-Bacchi V, Rodriguez de Cordoba S, et al. Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype. J Am Soc Nephrol (2013) 24:475-86. doi:10.1681/ASN.2012090884
-
(2013)
J Am Soc Nephrol
, vol.24
, pp. 475-486
-
-
Bresin, E.1
Rurali, E.2
Caprioli, J.3
Sanchez-Corral, P.4
Fremeaux-Bacchi, V.5
Rodriguez de Cordoba, S.6
-
62
-
-
84917673672
-
Atypical hemolytic uremic syndrome recurrence after kidney transplantation
-
Matar D, Naqvi F, Racusen LC, Carter-Monroe N, Montgomery RA, Alachkar N. Atypical hemolytic uremic syndrome recurrence after kidney transplantation. Transplantation (2014) 98(11):1205-12. doi:10.1097/TP.0000000000000200
-
(2014)
Transplantation
, vol.98
, Issue.11
, pp. 1205-1212
-
-
Matar, D.1
Naqvi, F.2
Racusen, L.C.3
Carter-Monroe, N.4
Montgomery, R.A.5
Alachkar, N.6
-
63
-
-
0036284207
-
Local synthesis of complement component C3 regulates acute renal transplant rejection
-
Pratt JR, Basheer SA, Sacks SH. Local synthesis of complement component C3 regulates acute renal transplant rejection. Nat Med (2002) 8:582-7. doi:10.1038/nm0602-582
-
(2002)
Nat Med
, vol.8
, pp. 582-587
-
-
Pratt, J.R.1
Basheer, S.A.2
Sacks, S.H.3
-
64
-
-
33746897348
-
Preventing renal ischemia-reperfusion injury using small interfering RNA by targeting complement 3 gene
-
Zheng X, Feng B, Chen G, Zhang X, Li M, Sun H, et al. Preventing renal ischemia-reperfusion injury using small interfering RNA by targeting complement 3 gene. Am J Transplant (2006) 6:2099-108. doi:10.1111/j.1600-6143.2006.01427.x
-
(2006)
Am J Transplant
, vol.6
, pp. 2099-2108
-
-
Zheng, X.1
Feng, B.2
Chen, G.3
Zhang, X.4
Li, M.5
Sun, H.6
-
65
-
-
70350475255
-
Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome
-
Roumenina LT, Jablonski M, Hue C, Blouin J, Dimitrov JD, Dragon-Durey MA, et al. Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome. Blood (2009) 114:2837-45. doi:10.1182/blood-2009-01-197640
-
(2009)
Blood
, vol.114
, pp. 2837-2845
-
-
Roumenina, L.T.1
Jablonski, M.2
Hue, C.3
Blouin, J.4
Dimitrov, J.D.5
Dragon-Durey, M.A.6
-
66
-
-
84876044818
-
Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults
-
Fremeaux-Bacchi V, Fakhouri F, Garnier A, Bienaimé 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) 8:554-62. doi:10.2215/CJN.04760512
-
(2013)
Clin J Am Soc Nephrol
, vol.8
, pp. 554-562
-
-
Fremeaux-Bacchi, V.1
Fakhouri, F.2
Garnier, A.3
Bienaimé, F.4
Dragon-Durey, M.A.5
Ngo, S.6
-
67
-
-
0032571989
-
Recurrence of hemolytic-uremic syndrome in renal transplant recipients: a meta-analysis
-
Ducloux D, Rebibou JM, Semhoun-Ducloux S, Jamali M, Fournier V, Bresson-Vautrin C, et al. Recurrence of hemolytic-uremic syndrome in renal transplant recipients: a meta-analysis. Transplantation (1998) 65:1405-7. doi:10.1097/00007890-199805270-00023
-
(1998)
Transplantation
, vol.65
, pp. 1405-1407
-
-
Ducloux, D.1
Rebibou, J.M.2
Semhoun-Ducloux, S.3
Jamali, M.4
Fournier, V.5
Bresson-Vautrin, C.6
-
68
-
-
68049125195
-
Expression of complement components differs between kidney allografts from living and deceased donors
