-
1
-
-
0015689465
-
Idiopathic membranoproliferative glomerulonephritis. Morphology and natural history
-
4536440
-
Habib R, Kleinknecht C, Gubler MC, Maiz HB (1973) Idiopathic membranoproliferative glomerulonephritis. Morphology and natural history. Perspect Nephrol Hypertens 1:491-514
-
(1973)
Perspect Nephrol Hypertens
, vol.1
, pp. 491-514
-
-
Habib, R.1
Kleinknecht, C.2
Gubler, M.C.3
Maiz, H.B.4
-
2
-
-
0017361295
-
Membranoproliferative glomerulonephritis with disruption of the glomerular basement membrane
-
844227 1:STN:280:DyaE2s7jslSqtQ%3D%3D
-
Strife CF, McEnery PT, McAdams AJ, West CD (1977) Membranoproliferative glomerulonephritis with disruption of the glomerular basement membrane. Clin Nephrol 7:65-72
-
(1977)
Clin Nephrol
, vol.7
, pp. 65-72
-
-
Strife, C.F.1
McEnery, P.T.2
McAdams, A.J.3
West, C.D.4
-
3
-
-
84886614258
-
Immunopathology of membranoproliferative glomerulonephritis with subendothelial deposits (type i MPGN)
-
357058 10.1016/0090-1229(78)90160-5 1:CAS:528:DyaE1cXlt1Ogs78%3D
-
Levy M, Gubler MC, Sich M, Beziau A, Habib R (1978) Immunopathology of membranoproliferative glomerulonephritis with subendothelial deposits (type I MPGN). Clin Immunol Immunopathol 10:477-492
-
(1978)
Clin Immunol Immunopathol
, vol.10
, pp. 477-492
-
-
Levy, M.1
Gubler, M.C.2
Sich, M.3
Beziau, A.4
Habib, R.5
-
4
-
-
77955085990
-
C3 glomerulopathy: A new classification
-
20606628 10.1038/nrneph.2010.85 1:CAS:528:DC%2BC3cXptlyrsLg%3D
-
Fakhouri F, Fremeaux-Bacchi V, Noel LH, Cook HT, Pickering MC (2010) C3 glomerulopathy: a new classification. Nat Rev Nephrol 6:494-499
-
(2010)
Nat Rev Nephrol
, vol.6
, pp. 494-499
-
-
Fakhouri, F.1
Fremeaux-Bacchi, V.2
Noel, L.H.3
Cook, H.T.4
Pickering, M.C.5
-
5
-
-
34147180032
-
Primary glomerulonephritis with isolated C3 deposits: A new entity which shares common genetic risk factors with haemolytic uraemic syndrome
-
17018561 10.1136/jmg.2006.045328 1:CAS:528:DC%2BD2sXkvFehtLc%3D
-
Servais A, Fremeaux-Bacchi V, Lequintrec M, Salomon R, Blouin J, Knebelmann B, Grunfeld JP, Lesavre P, Noel LH, Fakhouri F (2007) Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome. J Med Genet 44:193-199
-
(2007)
J Med Genet
, vol.44
, pp. 193-199
-
-
Servais, A.1
Fremeaux-Bacchi, V.2
Lequintrec, M.3
Salomon, R.4
Blouin, J.5
Knebelmann, B.6
Grunfeld, J.P.7
Lesavre, P.8
Noel, L.H.9
Fakhouri, F.10
-
6
-
-
79957858528
-
Proliferative glomerulonephritis secondary to dysfunction of the alternative pathway of complement
-
21415311 10.2215/CJN.07110810
-
Sethi S, Fervenza FC, Zhang Y, Nasr SH, Leung N, Vrana J, Cramer C, Nester CM, Smith RJ (2011) Proliferative glomerulonephritis secondary to dysfunction of the alternative pathway of complement. Clin J Am Soc Nephrol 6:1009-1017
-
(2011)
Clin J Am Soc Nephrol
, vol.6
, pp. 1009-1017
-
-
Sethi, S.1
Fervenza, F.C.2
Zhang, Y.3
Nasr, S.H.4
Leung, N.5
Vrana, J.6
Cramer, C.7
Nester, C.M.8
Smith, R.J.9
-
7
-
-
64049119966
-
Dense deposit disease: Clinicopathologic study of 32 pediatric and adult patients
-
18971369 10.2215/CJN.03480708
-
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
-
8
-
-
84858661698
-
Eculizumab for the treatment of dense deposit disease
-
22435383 10.1056/NEJMc1111953 1:CAS:528:DC%2BC38XktlCqtbY%3D
-
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
-
9
-
-
84860779074
-
Eculizumab for dense deposit disease and C3 glomerulonephritis
-
22403278 10.2215/CJN.12901211 1:CAS:528:DC%2BC38XpsVGqsbY%3D
-
