-
1
-
-
35548967700
-
Complement regulatory genes and hemolytic uremic syndromes
-
Kavanagh D., Richards A., Atkinson J. Complement regulatory genes and hemolytic uremic syndromes. Annu Rev Med 2008, 59:293-309.
-
(2008)
Annu Rev Med
, vol.59
, pp. 293-309
-
-
Kavanagh, D.1
Richards, A.2
Atkinson, J.3
-
2
-
-
33746508999
-
A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders
-
Besbas N., Karpman D., Landau D., Loirat C., Proesmans W., Remuzzi G., et al. A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders. Kidney Int 2006, 70:423-431.
-
(2006)
Kidney Int
, vol.70
, pp. 423-431
-
-
Besbas, N.1
Karpman, D.2
Landau, D.3
Loirat, C.4
Proesmans, W.5
Remuzzi, G.6
-
3
-
-
2542420109
-
Non-enteropathic hemolytic uremic syndrome: causes and short-term course
-
Constantinescu A.R., Bitzan M., Weiss L.S., Christen E., Kaplan B.S., Cnaan A., et al. Non-enteropathic hemolytic uremic syndrome: causes and short-term course. Am J Kidney Dis 2004, 43:976-982.
-
(2004)
Am J Kidney Dis
, vol.43
, pp. 976-982
-
-
Constantinescu, A.R.1
Bitzan, M.2
Weiss, L.S.3
Christen, E.4
Kaplan, B.S.5
Cnaan, A.6
-
5
-
-
77955883153
-
Complement: a key system for immune surveillance and homeostasis
-
Ricklin D., Hajishengallis G., Yang K., Lambris J.D. Complement: a key system for immune surveillance and homeostasis. Nat Immunol 2010, 11:785-797.
-
(2010)
Nat Immunol
, vol.11
, pp. 785-797
-
-
Ricklin, D.1
Hajishengallis, G.2
Yang, K.3
Lambris, J.D.4
-
6
-
-
33845905781
-
T-cell regulation: with complements from innate immunity
-
Kemper C., Atkinson J.P. T-cell regulation: with complements from innate immunity. Nat Rev Immunol 2007, 7:9-18.
-
(2007)
Nat Rev Immunol
, vol.7
, pp. 9-18
-
-
Kemper, C.1
Atkinson, J.P.2
-
7
-
-
0031970553
-
Genetic studies into inherited and sporadic hemolytic uremic syndrome
-
Warwicker P., Goodship T.H., Donne R.L., Pirson Y., Nicholls A., Ward R.M., 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
Pirson, Y.4
Nicholls, A.5
Ward, R.M.6
-
8
-
-
0035128326
-
Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognition
-
Richards A., Buddles M.R., Donne R.L., Kaplan B.S., Kirk E., Venning M.C., et al. Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognition. Am J Hum Genet 2001, 68:485-490.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 485-490
-
-
Richards, A.1
Buddles, M.R.2
Donne, R.L.3
Kaplan, B.S.4
Kirk, E.5
Venning, M.C.6
-
9
-
-
84872174501
-
Analysis of genetic and predisposing factors in Japanese patients with atypical hemolytic uremic syndrome
-
Fan X., Yoshida Y., Honda S., Matsumoto M., Sawada Y., Hattori M., et al. Analysis of genetic and predisposing factors in Japanese patients with atypical hemolytic uremic syndrome. Mol Immunol 2013, 54:238-246.
-
(2013)
Mol Immunol
, vol.54
, pp. 238-246
-
-
Fan, X.1
Yoshida, Y.2
Honda, S.3
Matsumoto, M.4
Sawada, Y.5
Hattori, M.6
-
10
-
-
84863985862
-
Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics
-
Geerdink L.M., Westra D., van Wijk J.A., Dorresteijn E.M., Lilien M.R., Davin J.C., 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
Dorresteijn, E.M.4
Lilien, M.R.5
Davin, J.C.6
-
11
-
-
77952682366
-
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome
-
Maga T.K., Nishimura C.J., Weaver A.E., Frees K.L., Smith R.J. Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. Hum Mutat 2010, 31:E1445-E1460.
-
(2010)
Hum Mutat
, vol.31
-
-
Maga, T.K.1
Nishimura, C.J.2
Weaver, A.E.3
Frees, K.L.4
Smith, R.J.5
-
12
-
-
0042329931
-
Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries
-
Neumann H.P., Salzmann M., Bohnert-Iwan B., Mannuelian T., Skerka C., Lenk D., et al. Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries. J Med Genet 2003, 40:676-681.
-
(2003)
J Med Genet
, vol.40
, pp. 676-681
-
-
Neumann, H.P.1
Salzmann, M.2
Bohnert-Iwan, B.3
Mannuelian, T.4
Skerka, C.5
Lenk, D.6
-
13
-
-
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 P.F., 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
-
14
-
-
0035121908
-
Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome
-
Perez-Caballero D., Gonzalez-Rubio C., Gallardo M.E., Vera M., Lopez-Trascasa M., Rodriguez de Cordoba S., et al. Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome. Am J Hum Genet 2001, 68:478-484.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 478-484
-
-
Perez-Caballero, D.1
Gonzalez-Rubio, C.2
Gallardo, M.E.3
Vera, M.4
Lopez-Trascasa, M.5
Rodriguez de Cordoba, S.6
-
15
-
-
1542318912
-
Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases
-
Dragon-Durey M.A., Fremeaux-Bacchi V., Loirat C., Blouin J., Niaudet P., Deschenes G., et al. Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases. J Am Soc Nephrol 2004, 15:787-795.
-
(2004)
J Am Soc Nephrol
, vol.15
, pp. 787-795
-
-
Dragon-Durey, M.A.1
Fremeaux-Bacchi, V.2
Loirat, C.3
Blouin, J.4
Niaudet, P.5
Deschenes, G.6
-
16
-
-
35548956373
-
Inherited complement regulatory protein deficiency predisposes to human disease in acute injury and chronic inflammatory statesthe examples of vascular damage in atypical hemolytic uremic syndrome and debris accumulation in age-related macular degeneration
-
Richards A., Kavanagh D., Atkinson J.P. Inherited complement regulatory protein deficiency predisposes to human disease in acute injury and chronic inflammatory statesthe examples of vascular damage in atypical hemolytic uremic syndrome and debris accumulation in age-related macular degeneration. Adv Immunol 2007, 96:141-177.
-
(2007)
Adv Immunol
, vol.96
, pp. 141-177
-
-
Richards, A.1
Kavanagh, D.2
Atkinson, J.P.3
-
17
-
-
53149104792
-
A new map of glycosaminoglycan and C3b binding sites on factor H
-
Schmidt C.Q., Herbert A.P., Kavanagh D., Gandy C., Fenton C.J., Blaum B.S., et al. A new map of glycosaminoglycan and C3b binding sites on factor H. J Immunol 2008, 181:2610-2619.
-
(2008)
J Immunol
, vol.181
, pp. 2610-2619
-
-
Schmidt, C.Q.1
Herbert, A.P.2
Kavanagh, D.3
Gandy, C.4
Fenton, C.J.5
Blaum, B.S.6
-
18
-
-
77954315059
-
Complement control protein factor H: the good, the bad, and the inadequate
-
Ferreira V.P., Pangburn M.K., Cortes C. Complement control protein factor H: the good, the bad, and the inadequate. Mol Immunol 2010, 47:2187-2197.
-
(2010)
Mol Immunol
, vol.47
, pp. 2187-2197
-
-
Ferreira, V.P.1
Pangburn, M.K.2
Cortes, C.3
-
19
-
-
84874253499
-
Tissue-specific host recognition by complement factor H is mediated by differential activities of its glycoaminoglycans-binding regions
-
Clark S.J., Ridge L.A., Herbert A.P., Hakobyan S., Mulloy B., Wurzner R., et al. Tissue-specific host recognition by complement factor H is mediated by differential activities of its glycoaminoglycans-binding regions. J Immunol 2013, 190:2049-2057.
-
(2013)
J Immunol
, vol.190
, pp. 2049-2057
-
-
Clark, S.J.1
Ridge, L.A.2
Herbert, A.P.3
Hakobyan, S.4
Mulloy, B.5
Wurzner, R.6
-
20
-
-
80053904386
-
Complement factor H binds malondialdehyde epitopes and protects from oxidative stress
-
Weismann D., Hartvigsen K., Lauer N., Bennett K.L., Scholl H.P., Charbel Issa P., et al. Complement factor H binds malondialdehyde epitopes and protects from oxidative stress. Nature 2011, 478:76-81.
-
(2011)
Nature
, vol.478
, pp. 76-81
-
-
Weismann, D.1
Hartvigsen, K.2
Lauer, N.3
Bennett, K.L.4
Scholl, H.P.5
Charbel Issa, P.6
-
21
-
-
34249740145
-
The factor H variant associated with age-related macular degeneration (His-384) and the non-disease-associated form bind differentially to C-reactive protein, fibromodulin, DNA, and necrotic cells
-
Sjoberg A.P., Trouw L.A., Clark S.J., Sjolander J., Heinegard D., Sim R.B., et al. The factor H variant associated with age-related macular degeneration (His-384) and the non-disease-associated form bind differentially to C-reactive protein, fibromodulin, DNA, and necrotic cells. J Biol Chem 2007, 282:10894-10900.
-
(2007)
J Biol Chem
, vol.282
, pp. 10894-10900
-
-
Sjoberg, A.P.1
Trouw, L.A.2
Clark, S.J.3
Sjolander, J.4
Heinegard, D.5
Sim, R.B.6
-
22
-
-
33947214392
-
Y402H polymorphism of complement factor H affects binding affinity to C-reactive protein
-
Laine M., Jarva H., Seitsonen S., Haapasalo K., Lehtinen M.J., Lindeman N., et al. Y402H polymorphism of complement factor H affects binding affinity to C-reactive protein. J Immunol 2007, 178:3831-3836.
-
(2007)
J Immunol
, vol.178
, pp. 3831-3836
-
-
Laine, M.1
Jarva, H.2
Seitsonen, S.3
Haapasalo, K.4
Lehtinen, M.J.5
Lindeman, N.6
-
23
-
-
57649155220
-
Complement factor H binds to denatured rather than to native pentameric C-reactive protein
-
Hakobyan S., Harris C.L., van den Berg C.W., Fernandez-Alonso M.C., de Jorge E.G., de Cordoba S.R., et al. Complement factor H binds to denatured rather than to native pentameric C-reactive protein. J Biol Chem 2008, 283:30451-30460.
-
(2008)
J Biol Chem
, vol.283
, pp. 30451-30460
-
-
Hakobyan, S.1
Harris, C.L.2
Van Den Berg, C.W.3
Fernandez-Alonso, M.C.4
De Jorge, E.G.5
de Cordoba, S.R.6
-
24
-
-
84864823657
-
Atypical hemolytic uremic syndrome-associated variants and autoantibodies impair binding of factor h and factor h-related protein 1 to pentraxin 3
-
Kopp A., Strobel S., Tortajada A., Rodriguez de Cordoba S., Sanchez-Corral P., Prohaszka Z, et al. Atypical hemolytic uremic syndrome-associated variants and autoantibodies impair binding of factor h and factor h-related protein 1 to pentraxin 3. J Immunol 2012, 189:1858-1867.
-
(2012)
J Immunol
, vol.189
, pp. 1858-1867
-
-
Kopp, A.1
Strobel, S.2
Tortajada, A.3
Rodriguez de Cordoba, S.4
Sanchez-Corral, P.5
Prohaszka, Z.6
-
25
-
-
67449119124
-
The binding of factor H to a complex of physiological polyanions and C3b on cells is impaired in atypical hemolytic uremic syndrome
-
Ferreira V.P., Herbert A.P., Cortes C., McKee K.A., Blaum B.S., Esswein S.T., et al. The binding of factor H to a complex of physiological polyanions and C3b on cells is impaired in atypical hemolytic uremic syndrome. J Immunol 2009, 182:7009-7018.
-
(2009)
J Immunol
, vol.182
, pp. 7009-7018
-
-
Ferreira, V.P.1
Herbert, A.P.2
Cortes, C.3
McKee, K.A.4
Blaum, B.S.5
Esswein, S.T.6
-
26
-
-
45449105770
-
Mutations in proteins of the alternative pathway of complement and the pathogenesis of atypical hemolytic uremic syndrome
-
Abarrategui-Garrido C., Melgosa M., Pena-Carrion A., de Jorge E.G., de Cordoba S.R., Lopez-Trascasa M., et al. Mutations in proteins of the alternative pathway of complement and the pathogenesis of atypical hemolytic uremic syndrome. Am J Kidney Dis 2008, 52:171-180.
-
(2008)
Am J Kidney Dis
, vol.52
, pp. 171-180
-
-
Abarrategui-Garrido, C.1
Melgosa, M.2
Pena-Carrion, A.3
de Jorge, E.G.4
de Cordoba, S.R.5
Lopez-Trascasa, M.6
-
27
-
-
33644870779
-
Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome
-
Vaziri-Sani F., Holmberg L., Sjoholm A.G., Kristoffersson A.C., Manea M., Fremeaux-Bacchi V., et al. Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome. Kidney Int 2006, 69:981-988.