-
Naesens M, Li L, Ying L, Sansanwal P, Sigdel TK, Hsieh SC, et al. Expression of complement components differs between kidney allografts from living and deceased donors. J Am Soc Nephrol (2009) 20:1839-51. doi:10.1681/ASN.2008111145
-
(2009)
J Am Soc Nephrol
, vol.20
, pp. 1839-1851
-
-
Naesens, M.1
Li, L.2
Ying, L.3
Sansanwal, P.4
Sigdel, T.K.5
Hsieh, S.C.6
-
69
-
-
84875701958
-
Complement mediated renal inflammation induced by donor brain death: role of renal C5a-C5aR interaction
-
van Werkhoven MB, Damman J, van Dijk MC, Daha MR, de Jong IJ, Leliveld A, et al. Complement mediated renal inflammation induced by donor brain death: role of renal C5a-C5aR interaction. Am J Transplant (2013) 13:875-82. doi:10.1111/ajt.12130
-
(2013)
Am J Transplant
, vol.13
, pp. 875-882
-
-
van Werkhoven, M.B.1
Damman, J.2
van Dijk, M.C.3
Daha, M.R.4
de Jong, I.J.5
Leliveld, A.6
-
70
-
-
78349277612
-
Acute ischemic injury to the renal microvasculature in human kidney transplantation
-
Snoeijs MG, Vink H, Voesten N, Christiaans MH, Daemen JW, Peppelenbosch AG, et al. Acute ischemic injury to the renal microvasculature in human kidney transplantation. Am J Physiol Renal Physiol (2010) 299:F1134-40. doi:10.1152/ajprenal.00158.2010
-
(2010)
Am J Physiol Renal Physiol
, vol.299
, pp. F1134-F1140
-
-
Snoeijs, M.G.1
Vink, H.2
Voesten, N.3
Christiaans, M.H.4
Daemen, J.W.5
Peppelenbosch, A.G.6
-
71
-
-
11144290605
-
Posttransplantation cytomegalovirus-induced recurrence of atypical hemolytic uremic syndrome associated with a factor H mutation: successful treatment with intensive plasma exchanges and ganciclovir
-
Olie KH, Goodship TH, Verlaak R, Florquin S, Groothoff JW, Strain L, et al. Posttransplantation cytomegalovirus-induced recurrence of atypical hemolytic uremic syndrome associated with a factor H mutation: successful treatment with intensive plasma exchanges and ganciclovir. Am J Kidney Dis (2005) 45:e12-5. doi:10.1053/j.ajkd.2004.09.012
-
(2005)
Am J Kidney Dis
, vol.45
, pp. e12-e15
-
-
Olie, K.H.1
Goodship, T.H.2
Verlaak, R.3
Florquin, S.4
Groothoff, J.W.5
Strain, L.6
-
72
-
-
79954443076
-
Eculizumab induces long-term remission in recurrent post-transplant HUS associated with C3 gene mutation
-
Al-Akash SI, Almond PS, Savell VH Jr, Gharaybeh SI, Hogue C. Eculizumab induces long-term remission in recurrent post-transplant HUS associated with C3 gene mutation. Pediatr Nephrol (2011) 26:613-9. doi:10.1007/s00467-010-1708-6
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 613-619
-
-
Al-Akash, S.I.1
Almond, P.S.2
Savell, V.H.3
Gharaybeh, S.I.4
Hogue, C.5
-
73
-
-
79952997596
-
Pandemic influenza A (H1N1) 2009-associated hemolytic uremic syndrome
-
Printza N, Roilides E, Kotsiou M, Zafeiriou D, Hatzidimitriou V, Papachristou F. Pandemic influenza A (H1N1) 2009-associated hemolytic uremic syndrome. Pediatr Nephrol (2011) 26:143-4. doi:10.1007/s00467-010-1603-1
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 143-144
-
