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Journal Abstract Search

215 related items for PubMed ID: 25711261

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  • 4. NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
    Guaragna MS, Cleto TL, Souza ML, Lutaif AC, de Castro LC, Penido MG, Maciel-Guerra AT, Belangero VM, Guerra-Junior G, De Mello MP.
    Nephrology (Carlton); 2016 Sep; 21(9):753-7. PubMed ID: 26560236
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  • 5. Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.
    Koziell A, Grech V, Hussain S, Lee G, Lenkkeri U, Tryggvason K, Scambler P.
    Hum Mol Genet; 2002 Feb 15; 11(4):379-88. PubMed ID: 11854170
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  • 11. 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. Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome.
    Sako M, Nakanishi K, Obana M, Yata N, Hoshii S, Takahashi S, Wada N, Takahashi Y, Kaku Y, Satomura K, Ikeda M, Honda M, Iijima K, Yoshikawa N.
    Kidney Int; 2005 Apr 15; 67(4):1248-55. PubMed ID: 15780077
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  • 17. No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations.
    Schultheiss M, Ruf RG, Mucha BE, Wiggins R, Fuchshuber A, Lichtenberger A, Hildebrandt F.
    Pediatr Nephrol; 2004 Dec 15; 19(12):1340-8. PubMed ID: 15338398
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  • 19. NPHS1 gene mutation in Japanese patients with congenital nephrotic syndrome.
    Aya K, Shimizu J, Ohtomo Y, Satomura K, Suzuki H, Yan K, Sado Y, Morishima T, Tanaka H.
    Nephrol Dial Transplant; 2009 Aug 15; 24(8):2411-4. PubMed ID: 19321760
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