-
1
-
-
84858668780
-
Membranoproliferative glomerulonephritis—a new look at an old entity
-
COI: 1:CAS:528:DC%2BC38XktlCqtLc%3D, PID: 22435371
-
Sethi S, Fervenza FC (2012) Membranoproliferative glomerulonephritis—a new look at an old entity. N Engl J Med 366:1119–1131
-
(2012)
N Engl J Med
, vol.366
, pp. 1119-1131
-
-
Sethi, S.1
Fervenza, F.C.2
-
2
-
-
79961214569
-
Membranoproliferative glomerulonephritis: pathogenetic heterogeneity and proposal for a new classification
-
COI: 1:CAS:528:DC%2BC3MXhtVelsrvM, PID: 21839367
-
Sethi S, Fervenza FC (2011) Membranoproliferative glomerulonephritis: pathogenetic heterogeneity and proposal for a new classification. Semin Nephrol 31:341–348
-
(2011)
Semin Nephrol
, vol.31
, pp. 341-348
-
-
Sethi, S.1
Fervenza, F.C.2
-
3
-
-
84888641200
-
C3 glomerulopathy: consensus report
-
PID: 24172683
-
Pickering MC, D'Agati VD, Nester CM, Smith RJ, Haas M, Appel GB, Alpers CE, Bajema IM, Bedrosian C, Braun M, Doyle M, Fakhouri F, Fervenza FC, Fogo AB, Fremeaux-Bacchi V, Gale DP, Goicoechea De Jorge E, Griffin G, Harris CL, Holers VM, Johnson S, Lavin PJ, Medjeral-Thomas N, Paul Morgan B, Nast CC, Noel LH, Peters DK, Rodriguez De Cordoba S, Servais A, Sethi S, Song WC, Tamburini P, Thurman JM, Zavros M, Cook HT (2013) C3 glomerulopathy: consensus report. Kidney Int 84:1079–1089
-
(2013)
Kidney Int
, vol.84
, pp. 1079-1089
-
-
Pickering, M.C.1
D'Agati, V.D.2
Nester, C.M.3
Smith, R.J.4
Haas, M.5
Appel, G.B.6
Alpers, C.E.7
Bajema, I.M.8
Bedrosian, C.9
Braun, M.10
Doyle, M.11
Fakhouri, F.12
Fervenza, F.C.13
Fogo, A.B.14
Fremeaux-Bacchi, V.15
Gale, D.P.16
Goicoechea De Jorge, E.17
Griffin, G.18
Harris, C.L.19
Holers, V.M.20
Johnson, S.21
Lavin, P.J.22
Medjeral-Thomas, N.23
Paul Morgan, B.24
Nast, C.C.25
Noel, L.H.26
Peters, D.K.27
Rodriguez De Cordoba, S.28
Servais, A.29
Sethi, S.30
Song, W.C.31
Tamburini, P.32
Thurman, J.M.33
Zavros, M.34
Cook, H.T.35
more..
-
4
-
-
84901000965
-
Membranoproliferative glomerulonephritis associated with autoimmune diseases
-
COI: 1:CAS:528:DC%2BC28Xhs1ykt78%3D, PID: 24500888
-
Zand L, Fervenza FC, Nasr SH, Sethi S (2014) Membranoproliferative glomerulonephritis associated with autoimmune diseases. J Nephrol 27:165–171
-
(2014)
J Nephrol
, vol.27
, pp. 165-171
-
-
Zand, L.1
Fervenza, F.C.2
Nasr, S.H.3
Sethi, S.4
-
5
-
-
84883236791
-
C3 glomerulonephritis associated with monoclonal gammopathy: a case series
-
COI: 1:CAS:528:DC%2BC3sXntValurk%3D, PID: 23623956
-
Zand L, Kattah A, Fervenza FC, Smith RJH, Nasr SH, Zhang Y, Vrana JA, Leung N, Cornell LD, Sethi S (2013) C3 glomerulonephritis associated with monoclonal gammopathy: a case series. Am J Kidney Dis 62:506–514
-
(2013)
Am J Kidney Dis
, vol.62
, pp. 506-514
-
-
Zand, L.1
Kattah, A.2
Fervenza, F.C.3
Smith, R.J.H.4
Nasr, S.H.5
Zhang, Y.6
Vrana, J.A.7
Leung, N.8
Cornell, L.D.9
Sethi, S.10
-
6
-
-
0028911904
-
Secondary membranoproliferative glomerulonephritis
-
COI: 1:STN:280:DyaK2M3jvF2rtA%3D%3D, PID: 7723253
-
Rennke HG (1995) Secondary membranoproliferative glomerulonephritis. Kidney Int 47:643–656
-
(1995)
Kidney Int
, vol.47
, pp. 643-656
-
-
Rennke, H.G.1
-
7
-
-
64949093413
-
Glomeruli of dense deposit disease contain components of the alternative and terminal complement pathway
-
COI: 1:CAS:528:DC%2BD1MXks1Sjtro%3D, PID: 19177158
-
Sethi S, Gamez JD, Vrana JA, Theis JD, Bergen HR 3rd, Zipfel PF, Dogan A, Smith RJH (2009) Glomeruli of dense deposit disease contain components of the alternative and terminal complement pathway. Kidney Int 75:952–960
-
(2009)
Kidney Int
, vol.75
, pp. 952-960
-
-
Sethi, S.1
Gamez, J.D.2
Vrana, J.A.3
Theis, J.D.4
Bergen, H.R.5
Zipfel, P.F.6
Dogan, A.7
Smith, R.J.H.8
-
8
-
-
84878872967
-
Mass spectrometry based proteomics in the diagnosis of kidney disease
-
COI: 1:CAS:528:DC%2BC3sXptVOlsbs%3D, PID: 23470817
-
Sethi S, Vrana JA, Theis JD, Dogan A (2013) Mass spectrometry based proteomics in the diagnosis of kidney disease. Curr Opin Nephrol Hypertens 22:273–280
-
(2013)
Curr Opin Nephrol Hypertens
, vol.22
, pp. 273-280
-
-
Sethi, S.1
Vrana, J.A.2
Theis, J.D.3
Dogan, A.4
-
9
-
-
84862610440
-
Association of a novel complement factor H mutation with severe crescentic and necrotizing glomerulonephritis
-
COI: 1:CAS:528:DC%2BC38XmtFGhu70%3D, PID: 22542290
-
Fervenza FC, Smith RJH, Sethi S (2012) Association of a novel complement factor H mutation with severe crescentic and necrotizing glomerulonephritis. Am J Kidney Dis 60:126–132
-
(2012)
Am J Kidney Dis
, vol.60
, pp. 126-132
-
-
Fervenza, F.C.1
Smith, R.J.H.2
Sethi, S.3
-
10
-
-
84927175264
-
Histopathology of MPGN and C3 glomerulopathies
-
COI: 1:CAS:528:DC%2BC2cXitVemsr%2FN, PID: 25447133
-
Cook HT, Pickering MC (2015) Histopathology of MPGN and C3 glomerulopathies. Nat Rev Nephrol 11:14–22
-
(2015)
Nat Rev Nephrol
, vol.11
, pp. 14-22
-
-
Cook, H.T.1
Pickering, M.C.2
-
11
-
-
34247231531
-
Dense deposit disease: new insights
-
PID: 17420663
-
Walker PD (2007) Dense deposit disease: new insights. Curr Opin Nephrol Hypertens 16:204–212
-
(2007)
Curr Opin Nephrol Hypertens
, vol.16
, pp. 204-212
-
-
Walker, P.D.1
-
12
-
-
84873405017
-
Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement
-
COI: 1:CAS:528:DC%2BC3sXhvFGhsLs%3D, PID: 23235567
-
Sethi S, Fervenza FC, Zhang Y, Zand L, Meyer NC, Borsa N, Nasr SH, Smith RJH (2013) Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement. Kidney Int 83:293–299
-
(2013)
Kidney Int
, vol.83
, pp. 293-299
-
-
Sethi, S.1
Fervenza, F.C.2
Zhang, Y.3
Zand, L.4
Meyer, N.C.5
Borsa, N.6
Nasr, S.H.7
Smith, R.J.H.8
-
13
-
-
84895905249
-
Toward a working definition of C3 glomerulopathy by immunofluorescence
-
COI: 1:CAS:528:DC%2BC3sXhsFeqtLbN, PID: 24067430
-
Hou J, Markowitz GS, Bomback AS, Appel GB, Herlitz LC, Barry Stokes M, D'Agati VD (2014) Toward a working definition of C3 glomerulopathy by immunofluorescence. Kidney Int 85:450–456
-
(2014)
Kidney Int
, vol.85
, pp. 450-456
-
-
Hou, J.1
Markowitz, G.S.2
Bomback, A.S.3
Appel, G.B.4
Herlitz, L.C.5
Barry Stokes, M.6
D'Agati, V.D.7
-
14
-
-
84946046875
-
C4d as a diagnostic tool in proliferative GN
-
COI: 1:CAS:528:DC%2BC28Xls1yrsL0%3D, PID: 25991041
-
Sethi S, Nasr SH, De Vriese AS, Fervenza FC (2015) C4d as a diagnostic tool in proliferative GN. J Am Soc Nephrol 26:2852–2859
-
(2015)
J Am Soc Nephrol
, vol.26
, pp. 2852-2859
-
-
Sethi, S.1
Nasr, S.H.2
De Vriese, A.S.3
Fervenza, F.C.4
-
15
-
-
0021714061
-
Mycoplasmal pneumonia associated with mesangiocapillary glomerulonephritis type II (dense deposit disease)
-
Bonsdorff M, Ponka A, Tornroth T (1984) Mycoplasmal pneumonia associated with mesangiocapillary glomerulonephritis type II (dense deposit disease). Acta Med Scand 216:427–429
-
(1984)
Acta Med Scand
, vol.216
, pp. 427-429
-
-
Bonsdorff, M.1
Ponka, A.2
Tornroth, T.3
-
16
-
-
64049119966
-
Dense deposit disease: clinicopathologic study of 32 pediatric and adult patients
-
PID: 18971369
-
Nasr SH, Valeri AM, Appel GB, Sherwinter J, Stokes MB, Said SM, Markowitz GS, D'Agati VD (2009) Dense deposit disease: clinicopathologic study of 32 pediatric and adult patients. Clin J Am Soc Nephrol 4:22–32
-
(2009)
Clin J Am Soc Nephrol
, vol.4
, pp. 22-32
-
-
Nasr, S.H.1
Valeri, A.M.2
Appel, G.B.3
Sherwinter, J.4
Stokes, M.B.5
Said, S.M.6
Markowitz, G.S.7
D'Agati, V.D.8
-
18
-
-
84886309053
-
Overview of complement activation and regulation
-
COI: 1:CAS:528:DC%2BC3sXhs1yitbjF, PID: 24161035
-
Noris M, Remuzzi G (2013) Overview of complement activation and regulation. Semin Nephrol 33:479–492
-
(2013)
Semin Nephrol
, vol.33
, pp. 479-492
-
-
Noris, M.1