-
(2006)
Kidney Int
, vol.69
, pp. 981-988
-
-
Vaziri-Sani, F.1
Holmberg, L.2
Sjoholm, A.G.3
Kristoffersson, A.C.4
Manea, M.5
Fremeaux-Bacchi, V.6
-
28
-
-
45949108983
-
Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation
-
Stahl A.L., Vaziri-Sani F., Heinen S., Kristoffersson A.C., Gydell K.H., Raafat R., et al. Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation. Blood 2008, 111:5307-5315.
-
(2008)
Blood
, vol.111
, pp. 5307-5315
-
-
Stahl, A.L.1
Vaziri-Sani, F.2
Heinen, S.3
Kristoffersson, A.C.4
Gydell, K.H.5
Raafat, R.6
-
29
-
-
79953190798
-
Disease-associated N-terminal complement factor H mutations perturb cofactor and decay-accelerating activities
-
Pechtl I.C., Kavanagh D., McIntosh N., Harris C.L., Barlow P.N. Disease-associated N-terminal complement factor H mutations perturb cofactor and decay-accelerating activities. J Biol Chem 2011, 286:11082-11090.
-
(2011)
J Biol Chem
, vol.286
, pp. 11082-11090
-
-
Pechtl, I.C.1
Kavanagh, D.2
McIntosh, N.3
Harris, C.L.4
Barlow, P.N.5
-
30
-
-
83655191999
-
Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance
-
Tortajada A., Pinto S., Martinez-Ara J., Lopez-Trascasa M., Sanchez-Corral P., de Cordoba S.R. Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance. Kidney Int 2012, 81:56-63.
-
(2012)
Kidney Int
, vol.81
, pp. 56-63
-
-
Tortajada, A.1
Pinto, S.2
Martinez-Ara, J.3
Lopez-Trascasa, M.4
Sanchez-Corral, P.5
de Cordoba, S.R.6
-
31
-
-
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 M.S., Strain L., Goodship J.A., Kemp E.J., 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
Strain, L.4
Goodship, J.A.5
Kemp, E.J.6
-
32
-
-
33750855444
-
Atypical haemolytic uraemic syndrome associated with a hybrid complement gene
-
Venables J.P., Strain L., Routledge D., Bourn D., Powell H.M., Warwicker P., et al. Atypical haemolytic uraemic syndrome associated with a hybrid complement gene. PLoS Med 2006, 3:e431.
-
(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
-
33
-
-
84855862414
-
A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome
-
Francis N.J., 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.
-
(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
-
34
-
-
34250329129
-
Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains
-
Pickering M.C., de Jorge E.G., Martinez-Barricarte R., Recalde S., Garcia-Layana A., Rose K.L., et al. Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains. J Exp Med 2007, 204:1249-1256.
-
(2007)
J Exp Med
, vol.204
, pp. 1249-1256
-
-
Pickering, M.C.1
de Jorge, E.G.2
Martinez-Barricarte, R.3
Recalde, S.4
Garcia-Layana, A.5
Rose, K.L.6
-
35
-
-
68549099868
-
Pathogenesis of thrombotic microangiopathy: insights from animal models
-
Richards A., Kavanagh D. Pathogenesis of thrombotic microangiopathy: insights from animal models. Nephron Exp Nephrol 2009, 113:e97-103.
-
(2009)
Nephron Exp Nephrol
, vol.113
-
-
Richards, A.1
Kavanagh, D.2
-
36
-
-
78651410434
-
The development of atypical hemolytic uremic syndrome depends on complement C5
-
Goicoechea de Jorge E., Macor P., Paixao-Cavalcante D., Rose K.L., Tedesco F., Cook H.T., et al. The development of atypical hemolytic uremic syndrome depends on complement C5. J Am Soc Nephrol 2011, 22:137-145.
-
(2011)
J Am Soc Nephrol
, vol.22
, pp. 137-145
-
-
Goicoechea de Jorge, E.1
Macor, P.2
Paixao-Cavalcante, D.3
Rose, K.L.4
Tedesco, F.5
Cook, H.T.6
-
37
-
-
19444369542
-
Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome
-
Fremeaux-Bacchi V., Dragon-Durey M.A., 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.
-
(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
-
38
-
-
27744452766
-
Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome
-
Kavanagh D., Kemp E.J., Mayland E., Winney R.J., Duffield J.S., Warwick G., et al. Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome. J Am Soc Nephrol 2005, 16:2150-2155.
-
(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
-
39
-
-
34548309310
-
Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome
-
Kavanagh D., Richards A., Noris M., Hauhart R., Liszewski M.K., Karpman D., et al. Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome. Mol Immunol 2008, 45:95-105.
-
(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
-
40
-
-
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, 108:1267-1279.
-
(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
-
41
-
-
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 S.C., Kalchishkova N., Trouw L.A., Fremeaux-Bacchi V., Villoutreix B.O., Blom A.M. 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, 40:172-185.
-
(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
-
42
-
-
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 S.C., Karpman D., Vaziri-Sani F., Kristoffersson A.C., 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, 44:1835-1844.
-
(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
-
43
-
-
77954328285
-
Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS)
-
Westra D., Volokhina E., van der Heijden E., Vos A., Huigen M., Jansen J., 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
Vos, A.4
Huigen, M.5
Jansen, J.6
-
44
-
-
72549097037
-
Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome
-
Sullivan M., Erlic Z., Hoffmann M.M., Arbeiter K., Patzer L., Budde K., et al. Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome. Ann Hum Genet 2010, 74:17-26.
-
(2010)
Ann Hum Genet
, vol.74
, pp. 17-26
-
-
Sullivan, M.1
Erlic, Z.2
Hoffmann, M.M.3
Arbeiter, K.4
Patzer, L.5
Budde, K.6
-
45
-
-
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., Goodship J.A., Lampe A.K., 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, 100:12966-12971.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 12966-12971
-
-
Richards, A.1
Kemp, E.J.2
Liszewski, M.K.3
Goodship, J.A.4
Lampe, A.K.5
Decorte, R.6
-
46
-
-
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, 24:475-486.
-
(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
-
47
-
-
33745812440
-
Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome
-
Fremeaux-Bacchi V., Moulton E.A., Kavanagh D., Dragon-Durey M.A., 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, 17:2017-2025.
-
(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
-
48
-
-
33751035523
-
Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome
-
Richards A., Liszewski K.M., Kavanagh D., Fang C.J., Moulton E., Fremeaux-Bacchi V., et al. Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome. Mol Immunol 2007, 44:111-122.
-
(2007)
Mol Immunol
, vol.44
, pp. 111-122
-
-
Richards, A.1
Liszewski, K.M.2
Kavanagh, D.3
Fang, C.J.4
Moulton, E.5
Fremeaux-Bacchi, V.6
-
49
-
-
84876044818
-
Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide french series comparing children and adults
-
Fremeaux-Bacchi V., Fakhouri F., Garnier A., Bienaime F., Dragon-Durey M.A., 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, 8:554-562.
-
(2013)
Clin J Am Soc Nephrol
, vol.8
, pp. 554-562
-
-
Fremeaux-Bacchi, V.1
Fakhouri, F.2
Garnier, A.3
Bienaime, F.4
Dragon-Durey, M.A.5
Ngo, S.6
-
50
-
-
54049137505
-
Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome
-
Fremeaux-Bacchi V., Miller E.C., Liszewski M.K., Strain L., Blouin J., Brown A.L., 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
Strain, L.4
Blouin, J.5
Brown, A.L.6
-
51
-
-
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, 5:1844-1859.
-
(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
-
52
-
-
84856863401
-
A novel C3 mutation causing increased formation of the C3 convertase in familial atypical hemolytic uremic syndrome
-
Sartz L., Olin A.I., Kristoffersson A.C., Stahl A.L., Johansson M.E., Westman K., et al. A novel C3 mutation causing increased formation of the C3 convertase in familial atypical hemolytic uremic syndrome. J Immunol 2012, 188:2030-2037.
-
(2012)
J Immunol
, vol.188
, pp. 2030-2037
-
-
Sartz, L.1
Olin, A.I.2
Kristoffersson, A.C.3
Stahl, A.L.4
Johansson, M.E.5
Westman, K.6
-
53
-
-
70349923265
-
A large family with a gain-of-function mutation of complement C3 predisposing to atypical hemolytic uremic syndrome, microhematuria, hypertension and chronic renal failure
-
Lhotta K., Janecke A.R., Scheiring J., Petzlberger B., Giner T., Fally V., et al. A large family with a gain-of-function mutation of complement C3 predisposing to atypical hemolytic uremic syndrome, microhematuria, hypertension and chronic renal failure. Clin J Am Soc Nephrol 2009, 4:1356-1362.
-
(2009)
Clin J Am Soc Nephrol
, vol.4
, pp. 1356-1362
-
-
Lhotta, K.1
Janecke, A.R.2
Scheiring, J.3
Petzlberger, B.4
Giner, T.5
Fally, V.6
-
54
-
-
84860711841
-
A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function
-
Roumenina L.T., Frimat M., Miller E.C., Provot F., Dragon-Durey M.A., Bordereau P., et al. A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function. Blood 2012, 119:4182-4191.
-
(2012)
Blood
, vol.119
, pp. 4182-4191
-
-
Roumenina, L.T.1
Frimat, M.2
Miller, E.C.3
Provot, F.4
Dragon-Durey, M.A.5
Bordereau, P.6
-
55
-
-
70350475255
-
Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome
-
Roumenina L.T., Jablonski M., Hue C., Blouin J., Dimitrov J.D., Dragon-Durey M.A., et al. Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome. Blood 2009, 114:2837-2845.
-
(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
-
56
-
-
33846094404
-
Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome
-
Goicoechea de Jorge E., Harris C.L., Esparza-Gordillo J., Carreras L., Arranz E.A., Garrido C.A., 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, 104:240-245.
-
(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
Carreras, L.4
Arranz, E.A.5
Garrido, C.A.6
-
57
-
-
29144497930
-
Does complement factor B have a role in the pathogenesis of atypical HUS?
-
Kavanagh D., Kemp E.J., Richards A., Burgess R.M., Mayland E., Goodship J.A., et al. Does complement factor B have a role in the pathogenesis of atypical HUS?. Mol Immunol 2006, 43:856-859.
-
(2006)
Mol Immunol
, vol.43
, pp. 856-859
-
-
Kavanagh, D.1
Kemp, E.J.2
Richards, A.3
Burgess, R.M.4
Mayland, E.5
Goodship, J.A.6
-
58
-
-
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 R.J., Schoeneman M. A novel mutation in the complement factor B gene (CFB) and atypical hemolytic uremic syndrome. Pediatr Nephrol 2010, 25:947-951.
-
(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
-
60
-
-
67651166873
-
Thrombomodulin mutations in atypical hemolytic-uremic syndrome
-
Delvaeye M., Noris M., De Vriese A., Esmon C.T., Esmon N.L., Ferrell G., 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
Esmon, C.T.4
Esmon, N.L.5
Ferrell, G.6
-
61
-
-
84864374494
-
Atypical hemolytic uremic syndrome and genetic aberrations in the complement factor H-related 5 gene
-
Westra D., Vernon K.A., Volokhina E.B., Pickering M.C., van de Kar N.C., van den Heuvel L.P. Atypical hemolytic uremic syndrome and genetic aberrations in the complement factor H-related 5 gene. J Hum Genet 2012, 57:459-464.
-
(2012)
J Hum Genet
, vol.57
, pp. 459-464
-
-
Westra, D.1
Vernon, K.A.2
Volokhina, E.B.3
Pickering, M.C.4
Van De Kar, N.C.5
Van Den Heuvel, L.P.6
-
62
-
-
33751329318
-
Genetic analysis of the complement factor H related 5 gene in haemolytic uraemic syndrome
-
Monteferrante G., Brioschi S., Caprioli J., Pianetti G., Bettinaglio P., Bresin E., et al. Genetic analysis of the complement factor H related 5 gene in haemolytic uraemic syndrome. Mol Immunol 2007, 44:1704-1708.
-
(2007)
Mol Immunol
, vol.44
, pp. 1704-1708
-
-
Monteferrante, G.1
Brioschi, S.2
Caprioli, J.3
Pianetti, G.4
Bettinaglio, P.5
Bresin, E.6
-
63
-
-
67349259594
-
A novel mutation in the complement regulator clusterin in recurrent hemolytic uremic syndrome
-
Stahl A.L., Kristoffersson A., Olin A.I., Olsson M.L., Roodhooft A.M., Proesmans W., et al. A novel mutation in the complement regulator clusterin in recurrent hemolytic uremic syndrome. Mol Immunol 2009, 46:2236-2243.
-
(2009)
Mol Immunol
, vol.46
, pp. 2236-2243
-
-
Stahl, A.L.1
Kristoffersson, A.2
Olin, A.I.3
Olsson, M.L.4
Roodhooft, A.M.5
Proesmans, W.6
-
64
-
-
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., Martinez-Barricarte R., Lopez-Trascasa M., de Cordoba S.R., Sanchez-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, 114:4261-4271.
