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372 related items for PubMed ID: 16518627

  • 1. Recurrence of proteinuria following renal transplantation in congenital nephrotic syndrome of the Finnish type.
    Srivastava T, Garola RE, Kestila M, Tryggvason K, Ruotsalainen V, Sharma M, Savin VJ, Jalanko H, Warady BA.
    Pediatr Nephrol; 2006 May; 21(5):711-8. PubMed ID: 16518627
    [Abstract] [Full Text] [Related]

  • 2. Recurrence of nephrotic syndrome in kidney grafts of patients with congenital nephrotic syndrome of the Finnish type: role of nephrin.
    Patrakka J, Ruotsalainen V, Reponen P, Qvist E, Laine J, Holmberg C, Tryggvason K, Jalanko H.
    Transplantation; 2002 Feb 15; 73(3):394-403. PubMed ID: 11884936
    [Abstract] [Full Text] [Related]

  • 3. Plasma exchange and retransplantation in recurrent nephrosis of patients with congenital nephrotic syndrome of the Finnish type (NPHS1).
    Kuusniemi AM, Qvist E, Sun Y, Patrakka J, Rönnholm K, Karikoski R, Jalanko H.
    Transplantation; 2007 May 27; 83(10):1316-23. PubMed ID: 17519780
    [Abstract] [Full Text] [Related]

  • 4. Congenital nephrotic syndrome and recurrence of proteinuria after renal transplantation.
    Holmberg C, Jalanko H.
    Pediatr Nephrol; 2014 Dec 27; 29(12):2309-17. PubMed ID: 24682440
    [Abstract] [Full Text] [Related]

  • 5. [Congenital nephrotic syndrome].
    Hattori M.
    Nihon Rinsho; 2004 Oct 27; 62(10):1861-6. PubMed ID: 15500131
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  • 7. Recurrence of nephrotic syndrome after transplantation in CNF is due to autoantibodies to nephrin.
    Wang SX, Ahola H, Palmen T, Solin ML, Luimula P, Holthöfer H.
    Exp Nephrol; 2001 Oct 27; 9(5):327-31. PubMed ID: 11549850
    [Abstract] [Full Text] [Related]

  • 8. Cyclosporine A responsive congenital nephrotic syndrome with single heterozygous variants in NPHS1, NPHS2, and PLCE1.
    Eichinger A, Ponsel S, Bergmann C, Günthner R, Hoefele J, Amann K, Lange-Sperandio B.
    Pediatr Nephrol; 2018 Jul 27; 33(7):1269-1272. PubMed ID: 29663071
    [Abstract] [Full Text] [Related]

  • 9. Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome.
    Carraro M, Caridi G, Bruschi M, Artero M, Bertelli R, Zennaro C, Musante L, Candiano G, Perfumo F, Ghiggeri GM.
    J Am Soc Nephrol; 2002 Jul 27; 13(7):1946-52. PubMed ID: 12089392
    [Abstract] [Full Text] [Related]

  • 10. Recurrence of nephrotic syndrome after renal transplantation: influence of increased immunosuppression.
    Nathanson S, Cochat P, André JL, Guyot C, Loirat C, Nivet H, Deschênes G.
    Pediatr Nephrol; 2005 Dec 27; 20(12):1801-4. PubMed ID: 16228184
    [Abstract] [Full Text] [Related]

  • 11. Early recurrence of nephrotic syndrome (immunoglobulin m nephropathy) after renal transplantation successfully treated with combinations of plasma exchanges, immunoglobulin, and rituximab.
    Westphal S, Hansson S, Mjörnstedt L, Mölne J, Swerkersson S, Friman S.
    Transplant Proc; 2006 Oct 27; 38(8):2659-60. PubMed ID: 17098031
    [Abstract] [Full Text] [Related]