Remuzzi, G.2
-
19
-
-
84902134692
-
The spectrum of complement-mediated thrombotic microangiopathies—pathogenetic insights identifying novel treatment approaches
-
PID: 24911558
-
Riedl M, Fakhouri F, Lequintrec M, Noone D, Jungraithmayr TC, Fremeaux-Bacchi V, Licht C (2014) The spectrum of complement-mediated thrombotic microangiopathies—pathogenetic insights identifying novel treatment approaches. Semin Thromb Hemost 40:444–464
-
(2014)
Semin Thromb Hemost
, vol.40
, pp. 444-464
-
-
Riedl, M.1
Fakhouri, F.2
Lequintrec, M.3
Noone, D.4
Jungraithmayr, T.C.5
Fremeaux-Bacchi, V.6
Licht, C.7
-
20
-
-
84865611225
-
Antibody mediated rejection associated with complement factor H-related protein 3/1 deficiency successfully treated with Eculizumab
-
COI: 1:CAS:528:DC%2BC38XhsVyrurvE, PID: 22681773
-
Noone D, Al-Matrafi J, Tinckam K, Zipfel PF, Herzenberg AM, Thorner PS, Pluthero FG, Kahr WHA, Filler G, Hebert D, Harvey E, Licht C (2012) Antibody mediated rejection associated with complement factor H-related protein 3/1 deficiency successfully treated with Eculizumab. Am J Transplant 12:2546–2553
-
(2012)
Am J Transplant
, vol.12
, pp. 2546-2553
-
-
Noone, D.1
Al-Matrafi, J.2
Tinckam, K.3
Zipfel, P.F.4
Herzenberg, A.M.5
Thorner, P.S.6
Pluthero, F.G.7
Kahr, W.H.A.8
Filler, G.9
Hebert, D.10
Harvey, E.11
Licht, C.12
-
21
-
-
84864554927
-
Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies
-
COI: 1:CAS:528:DC%2BC38XhtFCku73K, PID: 22456601
-
Servais A, Noel L-H, Roumenina LT, Le Quintrec M, Ngo S, Dragon-Durey M-A, Macher M-A, Zuber J, Karras A, Provot F, Moulin B, Grunfeld J-P, Niaudet P, Lesavre P, Fremeaux-Bacchi V (2012) Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies. Kidney Int 82:454–464
-
(2012)
Kidney Int
, vol.82
, pp. 454-464
-
-
Servais, A.1
Noel, L.-H.2
Roumenina, L.T.3
Le Quintrec, M.4
Ngo, S.5
Dragon-Durey, M.-A.6
Macher, M.-A.7
Zuber, J.8
Karras, A.9
Provot, F.10
Moulin, B.11
Grunfeld, J.-P.12
Niaudet, P.13
Lesavre, P.14
Fremeaux-Bacchi, V.15
-
22
-
-
70349441306
-
Factor H-related protein 1 (CFHR-1) inhibits complement C5 convertase activity and terminal complex formation
-
COI: 1:CAS:528:DC%2BD1MXht1WktrzL, PID: 19528535
-
Heinen S, Hartmann A, Lauer N, Wiehl U, Dahse HM, Schirmer S, Gropp K, Enghardt T, Wallich R, Halbich S, Mihlan M, Schlotzer-Schrehardt U, Zipfel PF, Skerka C (2009) Factor H-related protein 1 (CFHR-1) inhibits complement C5 convertase activity and terminal complex formation. Blood 114:2439–2447
-
(2009)
Blood
, vol.114
, pp. 2439-2447
-
-
Heinen, S.1
Hartmann, A.2
Lauer, N.3
Wiehl, U.4
Dahse, H.M.5
Schirmer, S.6
Gropp, K.7
Enghardt, T.8
Wallich, R.9
Halbich, S.10
Mihlan, M.11
Schlotzer-Schrehardt, U.12
Zipfel, P.F.13
Skerka, C.14
-
23
-
-
84875239064
-
Dimerization of complement factor H-related proteins modulates complement activation in vivo
-
COI: 1:CAS:528:DC%2BC3sXms12msr8%3D, PID: 23487775
-
Goicoechea de Jorge E, Caesar JJ, Malik TH, Patel M, Colledge M, Johnson S, Hakobyan S, Morgan BP, Harris CL, Pickering MC, Lea SM (2013) Dimerization of complement factor H-related proteins modulates complement activation in vivo. Proc Natl Acad Sci USA 110:4685–4690
-
(2013)
Proc Natl Acad Sci USA
, vol.110
, pp. 4685-4690
-
-
Goicoechea de Jorge, E.1
Caesar, J.J.2
Malik, T.H.3
Patel, M.4
Colledge, M.5
Johnson, S.6
Hakobyan, S.7
Morgan, B.P.8
Harris, C.L.9
Pickering, M.C.10
Lea, S.M.11
-
24
-
-
84902291006
-
C3 glomerulopathy: the genetic and clinical findings in dense deposit disease and c3 glomerulonephritis
-
COI: 1:CAS:528:DC%2BC2cXht1ansLjL, PID: 24799308
-
Xiao X, Pickering MC, Smith RJ (2014) C3 glomerulopathy: the genetic and clinical findings in dense deposit disease and c3 glomerulonephritis. Semin Thromb Hemost 40:465–471
-
(2014)
Semin Thromb Hemost
, vol.40
, pp. 465-471
-
-
Xiao, X.1
Pickering, M.C.2
Smith, R.J.3
-
25
-
-
0031885010
-
In situ complement activation in porcine membranoproliferative glomerulonephritis type II
-
COI: 1:CAS:528:DyaK1cXhtVGhs7k%3D, PID: 9461093
-
Jansen JH, Hogasen K, Harboe M, Hovig T (1998) In situ complement activation in porcine membranoproliferative glomerulonephritis type II. Kidney Int 53:331–349
-
(1998)
Kidney Int
, vol.53
, pp. 331-349
-
-
Jansen, J.H.1
Hogasen, K.2
Harboe, M.3
Hovig, T.4
-
26
-
-
0036699540
-
Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H
-
COI: 1:CAS:528:DC%2BD38Xls1Orsr0%3D, PID: 12091909
-
Pickering MC, Cook HT, Warren J, Bygrave AE, Moss J, Walport MJ, Botto M (2002) Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H. Nat Genet 31:424–428
-
(2002)
Nat Genet
, vol.31
, pp. 424-428
-
-
Pickering, M.C.1
Cook, H.T.2
Warren, J.3
Bygrave, A.E.4
Moss, J.5
Walport, M.J.6
Botto, M.7
-
27
-
-
38849102544
-
Factor I is required for the development of membranoproliferative glomerulonephritis in factor H-deficient mice
-
COI: 1:CAS:528:DC%2BD1cXhsFOmsrk%3D, PID: 18202746
-
Rose KL, Paixao-Cavalcante D, Fish J, Manderson AP, Malik TH, Bygrave AE, Lin T, Sacks SH, Walport MJ, Cook HT, Botto M, Pickering MC (2008) Factor I is required for the development of membranoproliferative glomerulonephritis in factor H-deficient mice. J Clin Invest 118:608–618
-
(2008)
J Clin Invest
, vol.118
, pp. 608-618
-
-
Rose, K.L.1
Paixao-Cavalcante, D.2
Fish, J.3
Manderson, A.P.4
Malik, T.H.5
Bygrave, A.E.6
Lin, T.7
Sacks, S.H.8
Walport, M.J.9
Cook, H.T.10
Botto, M.11
Pickering, M.C.12
-
28
-
-
33745441327
-
Prevention of C5 activation ameliorates spontaneous and experimental glomerulonephritis in factor H-deficient mice
-
COI: 1:CAS:528:DC%2BD28XmsFOqs7o%3D, PID: 16769899
-
Pickering MC, Warren J, Rose KL, Carlucci F, Wang Y, Walport MJ, Cook HT, Botto M (2006) Prevention of C5 activation ameliorates spontaneous and experimental glomerulonephritis in factor H-deficient mice. Proc Natl Acad Sci USA 103:9649–9654
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 9649-9654
-
-
Pickering, M.C.1
Warren, J.2
Rose, K.L.3
Carlucci, F.4
Wang, Y.5
Walport, M.J.6
Cook, H.T.7
Botto, M.8
-
29
-
-
78651410434
-
The development of atypical hemolytic uremic syndrome depends on complement C5
-
PID: 21148255
-
de Jorge EG, Macor P, Paixao-Cavalcante D, Rose KL, Tedesco F, Cook HT, Botto M, Pickering MC (2011) The development of atypical hemolytic uremic syndrome depends on complement C5. J Am Soc Nephrol 22:137–145
-
(2011)
J Am Soc Nephrol
, vol.22
, pp. 137-145
-
-
de Jorge, E.G.1
Macor, P.2
Paixao-Cavalcante, D.3
Rose, K.L.4
Tedesco, F.5
Cook, H.T.6
Botto, M.7
Pickering, M.C.8
-
30
-
-
34250329129
-
Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains
-
COI: 1:CAS:528:DC%2BD2sXms1aktro%3D, PID: 17517971
-
Pickering MC, de Jorge EG, Martinez-Barricarte R, Recalde S, Garcia-Layana A, Rose KL, Moss J, Walport MJ, Cook HT, de Cordoba SR, Botto M (2007) Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains. J Exp Med 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
Moss, J.7
Walport, M.J.8
Cook, H.T.9
de Cordoba, S.R.10
Botto, M.11
-
31
-
-
84868585648
-
Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation
-
COI: 1:CAS:528:DC%2BC38Xhs1artLvF, PID: 22854646
-
Paixao-Cavalcante D, Lopez-Trascasa M, Skattum L, Giclas PC, Goodship TH, de Cordoba SR, Truedsson L, Morgan BP, Harris CL (2012) Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation. Kidney Int 82:1084–1092
-
(2012)
Kidney Int
, vol.82
, pp. 1084-1092
-
-
Paixao-Cavalcante, D.1
Lopez-Trascasa, M.2
Skattum, L.3
Giclas, P.C.4
Goodship, T.H.5
de Cordoba, S.R.6
Truedsson, L.7
Morgan, B.P.8
Harris, C.L.9
-
32
-
-
33745697887
-
Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II)
-