-
(2009)
Blood
, vol.114
, pp. 4261-4271
-
-
Abarrategui-Garrido, C.1
Martinez-Barricarte, R.2
Lopez-Trascasa, M.3
de Cordoba, S.R.4
Sanchez-Corral, P.5
-
65
-
-
78649863686
-
Clinical features of anti-factor H autoantibody-associated hemolytic uremic syndrome
-
Dragon-Durey M.A., Sethi S.K., Bagga A., Blanc C., Blouin J., Ranchin B., 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
Blanc, C.4
Blouin, J.5
Ranchin, B.6
-
66
-
-
38949155911
-
Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency
-
Jozsi M., Licht C., Strobel S., Zipfel S.L., Richter H., Heinen 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
Zipfel, S.L.4
Richter, H.5
Heinen, S.6
-
67
-
-
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 P.N., Herbert A.P., 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
Kavanagh, D.4
Barlow, P.N.5
Herbert, A.P.6
-
68
-
-
84864925248
-
Factor H autoantibodies and deletion of complement factor H-related protein-1 in rheumatic diseases in comparison to atypical hemolytic uremic syndrome
-
Foltyn Zadura A., Zipfel P.F., Bokarewa M.I., Sturfelt G., Jonsen A., Nilsson S.C., et al. Factor H autoantibodies and deletion of complement factor H-related protein-1 in rheumatic diseases in comparison to atypical hemolytic uremic syndrome. Arthritis Res Ther 2012, 14:R185.
-
(2012)
Arthritis Res Ther
, vol.14
-
-
Foltyn Zadura, A.1
Zipfel, P.F.2
Bokarewa, M.I.3
Sturfelt, G.4
Jonsen, A.5
Nilsson, S.C.6
-
69
-
-
84875029270
-
Complement factor H-related protein 1 deficiency and factor H antibodies in pediatric patients with atypical hemolytic uremic syndrome
-
Hofer J., Janecke A.R., Zimmerhackl L.B., 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, 8:407-415.
-
(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
-
70
-
-
34047200899
-
Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome
-
Zipfel P.F., Edey M., Heinen S., Jozsi M., Richter H., Misselwitz J., et al. Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome. PLoS Genet 2007, 3:e41.
-
(2007)
PLoS Genet
, vol.3
-
-
Zipfel, P.F.1
Edey, M.2
Heinen, S.3
Jozsi, M.4
Richter, H.5
Misselwitz, J.6
-
71
-
-
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., Martinez-Barricarte R., Lopez-Trascasa M., Rodriguez de Cordoba S., Sanchez-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, 114:4261-4271.
-
(2009)
Blood
, vol.114
, pp. 4261-4271
-
-
Abarrategui-Garrido, C.1
Martinez-Barricarte, R.2
Lopez-Trascasa, M.3
Rodriguez de Cordoba, S.4
Sanchez-Corral, P.5
-
72
-
-
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 haemolytic uraemic syndrome
-
Moore I., Strain L., Pappworth I., Kavanagh D., Barlow P.N., Herbert A.P., 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 haemolytic uraemic syndrome. Blood 2010, 115:379-387.
-
(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
-
73
-
-
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 M.A., 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, 46:447-450.
-
(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
-
74
-
-
80052272216
-
Factor H-related protein 1 neutralizes anti-factor H autoantibodies in autoimmune hemolytic uremic syndrome
-
Strobel S., Abarrategui-Garrido C., Fariza-Requejo E., Seeberger H., Sanchez-Corral P., Jozsi M. Factor H-related protein 1 neutralizes anti-factor H autoantibodies in autoimmune hemolytic uremic syndrome. Kidney Int 2011, 80:397-404.
-
(2011)
Kidney Int
, vol.80
, pp. 397-404
-
-
Strobel, S.1
Abarrategui-Garrido, C.2
Fariza-Requejo, E.3
Seeberger, H.4
Sanchez-Corral, P.5
Jozsi, M.6
-
75
-
-
34548853385
-
Anti factor H autoantibodies block C-terminal recognition function of factor H in hemolytic uremic syndrome
-
Jozsi M., Strobel S., Dahse H.M., Liu W.S., Hoyer P.F., Oppermann M., et al. Anti factor H autoantibodies block C-terminal recognition function of factor H in hemolytic uremic syndrome. Blood 2007, 110:1516-1518.
-
(2007)
Blood
, vol.110
, pp. 1516-1518
-
-
Jozsi, M.1
Strobel, S.2
Dahse, H.M.3
Liu, W.S.4
Hoyer, P.F.5
Oppermann, M.6
-
76
-
-
20544437666
-
Anti-factor H autoantibodies associated with atypical hemolytic uremic syndrome
-
Dragon-Durey M.A., Loirat C., Cloarec S., Macher M.A., Blouin J., Nivet H., 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
Macher, M.A.4
Blouin, J.5
Nivet, H.6
-
77
-
-
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 L.T., Ashraf Y., Hyvarinen S., Sethi S.K., Ranchin B., 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
Hyvarinen, S.4
Sethi, S.K.5
Ranchin, B.6
-
78
-
-
84858029055
-
Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon?
-
Kavanagh D., Pappworth I.Y., Anderson H., Hayes C.M., Moore I., Hunze E.M., et al. Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon?. Clin J Am Soc Nephrol 2012, 7:417-426.
-
(2012)
Clin J Am Soc Nephrol
, vol.7
, pp. 417-426
-
-
Kavanagh, D.1
Pappworth, I.Y.2
Anderson, H.3
Hayes, C.M.4
Moore, I.5
Hunze, E.M.6
-
79
-
-
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., Bettinaglio P., Bresin E., Pianetti G., et al. 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 2003, 12:3385-3395.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 3385-3395
-
-
Caprioli, J.1
Castelletti, F.2
Bucchioni, S.3
Bettinaglio, P.4
Bresin, E.5
Pianetti, G.6
-
80
-
-
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., Carreras Berges L., Lopez-Trascasa M., Sanchez-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, 14:703-712.
-
(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
Lopez-Trascasa, M.5
Sanchez-Corral, P.6
-
81
-
-
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 E.J., Goodship J.A., Dragon-Durey M.A., 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, 42:852-856.
-
(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
-
82
-
-
84655168091
-
Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS
-
Ermini L., Goodship T.H., Strain L., Weale M.E., Sacks S.H., Cordell H.J., et al. Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS. Mol Immunol 2012, 49:640-648.
-
(2012)
Mol Immunol
, vol.49
, pp. 640-648
-
-
Ermini, L.1
Goodship, T.H.2
Strain, L.3
Weale, M.E.4
Sacks, S.H.5
Cordell, H.J.6
-
83
-
-
84866753225
-
The complotype: dictating risk for inflammation and infection
-
Harris C.L., Heurich M., Rodriguez de Cordoba S., Morgan B.P. The complotype: dictating risk for inflammation and infection. Trends Immunol 2012, 33:513-521.
-
(2012)
Trends Immunol
, vol.33
, pp. 513-521
-
-
Harris, C.L.1
Heurich, M.2
Rodriguez de Cordoba, S.3
Morgan, B.P.4
-
84
-
-
69449090499
-
De Cordoba SR. The disease-protective complement factor H allotypic variant Ile62 shows increased binding affinity for C3b and enhanced cofactor activity
-
Tortajada A., Montes T., Martinez-Barricarte R., Morgan B.P., Harris C.L. de Cordoba SR. The disease-protective complement factor H allotypic variant Ile62 shows increased binding affinity for C3b and enhanced cofactor activity. Hum Mol Genet 2009, 18:3452-3461.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 3452-3461
-
-
Tortajada, A.1
Montes, T.2
Martinez-Barricarte, R.3
Morgan, B.P.4
Harris, C.L.5
-
85
-
-
44049086967
-
Structure of the N-terminal region of complement factor H and conformational implications of disease-linked sequence variations
-
Hocking H.G., Herbert A.P., Kavanagh D., Soares D.C., Ferreira V.P., Pangburn M.K., et al. Structure of the N-terminal region of complement factor H and conformational implications of disease-linked sequence variations. J Biol Chem 2008, 283:9475-9487.
-
(2008)
J Biol Chem
, vol.283
, pp. 9475-9487
-
-
Hocking, H.G.1
Herbert, A.P.2
Kavanagh, D.3
Soares, D.C.4
Ferreira, V.P.5
Pangburn, M.K.6
-
86
-
-
33644964155
-
Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree
-
Esparza-Gordillo J., Jorge E.G., Garrido C.A., Carreras L., Lopez-Trascasa M., Sanchez-Corral P., et al. Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree. Mol Immunol 2006, 43:1769-1775.
-
(2006)
Mol Immunol
, vol.43
, pp. 1769-1775
-
-
Esparza-Gordillo, J.1
Jorge, E.G.2
Garrido, C.A.3
Carreras, L.4
Lopez-Trascasa, M.5
Sanchez-Corral, P.6
-
87
-
-
84886257408
-
Membrane cofactor protein (MCP) haplotype, which predisposes to atypical hemolytic and uremic syndrome, has no consequence on neutrophils and endothelial cells MCP levels or on HUVECs ability to activate complement
-
Frimat M., Roumenina L., Tabarin F., Halbwachs-Mecarelli L., Fremeaux-Bacchi V. Membrane cofactor protein (MCP) haplotype, which predisposes to atypical hemolytic and uremic syndrome, has no consequence on neutrophils and endothelial cells MCP levels or on HUVECs ability to activate complement. Immunobiology 2012, 217:1187-1188.
-
(2012)
Immunobiology
, vol.217
, pp. 1187-1188
-
-
Frimat, M.1
Roumenina, L.2
Tabarin, F.3
Halbwachs-Mecarelli, L.4
Fremeaux-Bacchi, V.5
-
88
-
-
44449103295
-
A novel non-synonymous polymorphism (p.Arg240His) in C4b-binding protein is associated with atypical hemolytic uremic syndrome and leads to impaired alternative pathway cofactor activity
-
Blom A.M., Bergstrom F., Edey M., Diaz-Torres M., Kavanagh D., Lampe A., et al. A novel non-synonymous polymorphism (p.Arg240His) in C4b-binding protein is associated with atypical hemolytic uremic syndrome and leads to impaired alternative pathway cofactor activity. J Immunol 2008, 180:6385-6391.
-
(2008)
J Immunol
, vol.180
, pp. 6385-6391
-
-
Blom, A.M.1
Bergstrom, F.2
Edey, M.3
Diaz-Torres, M.4
Kavanagh, D.5
Lampe, A.6
-
89
-
-
57449108090
-
Lack of association between polymorphisms in C4b-binding protein and atypical haemolytic uraemic syndrome in the Spanish population
-
Martinez-Barricarte R., Goicoechea de Jorge E., Montes T., Layana A.G., Rodriguez de Cordoba S. Lack of association between polymorphisms in C4b-binding protein and atypical haemolytic uraemic syndrome in the Spanish population. Clin Exp Immunol 2009, 155:59-64.
-
(2009)
Clin Exp Immunol
, vol.155
, pp. 59-64
-
-
Martinez-Barricarte, R.1
Goicoechea de Jorge, E.2
Montes, T.3
Layana, A.G.4
Rodriguez de Cordoba, S.5
-
90
-
-
78449293078
-
Genetics and complement in atypical HUS
-
Kavanagh D., Goodship T. Genetics and complement in atypical HUS. Pediatr Nephrol 2010, 25:2431-2442.
-
(2010)
Pediatr Nephrol
, vol.25
, pp. 2431-2442
-
-
Kavanagh, D.1
Goodship, T.2
-
91
-
-
80053572803
-
Age-related penetrance of hereditary atypical hemolytic uremic syndrome
-
Sullivan M., Rybicki L.A., Winter A., Hoffmann M.M., Reiermann S., Linke H., et al. Age-related penetrance of hereditary atypical hemolytic uremic syndrome. Ann Hum Genet 2011, 75:639-647.
-
(2011)
Ann Hum Genet
, vol.75
, pp. 639-647
-
-
Sullivan, M.1
Rybicki, L.A.2
Winter, A.3
Hoffmann, M.M.4
Reiermann, S.5
Linke, H.6
-
92
-
-
66249101956
-
Successful renal transplantation in a patient with atypical hemolytic uremic syndrome carrying mutations in both factor I and MCP
-
Cruzado J.M., de Cordoba S.R., Melilli E., Bestard O., Rama I., Sanchez-Corral P., et al. Successful renal transplantation in a patient with atypical hemolytic uremic syndrome carrying mutations in both factor I and MCP. Am J Transplant 2009, 9:1477-1483.
-
(2009)
Am J Transplant
, vol.9
, pp. 1477-1483
-
-
Cruzado, J.M.1
de Cordoba, S.R.2
Melilli, E.3
Bestard, O.4
Rama, I.5
Sanchez-Corral, P.6
-
93
-
-
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., Nilsson S.C., Kwan W.H., Blouin J., et al. Mutations in components of complement influence the outcome of factor I-associated atypical hemolytic uremic syndrome. Kidney Int 2010, 77:339-349.
-
(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
-
94
-
-
34547633064
-
Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome
-
Sellier-Leclerc A.L., Fremeaux-Bacchi V., Dragon-Durey M.A., Macher M.A., Niaudet P., Guest G., et al. Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome. J Am Soc Nephrol 2007, 18:2392-2400.
-
(2007)
J Am Soc Nephrol
, vol.18
, pp. 2392-2400
-
-
Sellier-Leclerc, A.L.1
Fremeaux-Bacchi, V.2
Dragon-Durey, M.A.3
Macher, M.A.4
Niaudet, P.5
Guest, G.6
-
95
-
-
39449131108
-
Association of a factor H mutation with hemolytic uremic syndrome following a diarrheal illness
-
Edey M.M., Mead P.A., Saunders R.E., Strain L., Perkins S.J., Goodship T.H., et al. Association of a factor H mutation with hemolytic uremic syndrome following a diarrheal illness. Am J Kidney Dis 2008, 51:487-490.