Bomback AS, Smith RJ, Barile GR, Zhang Y, Heher EC, Herlitz L, Stokes MB, 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
Stokes, M.B.7
Markowitz, G.S.8
D'Agati, V.D.9
Canetta, P.A.10
Radhakrishnan, J.11
Appel, G.B.12
-
10
-
-
84858671433
-
Eculizumab in a patient with dense deposit disease
-
22435382 10.1056/NEJMc1112273 1:CAS:528:DC%2BC38XktlCqtbk%3D
-
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
-
11
-
-
84859421387
-
Recurrent dense deposit disease after renal transplantation: An emerging role for complementary therapies
-
22233157 10.1111/j.1600-6143.2011.03923.x 1:CAS:528:DC%2BC38XmvVynsbw%3D
-
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
-
12
-
-
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)
-
16299065 10.1136/jmg.2005.038315 1:CAS:528:DC%2BD28XotFarur4%3D
-
Abrera-Abeleda MA, Nishimura C, Smith JL, Sethi S, McRae JL, Murphy BF, Silvestri G, Skerka C, Jozsi M, Zipfel PF, Hageman GS, Smith RJ (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.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.12
-
13
-
-
84863115476
-
Causes of alternative pathway dysregulation in dense deposit disease
-
22223606 10.2215/CJN.07900811 1:CAS:528:DC%2BC38XktVyksrc%3D
-
Zhang Y, Meyer NC, Wang K, Nishimura C, Frees K, Jones M, Katz LM, Sethi S, Smith RJ (2012) Causes of alternative pathway dysregulation in dense deposit disease. Clin J Am Soc Nephrol 7:265-274
-
(2012)
Clin J Am Soc Nephrol
, vol.7
, pp. 265-274
-
-
Zhang, Y.1
Meyer, N.C.2
Wang, K.3
Nishimura, C.4
Frees, K.5
Jones, M.6
Katz, L.M.7
Sethi, S.8
Smith, R.J.9
-
14
-
-
77952682366
-
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome
-
20513133 10.1002/humu.21256 1:CAS:528:DC%2BC3cXosl2ksr0%3D
-
Maga TK, Nishimura CJ, Weaver AE, Frees KL, Smith RJ (2010) Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. Hum Mutat 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
-
15
-
-
37049016216
-
Activity and safety profile of low-dose rituximab for the treatment of autoimmune cytopenias in adults
-
18055995 10.3324/haematol.11709 1:CAS:528:DC%2BD1cXitVaiug%3D%3D
-
Provan D, Butler T, Evangelista ML, Amadori S, Newland AC, Stasi R (2007) Activity and safety profile of low-dose rituximab for the treatment of autoimmune cytopenias in adults. Haematologica 92:1695-1698
-
(2007)
Haematologica
, vol.92
, pp. 1695-1698
-
-
Provan, D.1
Butler, T.2
Evangelista, M.L.3
Amadori, S.4
Newland, A.C.5
Stasi, R.6
-
16
-
-
77956973924
-
Low-dose rituximab in adult patients with primary immune thrombocytopenia
-
20546023 10.1111/j.1600-0609.2010.01486.x 1:CAS:528:DC%2BC3cXhtlKgsLfO
-
Zaja F, Vianelli N, Volpetti S, Battista ML, Defina M, Palmieri S, Bocchia M, Medeot M, De Luca S, Ferrara F, Isola M, Baccarani M, Fanin R (2010) Low-dose rituximab in adult patients with primary immune thrombocytopenia. Eur J Haematol 85:329-334
-
(2010)
Eur J Haematol
, vol.85
, pp. 329-334
-
-
Zaja, F.1
Vianelli, N.2
Volpetti, S.3
Battista, M.L.4
Defina, M.5
Palmieri, S.6
Bocchia, M.7
Medeot, M.8
De Luca, S.9
Ferrara, F.10
Isola, M.11
Baccarani, M.12
Fanin, R.13
-
17
-
-
84857113842
-
Membranoproliferative glomerulonephritis and C3 glomerulopathy: Resolving the confusion
-
22157657 10.1038/ki.2011.399
-
Sethi S, Nester CM, Smith RJ (2012) Membranoproliferative glomerulonephritis and C3 glomerulopathy: resolving the confusion. Kidney Int 81:434-441
-
(2012)
Kidney Int
, vol.81
, pp. 434-441
-
-
Sethi, S.1
Nester, C.M.2
Smith, R.J.3
-
18
-
-
77957827919
-
Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation
-
20852386 10.1172/JCI43343 1:CAS:528:DC%2BC3cXht1Ggtb7J