COI: 1:CAS:528:DC%2BD28XmtlGlsbk%3D, PID: 16612335
-
Licht C, Heinen S, Jozsi M, Loschmann I, Saunders RE, Perkins SJ, Waldherr R, Skerka C, Kirschfink M, Hoppe B, Zipfel PF (2006) Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II). Kidney Int 70:42–50
-
(2006)
Kidney Int
, vol.70
, pp. 42-50
-
-
Licht, C.1
Heinen, S.2
Jozsi, M.3
Loschmann, I.4
Saunders, R.E.5
Perkins, S.J.6
Waldherr, R.7
Skerka, C.8
Kirschfink, M.9
Hoppe, B.10
Zipfel, P.F.11
-
33
-
-
77957827919
-
Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation
-
COI: 1:CAS:528:DC%2BC3cXht1Ggtb7J, PID: 20852386
-
Martinez-Barricarte R, Heurich M, Valdes-Canedo F, Vazquez-Martul E, Torreira E, Montes T, Tortajada A, Pinto S, Lopez-Trascasa M, Morgan BP, Llorca O, Harris CL, De Cordoba SR (2010) Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation. J Clin Invest 120:3702–3712
-
(2010)
J Clin Invest
, vol.120
, pp. 3702-3712
-
-
Martinez-Barricarte, R.1
Heurich, M.2
Valdes-Canedo, F.3
Vazquez-Martul, E.4
Torreira, E.5
Montes, T.6
Tortajada, A.7
Pinto, S.8
Lopez-Trascasa, M.9
Morgan, B.P.10
Llorca, O.11
Harris, C.L.12
De Cordoba, S.R.13
-
34
-
-
84902254536
-
Treatment of C3 glomerulopathy with complement blockers
-
COI: 1:CAS:528:DC%2BC2cXht1ansLjE, PID: 24799307
-
Vivarelli M, Emma F (2014) Treatment of C3 glomerulopathy with complement blockers. Semin Thromb Hemost 40:472–477
-
(2014)
Semin Thromb Hemost
, vol.40
, pp. 472-477
-
-
Vivarelli, M.1
Emma, F.2
-
35
-
-
0023710433
-
On the origin and control of C3NeF
-
COI: 1:STN:280:DyaK387jsFGmuw%3D%3D, PID: 2979821
-
Spitzer RE, Stitzel AE (1988) On the origin and control of C3NeF. In Vivo 2:79–81
-
(1988)
In Vivo
, vol.2
, pp. 79-81
-
-
Spitzer, R.E.1
Stitzel, A.E.2
-
36
-
-
0034943625
-
Complement analysis in children with idiopathic membranoproliferative glomerulonephritis: a long-term follow-up
-
COI: 1:STN:280:DC%2BD3MvjvFSmtQ%3D%3D, PID: 11473682
-
Schwertz R, Rother U, Anders D, Gretz N, Scharer K, Kirschfink M (2001) Complement analysis in children with idiopathic membranoproliferative glomerulonephritis: a long-term follow-up. Pediatr Allergy Immunol 12:166–172
-
(2001)
Pediatr Allergy Immunol
, vol.12
, pp. 166-172
-
-
Schwertz, R.1
Rother, U.2
Anders, D.3
Gretz, N.4
Scharer, K.5
Kirschfink, M.6
-
37
-
-
84890444436
-
C3 nephritic factor associated with C3 glomerulopathy in children
-
PID: 24068526
-
Nicolas C, Vuiblet V, Baudouin V, Macher M-A, Vrillon I, Biebuyck-Gouge N, Dehennault M, Gie S, Morin D, Nivet H, Nobili F, Ulinski T, Ranchin B, Marinozzi MC, Ngo S, Fremeaux-Bacchi V, Pietrement C (2014) C3 nephritic factor associated with C3 glomerulopathy in children. Pediatr Nephrol 29:85–94
-
(2014)
Pediatr Nephrol
, vol.29
, pp. 85-94
-
-
Nicolas, C.1
Vuiblet, V.2
Baudouin, V.3
Macher, M.-A.4
Vrillon, I.5
Biebuyck-Gouge, N.6
Dehennault, M.7
Gie, S.8
Morin, D.9
Nivet, H.10
Nobili, F.11
Ulinski, T.12
Ranchin, B.13
Marinozzi, M.C.14
Ngo, S.15
Fremeaux-Bacchi, V.16
Pietrement, C.17
-
38
-
-
0028245945
-
Selective disappearance of C3NeF IgG autoantibody in the plasma of a patient with membranoproliferative glomerulonephritis following renal transplantation
-
COI: 1:STN:280:DyaK2M%2FmtVWltg%3D%3D, PID: 7970124
-
Fremeaux-Bacchi V, Weiss L, Brun P, Kazatchkine MD (1994) Selective disappearance of C3NeF IgG autoantibody in the plasma of a patient with membranoproliferative glomerulonephritis following renal transplantation. Nephrol Dial Transplant 9:811–814
-
(1994)
Nephrol Dial Transplant
, vol.9
, pp. 811-814
-
-
Fremeaux-Bacchi, V.1
Weiss, L.2
Brun, P.3
Kazatchkine, M.D.4
-
39
-
-
0022000709
-
A circulating inhibitor of fluid-phase amplification. C3 convertase formation in systemic lupus erythematosus
-
COI: 1:CAS:528:DyaL2MXksFanurk%3D, PID: 3159752
-
Waldo FB, Forristal J, Beischel L, West CD (1985) A circulating inhibitor of fluid-phase amplification. C3 convertase formation in systemic lupus erythematosus. J Clin Invest 75:1786–1795
-
(1985)
J Clin Invest
, vol.75
, pp. 1786-1795
-
-
Waldo, F.B.1
Forristal, J.2
Beischel, L.3
West, C.D.4
-
40
-
-
0017089166
-
Activation of the alternative complement pathway in systemic lupus erythematosus
-
COI: 1:STN:280:DyaE2s%2FmslGjsA%3D%3D, PID: 826360
-
Wilson MR, Arroyave CM, Nakamura RM, Vaughan JH, Tan EM (1976) Activation of the alternative complement pathway in systemic lupus erythematosus. Clin Exp Immunol 26:11–20
-
(1976)
Clin Exp Immunol
, vol.26
, pp. 11-20
-
-
Wilson, M.R.1
Arroyave, C.M.2
Nakamura, R.M.3
Vaughan, J.H.4
Tan, E.M.5
-
41
-
-
84891649590
-
Meningococcal disease and the complement system
-
PID: 24104403
-
Lewis LA, Ram S (2014) Meningococcal disease and the complement system. Virulence 5:98–126
-
(2014)
Virulence
, vol.5
, pp. 98-126
-
-
Lewis, L.A.1
Ram, S.2
-
42
-
-
79955028622
-
Membranoproliferative glomerulonephritis with C3NeF and genetic complement dysregulation
-
PID: 21188423
-
Leroy V, Fremeaux-Bacchi V, Peuchmaur M, Baudouin V, Deschenes G, Macher M-A, Loirat C (2011) Membranoproliferative glomerulonephritis with C3NeF and genetic complement dysregulation. Pediatr Nephrol 26:419–424
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 419-424
-
-
Leroy, V.1
Fremeaux-Bacchi, V.2
Peuchmaur, M.3
Baudouin, V.4
Deschenes, G.5
Macher, M.-A.6
Loirat, C.7
-
43
-
-
84855161508
-
Combined C3b and factor B autoantibodies and MPGN type II
-
COI: 1:CAS:528:DC%2BC3MXhs1OgsbbL, PID: 22168663
-
Chen Q, Muller D, Rudolph B, Hartmann A, Kuwertz-Broking E, Wu K, Kirschfink M, Skerka C, Zipfel PF (2011) Combined C3b and factor B autoantibodies and MPGN type II. N Engl J Med 365:2340–2342
-
(2011)
N Engl J Med
, vol.365
, pp. 2340-2342
-
-
Chen, Q.1
Muller, D.2
Rudolph, B.3
Hartmann, A.4
Kuwertz-Broking, E.5
Wu, K.6
Kirschfink, M.7
Skerka, C.8
Zipfel, P.F.9
-
44
-
-
77950628002
-
Anti-factor B autoantibody in dense deposit disease
-
COI: 1:CAS:528:DC%2BC3cXkt1Khu70%3D, PID: 20193965
-
Strobel S, Zimmering M, Papp K, Prechl J, Jozsi M (2010) Anti-factor B autoantibody in dense deposit disease. Mol Immunol 47:1476–1483
-
(2010)
Mol Immunol
, vol.47
, pp. 1476-1483
-
-
Strobel, S.1
Zimmering, M.2
Papp, K.3
Prechl, J.4
Jozsi, M.5
-
45
-
-
84875029270
-
Complement factor H-related protein 1 deficiency and factor H antibodies in pediatric patients with atypical hemolytic uremic syndrome
-
COI: 1:CAS:528:DC%2BC3sXltVejsbw%3D, PID: 23243267
-
Hofer J, Janecke AR, Zimmerhackl LB, Riedl M, Rosales A, Giner T, Cortina G, Haindl CJ, Petzelberger B, Pawlik M, Jeller V, Vester U, Gadner B, van Husen M, Moritz ML, Wurzner R, Jungraithmayr T (2013) Complement factor H-related protein 1 deficiency and factor H antibodies in pediatric patients with atypical hemolytic uremic syndrome. Clin J Am Soc Nephrol 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
Cortina, G.7
Haindl, C.J.8
Petzelberger, B.9
Pawlik, M.10
Jeller, V.11
Vester, U.12
Gadner, B.13
van Husen, M.14
Moritz, M.L.15
Wurzner, R.16
Jungraithmayr, T.17
-
46
-
-
0032875669
-
Nephritogenic lambda light chain dimer: a unique human miniautoantibody against complement factor H
-
COI: 1:CAS:528:DyaK1MXmsleltb8%3D, PID: 10510403
-
Jokiranta TS, Solomon A, Pangburn MK, Zipfel PF, Meri S (1999) Nephritogenic lambda light chain dimer: a unique human miniautoantibody against complement factor H. J Immunol 163:4590–4596
-
(1999)
J Immunol
, vol.163
, pp. 4590-4596
-
-
Jokiranta, T.S.1
Solomon, A.2
Pangburn, M.K.3
Zipfel, P.F.4
Meri, S.5
-
47
-
-
84894213015
-
C4 dense-deposit disease
-
COI: 1:CAS:528:DC%2BC2cXjt1aks7o%3D, PID: 24552345
-
Sethi S, Sullivan A, Smith RJ (2014) C4 dense-deposit disease. N Engl J Med 370:784–786
-
(2014)
N Engl J Med