-
(2008)
Am J Kidney Dis
, vol.51
, pp. 487-490
-
-
Edey, M.M.1
Mead, P.A.2
Saunders, R.E.3
Strain, L.4
Perkins, S.J.5
Goodship, T.H.6
-
96
-
-
77952556624
-
Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations
-
Fakhouri F., Roumenina L., Provot F., Sallee M., Caillard S., Couzi L., et al. Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations. J Am Soc Nephrol 2010, 21:859-867.
-
(2010)
J Am Soc Nephrol
, vol.21
, pp. 859-867
-
-
Fakhouri, F.1
Roumenina, L.2
Provot, F.3
Sallee, M.4
Caillard, S.5
Couzi, L.6
-
97
-
-
77952580558
-
Pulling the trigger in atypical hemolytic uremic syndrome: the role of pregnancy
-
Goodship T.H., Kavanagh D. Pulling the trigger in atypical hemolytic uremic syndrome: the role of pregnancy. J Am Soc Nephrol 2010, 21:731-732.
-
(2010)
J Am Soc Nephrol
, vol.21
, pp. 731-732
-
-
Goodship, T.H.1
Kavanagh, D.2
-
98
-
-
77952556624
-
Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations
-
Fakhouri F., Roumenina L., Provot F., Sallee M., Caillard S., Couzi L., et al. Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations. J Am Soc Nephrol 2010, 21:859-867.
-
(2010)
J Am Soc Nephrol
, vol.21
, pp. 859-867
-
-
Fakhouri, F.1
Roumenina, L.2
Provot, F.3
Sallee, M.4
Caillard, S.5
Couzi, L.6
-
99
-
-
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, 13:663-675.
-
(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
-
101
-
-
34548313714
-
Screening for complement system abnormalities in patients with atypical hemolytic uremic syndrome
-
Kavanagh D., Richards A., Fremeaux-Bacchi V., Noris M., Goodship T., Remuzzi G., et al. Screening for complement system abnormalities in patients with atypical hemolytic uremic syndrome. Clin J Am Soc Nephrol 2007, 2:591-596.
-
(2007)
Clin J Am Soc Nephrol
, vol.2
, pp. 591-596
-
-
Kavanagh, D.1
Richards, A.2
Fremeaux-Bacchi, V.3
Noris, M.4
Goodship, T.5
Remuzzi, G.6
-
102
-
-
83655198117
-
Interpretation of genetic variants of uncertain significance in atypical hemolytic uremic syndrome
-
Kavanagh D., Anderson H.E. Interpretation of genetic variants of uncertain significance in atypical hemolytic uremic syndrome. Kidney Int 2012, 81:11-13.
-
(2012)
Kidney Int
, vol.81
, pp. 11-13
-
-
Kavanagh, D.1
Anderson, H.E.2
-
103
-
-
78449308775
-
Neurological involvement in a child with atypical hemolytic uremic syndrome
-
Koehl B., Boyer O., Biebuyck-Gouge N., Kossorotoff M., Fremeaux-Bacchi V., Boddaert N., et al. Neurological involvement in a child with atypical hemolytic uremic syndrome. Pediatr Nephrol 2010, 25:2539-2542.
-
(2010)
Pediatr Nephrol
, vol.25
, pp. 2539-2542
-
-
Koehl, B.1
Boyer, O.2
Biebuyck-Gouge, N.3
Kossorotoff, M.4
Fremeaux-Bacchi, V.5
Boddaert, N.6
-
104
-
-
61549117207
-
Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome
-
Ariceta G., Besbas N., Johnson S., Karpman D., Landau D., Licht C., 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
Karpman, D.4
Landau, D.5
Licht, C.6
-
105
-
-
72249097911
-
Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom
-
Taylor C.M., Machin S., Wigmore S.J., Goodship T.H. Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom. Br J Haematol 2010, 148:37-47.
-
(2010)
Br J Haematol
, vol.148
, pp. 37-47
-
-
Taylor, C.M.1
Machin, S.2
Wigmore, S.J.3
Goodship, T.H.4
-
106
-
-
35948959015
-
Discovery and development of the complement inhibitor eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria
-
Rother R.P., Rollins S.A., Mojcik C.F., Brodsky R.A., Bell L. Discovery and development of the complement inhibitor eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria. Nat Biotechnol 2007, 25:1256-1264.
-
(2007)
Nat Biotechnol
, vol.25
, pp. 1256-1264
-
-
Rother, R.P.1
Rollins, S.A.2
Mojcik, C.F.3
Brodsky, R.A.4
Bell, L.5
-
107
-
-
59449088846
-
Eculizumab for congenital atypical hemolytic-uremic syndrome
-
Gruppo R.A., Rother R.P. Eculizumab for congenital atypical hemolytic-uremic 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
-
108
-
-
84859798441
-
Eculizumab in the treatment of atypical hemolytic uremic syndrome in infants
-
Ariceta G., Arrizabalaga B., Aguirre M., Morteruel E., Lopez-Trascasa M. Eculizumab in the treatment of atypical hemolytic uremic syndrome in infants. Am J Kidney Dis 2012, 59:707-710.
-
(2012)
Am J Kidney Dis
, vol.59
, pp. 707-710
-
-
Ariceta, G.1
Arrizabalaga, B.2
Aguirre, M.3
Morteruel, E.4
Lopez-Trascasa, M.5
-
109
-
-
84863981911
-
Eculizumab as rescue therapy for atypical hemolytic uremic syndrome with normal platelet count
-
Dorresteijn E.M., van de Kar NCAJ, Cransberg K. Eculizumab as rescue therapy for atypical hemolytic uremic syndrome with normal platelet count. Pediatr Nephrol 2012, 27:1193-1195.
-
(2012)
Pediatr Nephrol
, vol.27
, pp. 1193-1195
-
-
Dorresteijn, E.M.1
van de Kar, N.C.A.J.2
Cransberg, K.3
-
110
-
-
79954433046
-
Efficacy of eculizumab in a patient with factor-H-associated atypical hemolytic uremic syndrome
-
Lapeyraque A.-L., Fremeaux-Bacchi V., Robitaille P. Efficacy of eculizumab in a patient with factor-H-associated atypical hemolytic uremic syndrome. Pediatr Nephrol 2011, 26:621-624.
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 621-624
-
-
Lapeyraque, A.-L.1
Fremeaux-Bacchi, V.2
Robitaille, P.3
-
111
-
-
81255130615
-
Eculizumab safely reverses neurologic impairment and eliminates need for dialysis in severe atypical hemolytic uremic syndrome
-
Ohanian M., Cable C., Halka K. Eculizumab safely reverses neurologic impairment and eliminates need for dialysis in severe atypical hemolytic uremic syndrome. Clin Pharmacol 2011, 3:5-12.
-
(2011)
Clin Pharmacol
, vol.3
, pp. 5-12
-
-
Ohanian, M.1
Cable, C.2
Halka, K.3
-
112
-
-
78649513705
-
Eculizumab therapy in an adult with plasma exchange-refractory atypical hemolytic uremic syndrome
-
Prescott H.C., Wu H.M., Cataland S.R., Baiocchi R.A. Eculizumab therapy in an adult with plasma exchange-refractory atypical hemolytic uremic syndrome. Am J Hematol 2010, 85:976-977.
-
(2010)
Am J Hematol
, vol.85
, pp. 976-977
-
-
Prescott, H.C.1
Wu, H.M.2
Cataland, S.R.3
Baiocchi, R.A.4
-
113
-
-
83155172386
-
Eculizumab in atypical hemolytic uremic syndrome: long-term clinical course and histological findings
-
Tschumi S., Gugger M., Bucher B.S., Riedl M., Simonetti G.D. Eculizumab in atypical hemolytic uremic syndrome: long-term clinical course and histological findings. Pediatr Nephrol 2011, 26:2085-2088.
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 2085-2088
-
-
Tschumi, S.1
Gugger, M.2
Bucher, B.S.3
Riedl, M.4
Simonetti, G.D.5
-
114
-
-
77957602105
-
New treatment options for atypical hemolytic uremic syndrome with the complement inhibitor eculizumab
-
Koese O., Zimmerhackl L.-B., Jungraithmayr T., Mache C., Nuernberger J. New treatment options for atypical hemolytic uremic syndrome with the complement inhibitor eculizumab. Semin Thromb Hemost 2010, 36:669-672.
-
(2010)
Semin Thromb Hemost
, vol.36
, pp. 669-672
-
-
Koese, O.1
Zimmerhackl, L.-B.2
Jungraithmayr, T.3
Mache, C.4
Nuernberger, J.5
-
115
-
-
84898865896
-
-
Eculizumab in atypical haemolytic-uraemic syndrome allows cessation of plasma exchange and dialysis. Clin Kidney J.
-
Kim JJ, Waller SC, Reid CJ. Eculizumab in atypical haemolytic-uraemic syndrome allows cessation of plasma exchange and dialysis. Clin Kidney J. 2012;5:34-6.
-
(2012)
, vol.5
, pp. 34-36
-
-
Kim, J.J.1
Waller, S.C.2
Reid, C.J.3
-
116
-
-
84886258755
-
-
Peripheral gangrene in children with atypical hemolytic uremic syndrome. Paper presented at: 44th Annual Meeting of the European Society for Pediatric Nephrology 14 Sept Dubrovnik, Croatia
-
Malina M. Peripheral gangrene in children with atypical hemolytic uremic syndrome. Paper presented at: 44th Annual Meeting of the European Society for Pediatric Nephrology 14 Sept 2011 Dubrovnik, Croatia.
-
(2011)
-
-
Malina, M.1
-
117
-
-
84886255932
-
-
Eculizumab treatment for aHUS in a child with positive family history. Paper presented at: 42nd Annual Meeting of the American Society of Nephrology. 27 Oct San Diego CA
-
Fremont OT. Eculizumab treatment for aHUS in a child with positive family history. Paper presented at: 42nd Annual Meeting of the American Society of Nephrology. 27 Oct 2009 San Diego CA.
-
(2009)
-
-
Fremont, O.T.1
-
118
-
-
84867980876
-
Early treatment with eculizumab may be beneficial in atypical haemolytic uraemic syndrome
-
Garjau M. Early treatment with eculizumab may be beneficial in atypical haemolytic uraemic syndrome. Clin Kidney J 2012, 5:31-33.
-
(2012)
Clin Kidney J
, vol.5
, pp. 31-33
-
-
Garjau, M.1
-
119
-
-
84886260150
-
-
Effective eculizumab therapy of familiar atypical HUS in a 4 year old patient Paper presented at: 2nd International Conference on HUS, MPGN and PNH 13 June Innsbruck, Austria
-
Haffner K. Effective eculizumab therapy of familiar atypical HUS in a 4 year old patient Paper presented at: 2nd International Conference on HUS, MPGN and PNH 13 June 2010 Innsbruck, Austria.
-
(2010)
-
-
Haffner, K.1
-
120
-
-
84886260151
-
-
Safety and efficacy of eculizumab in aHUS patients on chronic plasma therapy: Interim analysis of a phase II trial. Paper presented at: 43rd Annual Meeting of the American Society of Nephrology November 16, Denver, CO
-
Muus P. Safety and efficacy of eculizumab in aHUS patients on chronic plasma therapy: Interim analysis of a phase II trial. Paper presented at: 43rd Annual Meeting of the American Society of Nephrology November 16, 2010; Denver, CO.
-
(2010)
-
-
Muus, P.1
-
121
-
-
84886258756
-
-
Phase II study of eculizumab in patients with atypical HUS receiving chronic plasma exchange/infusion. Paper presented at 44th Annual Meeting of the American Society of Nephrology November 8, Philadelphia, PA
-
Licht C. Phase II study of eculizumab in patients with atypical HUS receiving chronic plasma exchange/infusion. Paper presented at 44th Annual Meeting of the American Society of Nephrology November 8, 2011; Philadelphia, PA.
-
(2011)
-
-
Licht, C.1
-
122
-
-
84886257409
-
-
Eculizumab is an effective long-term treatment in patients with atypical haemolytic uremic syndrome previously receiving chronic plasma exchange/infusion: extension study results. Presented at the 53rd Annual Meeting of the American Society of Hematology; December 10, San Diego, CA
-
Greenbaum LA. Eculizumab is an effective long-term treatment in patients with atypical haemolytic uremic syndrome previously receiving chronic plasma exchange/infusion: extension study results. Presented at the 53rd Annual Meeting of the American Society of Hematology; December 10, 2011; San Diego, CA.
-
(2011)
-
-
Greenbaum, L.A.1
-
123
-
-
84886257410
-
-
Safety and efficacy of eculizumab in aHUS patients on chronic plasma therapy: interim analysis of a phase II trial. Presented at the 43rd Annual Meeting of the American Society of Nephrology; November 16, Denver, CO
-
Muus PM. Safety and efficacy of eculizumab in aHUS patients on chronic plasma therapy: interim analysis of a phase II trial. Presented at the 43rd Annual Meeting of the American Society of Nephrology; November 16, 2010; Denver, CO.