-
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, Rodriguez de Cordoba S (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
Rodriguez De Cordoba, S.13
-
19
-
-
77956394517
-
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis
-
20800271 10.1016/S0140-6736(10)60670-8 1:CAS:528:DC%2BC3cXhtFWqu7jE
-
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
-
20
-
-
67349180237
-
C3 deposition glomerulopathy due to a functional factor H defect
-
18633337 10.1038/ki.2008.354
-
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
-
21
-
-
79960437582
-
Dense deposit disease
-
21601923 10.1016/j.molimm.2011.04.005 1:CAS:528:DC%2BC3MXpt1ahurw%3D
-
Smith RJ, Harris CL, Pickering MC (2011) Dense deposit disease. Mol Immunol 48:1604-1610
-
(2011)
Mol Immunol
, vol.48
, pp. 1604-1610
-
-
Smith, R.J.1
Harris, C.L.2
Pickering, M.C.3
-
22
-
-
0020694279
-
Idiopathic mesangiocapillary glomerulonephritis. Comparison of types i and II in children and adults and long-term prognosis
-
6337487 10.1016/0002-9343(83)90606-X 1:STN:280:DyaL3s7isVSgug%3D%3D
-
Cameron JS, Turner DR, Heaton J, Williams DG, Ogg CS, Chantler C, Haycock GB, Hicks J (1983) Idiopathic mesangiocapillary glomerulonephritis. Comparison of types I and II in children and adults and long-term prognosis. Am J Med 74:175-192
-
(1983)
Am J Med
, vol.74
, pp. 175-192
-
-
Cameron, J.S.1
Turner, D.R.2
Heaton, J.3
Williams, D.G.4
Ogg, C.S.5
Chantler, C.6
Haycock, G.B.7
Hicks, J.8
-
23
-
-
0020378610
-
Biological significance of the C3 nephritic factor in membranoproliferative glomerulonephritis
-
7151338 1:STN:280:DyaL3s7gtlKrtw%3D%3D
-
Schena FP, Pertosa G, Stanziale P, Vox E, Pecoraro C, Andreucci VE (1982) Biological significance of the C3 nephritic factor in membranoproliferative glomerulonephritis. Clin Nephrol 18:240-246
-
(1982)
Clin Nephrol
, vol.18
, pp. 240-246
-
-
Schena, F.P.1
Pertosa, G.2
Stanziale, P.3
Vox, E.4
Pecoraro, C.5
Andreucci, V.E.6
-
24
-
-
0034943625
-
Complement analysis in children with idiopathic membranoproliferative glomerulonephritis: A long-term follow-up
-
11473682 10.1034/j.1399-3038.2001.012003166.x 1:STN:280: DC%2BD3MvjvFSmtQ%3D%3D
-
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
-
25
-
-
79958202220
-
Pre-emptive eculizumab and plasmapheresis for renal transplant in atypical hemolytic uremic syndrome
-
21617085 10.2215/CJN.10181110 1:CAS:528:DC%2BC3MXovFWntro%3D
-
Nester C, Stewart Z, Myers D, Jetton J, Nair R, Reed A, Thomas C, Smith R, Brophy P (2011) Pre-emptive eculizumab and plasmapheresis for renal transplant in atypical hemolytic uremic syndrome. Clin J Am Soc Nephrol 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
Thomas, C.7
Smith, R.8
Brophy, P.9
-
26
-
-
60649118722
-
Eculizumab for paroxysmal nocturnal haemoglobinuria
-
19144399 10.1016/S0140-6736(09)60001-5 1:CAS:528:DC%2BD1MXisVOrtrw%3D
-
Parker C (2009) Eculizumab for paroxysmal nocturnal haemoglobinuria. Lancet 373:759-767
-
(2009)
Lancet
, vol.373
, pp. 759-767
-
-
Parker, C.1
-
27
-
-
77957602105
-
New treatment options for atypical hemolytic uremic syndrome with the complement inhibitor eculizumab
-
20865644 10.1055/s-0030-1262889
-
Kose O, Zimmerhackl LB, Jungraithmayr T, Mache C, Nurnberger J (2010) New treatment options for atypical hemolytic uremic syndrome with the complement inhibitor eculizumab. Semin Thromb Hemost 36:669-672
-
(2010)
Semin Thromb Hemost
, vol.36
, pp. 669-672
-
-
Kose, O.1
Zimmerhackl, L.B.2
Jungraithmayr, T.3
Mache, C.4
Nurnberger, J.5
|