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Journal Abstract Search

230 related items for PubMed ID: 21696001

  • 1. [Congenital nephrotic syndrome of the Finnish type--key to the mechanisms of proteinuria].
    Holmberg C, Jalanko H.
    Duodecim; 2011; 127(10):1017-25. PubMed ID: 21696001
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  • 5. 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
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  • 7. Molecular basis of steroid-resistant nephrotic syndrome.
    Antignac C.
    Nefrologia; 2005 May 27; 25 Suppl 2():25-8. PubMed ID: 16050398
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  • 8. Proteinuria in congenital nephrotic syndrome of the Finnish type.
    Huttunen NP, Vehaskari M, Viikari M, Laipio ML.
    Clin Nephrol; 1980 Jan 27; 13(1):12-9. PubMed ID: 6988118
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  • 9. [New findings on the pathogenesis of nephrotic syndrome (review article)].
    Tesar V, Zima T, Kalousová M.
    Sb Lek; 2002 Jan 27; 103(3):379-95. PubMed ID: 12688182
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  • 11. 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
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  • 12. 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 15; 21(5):711-8. PubMed ID: 16518627
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  • 13. Discovery of the congenital nephrotic syndrome gene discloses the structure of the mysterious molecular sieve of the kidney.
    Tryggvason K, Ruotsalainen V, Wartiovaara J.
    Int J Dev Biol; 1999 May 15; 43(5):445-51. PubMed ID: 10535322
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  • 14. Genetic kidney diseases disclose the pathogenesis of proteinuria.
    Jalanko H, Patrakka J, Tryggvason K, Holmberg C.
    Ann Med; 2001 Nov 15; 33(8):526-33. PubMed ID: 11730159
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  • 16. [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 Nov 15; 63 Suppl 3():85-6. PubMed ID: 16898497
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  • 18. Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach.
    Gigante M, Monno F, Roberto R, Laforgia N, Assael MB, Livolti S, Caringella A, La Manna A, Masella L, Iolascon A.
    J Nephrol; 2002 Nov 15; 15(6):696-702. PubMed ID: 12495287
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  • 19. Congenital nephrotic syndrome of the Finnish type is not associated with the Pax-2 gene despite the promising transgenic animal model.
    Kestilä M, Männikkö M, Holmberg C, Tryggvason K, Peltonen L.
    Genomics; 1994 Feb 15; 19(3):570-2. PubMed ID: 8188301
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  • 20. [The genetic background of congenital nephrotic syndrome].
    Zwolińska D.
    Przegl Lek; 2006 Feb 15; 63 Suppl 3():10-1. PubMed ID: 16898476
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