-
(2010)
-
-
Muus, P.M.1
-
124
-
-
84886255931
-
-
Continued improvement in renal function with sustained eculizumab in patients with atypical HUS resistant to plasma exchange/infusion. Paper presented at 44th Annual Meeting of the American Society of Nephrology November 8, Philadelphia, PA
-
Greenbaum LA. Continued improvement in renal function with sustained eculizumab in patients with atypical HUS resistant to plasma exchange/infusion. Paper presented at 44th Annual Meeting of the American Society of Nephrology November 8, 2011; Philadelphia, PA.
-
(2011)
-
-
Greenbaum, L.A.1
-
125
-
-
84886255930
-
-
Eculizumab is an effective long-term treatment in patients with atypical haemolytic uremic syndrome previously receiving chronic plasma exchange/infusion: Extension study results. Presented at the 53rd Annual Meeting of the American Society of Hematology; December 10, San Diego, CA
-
Licht C. Eculizumab is an effective long-term treatment in patients with atypical haemolytic uremic syndrome previously receiving chronic plasma exchange/infusion: Extension study results. Presented at the 53rd Annual Meeting of the American Society of Hematology; December 10, 2011; San Diego, CA.
-
(2011)
-
-
Licht, C.1
-
126
-
-
84878589219
-
Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome
-
Legendre C.M., Licht C., Muus P., Greenbaum L.A., Babu S., Bedrosian C., et al. Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome. New Engl J Med 2013, 368:2169-2181.
-
(2013)
New Engl J Med
, vol.368
, pp. 2169-2181
-
-
Legendre, C.M.1
Licht, C.2
Muus, P.3
Greenbaum, L.A.4
Babu, S.5
Bedrosian, C.6
-
127
-
-
84880799517
-
-
Complement therapy in atypical haemolytic uraemic syndrome (aHUS). Mol Immunol.
-
Wong EK, Goodship TH, Kavanagh D. Complement therapy in atypical haemolytic uraemic syndrome (aHUS). Mol Immunol. 2013;56:199-212.
-
(2013)
, vol.56
, pp. 199-212
-
-
Wong, E.K.1
Goodship, T.H.2
Kavanagh, D.3
-
128
-
-
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.
-
(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
-
129
-
-
49349112382
-
Hemolytic uremic syndrome recurrence after renal transplantation
-
Loirat C., Fremeaux-Bacchi V. Hemolytic uremic syndrome recurrence after renal transplantation. Pediatr Transplant 2008, 12:619-629.
-
(2008)
Pediatr Transplant
, vol.12
, pp. 619-629
-
-
Loirat, C.1
Fremeaux-Bacchi, V.2
-
130
-
-
34447127478
-
Recurrence of HUS due to CD46/MCP mutation after renal transplantation: a role for endothelial microchimerism
-
Fremeaux-Bacchi V., Arzouk N., Ferlicot S., Charpentier B., Snanoudj R., Durrbach A. Recurrence of HUS due to CD46/MCP mutation after renal transplantation: a role for endothelial microchimerism. Am J Transplant 2007, 7:2047-2051.
-
(2007)
Am J Transplant
, vol.7
, pp. 2047-2051
-
-
Fremeaux-Bacchi, V.1
Arzouk, N.2
Ferlicot, S.3
Charpentier, B.4
Snanoudj, R.5
Durrbach, A.6
-
131
-
-
80155136247
-
Three kidneys, two diseases, one antibody?
-
Lorcy N., Rioux-Leclercq N., Lombard M.L., Le Pogamp P., Vigneau C. Three kidneys, two diseases, one antibody?. Nephrol Dial Transplant 2011, 26:3811-3813.
-
(2011)
Nephrol Dial Transplant
, vol.26
, pp. 3811-3813
-
-
Lorcy, N.1
Rioux-Leclercq, N.2
Lombard, M.L.3
Le Pogamp, P.4
Vigneau, C.5
-
132
-
-
65249156546
-
Anti-factor H autoantibodies in a fifth renal transplant recipient with atypical hemolytic and uremic syndrome
-
Le Quintrec M., Zuber J., Noel L.H., Thervet E., Fremeaux-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, 9:1223-1229.
-
(2009)
Am J Transplant
, vol.9
, pp. 1223-1229
-
-
Le Quintrec, M.1
Zuber, J.2
Noel, L.H.3
Thervet, E.4
Fremeaux-Bacchi, V.5
Niaudet, P.6
-
133
-
-
44449165673
-
Successful pre-transplant management of a patient with anti-factor H autoantibodies-associated haemolytic uraemic syndrome
-
Kwon T., Dragon-Durey M.A., Macher M.A., 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, 23:2088-2090.
-
(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
-
134
-
-
18744377731
-
Recurrence of hemolytic uremic syndrome after live related renal transplantation associated with subsequent de novo disease in the donor
-
Donne R.L., Abbs I., Barany P., Elinder C.G., Little M., Conlon P., et al. Recurrence of hemolytic uremic syndrome after live related renal transplantation associated with subsequent de novo disease in the donor. Am J Kidney Dis 2002, 40:E22.
-
(2002)
Am J Kidney Dis
, vol.40
-
-
Donne, R.L.1
Abbs, I.2
Barany, P.3
Elinder, C.G.4
Little, M.5
Conlon, P.6
-
135
-
-
0016258050
-
Hemolytic-uremic syndrome in adult sisters
-
Bergstein J., Michael A., Kellstrand C., Simmons R., Najarian J. Hemolytic-uremic syndrome in adult sisters. Transplantation 1974, 17:487-490.
-
(1974)
Transplantation
, vol.17
, pp. 487-490
-
-
Bergstein, J.1
Michael, A.2
Kellstrand, C.3
Simmons, R.4
Najarian, J.5
-
136
-
-
0030777598
-
Zulkharnain Renal transplantation in adults with autosomal recessive inheritance of hemolytic uremic syndrome
-
Kaplan B.S., Papadimitriou M., Brezin J.H., Tomlanovich S.J., Zulkharnain Renal transplantation in adults with autosomal recessive inheritance of hemolytic uremic syndrome. Am J Kidney Dis 1997, 30:760-765.
-
(1997)
Am J Kidney Dis
, vol.30
, pp. 760-765
-
-
Kaplan, B.S.1
Papadimitriou, M.2
Brezin, J.H.3
Tomlanovich, S.J.4
-
137
-
-
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, 359:1671-1672.
-
(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
-
138
-
-
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, 5:1146-1150.
-
(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
-
139
-
-
1842637606
-
Attempted treatment of factor H deficiency by liver transplantation
-
Cheong H.I., Lee B.S., Kang H.G., Hahn H., Suh K.S., Ha I.S., et al. Attempted treatment of factor H deficiency by liver transplantation. Pediatr Nephrol 2004, 19:454-458.
-
(2004)
Pediatr Nephrol
, vol.19
, pp. 454-458
-
-
Cheong, H.I.1
Lee, B.S.2
Kang, H.G.3
Hahn, H.4
Suh, K.S.5
Ha, I.S.6
-
140
-
-
37549018997
-
Successful liver-kidney transplantation in two children with aHUS caused by a mutation in complement factor H
-
Jalanko H., Peltonen S., Koskinen A., Puntila J., Isoniemi H., Holmberg C., et al. Successful liver-kidney transplantation in two children with aHUS caused by a mutation in complement factor H. Am J Transplant 2008, 8:216-221.
-
(2008)
Am J Transplant
, vol.8
, pp. 216-221
-
-
Jalanko, H.1
Peltonen, S.2
Koskinen, A.3
Puntila, J.4
Isoniemi, H.5
Holmberg, C.6
-
141
-
-
64049101602
-
Successful split liver-kidney transplant for factor H associated hemolytic uremic syndrome
-
Saland J.M., Shneider B.L., Bromberg J.S., Shi P.A., Ward S.C., Magid M.S., et al. Successful split liver-kidney transplant for factor H associated hemolytic uremic syndrome. Clin J Am Soc Nephrol 2009, 4:201-206.
-
(2009)
Clin J Am Soc Nephrol
, vol.4
, pp. 201-206
-
-
Saland, J.M.1
Shneider, B.L.2
Bromberg, J.S.3
Shi, P.A.4
Ward, S.C.5
Magid, M.S.6
-
142
-
-
77956135217
-
Successful isolated liver transplantation in a child with atypical hemolytic uremic syndrome and a mutation in complement factor H
-
Haller W., Milford D.V., Goodship T.H., Sharif K., Mirza D.F., McKiernan P.J. Successful isolated liver transplantation in a child with atypical hemolytic uremic syndrome and a mutation in complement factor H. Am J Transplant 2010, 10:2142-2147.
-
(2010)
Am J Transplant
, vol.10
, pp. 2142-2147
-
-
Haller, W.1
Milford, D.V.2
Goodship, T.H.3
Sharif, K.4
Mirza, D.F.5
McKiernan, P.J.6
-
143
-
-
79959342153
-
Successful simultaneous liver-kidney transplant in an adult with atypical hemolytic uremic syndrome associated with a mutation in complement factor H
-
Wilson C., Torpey N., Jaques B., Strain L., Talbot D., Manas D., et al. Successful simultaneous liver-kidney transplant in an adult with atypical hemolytic uremic syndrome associated with a mutation in complement factor H. Am J Kidney Dis 2011, 58:109-112.
-
(2011)
Am J Kidney Dis
, vol.58
, pp. 109-112
-
-
Wilson, C.1
Torpey, N.2
Jaques, B.3
Strain, L.4
Talbot, D.5
Manas, D.6
-
144
-
-
77955779512
-
Advances in understanding the aetiology of atypical haemolytic uraemic syndrome
-
Sanchez-Corral P., Melgosa M. Advances in understanding the aetiology of atypical haemolytic uraemic syndrome. Br J Haematol 2010, 150:529-542.
-
(2010)
Br J Haematol
, vol.150
, pp. 529-542
-
-
Sanchez-Corral, P.1
Melgosa, M.2
-
145
-
-
33745767079
-
Favorable long-term outcome after liver-kidney transplant for recurrent hemolytic uremic syndrome associated with a factor H mutation
-
Saland J.M., Emre S.H., Shneider B.L., Benchimol C., Ames S., Bromberg J.S., et al. Favorable long-term outcome after liver-kidney transplant for recurrent hemolytic uremic syndrome associated with a factor H mutation. Am J Transplant 2006, 6:1948-1952.
-
(2006)
Am J Transplant
, vol.6
, pp. 1948-1952
-
-
Saland, J.M.1
Emre, S.H.2
Shneider, B.L.3
Benchimol, C.4
Ames, S.5
Bromberg, J.S.6
-
146
-
-
77957602545
-
Transplantation in atypical hemolytic uremic syndrome
-
Kavanagh D., Richards A., Goodship T., Jalanko H. Transplantation in atypical hemolytic uremic syndrome. Semin Thromb Hemost 2010, 36:653-659.
-
(2010)
Semin Thromb Hemost
, vol.36
, pp. 653-659
-
-
Kavanagh, D.1
Richards, A.2
Goodship, T.3
Jalanko, H.4
-
147
-
-
65649106258
-
Liver-kidney transplantation to cure atypical hemolytic uremic syndrome
-
Saland J.M., Ruggenenti P., Remuzzi G. Liver-kidney transplantation to cure atypical hemolytic uremic syndrome. J Am Soc Nephrol 2009, 20:940-949.
-
(2009)
J Am Soc Nephrol
, vol.20
, pp. 940-949
-
-
Saland, J.M.1
Ruggenenti, P.2
Remuzzi, G.3
-
148
-
-
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, 8:1694-1701.
-
(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
-
149
-
-
84862780165
-
Postpartum aHUS secondary to a genetic abnormality in factor H acquired through liver transplantation
-
Brown J.H., Tellez J., Wilson V., Mackie I.J., Scully M., Tredger M.M., et al. Postpartum aHUS secondary to a genetic abnormality in factor H acquired through liver transplantation. Am J Transplant 2012, 12:1632-1636.
-
(2012)
Am J Transplant
, vol.12
, pp. 1632-1636
-
-
Brown, J.H.1
Tellez, J.2
Wilson, V.3
Mackie, I.J.4
Scully, M.5
Tredger, M.M.6
-
150
-
-
59449107473
-
Eculizumab for atypical hemolytic-uremic syndrome
-
Nuernberger J., Witzke O., Saez A.O., Vester U., Baba H.A., Kribben A., 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
-
-
Nuernberger, J.1
Witzke, O.2
Saez, A.O.3
Vester, U.4
Baba, H.A.5
Kribben, A.6
-
151
-
-
79954443076
-
Eculizumab induces long-term remission in recurrent post-transplant HUS associated with C3 gene mutation
-
Al-Akash S.I., Almond P.S., Savell V.H., Gharaybeh S.I., Hogue C. Eculizumab induces long-term remission in recurrent post-transplant HUS associated with C3 gene mutation. Pediatr Nephrol 2011, 26:613-619.
-
(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
-
152
-
-
70350130833
-
-
Safety and long-term efficacy of eculizumab in a renal transplant patient with recurrent atypical hemolytic-uremic syndrome. Am J Transplant.
-
Chatelet V, Fremeaux-Bacchi V, Lobbedez T, Ficheux M, de Ligny BH. 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.
