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Volumn 29, Issue 12, 2014, Pages 2309-2317

Congenital nephrotic syndrome and recurrence of proteinuria after renal transplantation

Author keywords

Anti nephrin antibodies; Congenital nephrotic syndrome; Renephrosis; Rituximab

Indexed keywords


EID: 84896689301     PISSN: 0931041X     EISSN: 1432198X     Source Type: Journal    
DOI: 10.1007/s00467-014-2781-z     Document Type: Article
Times cited : (61)

References (46)
  • 1
    • 16244390295 scopus 로고    scopus 로고
    • Congenital nephrotic syndrome
    • Avner D-D, Harmon W-E, Niaudet P, Yoshikawa N, (eds), Springer, Berlin Heidelberg New York:
    • Jalanko H, Holmberg C (2009) Congenital nephrotic syndrome. In: Avner D-D, Harmon W-E, Niaudet P, Yoshikawa N (eds) Pediatric Nephrology, 6th edn. Springer, Berlin Heidelberg New York, pp S601–S619
    • (2009) Pediatric Nephrology , pp. S601-S619
    • Jalanko, H.1    Holmberg, C.2
  • 2
    • 84855183026 scopus 로고    scopus 로고
    • Focal segmental glomerulosclerosis
    • PID: 22187987
    • Agati VD, Kaskel FJ, Falk RJ (2011) Focal segmental glomerulosclerosis. N Engl J Med 365:2398–2411
    • (2011) N Engl J Med , vol.365 , pp. 2398-2411
    • Agati, V.D.1    Kaskel, F.J.2    Falk, R.J.3
  • 3
    • 0001027729 scopus 로고
    • Nephrotic syndrome in newborn and young infants
    • PID: 13373132, COI: 1:STN:280:DyaG2s%2FhvFagsQ%3D%3D
    • Ahvenainen EK, Hallman N, Hjelt L (1956) Nephrotic syndrome in newborn and young infants. Ann Paediatr Fenn 2:227–241
    • (1956) Ann Paediatr Fenn , vol.2 , pp. 227-241
    • Ahvenainen, E.K.1    Hallman, N.2    Hjelt, L.3
  • 6
    • 34548526982 scopus 로고    scopus 로고
    • Nephrin—a unique structural and signalling protein of the kidney filter
    • PID: 17766183, COI: 1:CAS:528:DC%2BD2sXhtVCnsrnO
    • Patrakka J, Tryggvason K (2007) Nephrin—a unique structural and signalling protein of the kidney filter. Trends Mol Med 13:396–403
    • (2007) Trends Mol Med , vol.13 , pp. 396-403
    • Patrakka, J.1    Tryggvason, K.2
  • 13
    • 17344364993 scopus 로고    scopus 로고
    • Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database
    • PID: 9529364, COI: 1:CAS:528:DyaK1cXlvVahsrg%3D
    • Jeanpierre C, Denamur E, Henry I, Cabanis MO, Luce S, Cécille A, Elion J, Peuchmaur M, Loirat C, Niaudet P, Gubler MC, Junien C (1998) Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database. Am J Hum Genet 62:824–833
    • (1998) Am J Hum Genet , vol.62 , pp. 824-833
    • Jeanpierre, C.1    Denamur, E.2    Henry, I.3    Cabanis, M.O.4    Luce, S.5    Cécille, A.6    Elion, J.7    Peuchmaur, M.8    Loirat, C.9    Niaudet, P.10    Gubler, M.C.11    Junien, C.12
  • 19
    • 84874453469 scopus 로고    scopus 로고
    • Pediatric kidney transplant practice patterns and autcome benchmarks, 1987–2010: A report of the North American Pediatric Renal Trials and Collaborative Studies
    • PID: 23281637
    • Smith JM, Matz K, Blydt-Hansen TD (2013) Pediatric kidney transplant practice patterns and autcome benchmarks, 1987–2010: A report of the North American Pediatric Renal Trials and Collaborative Studies. Pediatr Transplant 17:149–157
    • (2013) Pediatr Transplant , vol.17 , pp. 149-157
    • Smith, J.M.1    Matz, K.2    Blydt-Hansen, T.D.3
  • 20
    • 81855212739 scopus 로고    scopus 로고
    • Association between age and graft failure rates in young kidney transplant recipients
    • PID: 22124283
    • Foster BJ, Dahhou M, Zhang X, Platt RW, Samuel SM, Hanley JA (2011) Association between age and graft failure rates in young kidney transplant recipients. Transplantation 92:1237–1243
    • (2011) Transplantation , vol.92 , pp. 1237-1243
    • Foster, B.J.1    Dahhou, M.2    Zhang, X.3    Platt, R.W.4    Samuel, S.M.5    Hanley, J.A.6
  • 22
    • 84856459779 scopus 로고    scopus 로고
    • Racial disparities in pediatric access to kidney transplantation: does socioeconomic status play a role?