, vol.370
, pp. 784-786
-
-
Sethi, S.1
Sullivan, A.2
Smith, R.J.3
-
48
-
-
0028290534
-
Occurrence of C3 nephritic factor and C4 nephritic factor in membranoproliferative glomerulonephritis (MPGN)
-
COI: 1:CAS:528:DyaK2cXhvV2mtbs%3D, PID: 8306508
-
Ohi H, Yasugi T (1994) Occurrence of C3 nephritic factor and C4 nephritic factor in membranoproliferative glomerulonephritis (MPGN). Clin Exp Immunol 95:316–321
-
(1994)
Clin Exp Immunol
, vol.95
, pp. 316-321
-
-
Ohi, H.1
Yasugi, T.2
-
49
-
-
67349180237
-
C3 deposition glomerulopathy due to a functional factor H defect
-
PID: 18633337
-
Habbig S, Mihatsch MJ, Heinen S, Beck B, Emmel M, Skerka C, Kirschfink M, Hoppe B, Zipfel PF, Licht C (2009) C3 deposition glomerulopathy due to a functional factor H defect. Kidney Int 75:1230–1234
-
(2009)
Kidney Int
, vol.75
, pp. 1230-1234
-
-
Habbig, S.1
Mihatsch, M.J.2
Heinen, S.3
Beck, B.4
Emmel, M.5
Skerka, C.6
Kirschfink, M.7
Hoppe, B.8
Zipfel, P.F.9
Licht, C.10
-
50
-
-
0022904646
-
H deficiency in two brothers with atypical dense intramembranous deposit disease
-
COI: 1:STN:280:DyaL2s7kt1GhtA%3D%3D, PID: 2950269
-
Levy M, Halbwachs-Mecarelli L, Gubler MC (1986) H deficiency in two brothers with atypical dense intramembranous deposit disease. Kidney Int 30:949–956
-
(1986)
Kidney Int
, vol.30
, pp. 949-956
-
-
Levy, M.1
Halbwachs-Mecarelli, L.2
Gubler, M.C.3
-
51
-
-
0030823285
-
Human factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolism
-
COI: 1:CAS:528:DyaK2sXms1ehsb8%3D, PID: 9312129
-
Ault BH, Schmidt BZ, Fowler NL, Kashtan CE, Ahmed AE, Vogt BA, Colten HR (1997) Human factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolism. J Biol Chem 272:25168–25175
-
(1997)
J Biol Chem
, vol.272
, pp. 25168-25175
-
-
Ault, B.H.1
Schmidt, B.Z.2
Fowler, N.L.3
Kashtan, C.E.4
Ahmed, A.E.5
Vogt, B.A.6
Colten, H.R.7
-
52
-
-
1542318912
-
Heterozygous and homozygous factor H deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases
-
COI: 1:CAS:528:DC%2BD2cXhtlShu7w%3D, PID: 14978182
-
Dragon-Durey MA, Fremeaux-Bacchi V, Loirat C, Blouin J, Niaudet P, Deschenes G, Coppo P, Fridman WH, Weiss L (2004) 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 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
Coppo, P.7
Fridman, W.H.8
Weiss, L.9
-
53
-
-
0028809266
-
Inherited factor H deficiency and collagen type III glomerulopathy
-
COI: 1:STN:280:DyaK2M3mtVOjsQ%3D%3D, PID: 7742208
-
Vogt BA, Wyatt RJ, Burke BA, Simonton SC, Kashtan CE (1995) Inherited factor H deficiency and collagen type III glomerulopathy. Pediatr Nephrol 9:11–15
-
(1995)
Pediatr Nephrol
, vol.9
, pp. 11-15
-
-
Vogt, B.A.1
Wyatt, R.J.2
Burke, B.A.3
Simonton, S.C.4
Kashtan, C.E.5
-
54
-
-
84929583971
-
Familial C3 glomerulonephritis associated with mutations in the gene for complement factor B
-
Imamura H, Konomoto T, Tanaka E, Hisano S, Yoshida Y, Fujimura Y, Miyata T, Nunoi H (2015) Familial C3 glomerulonephritis associated with mutations in the gene for complement factor B. Nephrol Dial Transplant 30(5):862–864
-
(2015)
Nephrol Dial Transplant
, vol.30
, Issue.5
, pp. 862-864
-
-
Imamura, H.1
Konomoto, T.2
Tanaka, E.3
Hisano, S.4
Yoshida, Y.5
Fujimura, Y.6
Miyata, T.7
Nunoi, H.8
-
55
-
-
77956394517
-
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis
-
COI: 1:CAS:528:DC%2BC3cXhtFWqu7jE, PID: 20800271
-
Gale DP, de Jorge EG, Cook HT, Martinez-Barricarte R, Hadjisavvas A, McLean AG, Pusey CD, Pierides A, Kyriacou K, Athanasiou Y, Voskarides K, Deltas C, Palmer A, Fremeaux-Bacchi V, de Cordoba SR, Maxwell PH, Pickering MC (2010) Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis. Lancet 376:794–801
-
(2010)
Lancet
, vol.376
, pp. 794-801
-
-
Gale, D.P.1
de Jorge, E.G.2
Cook, H.T.3
Martinez-Barricarte, R.4
Hadjisavvas, A.5
McLean, A.G.6
Pusey, C.D.7
Pierides, A.8
Kyriacou, K.9
Athanasiou, Y.10
Voskarides, K.11
Deltas, C.12
Palmer, A.13
Fremeaux-Bacchi, V.14
de Cordoba, S.R.15
Maxwell, P.H.16
Pickering, M.C.17
-
56
-
-
84892930196
-
Complement factor H-related hybrid protein deregulates complement in dense deposit disease
-
COI: 1:CAS:528:DC%2BC2cXntFehsA%3D%3D, PID: 24334459
-
Chen Q, Wiesener M, Eberhardt HU, Hartmann A, Uzonyi B, Kirschfink M, Amann K, Buettner M, Goodship T, Hugo C, Skerka C, Zipfel PF (2014) Complement factor H-related hybrid protein deregulates complement in dense deposit disease. J Clin Invest 124:145–155
-
(2014)
J Clin Invest
, vol.124
, pp. 145-155
-
-
Chen, Q.1
Wiesener, M.2
Eberhardt, H.U.3
Hartmann, A.4
Uzonyi, B.5
Kirschfink, M.6
Amann, K.7
Buettner, M.8
Goodship, T.9
Hugo, C.10
Skerka, C.11
Zipfel, P.F.12
-
57
-
-
84863511490
-
A hybrid CFHR3-1 gene causes familial C3 glomerulopathy
-
COI: 1:CAS:528:DC%2BC38XhtFOks7rJ, PID: 22626820
-
Malik TH, Lavin PJ, De Jorge EG, Vernon KA, Rose KL, Patel MP, De Leeuw M, Neary JJ, Conlon PJ, Winn MP, Pickering MC (2012) A hybrid CFHR3-1 gene causes familial C3 glomerulopathy. J Am Soc Nephrol 23:1155–1160
-
(2012)
J Am Soc Nephrol
, vol.23
, pp. 1155-1160
-
-
Malik, T.H.1
Lavin, P.J.2
De Jorge, E.G.3
Vernon, K.A.4
Rose, K.L.5
Patel, M.P.6
De Leeuw, M.7
Neary, J.J.8
Conlon, P.J.9
Winn, M.P.10
Pickering, M.C.11
-
58
-
-
84878548121
-
C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulation
-
COI: 1:CAS:528:DC%2BC3sXpsFWksbY%3D, PID: 23728178
-
Tortajada A, Yebenes H, Abarrategui-Garrido C, Anter J, Garcia-Fernandez JM, Martinez-Barricarte R, Alba-Dominguez M, Malik TH, Bedoya R, Cabrera Perez R, Lopez Trascasa M, Pickering MC, Harris CL, Sanchez-Corral P, Llorca O, Rodriguez de Cordoba S (2013) C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulation. J Clin Invest 123:2434–2446
-
(2013)
J Clin Invest
, vol.123
, pp. 2434-2446
-
-
Tortajada, A.1
Yebenes, H.2
Abarrategui-Garrido, C.3
Anter, J.4
Garcia-Fernandez, J.M.5
Martinez-Barricarte, R.6
Alba-Dominguez, M.7
Malik, T.H.8
Bedoya, R.9
Cabrera Perez, R.10
Lopez Trascasa, M.11
Pickering, M.C.12
Harris, C.L.13
Sanchez-Corral, P.14
Llorca, O.15
Rodriguez de Cordoba, S.16
-
59
-
-
33745716919
-
Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)
-
COI: 1:CAS:528:DC%2BD28XotFarur4%3D, PID: 16299065
-
Abrera-Abeleda MA, Nishimura C, Smith JLH, Sethi S, McRae JL, Murphy BF, Silvestri G, Skerka C, Jozsi M, Zipfel PF, Hageman GS, Smith RJH (2006) Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease). J Med Genet 43:582–589
-
(2006)
J Med Genet
, vol.43
, pp. 582-589
-
-
Abrera-Abeleda, M.A.1
Nishimura, C.2
Smith, J.L.H.3
Sethi, S.4
McRae, J.L.5
Murphy, B.F.6
Silvestri, G.7
Skerka, C.8
Jozsi, M.9
Zipfel, P.F.10
Hageman, G.S.11
Smith, R.J.H.12
-
60
-
-
21044453724
-
A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration
-
COI: 1:CAS:528:DC%2BD2MXks12ns7g%3D, PID: 15870199
-
Hageman GS, Anderson DH, Johnson LV, Hancox LS, Taiber AJ, Hardisty LI, Hageman JL, Stockman HA, Borchardt JD, Gehrs KM, Smith RJ, Silvestri G, Russell SR, Klaver CC, Barbazetto I, Chang S, Yannuzzi LA, Barile GR, Merriam JC, Smith RT, Olsh AK, Bergeron J, Zernant J, Merriam JE, Gold B, Dean M, Allikmets R (2005) A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration. Proc Natl Acad Sci USA 102:7227–7232
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 7227-7232
-
-
Hageman, G.S.1
Anderson, D.H.2
Johnson, L.V.3
Hancox, L.S.4
Taiber, A.J.5
Hardisty, L.I.6
Hageman, J.L.7
Stockman, H.A.8
Borchardt, J.D.9
Gehrs, K.M.10
Smith, R.J.11
Silvestri, G.12
Russell, S.R.13
Klaver, C.C.14
Barbazetto, I.15
Chang, S.16
Yannuzzi, L.A.17
Barile, G.R.18
Merriam, J.C.19
Smith, R.T.20
Olsh, A.K.21
Bergeron, J.22
Zernant, J.23
Merriam, J.E.24
Gold, B.25
Dean, M.26
Allikmets, R.27
more..