-
(2009)
, vol.9
, pp. 2644-2645
-
-
Chatelet, V.1
Fremeaux-Bacchi, V.2
Lobbedez, T.3
Ficheux, M.4
De Ligny, B.H.5
-
153
-
-
78650507665
-
Eculizumab: safety and efficacy after 17 months of treatment in a renal transplant patient with recurrent atypical hemolytic-uremic syndrome: case report
-
Chatelet V., Lobbedez T., Fremeaux-Bacchi V., Ficheux M., Ryckelynck J.P., de Ligny BH. Eculizumab: safety and efficacy after 17 months of treatment in a renal transplant patient with recurrent atypical hemolytic-uremic syndrome: case report. Transplant Proc 2010, 42:4353-4355.
-
(2010)
Transplant Proc
, vol.42
, pp. 4353-4355
-
-
Chatelet, V.1
Lobbedez, T.2
Fremeaux-Bacchi, V.3
Ficheux, M.4
Ryckelynck, J.P.5
de Ligny, B.H.6
-
154
-
-
77950955452
-
Efficacy of eculizumab in the treatment of recurrent atypical hemolytic-uremic syndrome after renal transplantation
-
Larrea CF-d Cofan F., Oppenheimer F., Campistol J.M., Escolar G., Lozano M. Efficacy of eculizumab in the treatment of recurrent atypical hemolytic-uremic syndrome after renal transplantation. Transplantation 2010, 89:903-904.
-
(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
-
155
-
-
78650517945
-
New insights into postrenal transplant hemolytic uremic syndrome
-
Zuber J., Le Quintrec M., Sberro-Soussan R., Loirat C., Fremeaux-Bacchi V., Legendre C. New insights into postrenal transplant hemolytic uremic syndrome. Nat Rev Nephrol 2011, 7:23-35.
-
(2011)
Nat Rev Nephrol
, vol.7
, pp. 23-35
-
-
Zuber, J.1
Le Quintrec, M.2
Sberro-Soussan, R.3
Loirat, C.4
Fremeaux-Bacchi, V.5
Legendre, C.6
-
156
-
-
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, 6:1488-1494.
-
(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
-
157
-
-
84863208524
-
Renal transplantation under prophylactic eculizumab in atypical hemolytic uremic syndrome with CFH/CFHR1 hybrid protein
-
Krid S., Roumenina L., Beury D., Charbit M., Boyer O., Fremeaux-Bacchi V., et al. Renal transplantation under prophylactic eculizumab in atypical hemolytic uremic syndrome with CFH/CFHR1 hybrid protein. Am J Transplant 2012, 12:1938-1944.
-
(2012)
Am J Transplant
, vol.12
, pp. 1938-1944
-
-
Krid, S.1
Roumenina, L.2
Beury, D.3
Charbit, M.4
Boyer, O.5
Fremeaux-Bacchi, V.6
-
158
-
-
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, 26:1325-1329.
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 1325-1329
-
-
Weitz, M.1
Amon, O.2
Bassler, D.3
Koenigsrainer, A.4
Nadalin, S.5
-
159
-
-
77951876953
-
Prophylactic eculizumab after renal transplantation in atypical hemolytic-uremic syndrome
-
Zimmerhackl L.B., Hofer J., Cortina G., Mark W., Wurzner R., Jungraithmayr T.C., et al. Prophylactic eculizumab after renal transplantation in atypical hemolytic-uremic syndrome. N Engl J Med 2010, 362:1746-1748.
-
(2010)
N Engl J Med
, vol.362
, pp. 1746-1748
-
-
Zimmerhackl, L.B.1
Hofer, J.2
Cortina, G.3
Mark, W.4
Wurzner, R.5
Jungraithmayr, T.C.6
-
160
-
-
84870534251
-
Atypical HUS. Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation
-
French Study Group
-
Zuber J., Le Quintrec M., Krid S., Bertoye C., Gueutin V., Lahoche A., et al. Atypical HUS. Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation. Am J Transplant 2012, 12:3337-3354. French Study Group.
-
(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
-
161
-
-
79961235437
-
Structural basis for complement factor I control and its disease-associated sequence polymorphisms
-
Roversi P., Johnson S., Caesar J.J., McLean F., Leath K.J., Tsiftsoglou S.A., et al. Structural basis for complement factor I control and its disease-associated sequence polymorphisms. Proc Natl Acad Sci U S A 2011, 108:12839-12844.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 12839-12844
-
-
Roversi, P.1
Johnson, S.2
Caesar, J.J.3
McLean, F.4
Leath, K.J.5
Tsiftsoglou, S.A.6
-
162
-
-
34547843562
-
Haemolytic uraemic syndrome complicated with norovirus-associated gastroenteritis
-
Sugimoto T., Ogawa N., Aoyama M., Sakaguchi M., Isshiki K., Kanasaki M., et al. Haemolytic uraemic syndrome complicated with norovirus-associated gastroenteritis. Nephrol Dial Transplant 2007, 22:2098-2099.
-
(2007)
Nephrol Dial Transplant
, vol.22
, pp. 2098-2099
-
-
Sugimoto, T.1
Ogawa, N.2
Aoyama, M.3
Sakaguchi, M.4
Isshiki, K.5
Kanasaki, M.6
-
163
-
-
70350448229
-
Atypical hemolytic uremic syndrome associated with complement factor H autoantibodies and CFHR1/CFHR3 deficiency
-
Lee B.H., Kwak S.H., Shin J.I., Lee S.H., Choi H.J., Kang H.G., et al. Atypical hemolytic uremic syndrome associated with complement factor H autoantibodies and CFHR1/CFHR3 deficiency. Pediatr Res 2009, 66:336-340.
-
(2009)
Pediatr Res
, vol.66
, pp. 336-340
-
-
Lee, B.H.1
Kwak, S.H.2
Shin, J.I.3
Lee, S.H.4
Choi, H.J.5
Kang, H.G.6
-
164
-
-
0030345735
-
Hemolytic-uremic syndrome associated with acute Campylobacter upsaliensis gastroenteritis
-
Carter J.E., Cimolai N. Hemolytic-uremic syndrome associated with acute Campylobacter upsaliensis gastroenteritis. Nephron 1996, 74:489.
-
(1996)
Nephron
, vol.74
, pp. 489
-
-
Carter, J.E.1
Cimolai, N.2
-
165
-
-
84886260147
-
Hemolytic uremic syndrome associated with Clostridium difficile infection
-
(Epub ahead of print).
-
Alvarado A.S., Brodsky S.V., Nadasdy T., Singh N. Hemolytic uremic syndrome associated with Clostridium difficile infection. Clin Nephrol 2013, (Epub ahead of print).
-
(2013)
Clin Nephrol
-
-
Alvarado, A.S.1
Brodsky, S.V.2
Nadasdy, T.3
Singh, N.4
-
166
-
-
0036940021
-
Hemolytic uremic syndrome due to an altered factor H triggered by neonatal pertussis
-
Berner R., Krause M.F., Gordjani N., Zipfel P.F., Boehm N., Krueger M., et al. Hemolytic uremic syndrome due to an altered factor H triggered by neonatal pertussis. Pediatr Nephrol 2002, 17:190-192.
-
(2002)
Pediatr Nephrol
, vol.17
, pp. 190-192
-
-
Berner, R.1
Krause, M.F.2
Gordjani, N.3
Zipfel, P.F.4
Boehm, N.5
Krueger, M.6
-
167
-
-
34447539658
-
Hemolytic uremic syndrome associated with invasive pneumococcal disease: the United Kingdom experience
-
Waters A.M., Kerecuk L., Luk D., Haq M.R., Fitzpatrick M.M., Gilbert R.D., et al. Hemolytic uremic syndrome associated with invasive pneumococcal disease: the United Kingdom experience. J Pediatr 2007, 151:140-144.
-
(2007)
J Pediatr
, vol.151
, pp. 140-144
-
-
Waters, A.M.1
Kerecuk, L.2
Luk, D.3
Haq, M.R.4
Fitzpatrick, M.M.5
Gilbert, R.D.6
-
168
-
-
0035286556
-
Hemolytic uremic syndrome in an adolescent with Fusobacterium necrophorum bacteremia
-
Chand D.H., Brady R.C., Bissler J.J. Hemolytic uremic syndrome in an adolescent with Fusobacterium necrophorum bacteremia. Am J Kidney Dis 2001, 37:E22.
-
(2001)
Am J Kidney Dis
, vol.37
-
-
Chand, D.H.1
Brady, R.C.2
Bissler, J.J.3
-
169
-
-
69249100433
-
Varicella as a trigger of atypical haemolytic uraemic syndrome associated with complement dysfunction: two cases
-
Kwon T., Belot A., Ranchin B., Baudouin V., Fremeaux-Bacchi V., Dragon-Durey M.A., et al. Varicella as a trigger of atypical haemolytic uraemic syndrome associated with complement dysfunction: two cases. Nephrol Dial Transplant 2009, 24:2752-2754.
-
(2009)
Nephrol Dial Transplant
, vol.24
, pp. 2752-2754
-
-
Kwon, T.1
Belot, A.2
Ranchin, B.3
Baudouin, V.4
Fremeaux-Bacchi, V.5
Dragon-Durey, M.A.6
-
170
-
-
0032855782
-
De novo hemolytic uremic syndrome postrenal transplant after cytomegalovirus infection
-
Waiser J., Budde K., Rudolph B., Ortner M.A., Neumayer H.H. De novo hemolytic uremic syndrome postrenal transplant after cytomegalovirus infection. Am J Kidney Dis 1999, 34:556-559.
-
(1999)
Am J Kidney Dis
, vol.34
, pp. 556-559
-
-
Waiser, J.1
Budde, K.2
Rudolph, B.3
Ortner, M.A.4
Neumayer, H.H.5
-
171
-
-
77953593277
-
Triggering of atypical hemolytic uremic syndrome by influenza A (H1N1)
-
Bento D., Mapril J., Rocha C., Marchbank K.J., Kavanagh D., Barge D., et al. Triggering of atypical hemolytic uremic syndrome by influenza A (H1N1). Ren Fail 2010, 32:753-756.
-
(2010)
Ren Fail
, vol.32
, pp. 753-756
-
-
Bento, D.1
Mapril, J.2
Rocha, C.3
Marchbank, K.J.4
Kavanagh, D.5
Barge, D.6
-
172
-
-
2342530459
-
[Relapsing viral hepatitis type A complicated with renal failure]
-
Tagle M., Barriga J.A., Gutierrez S., Valdez L.M., Castle J., Antunez De Mayolo A., et al. [Relapsing viral hepatitis type A complicated with renal failure]. Rev Gastroenterol Peru 2004, 24:92-96.
-
(2004)
Rev Gastroenterol Peru
, vol.24
, pp. 92-96
-
-
Tagle, M.1
Barriga, J.A.2
Gutierrez, S.3
Valdez, L.M.4
Castle, J.5
Antunez De Mayolo, A.6
-
173
-
-
0032898908
-
Renal thrombotic microangiopathy associated with anticardiolipin antibodies in hepatitis C-positive renal allograft recipients
-
Baid S., Pascual M., Williams W.W., Tolkoff-Rubin N., Johnson S.M., Collins B., et al. Renal thrombotic microangiopathy associated with anticardiolipin antibodies in hepatitis C-positive renal allograft recipients. J Am Soc Nephrol 1999, 10:146-153.
-
(1999)
J Am Soc Nephrol
, vol.10
, pp. 146-153
-
-
Baid, S.1
Pascual, M.2
Williams, W.W.3
Tolkoff-Rubin, N.4
Johnson, S.M.5
Collins, B.6
-
174
-
-
0031041121
-
Haemolytic-uraemic syndrome in a patient infected by HIV
-
Benitez M., Boto A., Colchero J., Fernandez-Giron F., Rodriguez P., Paralle M., et al. Haemolytic-uraemic syndrome in a patient infected by HIV. Nephrol Dial Transplant 1997, 12:362-363.
-
(1997)
Nephrol Dial Transplant
, vol.12
, pp. 362-363
-
-
Benitez, M.1
Boto, A.2
Colchero, J.3
Fernandez-Giron, F.4
Rodriguez, P.5
Paralle, M.6
-
175
-
-
0015828683
-
B infections and the hemolytic-uremic syndrome
-
Coxsackie virus group
-
Austin T.W., Ray C.G. B infections and the hemolytic-uremic syndrome. J Infect Dis 1973, 127:698-701. Coxsackie virus group.
-
(1973)
J Infect Dis
, vol.127
, pp. 698-701
-
-
Austin, T.W.1
Ray, C.G.2
-
176
-
-
2342634460
-
Hemolytic uremic syndrome associated with Epstein-Barr virus infection
-
Watanabe T. Hemolytic uremic syndrome associated with Epstein-Barr virus infection. Pediatr Nephrol 2004, 19:569.
-
(2004)
Pediatr Nephrol
, vol.19
, pp. 569
-
-
Watanabe, T.1
-
177
-
-
33748329422
-
Dengue fever-induced hemolytic uremic syndrome
-
Wiersinga W.J., Scheepstra C.G., Kasanardjo J.S., de Vries PJ, Zaaijer H, Geerlings SE. Dengue fever-induced hemolytic uremic syndrome. Clin Infect Dis 2006, 43:800-801.