-
Printza, N.1
Roilides, E.2
Kotsiou, M.3
Zafeiriou, D.4
Hatzidimitriou, V.5
Papachristou, F.6
-
74
-
-
79953019720
-
Atypical hemolytic uremic syndrome associated with H1N1 influenza A virus infection
-
Trachtman H, Sethna C, Epstein R, D'Souza M, Rubin LG, Ginocchio CC. Atypical hemolytic uremic syndrome associated with H1N1 influenza A virus infection. Pediatr Nephrol (2011) 26:145-6. doi:10.1007/s00467-010-1636-5
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 145-146
-
-
Trachtman, H.1
Sethna, C.2
Epstein, R.3
D'Souza, M.4
Rubin, L.G.5
Ginocchio, C.C.6
-
75
-
-
0034130092
-
Thrombotic microangiopathy associated with parvovirus B 19 infection after renal transplantation
-
Murer L, Zacchello G, Bianchi D, Dall'Amico R, Montini G, Andreetta B, et al. Thrombotic microangiopathy associated with parvovirus B 19 infection after renal transplantation. J Am Soc Nephrol (2000) 11:1132-7
-
(2000)
J Am Soc Nephrol
, vol.11
, pp. 1132-1137
-
-
Murer, L.1
Zacchello, G.2
Bianchi, D.3
Dall'Amico, R.4
Montini, G.5
Andreetta, B.6
-
76
-
-
0035950694
-
BK-related polyomavirus vasculopathy in a renal-transplant recipient
-
Petrogiannis-Haliotis T, Sakoulas G, Kirby J, Koralnik IJ, Dvorak AM, Monahan-Earley R, et al. BK-related polyomavirus vasculopathy in a renal-transplant recipient. N Engl J Med (2001) 345:1250-5. doi:10.1056/NEJMoa010319
-
(2001)
N Engl J Med
, vol.345
, pp. 1250-1255
-
-
Petrogiannis-Haliotis, T.1
Sakoulas, G.2
Kirby, J.3
Koralnik, I.J.4
Dvorak, A.M.5
Monahan-Earley, R.6
-
77
-
-
80052473232
-
Prophylactic eculizumab prior to kidney transplantation for atypical hemolytic uremic syndrome
-
Weitz M, Amon O, Bassler D, Koenigsrainer A, Nadalin S. Prophylactic eculizumab prior to kidney transplantation for atypical hemolytic uremic syndrome. Pediatr Nephrol (2011) 26:1325-9. doi:10.1007/s00467-011-1879-9
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 1325-1329
-
-
Weitz, M.1
Amon, O.2
Bassler, D.3
Koenigsrainer, A.4
Nadalin, S.5
-
78
-
-
79958202220
-
Pre-emptive eculizumab and plasmapheresis for renal transplant in atypical hemolytic uremic syndrome
-
Nester C, Stewart Z, Myers D, Jetton J, Nair R, Reed A, et al. Pre-emptive eculizumab and plasmapheresis for renal transplant in atypical hemolytic uremic syndrome. Clin J Am Soc Nephrol (2011) 6:1488-94. doi:10.2215/CJN.10181110
-
(2011)
Clin J Am Soc Nephrol
, vol.6
, pp. 1488-1494
-
-
Nester, C.1
Stewart, Z.2
Myers, D.3
Jetton, J.4
Nair, R.5
Reed, A.6
-
79
-
-
53749100296
-
Impact of immunosuppressive treatment on endothelial biomarkers after kidney transplantation
-
Al-Massarani G, Vacher-Coponat H, Paul P, Widemann A, Arnaud L, Loundou A, et al. Impact of immunosuppressive treatment on endothelial biomarkers after kidney transplantation. Am J Transplant (2008) 8:2360-7. doi:10.1111/j.1600-6143.2008.02399.x
-
(2008)
Am J Transplant
, vol.8
, pp. 2360-2367
-
-
Al-Massarani, G.1
Vacher-Coponat, H.2
Paul, P.3
Widemann, A.4
Arnaud, L.5
Loundou, A.6
-
80
-
-
33746929488
-