-
61
-
-
79960945115
-
Allelic variants of complement genes associated with dense deposit disease
-
COI: 1:CAS:528:DC%2BC3MXhtFSlsrvK, PID: 21784901
-
Abrera-Abeleda MA, Nishimura C, Frees K, Jones M, Maga T, Katz LM, Zhang Y, Smith RJH (2011) Allelic variants of complement genes associated with dense deposit disease. J Am Soc Nephrol 22:1551–1559
-
(2011)
J Am Soc Nephrol
, vol.22
, pp. 1551-1559
-
-
Abrera-Abeleda, M.A.1
Nishimura, C.2
Frees, K.3
Jones, M.4
Maga, T.5
Katz, L.M.6
Zhang, Y.7
Smith, R.J.H.8
-
62
-
-
34548491156
-
New approaches to the treatment of dense deposit disease
-
Dense Deposit Disease Focus Group, Smith RJH, Alexander J, Barlow PN, Botto M, Cassavant TL, Cook HT, de Cordoba SR, Hageman GS, Jokiranta TS, Kimberling WJ, Lambris JD, Lanning LD, Levidiotis V, Licht C, Lutz HU, Meri S, Pickering MC, Quigg RJ, Rops AL, Salant DJ, Sethi S, Thurman JM, Tully HF, Tully SP, van der Vlag J, Walker PD, Wurzner R, Zipfel PF (2007) New approaches to the treatment of dense deposit disease. J Am Soc Nephrol 18:2447–2456
-
(2007)
J Am Soc Nephrol
, vol.18
, pp. 2447-2456
-
-
Smith, R.J.H.1
Alexander, J.2
Barlow, P.N.3
Botto, M.4
Cassavant, T.L.5
Cook, H.T.6
de Cordoba, S.R.7
Hageman, G.S.8
Jokiranta, T.S.9
Kimberling, W.J.10
Lambris, J.D.11
Lanning, L.D.12
Levidiotis, V.13
Licht, C.14
Lutz, H.U.15
Meri, S.16
Pickering, M.C.17
Quigg, R.J.18
Rops, A.L.19
Salant, D.J.20
Sethi, S.21
Thurman, J.M.22
Tully, H.F.23
Tully, S.P.24
van der Vlag, J.25
Walker, P.D.26
Wurzner, R.27
Zipfel, P.F.28
more..
-
63
-
-
84876044818
-
Genetics and outcome of atypical hemolytic uremic syndrome: A nationwide French series comparing children and adults
-
COI: 1:CAS:528:DC%2BC3sXmt1elu7Y%3D, PID: 23307876
-
Fremeaux-Bacchi V, Fakhouri F, Garnier A, Bienaime F, Dragon-Durey MA, Ngo S, Moulin B, Servais A, Provot F, Rostaing L, Burtey S, Niaudet P, Deschenes G, Lebranchu Y, Zuber J, Loirat C (2013) Genetics and outcome of atypical hemolytic uremic syndrome: A nationwide French series comparing children and adults. Clin J Am Soc Nephrol 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
Moulin, B.7
Servais, A.8
Provot, F.9
Rostaing, L.10
Burtey, S.11
Niaudet, P.12
Deschenes, G.13
Lebranchu, Y.14
Zuber, J.15
Loirat, C.16
-
64
-
-
0031965358
-
Frequency of renal diseases and clinical indications for renal biopsy in children (report of the Italian National Registry of Renal Biopsies in Children). Group of Renal Immunopathology of the Italian Society of Pediatric Nephrology and Group of Renal Immunopathology of the Italian Society of Nephrology
-
COI: 1:STN:280:DyaK1c7ntVWktA%3D%3D, PID: 9509437
-
Coppo R, Gianoglio B, Porcellini MG, Maringhini S (1998) Frequency of renal diseases and clinical indications for renal biopsy in children (report of the Italian National Registry of Renal Biopsies in Children). Group of Renal Immunopathology of the Italian Society of Pediatric Nephrology and Group of Renal Immunopathology of the Italian Society of Nephrology. Nephrol Dial Transplant 13:293–297
-
(1998)
Nephrol Dial Transplant
, vol.13
, pp. 293-297
-
-
Coppo, R.1
Gianoglio, B.2
Porcellini, M.G.3
Maringhini, S.4
-
65
-
-
84891885176
-
C3 glomerulopathy: clinicopathologic features and predictors of outcome
-
COI: 1:CAS:528:DC%2BC2cXjtlyjs7c%3D, PID: 24178974
-
Medjeral-Thomas NR, O'Shaughnessy MM, O'Regan JA, Traynor C, Flanagan M, Wong L, Teoh CW, Awan A, Waldron M, Cairns T, O'Kelly P, Dorman AM, Pickering MC, Conlon PJ, Cook HT (2014) C3 glomerulopathy: clinicopathologic features and predictors of outcome. Clin J Am Soc Nephrol 9:46–53
-
(2014)
Clin J Am Soc Nephrol
, vol.9
, pp. 46-53
-
-
Medjeral-Thomas, N.R.1
O'Shaughnessy, M.M.2
O'Regan, J.A.3
Traynor, C.4
Flanagan, M.5
Wong, L.6
Teoh, C.W.7
Awan, A.8
Waldron, M.9
Cairns, T.10
O'Kelly, P.11
Dorman, A.M.12
Pickering, M.C.13
Conlon, P.J.14
Cook, H.T.15
-
66
-
-
84863442729
-
Clinical features and outcomes of 98 children and adults with dense deposit disease
-
PID: 22105967
-
Lu D-F, Moon M, Lanning LD, McCarthy AM, Smith RJH (2012) Clinical features and outcomes of 98 children and adults with dense deposit disease. Pediatr Nephrol 27:773–781
-
(2012)
Pediatr Nephrol
, vol.27
, pp. 773-781
-
-
Lu, D.-F.1
Moon, M.2
Lanning, L.D.3
McCarthy, A.M.4
Smith, R.J.H.5
-
67
-
-
84887118518
-
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration
-
COI: 1:CAS:528:DC%2BC3sXhsVertLzO, PID: 24036949
-
Zhan X, Larson DE, Wang C, Koboldt DC, Sergeev YV, Fulton RS, Fulton LL, Fronick CC, Branham KE, Bragg-Gresham J, Jun G, Hu Y, Kang HM, Liu D, Othman M, Brooks M, Ratnapriya R, Boleda A, Grassmann F, Von Strachwitz C, Olson LM, Buitendijk GHS, Hofman A, Van Duijn CM, Cipriani V, Moore AT, Shahid H, Jiang Y, Conley YP, Morgan DJ, Kim IK, Johnson MP, Cantsilieris S, Richardson AJ, Guymer RH, Luo H, Ouyang H, Licht C, Pluthero FG, Zhang MM, Zhang K, Baird PN, Blangero J, Klein ML, Farrer LA, DeAngelis MM, Weeks DE, Gorin MB, Yates JRW, Klaver CCW, Pericak-Vance MA, Haines JL, Weber BHF, Wilson RK, Heckenlively JR, Chew EY, Stambolian D, Mardis ER, Swaroop A, Abecasis GR (2013) Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. Nat Genet 45:1375–1381
-
(2013)
Nat Genet
, vol.45
, pp. 1375-1381
-
-
Zhan, X.1
Larson, D.E.2
Wang, C.3
Koboldt, D.C.4
Sergeev, Y.V.5
Fulton, R.S.6
Fulton, L.L.7
Fronick, C.C.8
Branham, K.E.9
Bragg-Gresham, J.10
Jun, G.11
Hu, Y.12
Kang, H.M.13
Liu, D.14
Othman, M.15
Brooks, M.16
Ratnapriya, R.17
Boleda, A.18
Grassmann, F.19
Von Strachwitz, C.20
Olson, L.M.21
Buitendijk, G.H.S.22
Hofman, A.23
Van Duijn, C.M.24
Cipriani, V.25
Moore, A.T.26
Shahid, H.27
Jiang, Y.28
Conley, Y.P.29
Morgan, D.J.30
Kim, I.K.31
Johnson, M.P.32
Cantsilieris, S.33
Richardson, A.J.34
Guymer, R.H.35
Luo, H.36
Ouyang, H.37
Licht, C.38
Pluthero, F.G.39
Zhang, M.M.40
Zhang, K.41
Baird, P.N.42
Blangero, J.43
Klein, M.L.44
Farrer, L.A.45
DeAngelis, M.M.46
Weeks, D.E.47
Gorin, M.B.48
Yates, J.R.W.49
Klaver, C.C.W.50
Pericak-Vance, M.A.51
Haines, J.L.52
Weber, B.H.F.53
Wilson, R.K.54
Heckenlively, J.R.55
Chew, E.Y.56
Stambolian, D.57
Mardis, E.R.58
Swaroop, A.59
Abecasis, G.R.60
more..
-
68
-
-
0034012166
-
Drusen associated with aging and age-related macular degeneration contain proteins common to extracellular deposits associated with atherosclerosis, elastosis, amyloidosis, and dense deposit disease
-
COI: 1:CAS:528:DC%2BD3cXjtVejtb0%3D, PID: 10783137
-
Mullins RF, Russell SR, Anderson DH, Hageman GS (2000) Drusen associated with aging and age-related macular degeneration contain proteins common to extracellular deposits associated with atherosclerosis, elastosis, amyloidosis, and dense deposit disease. FASEB J 14:835–846
-
(2000)
FASEB J
, vol.14
, pp. 835-846
-
-
Mullins, R.F.1
Russell, S.R.2
Anderson, D.H.3
Hageman, G.S.4
-
69
-
-
0034954060
-
Structure and composition of drusen associated with glomerulonephritis: implications for the role of complement activation in drusen biogenesis
-
COI: 1:STN:280:DC%2BD3MzpvV2nuw%3D%3D, PID: 11450763
-
Mullins RF, Aptsiauri N, Hageman GS (2001) Structure and composition of drusen associated with glomerulonephritis: implications for the role of complement activation in drusen biogenesis. Eye 15:390–395
-
(2001)
Eye
, vol.15
, pp. 390-395
-
-
Mullins, R.F.1
Aptsiauri, N.2
Hageman, G.S.3
-
70
-
-
0027158913
-
Complement-mediated adipocyte lysis by nephritic factor sera
-
COI: 1:CAS:528:DyaK3sXitFWhs7c%3D, PID: 8496694
-
Mathieson PW, Wurzner R, Oliveria DB, Lachmann PJ, Peters DK (1993) Complement-mediated adipocyte lysis by nephritic factor sera. J Exp Med 177:1827–1831
-
(1993)
J Exp Med
, vol.177
, pp. 1827-1831
-
-
Mathieson, P.W.1
Wurzner, R.2
Oliveria, D.B.3
Lachmann, P.J.4
Peters, D.K.5
-
71
-
-
1542642958
-
Clinical features and metabolic and autoimmune derangements in acquired partial lipodystrophy: report of 35 cases and review of the literature
-
COI: 1:CAS:528:DC%2BD2cXntFShsQ%3D%3D, PID: 14747765
-
Misra A, Peethambaram A, Garg A (2004) Clinical features and metabolic and autoimmune derangements in acquired partial lipodystrophy: report of 35 cases and review of the literature. Medicine 83:18–34
-
(2004)
Medicine
, vol.83
, pp. 18-34
-
-
Misra, A.1
Peethambaram, A.2
Garg, A.3
-
72
-
-
37849022343
-
Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals
-
COI: 1:CAS:528:DC%2BD1cXitVWntL0%3D, PID: 18190458
-
Pickering MC, Cook HT (2008) Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals. Clin Exp Immunol 151:210–230
-
(2008)
Clin Exp Immunol
, vol.151
, pp. 210-230
-
-
Pickering, M.C.1
Cook, H.T.2
-
73
-
-
84863881370
-
Thrombotic microangiopathy mimicking membranoproliferative glomerulonephritis
-
PID: 21810760
-
Brackman D, Sartz L, Leh S, Kristoffersson AC, Bjerre A, Tati R, Fremeaux-Bacchi V, Karpman D (2011) Thrombotic microangiopathy mimicking membranoproliferative glomerulonephritis. Nephrol Dial Transplant 26:3399–3403
-
(2011)
Nephrol Dial Transplant
, vol.26
, pp. 3399-3403
-
-
Brackman, D.1
Sartz, L.2
Leh, S.3
Kristoffersson, A.C.4
Bjerre, A.5
Tati, R.6
Fremeaux-Bacchi, V.7
Karpman, D.8
-
74
-
-
80155136247
-
Three kidneys, two diseases, one antibody?