-
(2006)
Clin Infect Dis
, vol.43
, pp. 800-801
-
-
Wiersinga, W.J.1
Scheepstra, C.G.2
Kasanardjo, J.S.3
de Vries, P.J.4
Zaaijer, H.5
Geerlings, S.E.6
-
178
-
-
0032757354
-
Thrombotic microangiopathy associated with reactivation of human herpesvirus-6 following high-dose chemotherapy with autologous bone marrow transplantation in young children
-
Matsuda Y., Hara J., Miyoshi H., Osugi Y., Fujisaki H., Takai K., et al. Thrombotic microangiopathy associated with reactivation of human herpesvirus-6 following high-dose chemotherapy with autologous bone marrow transplantation in young children. Bone Marrow Transplant 1999, 24:919-923.
-
(1999)
Bone Marrow Transplant
, vol.24
, pp. 919-923
-
-
Matsuda, Y.1
Hara, J.2
Miyoshi, H.3
Osugi, Y.4
Fujisaki, H.5
Takai, K.6
-
179
-
-
34250371425
-
Renal complications associated with human parvovirus B19 infection in early childhood
-
Hartel C., Herz A., Vieth S., Lensing C., Schultz C. Renal complications associated with human parvovirus B19 infection in early childhood. Klin Padiatr 2007, 219:74-75.
-
(2007)
Klin Padiatr
, vol.219
, pp. 74-75
-
-
Hartel, C.1
Herz, A.2
Vieth, S.3
Lensing, C.4
Schultz, C.5
-
180
-
-
0346368326
-
[May Plasmodium falciparum induce a hemolytic uremic syndrome?]
-
Adonis-Koffy L. [May Plasmodium falciparum induce a hemolytic uremic syndrome?]. Arch Pediatr 2004, 11:55-56.
-
(2004)
Arch Pediatr
, vol.11
, pp. 55-56
-
-
Adonis-Koffy, L.1
-
181
-
-
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
-
182
-
-
0028035370
-
Cisplatin-associated hemolytic uremic syndrome
-
Canpolat C., Pearson P., Jaffe N. Cisplatin-associated hemolytic uremic syndrome. Cancer 1994, 74:3059-3062.
-
(1994)
Cancer
, vol.74
, pp. 3059-3062
-
-
Canpolat, C.1
Pearson, P.2
Jaffe, N.3
-
183
-
-
42449105802
-
Hemolytic-uremic syndrome associated with gemcitabine treatment for metastatic pancreatic cancer
-
Boeck S., Geiger S., Schulz C., Heinemann V. Hemolytic-uremic syndrome associated with gemcitabine treatment for metastatic pancreatic cancer. J Clin Gastroenterol 2008, 42:551-552.
-
(2008)
J Clin Gastroenterol
, vol.42
, pp. 551-552
-
-
Boeck, S.1
Geiger, S.2
Schulz, C.3
Heinemann, V.4
-
184
-
-
0031042555
-
Thrombotic thrombocytopenic purpura caused by ticlopidine, successfully treated by plasmapheresis
-
Ariyoshi K., Shinohara K., Ruirong X. Thrombotic thrombocytopenic purpura caused by ticlopidine, successfully treated by plasmapheresis. Am J Hematol 1997, 54:175-176.
-
(1997)
Am J Hematol
, vol.54
, pp. 175-176
-
-
Ariyoshi, K.1
Shinohara, K.2
Ruirong, X.3
-
185
-
-
4644354632
-
Thrombotic thrombocytopenic purpura/haemolytic uraemic syndrome associated with clopidogrel: report of two new cases
-
Andersohn F., Hagmann F.G., Garbe E. Thrombotic thrombocytopenic purpura/haemolytic uraemic syndrome associated with clopidogrel: report of two new cases. Heart 2004, 90:e57.
-
(2004)
Heart
, vol.90
-
-
Andersohn, F.1
Hagmann, F.G.2
Garbe, E.3
-
186
-
-
0027424961
-
Quinine sensitivity: a new cause of the hemolytic uremic syndrome
-
Aster R.H. Quinine sensitivity: a new cause of the hemolytic uremic syndrome. Ann Intern Med 1993, 119:243-244.
-
(1993)
Ann Intern Med
, vol.119
, pp. 243-244
-
-
Aster, R.H.1
-
187
-
-
0028131634
-
Quinine-induced immune thrombocytopenia with hemolytic uremic syndrome: clinical and serological findings in nine patients and review of literature
-
Gottschall J.L., Neahring B., McFarland J.G., Wu G.G., Weitekamp L.A., Aster R.H. Quinine-induced immune thrombocytopenia with hemolytic uremic syndrome: clinical and serological findings in nine patients and review of literature. Am J Hematol 1994, 47:283-289.
-
(1994)
Am J Hematol
, vol.47
, pp. 283-289
-
-
Gottschall, J.L.1
Neahring, B.2
McFarland, J.G.3
Wu, G.G.4
Weitekamp, L.A.5
Aster, R.H.6
-
188
-
-
0031693509
-
Hemolytic uremic syndrome associated with beta-interferon therapy for chronic hepatitis C
-
Ubara Y., Hara S., Takedatu H., Katori H., Yamada K., Yoshihara K., et al. Hemolytic uremic syndrome associated with beta-interferon therapy for chronic hepatitis C. Nephron 1998, 80:107-108.
-
(1998)
Nephron
, vol.80
, pp. 107-108
-
-
Ubara, Y.1
Hara, S.2
Takedatu, H.3
Katori, H.4
Yamada, K.5
Yoshihara, K.6
-
189
-
-
0035083320
-
Renal thrombotic microangiopathy induced by interferon-alpha
-
Badid C., McGregor B., Faivre J.M., Guerard A., Juillard L., Fouque D., et al. Renal thrombotic microangiopathy induced by interferon-alpha. Nephrol Dial Transplant 2001, 16:846-848.
-
(2001)
Nephrol Dial Transplant
, vol.16
, pp. 846-848
-
-
Badid, C.1
McGregor, B.2
Faivre, J.M.3
Guerard, A.4
Juillard, L.5
Fouque, D.6
-
190
-
-
84862118558
-
Beware renal adverse effects of anti-vascular endothelial growth factor treatment
-
Keir L., Moorsel F., Saleem M.A., Richards A. Beware renal adverse effects of anti-vascular endothelial growth factor treatment. BMJ 2012, 344:e3838.
-
(2012)
BMJ
, vol.344
-
-
Keir, L.1
Moorsel, F.2
Saleem, M.A.3
Richards, A.4
-
191
-
-
33847223122
-
Hemolytic uremic syndrome following Campath-1H induction
-
Bonatti H., Brandacher G., Boesmueller C., Cont M., Hengster P., Rosenkranz A.R., et al. Hemolytic uremic syndrome following Campath-1H induction. Transpl Int 2007, 20:386-389.
-
(2007)
Transpl Int
, vol.20
, pp. 386-389
-
-
Bonatti, H.1
Brandacher, G.2
Boesmueller, C.3
Cont, M.4
Hengster, P.5
Rosenkranz, A.R.6
-
192
-
-
0033638483
-
Hemolytic-uremic syndrome in association with both cyclosporine and tacrolimus
-
Abraham K.A., Little M.A., Dorman A.M., Walshe J.J. Hemolytic-uremic syndrome in association with both cyclosporine and tacrolimus. Transpl Int 2000, 13:443-447.
-
(2000)
Transpl Int
, vol.13
, pp. 443-447
-
-
Abraham, K.A.1
Little, M.A.2
Dorman, A.M.3
Walshe, J.J.4
-
193
-
-
0036014068
-
Ciprofloxacin-associated hemolytic-uremic syndrome
-
Allan D.S., Thompson C.M., Barr R.M., Clark W.F., Chin-Yee I.H. Ciprofloxacin-associated hemolytic-uremic syndrome. Ann Pharmacother 2002, 36:1000-1002.
-
(2002)
Ann Pharmacother
, vol.36
, pp. 1000-1002
-
-
Allan, D.S.1
Thompson, C.M.2
Barr, R.M.3
Clark, W.F.4
Chin-Yee, I.H.5
-
194
-
-
0016849584
-
[Hemolytic-uremic syndrome in a young woman following the use of ovulation inhibitors]
-
Blumberg A., Studer U., Briner J. [Hemolytic-uremic syndrome in a young woman following the use of ovulation inhibitors]. Schweiz Med Wochenschr 1975, 105:1324-1327.
-
(1975)
Schweiz Med Wochenschr
, vol.105
, pp. 1324-1327
-
-
Blumberg, A.1
Studer, U.2
Briner, J.3
-
195
-
-
0020061883
-
Hemolytic uremic syndrome in two postmenopausal women taking a conjugated estrogen preparation
-
Ashouri O.S., Marbury T.C., Fuller T.J., Gaffney E., Grubb W.G., Cade J.R. Hemolytic uremic syndrome in two postmenopausal women taking a conjugated estrogen preparation. Clin Nephrol 1982, 17:212-215.
-
(1982)
Clin Nephrol
, vol.17
, pp. 212-215
-
-
Ashouri, O.S.1
Marbury, T.C.2
Fuller, T.J.3
Gaffney, E.4
Grubb, W.G.5
Cade, J.R.6
-
196
-
-
0036735327
-
A post-menopausal woman with anuria and uterus bulk: the spectrum of estrogen-induced TTP/HUS
-
Au W.Y., Chan K.W., Lam C.C., Young K. A post-menopausal woman with anuria and uterus bulk: the spectrum of estrogen-induced TTP/HUS. Am J Hematol 2002, 71:59-60.
-
(2002)
Am J Hematol
, vol.71
, pp. 59-60
-
-
Au, W.Y.1
Chan, K.W.2
Lam, C.C.3
Young, K.4
-
197
-
-
0025315459
-
Hemolytic-uremic syndrome following "crack" cocaine inhalation
-
Tumlin J.A., Sands J.M., Someren A. Hemolytic-uremic syndrome following "crack" cocaine inhalation. Am J Med Sci 1990, 299:366-371.
-
(1990)
Am J Med Sci
, vol.299
, pp. 366-371
-
-
Tumlin, J.A.1
Sands, J.M.2
Someren, A.3
-
198
-
-
0031913280
-
Anticardiolipin antibodies in classic pediatric hemolytic-uremic syndrome: a possible pathogenic role
-
Ardiles L.G., Olavarria F., Elgueta M., Moya P., Mezzano S. Anticardiolipin antibodies in classic pediatric hemolytic-uremic syndrome: a possible pathogenic role. Nephron 1998, 78:278-283.
-
(1998)
Nephron
, vol.78
, pp. 278-283
-
-
Ardiles, L.G.1
Olavarria, F.2
Elgueta, M.3
Moya, P.4
Mezzano, S.5
-
199
-
-
0017737237
-
Hemolytic uremic syndrome with hypocomplementemia, serum C3NeF, and glomerular deposits of C3
-
Barre P., Kaplan B.S., de Chadarevian JP, Drummond KN. 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
Drummond, K.N.4
-
200
-
-
0028567103
-
Thrombotic microangiographic hemolytic anemia in systemic lupus erythematosus
-
Nesher G., Hanna V.E., Moore T.L., Hersh M., Osborn T.G. Thrombotic microangiographic hemolytic anemia in systemic lupus erythematosus. Semin Arthritis Rheum 1994, 24:165-172.
-
(1994)
Semin Arthritis Rheum
, vol.24
, pp. 165-172
-
-
Nesher, G.1
Hanna, V.E.2
Moore, T.L.3
Hersh, M.4
Osborn, T.G.5
-
201
-
-
27844507105
-
Hemolytic uremic syndrome after bone marrow transplantation: clinical characteristics and outcome in children
-
Hale G.A., Bowman L.C., Rochester RJ, Benaim E, Heslop HE, Krance RA, et al. Hemolytic uremic syndrome after bone marrow transplantation: clinical characteristics and outcome in children. Biol Blood Marrow Transplant 2005, 11:912-920.
-
(2005)
Biol Blood Marrow Transplant
, vol.11
, pp. 912-920
-
-
Hale, G.A.1
Bowman, L.C.2
Rochester, R.J.3
Benaim, E.4
Heslop, H.E.5
Krance, R.A.6
-
202
-
-
84863719861
-
Cancer-related microangiopathic hemolytic anemia: clinical and laboratory features in 168 reported cases
-
Lechner K., Obermeier H.L. Cancer-related microangiopathic hemolytic anemia: clinical and laboratory features in 168 reported cases. Medicine (Baltimore) 2012, 91:195-205.
-
(2012)
Medicine (Baltimore)
, vol.91
, pp. 195-205
-
-
Lechner, K.1
Obermeier, H.L.2
-
203
-
-
0036250547
-
Cobalamin C disease presenting as hemolytic-uremic syndrome in the neonatal period
-
Kind T., Levy J., Lee M., Kaicker S., Nicholson J.F., Kane S.A. Cobalamin C disease presenting as hemolytic-uremic syndrome in the neonatal period. J Pediatr Hematol Oncol 2002, 24:327-329.
-
(2002)
J Pediatr Hematol Oncol
, vol.24
, pp. 327-329
-
-
Kind, T.1
Levy, J.2
Lee, M.3
Kaicker, S.4
Nicholson, J.F.5
Kane, S.A.6
-
204
-
-
67650129379
-
Mutations of factor H impair regulation of surface-bound C3b by three mechanisms in atypical hemolytic uremic syndrome
-
Lehtinen M.J., Rops A.L., Isenman D.E., van der Vlag J., Jokiranta T.S. Mutations of factor H impair regulation of surface-bound C3b by three mechanisms in atypical hemolytic uremic syndrome. J Biol Chem 2009, 284:15650-15658.