mTOR inhibition induces endothelial progenitor cell death
-
Miriuka SG, Rao V, Peterson M, Tumiati L, Delgado DH, Mohan R, et al. mTOR inhibition induces endothelial progenitor cell death. Am J Transplant (2006) 6:2069-79. doi:10.1111/j.1600-6143.2006.01433.x
-
(2006)
Am J Transplant
, vol.6
, pp. 2069-2079
-
-
Miriuka, S.G.1
Rao, V.2
Peterson, M.3
Tumiati, L.4
Delgado, D.H.5
Mohan, R.6
-
81
-
-
34250166544
-
De novo thrombotic microangiopathy An underrated complication of renal transplantation
-
Ponticelli C. De novo thrombotic microangiopathy. An underrated complication of renal transplantation. Clin Nephrol (2007) 67:335-40. doi:10.5414/CNP67335
-
(2007)
Clin Nephrol
, vol.67
, pp. 335-340
-
-
Ponticelli, C.1
-
82
-
-
48349086641
-
Complement mutation-associated de novo thrombotic microangiopathy following kidney transplantation
-
Le Quintrec M, Lionet A, Kamar N, Karras A, Barbier S, Buchler M, et al. Complement mutation-associated de novo thrombotic microangiopathy following kidney transplantation. Am J Transplant (2008) 8:1694-701. doi:10.1111/j.1600-6143.2008.02297.x
-
(2008)
Am J Transplant
, vol.8
, pp. 1694-1701
-
-
Le Quintrec, M.1
Lionet, A.2
Kamar, N.3
Karras, A.4
Barbier, S.5
Buchler, M.6
-
83
-
-
0037308113
-
De novo thrombotic microangiopathy in renal transplant recipients: a comparison of hemolytic uremic syndrome with localized renal thrombotic microangiopathy
-
Schwimmer J, Nadasdy TA, Spitalnik PF, Kaplan KL, Zand MS. De novo thrombotic microangiopathy in renal transplant recipients: a comparison of hemolytic uremic syndrome with localized renal thrombotic microangiopathy. Am J Kidney Dis (2003) 41:471-9. doi:10.1053/ajkd.2003.50058
-
(2003)
Am J Kidney Dis
, vol.41
, pp. 471-479
-
-
Schwimmer, J.1
Nadasdy, T.A.2
Spitalnik, P.F.3
Kaplan, K.L.4
Zand, M.S.5
-
84
-
-
80054767700
-
Successful treatment of de novo posttransplant thrombotic microangiopathy with eculizumab
-
Wilson CH, Brown AL, White SA, Goodship TH, Sheerin NS, Manas DM. Successful treatment of de novo posttransplant thrombotic microangiopathy with eculizumab. Transplantation (2011) 92:e42-3. doi:10.1097/TP.0b013e318230c0bd
-
(2011)
Transplantation
, vol.92
, pp. e42-e43
-
-
Wilson, C.H.1
Brown, A.L.2
White, S.A.3
Goodship, T.H.4
Sheerin, N.S.5
Manas, D.M.6
-
85
-
-
20444446312
-
Recent advances in thrombotic thrombocytopenic purpura
-
Sadler JE, Moake JL, Miyata T, George JN. Recent advances in thrombotic thrombocytopenic purpura. Hematology Am Soc Hematol Educ Program (2004) 2004(1):407-23. doi:10.1182/asheducation-2004.1.407
-
(2004)
Hematology Am Soc Hematol Educ Program
, vol.2004
, Issue.1
, pp. 407-423
-
-
Sadler, J.E.1
Moake, J.L.2
Miyata, T.3
George, J.N.4
-
86
-
-
77950805395
-
Cardiovascular manifestations in patients with thrombotic thrombocytopenic purpura: a single-center experience
-
Gandhi K, Aronow WS, Desai H, Amin H, Sharma M, Lai HM, et al. Cardiovascular manifestations in patients with thrombotic thrombocytopenic purpura: a single-center experience. Clin Cardiol (2010) 33:213-6. doi:10.1002/clc.20731