-
PID: 21813829
-
Lorcy N, Rioux-Leclercq N, Lombard ML, Le Pogamp P, Vigneau C (2011) Three kidneys, two diseases, one antibody? Nephrol Dial Transplant 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
-
75
-
-
77958587405
-
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype
-
COI: 1:CAS:528:DC%2BC3cXhsVaqur7K, PID: 20595690
-
Noris M, Caprioli J, Bresin E, Mossali C, Pianetti G, Gamba S, Daina E, Fenili C, Castelletti F, Sorosina A, Piras R, Donadelli R, Maranta R, van der Meer I, Conway EM, Zipfel PF, Goodship TH, Remuzzi G (2010) Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype. Clin J Am Soc Nephrol 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
Daina, E.7
Fenili, C.8
Castelletti, F.9
Sorosina, A.10
Piras, R.11
Donadelli, R.12
Maranta, R.13
van der Meer, I.14
Conway, E.M.15
Zipfel, P.F.16
Goodship, T.H.17
Remuzzi, G.18
-
76
-
-
0015939075
-
Plasma C3 and C4 concentrations in management of glomerulonephritis
-
COI: 1:STN:280:DyaE2c%2FgsVyrtA%3D%3D, PID: 4200478
-
Cameron JS, Vick RM, Ogg CS, Seymour WM, Chantler C, Turner DR (1973) Plasma C3 and C4 concentrations in management of glomerulonephritis. Br Med J 3:668–672
-
(1973)
Br Med J
, vol.3
, pp. 668-672
-
-
Cameron, J.S.1
Vick, R.M.2
Ogg, C.S.3
Seymour, W.M.4
Chantler, C.5
Turner, D.R.6
-
77
-
-
77956394088
-
A complement to kidney disease: CFHR5 nephropathy
-
PID: 20800272
-
Karumanchi SA, Thadhani R (2010) A complement to kidney disease: CFHR5 nephropathy. Lancet 376:748–750
-
(2010)
Lancet
, vol.376
, pp. 748-750
-
-
Karumanchi, S.A.1
Thadhani, R.2
-
78
-
-
0022202346
-
Prednisone therapy of membranoproliferative glomerulonephritis in children
-
COI: 1:STN:280:DyaL28%2Fjs1Kgsw%3D%3D, PID: 3903090
-
Warady BA, Guggenheim SJ, Sedman A, Lum GM (1985) Prednisone therapy of membranoproliferative glomerulonephritis in children. J Pediatr 107:702–707
-
(1985)
J Pediatr
, vol.107
, pp. 702-707
-
-
Warady, B.A.1
Guggenheim, S.J.2
Sedman, A.3
Lum, G.M.4
-
79
-
-
0032717001
-
Differences between membranoproliferative glomerulonephritis types I and III in long-term response to an alternate-day prednisone regimen
-
COI: 1:CAS:528:DC%2BD3cXhsValtg%3D%3D, PID: 10585311
-
Braun MC, West CD, Strife CF (1999) Differences between membranoproliferative glomerulonephritis types I and III in long-term response to an alternate-day prednisone regimen. Am J Kidney Dis 34:1022–1032
-
(1999)
Am J Kidney Dis
, vol.34
, pp. 1022-1032
-
-
Braun, M.C.1
West, C.D.2
Strife, C.F.3
-
80
-
-
0026573776
-
Treatment of mesangiocapillary glomerulonephritis with alternate-day prednisone—a report of the international study of kidney disease in children
-
COI: 1:STN:280:DyaK383jvFaltg%3D%3D, PID: 1571205
-
Tarshish P, Bernstein J, Tobin JN, Edelmann CM Jr (1992) Treatment of mesangiocapillary glomerulonephritis with alternate-day prednisone—a report of the international study of kidney disease in children. Pediatr Nephrol 6:123–130
-
(1992)
Pediatr Nephrol
, vol.6
, pp. 123-130
-
-
Tarshish, P.1
Bernstein, J.2
Tobin, J.N.3
Edelmann, C.M.4
-
81
-
-
77951663701
-
Combination therapy with mycophenolate mofetil and prednisone in steroid-resistant idiopathic membranoproliferative glomerulonephritis
-
COI: 1:CAS:528:DC%2BC3cXot1eqsbs%3D, PID: 20420795
-
Yuan M, Zou J, Zhang X, Liu H, Teng J, Zhong Y, Ding X (2010) Combination therapy with mycophenolate mofetil and prednisone in steroid-resistant idiopathic membranoproliferative glomerulonephritis. Clin Nephrol 73:354–359
-
(2010)
Clin Nephrol
, vol.73
, pp. 354-359
-
-
Yuan, M.1
Zou, J.2
Zhang, X.3
Liu, H.4
Teng, J.5
Zhong, Y.6
Ding, X.7
-
82
-
-
59249099144
-
Mycophenolate mofetil in high-risk patients with primary glomerulonephritis: Results of a 1-year prospective study
-
COI: 1:CAS:528:DC%2BD1MXltVaisbk%3D, PID: 19194109
-
Dimkovic N, Jovanovic D, Kovacevic Z, Rabrenovic V, Nesic V, Savin M, Mitic B, Ratkovic M, Curic S, Mitic I, Pljesa S, Perunicic-Pekovic G, Marinkovic J, Popovic J, Vujic D (2009) Mycophenolate mofetil in high-risk patients with primary glomerulonephritis: Results of a 1-year prospective study. Nephron Clin Pract 111:c189–c196
-
(2009)
Nephron Clin Pract
, vol.111
, pp. c189-c196
-
-
Dimkovic, N.1
Jovanovic, D.2
Kovacevic, Z.3
Rabrenovic, V.4
Nesic, V.5
Savin, M.6
Mitic, B.7
Ratkovic, M.8
Curic, S.9
Mitic, I.10
Pljesa, S.11
Perunicic-Pekovic, G.12
Marinkovic, J.13
Popovic, J.14
Vujic, D.15
-
83
-
-
84957650960
-
The treatment of membranoproliferative glomerulonephritis in children with mycophenolate mofetil
-
Mazo A, Margieva T, Vashurina T, Zrobok O, Tsygin A (2013) The treatment of membranoproliferative glomerulonephritis in children with mycophenolate mofetil. Pediatr Nephrol 28:1607–1608
-
(2013)
Pediatr Nephrol
, vol.28
, pp. 1607-1608
-
-
Mazo, A.1
Margieva, T.2
Vashurina, T.3
Zrobok, O.4
Tsygin, A.5
-
84
-
-
39049084807
-
Cyclosporine in the treatment of membranoproliferative glomerulonephritis
-
COI: 1:CAS:528:DC%2BD1cXjt12ktro%3D, PID: 18154419
-
Bagheri N, Nemati E, Rahbar K, Nobakht A, Einollahi B, Taheri S (2008) Cyclosporine in the treatment of membranoproliferative glomerulonephritis. Arch Iran Med 11:26–29
-
(2008)
Arch Iran Med
, vol.11
, pp. 26-29
-
-
Bagheri, N.1
Nemati, E.2
Rahbar, K.3
Nobakht, A.4
Einollahi, B.5
Taheri, S.6
-
85
-
-
84880747699
-
Tacrolimus is an alternative therapy option for the treatment of adult steroid-resistant nephrotic syndrome: a prospective, multicenter clinical trial
-
COI: 1:CAS:528:DC%2BC3sXktlKhtLw%3D, PID: 22684795
-
Fan L, Liu Q, Liao Y, Li Z, Ji Y, Yang Z, Chen J, Fu J, Zhang J, Kong Y, Fu P, Lou T, Liu Z, Yu X, Chen W (2013) Tacrolimus is an alternative therapy option for the treatment of adult steroid-resistant nephrotic syndrome: a prospective, multicenter clinical trial. Int Urol Nephrol 45:459–468
-
(2013)
Int Urol Nephrol
, vol.45
, pp. 459-468
-
-
Fan, L.1
Liu, Q.2
Liao, Y.3
Li, Z.4
Ji, Y.5
Yang, Z.6
Chen, J.7
Fu, J.8
Zhang, J.9
Kong, Y.10
Fu, P.11
Lou, T.12
Liu, Z.13
Yu, X.14
Chen, W.15
-
86
-
-
67449152260
-
Tacrolimus therapy in adults with steroid- and cyclophosphamide-resistant nephrotic syndrome and normal or mildly reduced GFR
-
COI: 1:CAS:528:DC%2BD1MXptVKqs7o%3D, PID: 19406543
-
Li X, Li H, Ye H, Li Q, He X, Zhang X, Chen Y, Han F, He Q, Wang H, Chen J (2009) Tacrolimus therapy in adults with steroid- and cyclophosphamide-resistant nephrotic syndrome and normal or mildly reduced GFR. Am J Kidney Dis 54:51–58
-
(2009)
Am J Kidney Dis
, vol.54
, pp. 51-58
-
-
Li, X.1
Li, H.2
Ye, H.3
Li, Q.4
He, X.5
Zhang, X.6
Chen, Y.7
Han, F.8
He, Q.9
Wang, H.10
Chen, J.11
-
87
-
-
34548312531
-
Remission of membranoproliferative glomerulonephritis type I with the use of tacrolimus
-
PID: 17609987
-
Haddad M, Lau K, Butani L (2007) Remission of membranoproliferative glomerulonephritis type I with the use of tacrolimus. Pediatr Nephrol 22:1787–1791
-
(2007)
Pediatr Nephrol
, vol.22
, pp. 1787-1791
-
-
Haddad, M.1
Lau, K.2
Butani, L.3
-
88
-
-
23944468114
-
Membranoproliferative glomerulonephritis type II (dense deposit disease): an update
-
PID: 15800116
-
Appel GB, Cook HT, Hageman G, Jennette JC, Kashgarian M, Kirschfink M, Lambris JD, Lanning L, Lutz HU, Meri S, Rose NR, Salant DJ, Sethi S, Smith RJ, Smoyer W, Tully HF, Tully SP, Walker P, Welsh M, Wurzner R, Zipfel PF (2005) Membranoproliferative glomerulonephritis type II (dense deposit disease): an update. J Am Soc Nephrol 16:1392–1403
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 1392-1403
-
-
Appel, G.B.1
Cook, H.T.2
Hageman, G.3
Jennette, J.C.4
Kashgarian, M.5
Kirschfink, M.6
Lambris, J.D.7
Lanning, L.8
Lutz, H.U.9
Meri, S.10
Rose, N.R.11
Salant, D.J.12
Sethi, S.13
Smith, R.J.14
Smoyer, W.15
Tully, H.F.16
Tully, S.P.17
Walker, P.18
Welsh, M.19
Wurzner, R.20
Zipfel, P.F.21
more..