    • PID: 22226039, COI: 1:STN:280:DC%2BC387nvVOrtQ%3D%3D
    • Patzer RE, Amaral S, Klein M, Kutner N, Perryman JP, Gazmararian JA, McCellan WM (2012) Racial disparities in pediatric access to kidney transplantation: does socioeconomic status play a role? Am J Transplant 12:369–378
    • (2012) Am J Transplant , vol.12 , pp. 369-378
    • Patzer, R.E.1    Amaral, S.2    Klein, M.3    Kutner, N.4    Perryman, J.P.5    Gazmararian, J.A.6    McCellan, W.M.7
  • 23
    • 84872952913 scopus 로고    scopus 로고
    • Kidney graft survival in Europe and the United States: strikingly different long-term outcomes
    • PID: 23060279
    • Gondos A, Döhler B, Brenner H, Opelz G (2013) Kidney graft survival in Europe and the United States: strikingly different long-term outcomes. Transplantation 95:267–274
    • (2013) Transplantation , vol.95 , pp. 267-274
    • Gondos, A.1    Döhler, B.2    Brenner, H.3    Opelz, G.4
  • 25
    • 84870409438 scopus 로고    scopus 로고
    • Growth hormone treatment after renal transplantation: a promising but underused chance to improve growth
    • PID: 22948320
    • Mehls O, Fine RN (2013) Growth hormone treatment after renal transplantation: a promising but underused chance to improve growth. Pediatr Nephrol 28:1–4
    • (2013) Pediatr Nephrol , vol.28 , pp. 1-4
    • Mehls, O.1    Fine, R.N.2
  • 27
    • 84892825163 scopus 로고    scopus 로고
    • Parent-child and spousal relationship in families with a young child with end-stage renal disease
    • PID: 24018797
    • Laakkonen H, Taskinen S, Rönnholm K, Holmberg C, Sandberg S (2014) Parent-child and spousal relationship in families with a young child with end-stage renal disease. Pediatr Nephrol 29:289–295
    • (2014) Pediatr Nephrol , vol.29 , pp. 289-295
    • Laakkonen, H.1    Taskinen, S.2    Rönnholm, K.3    Holmberg, C.4    Sandberg, S.5
  • 31
    • 84875727696 scopus 로고    scopus 로고
    • TNFα pathway blockade ameliorate toxic effects of FSGS plasma on podocyte cytoskeleton and 3 integrin activation
    • PID: 22538781
    • Bitzan M, Babayeva S, Vasudevan A, Goodyear P, Torban E (2012) TNFα pathway blockade ameliorate toxic effects of FSGS plasma on podocyte cytoskeleton and 3 integrin activation. Pediatr Nephrol 27:2217–2226
    • (2012) Pediatr Nephrol , vol.27 , pp. 2217-2226
    • Bitzan, M.1    Babayeva, S.2    Vasudevan, A.3    Goodyear, P.4    Torban, E.5
  • 33
    • 0008520063 scopus 로고
    • Long-term survival of a girl with congenital nephrotic syndrome and recurrence of proteinuria after transplantation (abstr)
    • Sigström L, Hansson S, Jodal U (1989) Long-term survival of a girl with congenital nephrotic syndrome and recurrence of proteinuria after transplantation (abstr). Pediatr Nephrol 3:C169
    • (1989) Pediatr Nephrol , vol.3 , pp. C169
    • Sigström, L.1    Hansson, S.2    Jodal, U.3
  • 34
    • 0025727670 scopus 로고
    • Steroid-dependent nephrotic syndrome following renal transplantation for congenital nephrotic syndrome
    • PID: 1867984, COI: 1:STN:280:DyaK3MzivFWquw%3D%3D
    • Lane PH, Schnaper HW, Vernier RL, Bunchman TE (1991) Steroid-dependent nephrotic syndrome following renal transplantation for congenital nephrotic syndrome. Pediatr Nephrol 5:300–303
    • (1991) Pediatr Nephrol , vol.5 , pp. 300-303
    • Lane, P.H.1    Schnaper, H.W.2    Vernier, R.L.3    Bunchman, T.E.4
  • 35
    • 0027048991 scopus 로고
    • Treatment of steroid-resistant post-transplant nephrotic syndrome with cyclophosphamide in a child with congenital nephrotic syndrome
    • PID: 1482645, COI: 1:STN:280:DyaK3s7ivFGntQ%3D%3D
    • Flynn JT, Schulman SL, Dechaderevian J-P, Dunn SP, Kaiser BA, Polinsky MS, Baluarte HJ (1992) Treatment of steroid-resistant post-transplant nephrotic syndrome with cyclophosphamide in a child with congenital nephrotic syndrome. Pediatr Nephrol 6:553–555
    • (1992) Pediatr Nephrol , vol.6 , pp. 553-555