-
(2010)
Clin Cardiol
, vol.33
, pp. 213-216
-
-
Gandhi, K.1
Aronow, W.S.2
Desai, H.3
Amin, H.4
Sharma, M.5
Lai, H.M.6
-
87
-
-
4844226603
-
Atypical relapse of hemolytic uremic syndrome after transplantation
-
Olie KH, Florquin S, Groothoff JW, Verlaak R, Strain L, Goodship TH, et al. Atypical relapse of hemolytic uremic syndrome after transplantation. Pediatr Nephrol (2004) 19:1173-6. doi:10.1007/s00467-004-1565-2
-
(2004)
Pediatr Nephrol
, vol.19
, pp. 1173-1176
-
-
Olie, K.H.1
Florquin, S.2
Groothoff, J.W.3
Verlaak, R.4
Strain, L.5
Goodship, T.H.6
-
88
-
-
84921945959
-
Atypical HUS associated with severe, unexpected antibody-mediated rejection post kidney transplant
-
Stevenson S, Mallett A, Oliver K, Hyland V, Hawley C, Malmanche T, et al. Atypical HUS associated with severe, unexpected antibody-mediated rejection post kidney transplant. Nephrology (Carlton) (2014) 19(Suppl 1):22-6. doi:10.1111/nep.12195
-
(2014)
Nephrology (Carlton)
, vol.19
, pp. 22-26
-
-
Stevenson, S.1
Mallett, A.2
Oliver, K.3
Hyland, V.4
Hawley, C.5
Malmanche, T.6
-
89
-
-
84865611225
-
Antibody mediated rejection associated with complement factor h-related protein 3/1 deficiency successfully treated with eculizumab
-
Noone D, Al-Matrafi J, Tinckam K, Zipfel PF, Herzenberg AM, Thorner PS, et al. Antibody mediated rejection associated with complement factor h-related protein 3/1 deficiency successfully treated with eculizumab. Am J Transplant (2012) 12:2546-53. doi:10.1111/j.1600-6143.2012.04124.x
-
(2012)
Am J Transplant
, vol.12
, pp. 2546-2553
-
-
Noone, D.1
Al-Matrafi, J.2
Tinckam, K.3
Zipfel, P.F.4
Herzenberg, A.M.5
Thorner, P.S.6
-
90
-
-
84867993256
-
Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies
-
Zuber J, Fakhouri F, Roumenina LT, Loirat C, Frémeaux-Bacchi V, French Study Group for aHUS/C3G. Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies. Nat Rev Nephrol (2012) 8:643-57. doi:10.1038/nrneph.2012.214
-
(2012)
Nat Rev Nephrol
, vol.8
, pp. 643-657
-
-
Zuber, J.1
Fakhouri, F.2
Roumenina, L.T.3
Loirat, C.4
Frémeaux-Bacchi, V.5
-
91
-
-
47749148096
-
Plasma therapy in atypical haemolytic uremic syndrome: lessons from a family with a factor H mutation
-
Davin JC, Strain L, Goodship TH. Plasma therapy in atypical haemolytic uremic syndrome: lessons from a family with a factor H mutation. Pediatr Nephrol (2008) 23:1517-21. doi:10.1007/s00467-008-0833-y
-
(2008)
Pediatr Nephrol
, vol.23
, pp. 1517-1521
-
-
Davin, J.C.1
Strain, L.2
Goodship, T.H.3
-
92
-
-
84857442742
-
Management of hemolytic uremic syndrome
-
Loirat C, Saland J, Bitzan M. Management of hemolytic uremic syndrome. Presse Med (2012) 41(3 Pt 2):e115-35. doi:10.1016/j.lpm.2011.11.013
-
(2012)
Presse Med
, vol.41
, Issue.3
, pp. e115-e135
-
-
Loirat, C.1
Saland, J.2
Bitzan, M.3
-
93
-
-
0037062233
-
Combined kidney and liver transplantation for familial haemolytic uraemic syndrome
-