  • 12. [Congenital nephrotic syndrome of the Finnish type--key to the mechanisms of proteinuria].
    Holmberg C, Jalanko H.
    Duodecim; 2011 Oct 27; 127(10):1017-25. PubMed ID: 21696001
    [Abstract] [Full Text] [Related]

  • 13. Glomerular sclerosis in kidneys with congenital nephrotic syndrome (NPHS1).
    Kuusniemi AM, Merenmies J, Lahdenkari AT, Holmberg C, Salmela K, Karikoski R, Rapola J, Jalanko H.
    Kidney Int; 2006 Oct 27; 70(8):1423-31. PubMed ID: 16941028
    [Abstract] [Full Text] [Related]

  • 14. [Heterozygotic mutation in NPHS2 gene as a cause of familial steroid resistant nephrotic syndrome in two siblings--case report].
    Drozdz D, Pietrzyk JA, Wierzchowska-Słowiaczek E, Sancewicz-Pach K, Antignac C, Miezyński W.
    Przegl Lek; 2006 Oct 27; 63 Suppl 3():85-6. PubMed ID: 16898497
    [Abstract] [Full Text] [Related]

  • 15. Genetic kidney diseases disclose the pathogenesis of proteinuria.
    Jalanko H, Patrakka J, Tryggvason K, Holmberg C.
    Ann Med; 2001 Nov 27; 33(8):526-33. PubMed ID: 11730159
    [Abstract] [Full Text] [Related]

  • 16. Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.
    Trautmann A, Bodria M, Ozaltin F, Gheisari A, Melk A, Azocar M, Anarat A, Caliskan S, Emma F, Gellermann J, Oh J, Baskin E, Ksiazek J, Remuzzi G, Erdogan O, Akman S, Dusek J, Davitaia T, Özkaya O, Papachristou F, Firszt-Adamczyk A, Urasinski T, Testa S, Krmar RT, Hyla-Klekot L, Pasini A, Özcakar ZB, Sallay P, Cakar N, Galanti M, Terzic J, Aoun B, Caldas Afonso A, Szymanik-Grzelak H, Lipska BS, Schnaidt S, Schaefer F, PodoNet Consortium.
    Clin J Am Soc Nephrol; 2015 Apr 07; 10(4):592-600. PubMed ID: 25635037
    [Abstract] [Full Text] [Related]

  • 17. Glomerular endothelium in kidneys with congenital nephrotic syndrome of the Finnish type (NPHS1).
    Kaukinen A, Kuusniemi AM, Lautenschlager I, Jalanko H.
    Nephrol Dial Transplant; 2008 Apr 07; 23(4):1224-32. PubMed ID: 18048423
    [Abstract] [Full Text] [Related]

  • 18. Glomerular abundance of nephrin and podocin in experimental nephrotic syndrome: different effects of antiproteinuric therapies.
    Nakhoul F, Ramadan R, Khankin E, Yaccob A, Kositch Z, Lewin M, Assady S, Abassi Z.
    Am J Physiol Renal Physiol; 2005 Oct 07; 289(4):F880-90. PubMed ID: 15942045
    [Abstract] [Full Text] [Related]

  • 19. Congenital nephrotic syndrome of NPHS1 associated with cardiac malformation.
    Uysal B, Dönmez O, Uysal F, Akacı O, Vuruşkan BA, Berdeli A.
    Pediatr Int; 2015 Oct 07; 57(1):177-9. PubMed ID: 25711261
    [Abstract] [Full Text] [Related]

  • 20. Prediction and treatment of recurrent focal segmental glomerulosclerosis after renal transplantation in children.
    Dall'Amico R, Ghiggeri G, Carraro M, Artero M, Ghio L, Zamorani E, Zennaro C, Basile G, Montini G, Rivabella L, Cardillo M, Scalamogna M, Ginevri F.
    Am J Kidney Dis; 1999 Dec 07; 34(6):1048-55. PubMed ID: 10585314
    [Abstract] [Full Text] [Related]

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