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Journal Abstract Search

225 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
    [Abstract] [Full Text] [Related]

  • 2. Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients.
    Patrakka J, Kestilä M, Wartiovaara J, Ruotsalainen V, Tissari P, Lenkkeri U, Männikkö M, Visapää I, Holmberg C, Rapola J, Tryggvason K, Jalanko H.
    Kidney Int; 2000 Sep; 58(3):972-80. PubMed ID: 10972661
    [Abstract] [Full Text] [Related]

  • 3. [Congenital nephrotic syndrome].
    Hattori M.
    Nihon Rinsho; 2004 Oct; 62(10):1861-6. PubMed ID: 15500131
    [Abstract] [Full Text] [Related]

  • 4. Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.
    Beltcheva O, Martin P, Lenkkeri U, Tryggvason K.
    Hum Mutat; 2001 May; 17(5):368-73. PubMed ID: 11317351
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 6. [Responsible genes for proteinuria and concept of the treatment for proteinuria].
    Shimizu F.
    Nihon Rinsho; 2004 Oct 27; 62(10):1800-4. PubMed ID: 15500121
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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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  • 14. 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]

  • 15. Podocyte differentiation and hereditary proteinuria/nephrotic syndromes.
    Gubler MC.
    J Am Soc Nephrol; 2003 Jun 27; 14 Suppl 1():S22-6. PubMed ID: 12761234
    [Abstract] [Full Text] [Related]

  • 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 Jun 27; 63 Suppl 3():85-6. PubMed ID: 16898497
    [Abstract] [Full Text] [Related]

  • 17. Nephrin-signature molecule of the glomerular podocyte?
    Welsh GI, Saleem MA.
    J Pathol; 2010 Feb 27; 220(3):328-37. PubMed ID: 19950250
    [Abstract] [Full Text] [Related]

  • 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 Feb 27; 15(6):696-702. PubMed ID: 12495287
    [Abstract] [Full Text] [Related]

  • 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 27; 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 27; 63 Suppl 3():10-1. PubMed ID: 16898476
    [No Abstract] [Full Text] [Related]

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