Remuzzi G, Ruggenenti P, Codazzi D, Noris M, Caprioli J, Locatelli G, et al. Combined kidney and liver transplantation for familial haemolytic uraemic syndrome. Lancet (2002) 359:1671-2. doi:10.1016/S0140-6736(02)08560-4
-
(2002)
Lancet
, vol.359
, pp. 1671-1672
-
-
Remuzzi, G.1
Ruggenenti, P.2
Codazzi, D.3
Noris, M.4
Caprioli, J.5
Locatelli, G.6
-
94
-
-
20244377213
-
Hemolytic uremic syndrome: a fatal outcome after kidney and liver transplantation performed to correct factor h gene mutation
-
Remuzzi G, Ruggenenti P, Colledan M, Gridelli B, Bertani A, Bettinaglio P, et al. Hemolytic uremic syndrome: a fatal outcome after kidney and liver transplantation performed to correct factor h gene mutation. Am J Transplant (2005) 5:1146-50. doi:10.1111/j.1600-6143.2005.00783.x
-
(2005)
Am J Transplant
, vol.5
, pp. 1146-1150
-
-
Remuzzi, G.1
Ruggenenti, P.2
Colledan, M.3
Gridelli, B.4
Bertani, A.5
Bettinaglio, P.6
-
95
-
-
84861130721
-
Hyaluronan regulation of vascular integrity
-
Lennon FE, Singleton PA. Hyaluronan regulation of vascular integrity. Am J Cardiovasc Dis (2011) 1:200-13
-
(2011)
Am J Cardiovasc Dis
, vol.1
, pp. 200-213
-
-
Lennon, F.E.1
Singleton, P.A.2
-
96
-
-
37349124206
-
Shedding of the endothelial glycocalyx in patients undergoing major vascular surgery with global and regional ischemia
-
Rehm M, Bruegger D, Christ F, Conzen P, Thiel M, Jacob M, et al. Shedding of the endothelial glycocalyx in patients undergoing major vascular surgery with global and regional ischemia. Circulation (2007) 116:1896-906. doi:10.1161/CIRCULATIONAHA.106.684852
-
(2007)
Circulation
, vol.116
, pp. 1896-1906
-
-
Rehm, M.1
Bruegger, D.2
Christ, F.3
Conzen, P.4
Thiel, M.5
Jacob, M.6
-
97
-
-
84894107600
-
Liver-kidney transplantation to cure atypical HUS: still an option post-eculizumab?
-
Saland J. Liver-kidney transplantation to cure atypical HUS: still an option post-eculizumab? Pediatr Nephrol (2014) 29:329-32. doi:10.1007/s00467-013-2722-2
-
(2014)
Pediatr Nephrol
, vol.29
, pp. 329-332
-
-
Saland, J.1
-
98
-
-
84870534251
-
Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation
-
Zuber J, Le Quintrec M, Krid S, Bertoye C, Gueutin V, Lahoche A, et al. Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation. Am J Transplant (2012) 12:3337-54. doi:10.1111/j.1600-6143.2012.04252.x
-
(2012)
Am J Transplant
, vol.12
, pp. 3337-3354
-
-
Zuber, J.1
Le Quintrec, M.2
Krid, S.3
Bertoye, C.4
Gueutin, V.5
Lahoche, A.6
-
99
-
-
70350130833
-
Safety and long-term efficacy of eculizumab in a renal transplant patient with recurrent atypical hemolytic-uremic syndrome
-
Chatelet V, Frémeaux-Bacchi V, Lobbedez T, Ficheux M, Hurault de Ligny B. Safety and long-term efficacy of eculizumab in a renal transplant patient with recurrent atypical hemolytic-uremic syndrome. Am J Transplant (2009) 9:2644-5. doi:10.1111/j.1600-6143.2009.02817.x
-
(2009)
Am J Transplant
, vol.9
, pp. 2644-2645
-
-
Chatelet, V.1
Frémeaux-Bacchi, V.2
Lobbedez, T.3
Ficheux, M.4
Hurault de Ligny, B.5
-
100
-
-
80052268538
-