-
89
-
-
84861493758
-
Rituximab therapy for Type I membranoproliferative glomerulonephritis
-
COI: 1:CAS:528:DC%2BC38Xot1ylu7w%3D, PID: 22445472
-
Dillon JJ, Hladunewich M, Haley WE, Reich HN, Cattran DC, Fervenza FC (2012) Rituximab therapy for Type I membranoproliferative glomerulonephritis. Clin Nephrol 77:290–295
-
(2012)
Clin Nephrol
, vol.77
, pp. 290-295
-
-
Dillon, J.J.1
Hladunewich, M.2
Haley, W.E.3
Reich, H.N.4
Cattran, D.C.5
Fervenza, F.C.6
-
90
-
-
84879500739
-
Our experience with rituximab therapy for adult-onset primary glomerulonephritis and review of literature
-
COI: 1:CAS:528:DC%2BC3sXhtVahtbjJ, PID: 22798030
-
Kong WY, Swaminathan R, Irish A (2013) Our experience with rituximab therapy for adult-onset primary glomerulonephritis and review of literature. Int Urol Nephrol 45:795–802
-
(2013)
Int Urol Nephrol
, vol.45
, pp. 795-802
-
-
Kong, W.Y.1
Swaminathan, R.2
Irish, A.3
-
91
-
-
83655180822
-
Recurrent membranoproliferative glomerulonephritis after second renal graft treated with plasmapheresis and rituximab
-
COI: 1:STN:280:DC%2BC38%2Fnsl2msg%3D%3D, PID: 22172889
-
Perez-Saez MJ, Toledo K, Navarro MD, Lopez-Andreu M, Redondo MD, Ortega R, Perez-Seoane C, Aguera ML, Rodriguez-Benot A, Aljama P (2011) Recurrent membranoproliferative glomerulonephritis after second renal graft treated with plasmapheresis and rituximab. Transplant Proc 43:4005–4009
-
(2011)
Transplant Proc
, vol.43
, pp. 4005-4009
-
-
Perez-Saez, M.J.1
Toledo, K.2
Navarro, M.D.3
Lopez-Andreu, M.4
Redondo, M.D.5
Ortega, R.6
Perez-Seoane, C.7
Aguera, M.L.8
Rodriguez-Benot, A.9
Aljama, P.10
-
92
-
-
77955193837
-
Effect of single-dose rituximab on primary glomerular diseases
-
COI: 1:CAS:528:DC%2BC3MXhtlWjs78%3D, PID: 20693810
-
Sugiura H, Takei T, Itabashi M, Tsukada M, Moriyama T, Kojima C, Shiohira T, Shimizu A, Tsuruta Y, Amemiya N, Ogawa T, Uchida K, Tsuchiya K, Nitta K (2011) Effect of single-dose rituximab on primary glomerular diseases. Nephron Clin Pract 117:c98–c105
-
(2011)
Nephron Clin Pract
, vol.117
, pp. c98-c105
-
-
Sugiura, H.1
Takei, T.2
Itabashi, M.3
Tsukada, M.4
Moriyama, T.5
Kojima, C.6
Shiohira, T.7
Shimizu, A.8
Tsuruta, Y.9
Amemiya, N.10
Ogawa, T.11
Uchida, K.12
Tsuchiya, K.13
Nitta, K.14
-
93
-
-
79960338674
-
Patterns of noncryoglobulinemic glomerulonephritis with monoclonal Ig deposits: correlation with IgG subclass and response to rituximab
-
COI: 1:CAS:528:DC%2BC3MXhtValsb%2FJ, PID: 21700823
-
Guiard E, Karras A, Plaisier E, Duong Van Huyen J-P, Fakhouri F, Rougier J-P, Noel L-H, Callard P, Delahousse M, Ronco P (2011) Patterns of noncryoglobulinemic glomerulonephritis with monoclonal Ig deposits: correlation with IgG subclass and response to rituximab. Clin J Am Soc Nephrol 6:1609–1616
-
(2011)
Clin J Am Soc Nephrol
, vol.6
, pp. 1609-1616
-
-
Guiard, E.1
Karras, A.2
Plaisier, E.3
Duong Van Huyen, J.-P.4
Fakhouri, F.5
Rougier, J.-P.6
Noel, L.-H.7
Callard, P.8
Delahousse, M.9
Ronco, P.10
-
94
-
-
84859421387
-
Recurrent dense deposit disease after renal transplantation: an emerging role for complementary therapies
-
COI: 1:CAS:528:DC%2BC38XmvVynsbw%3D, PID: 22233157
-
McCaughan JA, O'Rourke DM, Courtney AE (2012) Recurrent dense deposit disease after renal transplantation: an emerging role for complementary therapies. Am J Transplant 12:1046–1051
-
(2012)
Am J Transplant
, vol.12
, pp. 1046-1051
-
-
McCaughan, J.A.1
O'Rourke, D.M.2
Courtney, A.E.3
-
95
-
-
84858671433
-
Eculizumab in a patient with dense-deposit disease
-
COI: 1:CAS:528:DC%2BC38XktlCqtbk%3D, PID: 22435382
-
Daina E, Noris M, Remuzzi G (2012) Eculizumab in a patient with dense-deposit disease. N Engl J Med 366:1161–1163
-
(2012)
N Engl J Med
, vol.366
, pp. 1161-1163
-
-
Daina, E.1
Noris, M.2
Remuzzi, G.3
-
96
-
-
84937856800
-
Management of dense deposit disease with plasmapheresis and eculizumab
-
Nord AT, Nord BL, Schmidt AE, Smith DS (2014) Management of dense deposit disease with plasmapheresis and eculizumab. J Clin Apher 29:28–29
-
(2014)
J Clin Apher
, vol.29
, pp. 28-29
-
-
Nord, A.T.1
Nord, B.L.2
Schmidt, A.E.3
Smith, D.S.4
-
97
-
-
0021857785
-
Plasma exchange in the treatment of mesangiocapillary glomerulonephritis
-
COI: 1:STN:280:DyaL2M3mvVanuw%3D%3D, PID: 4022205
-
McGinley E, Watkins R, McLay A, Boulton-Jones JM (1985) Plasma exchange in the treatment of mesangiocapillary glomerulonephritis. Nephron 40:385–390
-
(1985)
Nephron
, vol.40
, pp. 385-390
-
-
McGinley, E.1
Watkins, R.2
McLay, A.3
Boulton-Jones, J.M.4
-
98
-
-
84858633062
-
Eculizumab and refractory membranoproliferative glomerulonephritis
-
COI: 1:CAS:528:DC%2BC38XktlCqtbc%3D, PID: 22435384
-
Radhakrishnan S, Lunn A, Kirschfink M, Thorner P, Hebert D, Langlois V, Pluthero F, Licht C (2012) Eculizumab and refractory membranoproliferative glomerulonephritis. N Engl J Med 366:1165–1166
-
(2012)
N Engl J Med
, vol.366
, pp. 1165-1166
-
-
Radhakrishnan, S.1
Lunn, A.2
Kirschfink, M.3
Thorner, P.4
Hebert, D.5
Langlois, V.6
Pluthero, F.7
Licht, C.8
-
99
-
-
0023918184
-
Regression of recurrent membranoproliferative glomerulonephritis type II in a transplanted kidney after plasmapheresis therapy
-
COI: 1:STN:280:DyaL1c7lvFyhsQ%3D%3D, PID: 2964750
-
Oberkircher OR, Enama M, West JC, Campbell P, Moran J (1988) Regression of recurrent membranoproliferative glomerulonephritis type II in a transplanted kidney after plasmapheresis therapy. Transplant Proc 20:418–423
-
(1988)
Transplant Proc
, vol.20
, pp. 418-423
-
-
Oberkircher, O.R.1
Enama, M.2
West, J.C.3
Campbell, P.4
Moran, J.5
-
100
-
-
0036400061
-
Management of membranoproliferative glomerulonephritis type II with plasmapheresis
-
PID: 12378549
-
Kurtz KA, Schlueter AJ (2002) Management of membranoproliferative glomerulonephritis type II with plasmapheresis. J Clin Apher 17:135–137
-
(2002)
J Clin Apher
, vol.17
, pp. 135-137
-
-
Kurtz, K.A.1
Schlueter, A.J.2
-
101
-
-
0020486937
-
Acute renal failure in dense deposit disease: recovery after plasmapheresis
-
COI: 1:STN:280:DyaL383gslGqtA%3D%3D
-
Banks RA, May S, Wallington T (1982) Acute renal failure in dense deposit disease: recovery after plasmapheresis. Br Med J (Clin Res Ed) 284:1874–1875
-
(1982)
Br Med J (Clin Res Ed)
, vol.284
, pp. 1874-1875
-
-
Banks, R.A.1
May, S.2
Wallington, T.3
-
102
-
-
22244450678
-
Recurrent nephrotic syndrome after living-related renal transplantation resistant to plasma exchange: report of two cases
-
PID: 15955171
-
Masutani K, Katafuchi R, Ikeda H, Yamamoto H, Motoyama K, Sugitani A, Kanai H, Kumagai H, Hirakata H, Tanaka M, Iida M (2005) Recurrent nephrotic syndrome after living-related renal transplantation resistant to plasma exchange: report of two cases. Clin Transplant 19[Suppl 14]:59–64
-
(2005)
Clin Transplant
, vol.19
, pp. 59-64
-
-
Masutani, K.1
Katafuchi, R.2
Ikeda, H.3
Yamamoto, H.4
Motoyama, K.5
Sugitani, A.6
Kanai, H.7
Kumagai, H.8
Hirakata, H.9
Tanaka, M.10
Iida, M.11
-
103
-
-
0020651904
-
Plasmapheresis induced recovery from renal failure in mesangiocapillary glomerulonephritis of acute onset
-
COI: 1:STN:280:DyaL3s3ntlGrtg%3D%3D, PID: 6878267
-
Montoliu J, Bergada E, Botey A, Torras A, Darnell A, Arrizabalaga P, Lopez-Pedret J, Revert L (1983) Plasmapheresis induced recovery from renal failure in mesangiocapillary glomerulonephritis of acute onset. Proc Eur Dial Transplant Assoc 19:794–799
-
(1983)
Proc Eur Dial Transplant Assoc
, vol.19
, pp. 794-799
-
-
Montoliu, J.1
Bergada, E.2
Botey, A.3
Torras, A.4
Darnell, A.5
Arrizabalaga, P.6
Lopez-Pedret, J.7
Revert, L.8
-
104
-
-
0029050205
-
Plasmapheresis maintained renal function in an allograft with recurrent membranoproliferative glomerulonephritis type I
-
COI: 1:STN:280:DyaK28%2Fks12ltQ%3D%3D, PID: 7503148
-
Muczynski KA (1995) Plasmapheresis maintained renal function in an allograft with recurrent membranoproliferative glomerulonephritis type I. Am J Nephrol 15:446–449
-
(1995)
Am J Nephrol
, vol.15
, pp. 446-449
-
-
Muczynski, K.A.1