    • Flynn, J.T.1    Schulman, S.L.2    Dechaderevian, J.-P.3    Dunn, S.P.4    Kaiser, B.A.5    Polinsky, M.S.6    Baluarte, H.J.7
  • 37
    • 0032823921 scopus 로고    scopus 로고
    • Alport syndrome: an inherited disorder of renal, ocular and cochlear basement membranes
    • PID: 10499074, COI: 1:STN:280:DyaK1MvivVylsA%3D%3D
    • Kashtan CE (1999) Alport syndrome: an inherited disorder of renal, ocular and cochlear basement membranes. Medicine 78:338–360
    • (1999) Medicine , vol.78 , pp. 338-360
    • Kashtan, C.E.1
  • 38
    • 34249070747 scopus 로고    scopus 로고
    • Plasma exchange and retransplantation in recurrent nephrosis of patients with congenital nephrotic syndrome of the Finnish type
    • PID: 17519780
    • Kuusniemi A-M, Qvist E, Sun Y, Patrakka J, Rönnholm K, Karikoski R, Jalanko H (2007) Plasma exchange and retransplantation in recurrent nephrosis of patients with congenital nephrotic syndrome of the Finnish type. Transplantation 83:1316–1323
    • (2007) Transplantation , vol.83 , pp. 1316-1323
    • Kuusniemi, A.-M.1    Qvist, E.2    Sun, Y.3    Patrakka, J.4    Rönnholm, K.5    Karikoski, R.6    Jalanko, H.7
  • 40
    • 84863716525 scopus 로고    scopus 로고
    • Rituximab treatment for recurrence of nephrotic syndrome in a paediatric patient after renal transplantation for congenital nephrotic syndrome of the Finnish type
    • Chauduri A, Kambham N, Sutherland S, Grimm P, Alexander S, Conception W, Sarwal M, Wong C (2012) Rituximab treatment for recurrence of nephrotic syndrome in a paediatric patient after renal transplantation for congenital nephrotic syndrome of the Finnish type. Pediatric Transplant 16:E183–E187
    • (2012) Pediatric Transplant , vol.16 , pp. E183-E187
    • Chauduri, A.1    Kambham, N.2    Sutherland, S.3    Grimm, P.4    Alexander, S.5    Conception, W.6    Sarwal, M.7    Wong, C.8
  • 42
    • 33845633328 scopus 로고    scopus 로고
    • Recurrent nephrotic syndrome in homozygous truncating NPHS2 mutation is not due to anti-podocin antibodies
    • PID: 17109732, COI: 1:CAS:528:DC%2BD2sXps1Whug%3D%3D
    • Becker-Cohen R, Bruschi M, Rinat C, Feinstein S, Zennaro C, Ghicceri G, Frishberg Y (2007) Recurrent nephrotic syndrome in homozygous truncating NPHS2 mutation is not due to anti-podocin antibodies. Am J Transplant 7:256–260
    • (2007) Am J Transplant , vol.7 , pp. 256-260
    • Becker-Cohen, R.1    Bruschi, M.2    Rinat, C.3    Feinstein, S.4    Zennaro, C.5    Ghicceri, G.6    Frishberg, Y.7
  • 43
    • 3242795082 scopus 로고    scopus 로고
    • NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence
    • Weber S, Gribouval O, Esquivel E, Moriniere V, Tete M, Legendre C, Niaudet P, Antignac C (2004) NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence. Kidney Int 66:571–579
    • (2004) Kidney Int , vol.66 , pp. 571-579
    • Weber, S.1    Gribouval, O.2    Esquivel, E.3    Moriniere, V.4    Tete, M.5    Legendre, C.6    Niaudet, P.7    Antignac, C.8
  • 44
    • 33747845291 scopus 로고    scopus 로고
    • Recurrence of proteinuria 10 years post-transplant in NPHS2-associated focal segmental glomerulosclerosis after conversion from cyclosporin A to sirolimus
    • PID: 16721582
    • Höcker B, Knuppel T, Waldherr R, Schaefer F, Weber S, Tönshoff B (2006) Recurrence of proteinuria 10 years post-transplant in NPHS2-associated focal segmental glomerulosclerosis after conversion from cyclosporin A to sirolimus. Pediatr Nephrol 21:1476–1479
    • (2006) Pediatr Nephrol , vol.21 , pp. 1476-1479
    • Höcker, B.1    Knuppel, T.2    Waldherr, R.3    Schaefer, F.4    Weber, S.5    Tönshoff, B.6
  • 46
    • 79955086222 scopus 로고    scopus 로고
    • Living donor kidney transplantation in patients with hereditary nephropathies
    • PID: 20877305
    • Niaudet P (2010) Living donor kidney transplantation in patients with hereditary nephropathies. Nat Rev Nephrol 6:736–743
    • (2010) Nat Rev Nephrol , vol.6 , pp. 736-743
    • Niaudet, P.1


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