Complement activation during liver transplantation-special emphasis on patients with atypical hemolytic uremic syndrome
-
Koskinen AR, Tukiainen E, Arola J, Nordin A, Höckerstedt HK, Nilsson B, et al. Complement activation during liver transplantation-special emphasis on patients with atypical hemolytic uremic syndrome. Am J Transplant (2011) 11:1885-95. doi:10.1111/j.1600-6143.2011.03612.x
-
(2011)
Am J Transplant
, vol.11
, pp. 1885-1895
-
-
Koskinen, A.R.1
Tukiainen, E.2
Arola, J.3
Nordin, A.4
Höckerstedt, H.K.5
Nilsson, B.6
-
101
-
-
84877599866
-
Acute but transient release of terminal complement complex after reperfusion in clinical kidney transplantation
-
de Vries DK, van der Pol P, van Anken GE, van Gijlswijk DJ, Damman J, Lindeman JH, et al. Acute but transient release of terminal complement complex after reperfusion in clinical kidney transplantation. Transplantation (2013) 95:816-20. doi:10.1097/TP.0b013e31827e31c9
-
(2013)
Transplantation
, vol.95
, pp. 816-820
-
-
de Vries, D.K.1
van der Pol, P.2
van Anken, G.E.3
van Gijlswijk, D.J.4
Damman, J.5
Lindeman, J.H.6
-
102
-
-
79958849218
-
Long-term treatment with eculizumab in paroxysmal nocturnal hemoglobinuria: sustained efficacy and improved survival
-
Kelly RJ, Hill A, Arnold LM, Brooksbank GL, Richards SJ, Cullen M, et al. Long-term treatment with eculizumab in paroxysmal nocturnal hemoglobinuria: sustained efficacy and improved survival. Blood (2011) 117:6786-92. doi:10.1182/blood-2011-02-333997
-
(2011)
Blood
, vol.117
, pp. 6786-6792
-
-
Kelly, R.J.1
Hill, A.2
Arnold, L.M.3
Brooksbank, G.L.4
Richards, S.J.5
Cullen, M.6
-
103
-
-
78651410434
-
The development of atypical hemolytic uremic syndrome depends on complement C5
-
de Jorge EG, Macor P, Paixão-Cavalcante D, Rose KL, Tedesco F, Cook HT, et al. The development of atypical hemolytic uremic syndrome depends on complement C5. J Am Soc Nephrol (2011) 22:137-45. doi:10.1681/ASN.2010050451
-
(2011)
J Am Soc Nephrol
, vol.22
, pp. 137-145
-
-
de Jorge, E.G.1
Macor, P.2
Paixão-Cavalcante, D.3
Rose, K.L.4
Tedesco, F.5
Cook, H.T.6
-
104
-
-
59449107473
-
Eculizumab for atypical hemolytic-uremic syndrome
-
Nurnberger J, Philipp T, Witzke O, Opazo Saez A, Vester U, Baba HA, et al. Eculizumab for atypical hemolytic-uremic syndrome. N Engl J Med (2009) 360:542-4. doi:10.1056/NEJMc0808527
-
(2009)
N Engl J Med
, vol.360
, pp. 542-544
-
-
Nurnberger, J.1
Philipp, T.2
Witzke, O.3
Opazo Saez, A.4
Vester, U.5
Baba, H.A.6
-
105
-
-
77950955452
-
Efficacy of eculizumab in the treatment of recurrent atypical hemolytic-uremic syndrome after renal transplantation
-
Larrea CF, Cofan F, Oppenheimer F, Campistol JM, Escolar G, Lozano M. Efficacy of eculizumab in the treatment of recurrent atypical hemolytic-uremic syndrome after renal transplantation. Transplantation (2010) 89:903-4. doi:10.1097/TP.0b013e3181ccd80d
-
(2010)
Transplantation
, vol.89
, pp. 903-904
-
-
Larrea, C.F.1
Cofan, F.2
Oppenheimer, F.3
Campistol, J.M.4
Escolar, G.5
Lozano, M.6
-
106
-
-
84863724130
-
