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Journal Abstract Search

174 related items for PubMed ID: 8188301

  • 1. 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; 19(3):570-2. PubMed ID: 8188301
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  • 2. Deregulation of Pax-2 expression in transgenic mice generates severe kidney abnormalities.
    Dressler GR, Wilkinson JE, Rothenpieler UW, Patterson LT, Williams-Simons L, Westphal H.
    Nature; 1993 Mar 04; 362(6415):65-7. PubMed ID: 8383297
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  • 3. Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.
    Beltcheva O, Martin P, Lenkkeri U, Tryggvason K.
    Hum Mutat; 2001 May 04; 17(5):368-73. PubMed ID: 11317351
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  • 4. Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19.
    Kestilä M, Männikkö M, Holmberg C, Gyapay G, Weissenbach J, Savolainen ER, Peltonen L, Tryggvason K.
    Am J Hum Genet; 1994 May 04; 54(5):757-64. PubMed ID: 8178817
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  • 5. Noncollagenous matrix components of glomeruli in congenital nephrotic syndrome of the Finnish type: evidence of abnormal splitting of nidogen?
    Ljungberg P, Haltia A, Kuusela P, Jalanko H, Holmberg C, Holthöfer H.
    Exp Nephrol; 1996 May 04; 4(5):286-94. PubMed ID: 8931984
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  • 8. [Congenital and infantile nephrotic syndrome].
    Niaudet P.
    Nephrol Ther; 2005 Mar 04; 1(1):63-70. PubMed ID: 16895669
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  • 11. Genetic basis of nephrotic syndrome--review.
    Obeidová H, Merta M, Reiterová J, Maixnerová D, Stekrová J, Rysavá R, Tesar V.
    Prague Med Rep; 2006 Mar 04; 107(1):5-16. PubMed ID: 16752799
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  • 12. Exclusion of eight genes as mutated loci in congenital nephrotic syndrome of the Finnish type.
    Kestilä M, Männikkö M, Holmberg C, Korpela K, Savolainen ER, Peltonen L, Tryggvason K.
    Kidney Int; 1994 Apr 04; 45(4):986-90. PubMed ID: 8007602
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  • 13. Congenital nephrotic syndrome of Finnish type and other types of early familial nephrotic syndromes.
    Norio R.
    Birth Defects Orig Artic Ser; 1974 Apr 04; 10(4):69-72. PubMed ID: 4470912
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  • 14. Prenatal screening for congenital nephrosis in east Finland: results and impact on the birth prevalence of the disease.
    Heinonen S, Ryynänen M, Kirkinen P, Penttilä I, Syrjänen K, Seppälä M, Saarikoski S.
    Prenat Diagn; 1996 Mar 04; 16(3):207-13. PubMed ID: 8710773
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  • 15. The thickness of the glomerular basement membrane in congenital nephrotic syndrome of the Finnish type.
    Autio-Harmainen H, Rapola J.
    Nephron; 1983 Mar 04; 34(1):48-50. PubMed ID: 6855995
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  • 16. Renal pathology in congenital nephrotic syndrome of Finnish type: a quantitative light microscopic study on 50 patients.
    Huttunen NP, Rapola J, Vilska J, Hallman N.
    Int J Pediatr Nephrol; 1980 Mar 04; 1(1):10-6. PubMed ID: 7343522
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  • 17. [Congenital nephrotic syndrome of the Finnish type--key to the mechanisms of proteinuria].
    Holmberg C, Jalanko H.
    Duodecim; 2011 Mar 04; 127(10):1017-25. PubMed ID: 21696001
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  • 18. Molecular basis of steroid-resistant nephrotic syndrome.
    Antignac C.
    Nefrologia; 2005 Mar 04; 25 Suppl 2():25-8. PubMed ID: 16050398
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  • 19. [Genetic basis for malformation-associated uropathy and renal dysplasia].
    Oppezzo C, Barberis V, Edefonti A, Cusi D, Marra G.
    G Ital Nefrol; 2003 Mar 04; 20(2):120-6. PubMed ID: 12746796
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  • 20. [Genetic heterogeneity and pathology of congenital nephrotic syndrome and its significance in prenatal diagnosis].
    Braga S, Moser H, Zimmermann A, Oetliker O.
    J Genet Hum; 1985 Jun 04; 33(2):153-6. PubMed ID: 2410560
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