-
(2009)
J Biol Chem
, vol.284
, pp. 15650-15658
-
-
Lehtinen, M.J.1
Rops, A.L.2
Isenman, D.E.3
van der Vlag, J.4
Jokiranta, T.S.5
-
205
-
-
79953772478
-
Structural basis for engagement by complement factor H of C3b on a self surface
-
Morgan H.P., Schmidt C.Q., Guariento M., Blaum B.S., Gillespie D., Herbert A.P., et al. Structural basis for engagement by complement factor H of C3b on a self surface. Nat Struct Mol Biol 2011, 18:463-470.
-
(2011)
Nat Struct Mol Biol
, vol.18
, pp. 463-470
-
-
Morgan, H.P.1
Schmidt, C.Q.2
Guariento, M.3
Blaum, B.S.4
Gillespie, D.5
Herbert, A.P.6
-
206
-
-
33645451557
-
Factor H and atypical hemolytic uremic syndrome: mutations in the C-terminus cause structural changes and defective recognition functions
-
Jozsi M., Heinen S., Hartmann A., Ostrowicz C.W., Halbich S., Richter H., et al. Factor H and atypical hemolytic uremic syndrome: mutations in the C-terminus cause structural changes and defective recognition functions. J Am Soc Nephrol 2006, 17:170-177.
-
(2006)
J Am Soc Nephrol
, vol.17
, pp. 170-177
-
-
Jozsi, M.1
Heinen, S.2
Hartmann, A.3
Ostrowicz, C.W.4
Halbich, S.5
Richter, H.6
-
207
-
-
26244435599
-
Binding of complement factor H to endothelial cells is mediated by the carboxy-terminal glycosaminoglycan binding site
-
Jokiranta T.S., Cheng Z.Z., Seeberger H., Jozsi M., Heinen S., Noris M., et al. Binding of complement factor H to endothelial cells is mediated by the carboxy-terminal glycosaminoglycan binding site. Am J Pathol 2005, 167:1173-1181.
-
(2005)
Am J Pathol
, vol.167
, pp. 1173-1181
-
-
Jokiranta, T.S.1
Cheng, Z.Z.2
Seeberger, H.3
Jozsi, M.4
Heinen, S.5
Noris, M.6
-
208
-
-
0037396993
-
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome
-
Manuelian T., Hellwage J., Meri S., Caprioli J., Noris M., Heinen S., et al. Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome. J Clin Invest 2003, 111:1181-1190.
-
(2003)
J Clin Invest
, vol.111
, pp. 1181-1190
-
-
Manuelian, T.1
Hellwage, J.2
Meri, S.3
Caprioli, J.4
Noris, M.5
Heinen, S.6
-
209
-
-
2342582709
-
Functional analysis in serum from atypical hemolytic uremic syndrome patients reveals impaired protection of host cells associated with mutations in factor H
-
Sanchez-Corral P., Gonzalez-Rubio C., Rodriguez de Cordoba S, Lopez-Trascasa M. Functional analysis in serum from atypical hemolytic uremic syndrome patients reveals impaired protection of host cells associated with mutations in factor H. Mol Immunol 2004, 41:81-84.
-
(2004)
Mol Immunol
, vol.41
, pp. 81-84
-
-
Sanchez-Corral, P.1
Gonzalez-Rubio, C.2
Rodriguez de Cordoba, S.3
Lopez-Trascasa, M.4
-
210
-
-
0036908821
-
Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome
-
Sanchez-Corral P., Perez-Caballero D., Huarte O., Simckes A.M., Goicoechea E., Lopez-Trascasa M., et al. Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome. Am J Hum Genet 2002, 71:1285-1295.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1285-1295
-
-
Sanchez-Corral, P.1
Perez-Caballero, D.2
Huarte, O.3
Simckes, A.M.4
Goicoechea, E.5
Lopez-Trascasa, M.6
-
211
-
-
79959560322
-
Crystallographic determination of the disease-associated T1184R variant of complement regulator factor H
-
Morgan H.P., Jiang J., Herbert A.P., Kavanagh D., Uhrin D., Barlow P.N., et al. Crystallographic determination of the disease-associated T1184R variant of complement regulator factor H. Acta Crystallogr D Biol Crystallogr 2011, 67:593-600.
-
(2011)
Acta Crystallogr D Biol Crystallogr
, vol.67
, pp. 593-600
-
-
Morgan, H.P.1
Jiang, J.2
Herbert, A.P.3
Kavanagh, D.4
Uhrin, D.5
Barlow, P.N.6
-
212
-
-
84857828404
-
Structural and functional characterization of the product of disease-related factor H gene conversion
-
Herbert A.P., Kavanagh D., Johansson C., Morgan H.P., Blaum B.S., Hannan J.P., et al. Structural and functional characterization of the product of disease-related factor H gene conversion. Biochemistry 2012, 51:1874-1884.
-
(2012)
Biochemistry
, vol.51
, pp. 1874-1884
-
-
Herbert, A.P.1
Kavanagh, D.2
Johansson, C.3
Morgan, H.P.4
Blaum, B.S.5
Hannan, J.P.6
-
213
-
-
77951621575
-
Pulse cyclophosphamide therapy and clinical remission in atypical hemolytic uremic syndrome with anti-complement factor H autoantibodies
-
Boyer O., Balzamo E., Charbit M., Biebuyck-Gouge N., Salomon R., Dragon-Durey M.A., et al. Pulse cyclophosphamide therapy and clinical remission in atypical hemolytic uremic syndrome with anti-complement factor H autoantibodies. Am J Kidney Dis 2010, 55:923-927.
-
(2010)
Am J Kidney Dis
, vol.55
, pp. 923-927
-
-
Boyer, O.1
Balzamo, E.2
Charbit, M.3
Biebuyck-Gouge, N.4
Salomon, R.5
Dragon-Durey, M.A.6
-
214
-
-
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, 22:371-375.
-
(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
-
215
-
-
58249107188
-
Recurrent atypical hemolytic uremic syndrome associated with factor I mutation in a living related renal transplant recipient
-
Chan M.R., Thomas C.P., Torrealba J.R., Djamali A., Fernandez L.A., Nishimura C.J., et al. Recurrent atypical hemolytic uremic syndrome associated with factor I mutation in a living related renal transplant recipient. Am J Kidney Dis 2009, 53:321-326.
-
(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
-
216
-
-
84879308507
-
Eculizumab therapy in a child with hemolytic uremic syndrome and CFI mutation
-
Cayci F.S., Cakar N., Hancer V.S., Uncu N., Acar B., Gur G. Eculizumab therapy in a child with hemolytic uremic syndrome and CFI mutation. Pediatr Nephrol 2012, 27:2327-2331.
-
(2012)
Pediatr Nephrol
, vol.27
, pp. 2327-2331
-
-
Cayci, F.S.1
Cakar, N.2
Hancer, V.S.3
Uncu, N.4
Acar, B.5
Gur, G.6
-
217
-
-
38349172121
-
Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome
-
Fang C.J., Fremeaux-Bacchi V., Liszewski M.K., Pianetti G., Noris M., Goodship T.H., et al. Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome. Blood 2008, 111:624-632.
-
(2008)
Blood
, vol.111
, pp. 624-632
-
-
Fang, C.J.1
Fremeaux-Bacchi, V.2
Liszewski, M.K.3
Pianetti, G.4
Noris, M.5
Goodship, T.H.6
-
218
-
-
0242570482
-
Familial haemolytic uraemic syndrome and an MCP mutation
-
Noris M., Brioschi S., Caprioli J., Todeschini M., Bresin E., Porrati F., et al. Familial haemolytic uraemic syndrome and an MCP mutation. Lancet 2003, 362:1542-1547.
-
(2003)
Lancet
, vol.362
, pp. 1542-1547
-
-
Noris, M.1
Brioschi, S.2
Caprioli, J.3
Todeschini, M.4
Bresin, E.5
Porrati, F.6
-
219
-
-
33846611465
-
Unusual clinical severity of complement membrane cofactor protein-associated hemolytic-uremic syndrome and uniparental isodisomy
-
Fremeaux-Bacchi V., Sanlaville D., Menouer S., Blouin J., Dragon-Durey M.A., Fischbach M., et al. Unusual clinical severity of complement membrane cofactor protein-associated hemolytic-uremic syndrome and uniparental isodisomy. Am J Kidney Dis 2007, 49:323-329.
-
(2007)
Am J Kidney Dis
, vol.49
, pp. 323-329
-
-
Fremeaux-Bacchi, V.1
Sanlaville, D.2
Menouer, S.3
Blouin, J.4
Dragon-Durey, M.A.5
Fischbach, M.6
-
220
-
-
84864419719
-
Novel C3 mutation p.Lys65Gln in aHUS affects complement factor H binding
-
Volokhina E., Westra D., Xue X., Gros P., van de Kar N, van den Heuvel L. Novel C3 mutation p.Lys65Gln in aHUS affects complement factor H binding. Pediatr Nephrol 2012, 27:1519-1524.
-
(2012)
Pediatr Nephrol
, vol.27
, pp. 1519-1524
-
-
Volokhina, E.1
Westra, D.2
Xue, X.3
Gros, P.4
Van De Kar, N.5
Van Den Heuvel, L.6
-
221
-
-
84872858459
-
Peripheral gangrene in children with atypical hemolytic uremic syndrome
-
Malina M., Gulati A., Bagga A., Majid M.A., Simkova E., Schaefer F. Peripheral gangrene in children with atypical hemolytic uremic syndrome. Pediatrics 2013, 131:e331-e335.
-
(2013)
Pediatrics
, vol.131
-
-
Malina, M.1
Gulati, A.2
Bagga, A.3
Majid, M.A.4
Simkova, E.5
Schaefer, F.6
-
222
-
-
17944384021
-
Peripheral gangrene complicating hemolytic uremic syndrome in a child
-
Ozel A., Caliskan U., Gucer S. Peripheral gangrene complicating hemolytic uremic syndrome in a child. Pediatr Nephrol 2003, 18:465-467.
-
(2003)
Pediatr Nephrol
, vol.18
, pp. 465-467
-
-
Ozel, A.1
Caliskan, U.2
Gucer, S.3
-
223
-
-
0033869032
-
Peripheral gangrene complicating idiopathic and recessive hemolytic uremic syndromes
-
Kaplan B.S., Garcia C.D., Chesney R.W., Segar W.E., Giugno K., Chem R. Peripheral gangrene complicating idiopathic and recessive hemolytic uremic syndromes. Pediatr Nephrol 2000, 14:985-989.
-
(2000)
Pediatr Nephrol
, vol.14
, pp. 985-989
-
-
Kaplan, B.S.1
Garcia, C.D.2
Chesney, R.W.3
Segar, W.E.4
Giugno, K.5
Chem, R.6
-
224
-
-
77957221636
-
Non-atheromatous arterial stenoses in atypical haemolytic uraemic syndrome associated with complement dysregulation
-
Loirat C., Macher M.A., Elmaleh-Berges M., Kwon T., Deschenes G., Goodship T.H., et al. Non-atheromatous arterial stenoses in atypical haemolytic uraemic syndrome associated with complement dysregulation. Nephrol Dial Transplant 2010, 25:3421-3425.
-
(2010)
Nephrol Dial Transplant
, vol.25
, pp. 3421-3425
-
-
Loirat, C.1
Macher, M.A.2
Elmaleh-Berges, M.3
Kwon, T.4
Deschenes, G.5
Goodship, T.H.6
-
225
-
-
43649093598
-
Proximal cerebral artery stenosis in a patient with hemolytic uremic syndrome
-
Vergouwen M.D., Adriani K.S., Roos Y.B., Groothoff J.W., Majoie C.B. Proximal cerebral artery stenosis in a patient with hemolytic uremic syndrome. AJNR Am J Neuroradiol 2008, 29:e34.
-
(2008)
AJNR Am J Neuroradiol
, vol.29
-
-
Vergouwen, M.D.1
Adriani, K.S.2
Roos, Y.B.3
Groothoff, J.W.4
Majoie, C.B.5
-
226
-
-
77953008442
-
Myocardial infarction is a complication of factor H-associated atypical HUS
-
Sallee M., Daniel L., Piercecchi M.D., Jaubert D., Fremeaux-Bacchi V., Berland Y, et al. Myocardial infarction is a complication of factor H-associated atypical HUS. Nephrol Dial Transplant 2010, 25:2028-2032.
-
(2010)
Nephrol Dial Transplant
, vol.25
, pp. 2028-2032
-
-
Sallee, M.1
Daniel, L.2
Piercecchi, M.D.3
Jaubert, D.4
Fremeaux-Bacchi, V.5
Berland, Y.6
-
227
-
-
34848903255
-
Ocular involvement in hemolytic uremic syndrome due to factor H deficiency--are there therapeutic consequences?
-
Larakeb A., Leroy S., Fremeaux-Bacchi V., Montchilova M., Pelosse B., Dunand O., et al. Ocular involvement in hemolytic uremic syndrome due to factor H deficiency--are there therapeutic consequences?. Pediatr Nephrol 2007, 22:1967-1970.
-
(2007)
Pediatr Nephrol
, vol.22
, pp. 1967-1970
-
-
Larakeb, A.1
Leroy, S.2
Fremeaux-Bacchi, V.3
Montchilova, M.4
Pelosse, B.5
Dunand, O.6
|