Eculizumab for the treatment of two recurrences of atypical hemolytic uremic syndrome in a kidney allograft
-
Alachkar N, Bagnasco SM, Montgomery RA. Eculizumab for the treatment of two recurrences of atypical hemolytic uremic syndrome in a kidney allograft. Transpl Int (2012) 25:e93-5. doi:10.1111/j.1432-2277.2012.01497.x
-
(2012)
Transpl Int
, vol.25
, pp. e93-e95
-
-
Alachkar, N.1
Bagnasco, S.M.2
Montgomery, R.A.3
-
107
-
-
84880133478
-
Eculizumab in renal transplantation
-
Legendre C, Sberro-Soussan R, Zuber J, Rabant M, Loupy A, Timsit MO, et al. Eculizumab in renal transplantation. Transplant Rev (Orlando) (2013) 27:90-2. doi:10.1016/j.trre.2013.04.002
-
(2013)
Transplant Rev (Orlando)
, vol.27
, pp. 90-92
-
-
Legendre, C.1
Sberro-Soussan, R.2
Zuber, J.3
Rabant, M.4
Loupy, A.5
Timsit, M.O.6
-
108
-
-
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, Groothoff J, Strain L, Goodship T. 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) 55:708-11. doi:10.1053/j.ajkd.2009.08.011
-
(2010)
Am J Kidney Dis
, vol.55
, pp. 708-711
-
-
Davin, J.C.1
Gracchi, V.2
Bouts, A.3
Groothoff, J.4
Strain, L.5
Goodship, T.6
-
109
-
-
0030836462
-
Recurrence of haemolytic-uraemic syndrome in renal transplants: a single-centre report
-
Miller RB, Burke BA, Schmidt WJ, Gillingham KJ, Matas AJ, Mauer M, et al. Recurrence of haemolytic-uraemic syndrome in renal transplants: a single-centre report. Nephrol Dial Transplant (1997) 12:1425-30. doi:10.1093/ndt/12.7.1425
-
(1997)
Nephrol Dial Transplant
, vol.12
, pp. 1425-1430
-
-
Miller, R.B.1
Burke, B.A.2
Schmidt, W.J.3
Gillingham, K.J.4
Matas, A.J.5
Mauer, M.6
-
110
-
-
84870161966
-
Tailored eculizumab therapy in the management of complement factor H-mediated atypical hemolytic uremic syndrome in an adult kidney transplant recipient: a case report
-
Xie L, Nester CM, Reed AI, Zhang Y, Smith RJ, Thomas CP. Tailored eculizumab therapy in the management of complement factor H-mediated atypical hemolytic uremic syndrome in an adult kidney transplant recipient: a case report. Transplant Proc (2012) 44:3037-40. doi:10.1016/j.transproceed.2012.07.141
-
(2012)
Transplant Proc
, vol.44
, pp. 3037-3040
-
-
Xie, L.1
Nester, C.M.2
Reed, A.I.3
Zhang, Y.4
Smith, R.J.5
Thomas, C.P.6
-
111
-
-
77950628343
-
Successful treatment of transplantation-associated thrombotic microangiopathy with recombinant human soluble thrombomodulin
-
Sakai M, Ikezoe T, Bandobashi K, Togitani K, Yokoyama A. Successful treatment of transplantation-associated thrombotic microangiopathy with recombinant human soluble thrombomodulin. Bone Marrow Transplant (2010) 45:803-5. doi:10.1038/bmt.2009.242
-
(2010)
Bone Marrow Transplant
, vol.45
, pp. 803-805
-
-
Sakai, M.1
Ikezoe, T.2
Bandobashi, K.3
Togitani, K.4
Yokoyama, A.5
-
112
-
-
74149086780
-
Therapeutic potential of complement modulation
-
Wagner E, Frank MM. Therapeutic potential of complement modulation. Nat Rev Drug Discov (2010) 9:43-56. doi:10.1038/nrd3011
-
(2010)
Nat Rev Drug Discov
, vol.9
, pp. 43-56
-
-
Wagner, E.1
Frank, M.M.2
|