-
105
-
-
84937911001
-
Successful use of plasma exchange to prevent recurrence of C3 glomerulonephritis after kidney transplantation: a case report
-
Pipeleers L, Sennesael J, Massart A, Geers C, Goodship T, Stordeur P, Wissing KM (2012) Successful use of plasma exchange to prevent recurrence of C3 glomerulonephritis after kidney transplantation: a case report. Transplantation 94:1050
-
(2012)
Transplantation
, vol.94
, pp. 1050
-
-
Pipeleers, L.1
Sennesael, J.2
Massart, A.3
Geers, C.4
Goodship, T.5
Stordeur, P.6
Wissing, K.M.7
-
106
-
-
0034079690
-
Recurrent type I membranoproliferative glomerulonephritis in a renal allograft: successful treatment with plasmapheresis
-
COI: 1:STN:280:DC%2BD3c3gs1ejtQ%3D%3D, PID: 10739799
-
Saxena R, Frankel WL, Sedmak DD, Falkenhain ME, Cosio FG (2000) Recurrent type I membranoproliferative glomerulonephritis in a renal allograft: successful treatment with plasmapheresis. Am J Kidney Dis 35:749–752
-
(2000)
Am J Kidney Dis
, vol.35
, pp. 749-752
-
-
Saxena, R.1
Frankel, W.L.2
Sedmak, D.D.3
Falkenhain, M.E.4
Cosio, F.G.5
-
107
-
-
84997038692
-
Recurrent (MPGN) membranoproliferative glomerulonephritis type 1 successfully treated with plasma exchange (PE)
-
Yadav P, Ognjanovic M, Coulthard M, Moghal N, Lambert H, Tse Y (2011) Recurrent (MPGN) membranoproliferative glomerulonephritis type 1 successfully treated with plasma exchange (PE). Pediatr Nephrol 26:1665–1666
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 1665-1666
-
-
Yadav, P.1
Ognjanovic, M.2
Coulthard, M.3
Moghal, N.4
Lambert, H.5
Tse, Y.6
-
108
-
-
0027162122
-
Renal failure due to mesangiocapillary glomerulonephritis in pregnancy: use of plasma exchange therapy
-
COI: 1:STN:280:DyaK2c%2FjslKrtQ%3D%3D, PID: 8222375
-
Morton MR, Bannister KM (1993) Renal failure due to mesangiocapillary glomerulonephritis in pregnancy: use of plasma exchange therapy. Clin Nephrol 40:74–78
-
(1993)
Clin Nephrol
, vol.40
, pp. 74-78
-
-
Morton, M.R.1
Bannister, K.M.2
-
109
-
-
0024312719
-
Membranoproliferative glomerulonephritis in a patient with congenital deficiency of the third component of complement: effect of treatment with plasma
-
COI: 1:STN:280:DyaL1M3ksVyjsw%3D%3D, PID: 2719026
-
Roord JJ, van Diemen-van Steenvoorde RA, Schuurman HJ, Rijkers GT, Zegers BJ, Gmelig Meyling FH, Stoop JW (1989) Membranoproliferative glomerulonephritis in a patient with congenital deficiency of the third component of complement: effect of treatment with plasma. Am J Kidney Dis 13:413–417
-
(1989)
Am J Kidney Dis
, vol.13
, pp. 413-417
-
-
Roord, J.J.1
van Diemen-van Steenvoorde, R.A.2
Schuurman, H.J.3
Rijkers, G.T.4
Zegers, B.J.5
Gmelig Meyling, F.H.6
Stoop, J.W.7
-
110
-
-
84860779074
-
Eculizumab for dense deposit disease and C3 glomerulonephritis
-
COI: 1:CAS:528:DC%2BC38XpsVGqsbY%3D, PID: 22403278
-
Bomback AS, Smith RJ, Barile GR, Zhang Y, Heher EC, Herlitz L, Barry Stokes M, Markowitz GS, D'Agati VD, Canetta PA, Radhakrishnan J, Appel GB (2012) Eculizumab for dense deposit disease and C3 glomerulonephritis. Clin J Am Soc Nephrol 7:748–756
-
(2012)
Clin J Am Soc Nephrol
, vol.7
, pp. 748-756
-
-
Bomback, A.S.1
Smith, R.J.2
Barile, G.R.3
Zhang, Y.4
Heher, E.C.5
Herlitz, L.6
Barry Stokes, M.7
Markowitz, G.S.8
D'Agati, V.D.9
Canetta, P.A.10
Radhakrishnan, J.11
Appel, G.B.12
-
111
-
-
84858671433
-
Eculizumab in a patient with dense-deposit disease
-
COI: 1:CAS:528:DC%2BC38XktlCqtbk%3D, PID: 22435382, [Erratum appears in N Engl J Med. 2012 366:1454]
-
Daina E, Noris M, Remuzzi G (2012) Eculizumab in a patient with dense-deposit disease. N Engl J Med 366:1161–1163 [Erratum appears in N Engl J Med. 2012 366:1454]
-
(2012)
N Engl J Med
, vol.366
, pp. 1161-1163
-
-
Daina, E.1
Noris, M.2
Remuzzi, G.3
-
112
-
-
84858661698
-
Eculizumab for the treatment of dense-deposit disease
-
COI: 1:CAS:528:DC%2BC38XktlCqtbY%3D, PID: 22435383
-
Vivarelli M, Pasini A, Emma F (2012) Eculizumab for the treatment of dense-deposit disease. N Engl J Med 366:1163–1165
-
(2012)
N Engl J Med
, vol.366
, pp. 1163-1165
-
-
Vivarelli, M.1
Pasini, A.2
Emma, F.3
-
113
-
-
35948959015
-
Discovery and development of the complement inhibitor eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria
-
COI: 1:CAS:528:DC%2BD2sXht1Oru7zE, PID: 17989688
-
Rother RP, Rollins SA, Mojcik CF, Brodsky RA, Bell L (2007) Discovery and development of the complement inhibitor eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria. Nat Biotechnol 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
-
114
-
-
84883261341
-
Eculizumab and recurrent C3 glomerulonephritis
-
PID: 23689905
-
Gurkan S, Fyfe B, Weiss L, Xiao X, Zhang Y, Smith RJ (2013) Eculizumab and recurrent C3 glomerulonephritis. Pediatr Nephrol 28:1975–1981
-
(2013)
Pediatr Nephrol
, vol.28
, pp. 1975-1981
-
-
Gurkan, S.1
Fyfe, B.2
Weiss, L.3
Xiao, X.4
Zhang, Y.5
Smith, R.J.6
-
115
-
-
84901672159
-
Eculizumab therapy in a patient with dense-deposit disease associated with partial lipodystropy
-
PID: 24464478
-
Ozkaya O, Nalcacioglu H, Tekcan D, Genc G, Meydan BC, Ozdemir BH, Baysal MK, Keceligil HT (2014) Eculizumab therapy in a patient with dense-deposit disease associated with partial lipodystropy. Pediatr Nephrol 29:1283–1287
-
(2014)
Pediatr Nephrol
, vol.29
, pp. 1283-1287
-
-
Ozkaya, O.1
Nalcacioglu, H.2
Tekcan, D.3
Genc, G.4
Meydan, B.C.5
Ozdemir, B.H.6
Baysal, M.K.7
Keceligil, H.T.8
-
116
-
-
84901641827
-
Rituximab fails where eculizumab restores renal function in C3nef-related DDD
-
PID: 24408225
-
Rousset-Rouviere C, Cailliez M, Garaix F, Bruno D, Laurent D, Tsimaratos M (2014) Rituximab fails where eculizumab restores renal function in C3nef-related DDD. Pediatr Nephrol 29:1107–1111
-
(2014)
Pediatr Nephrol
, vol.29
, pp. 1107-1111
-
-
Rousset-Rouviere, C.1
Cailliez, M.2
Garaix, F.3
Bruno, D.4
Laurent, D.5
Tsimaratos, M.6
-
117
-
-
84942374688
-
Successful therapy of C3Nef-positive C3 glomerulopathy with plasma therapy and immunosuppression
-
PID: 25986912
-
Haffner K, Michelfelder S, Pohl M (2015) Successful therapy of C3Nef-positive C3 glomerulopathy with plasma therapy and immunosuppression. Pediatr Nephrol 30:1951–1959
-
(2015)
Pediatr Nephrol
, vol.30
, pp. 1951-1959
-
-
Haffner, K.1
Michelfelder, S.2
Pohl, M.3
-
118
-
-
78751637542
-
Allograft failure in kidney transplant recipients with membranoproliferative glomerulonephritis
-
PID: 21215503
-
Angelo JR, Bell CS, Braun MC (2011) Allograft failure in kidney transplant recipients with membranoproliferative glomerulonephritis. Am J Kidney Dis 57:291–299
-
(2011)
Am J Kidney Dis
, vol.57
, pp. 291-299
-
-
Angelo, J.R.1
Bell, C.S.2
Braun, M.C.3
-
119
-
-
84906557611
-
Clinical findings, pathology, and outcomes of C3GN after kidney transplantation
-
COI: 1:CAS:528:DC%2BC2cXps1Crt7w%3D, PID: 24357668
-
Zand L, Lorenz EC, Cosio FG, Fervenza FC, Nasr SH, Gandhi MJ, Smith RJ, Sethi S (2014) Clinical findings, pathology, and outcomes of C3GN after kidney transplantation. J Am Soc Nephrol 25:1110–1117
-
(2014)
J Am Soc Nephrol
, vol.25
, pp. 1110-1117
-
-
Zand, L.1
Lorenz, E.C.2
Cosio, F.G.3
Fervenza, F.C.4
Nasr, S.H.5
Gandhi, M.J.6
Smith, R.J.7
Sethi, S.8
-
120
-
-
84875977097
-
Impact of graft loss among kidney diseases with a high risk of post-transplant recurrence in the paediatric population
-
PID: 23300261
-
Van Stralen KJ, Verrina E, Belingheri M, Dudley J, Dusek J, Grenda R, Macher MA, Puretic Z, Rubic J, Rudaitis S, Rudin C, Schaefer F, Jager KJ; ESPN/ERA-EDTA Registry (2013) Impact of graft loss among kidney diseases with a high risk of post-transplant recurrence in the paediatric population. Nephrol Dial Transplant 28:1031–1038
-
(2013)
Nephrol Dial Transplant
, vol.28
, pp. 1031-1038
-
-
Van Stralen, K.J.1
Verrina, E.2
Belingheri, M.3
Dudley, J.4
Dusek, J.5
Grenda, R.6
Macher, M.A.7
Puretic, Z.8
Rubic, J.9
Rudaitis, S.10
Rudin, C.11
Schaefer, F.12
Jager, K.J.13
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