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Journal Abstract Search

272 related items for PubMed ID: 16898476

  • 1.
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  • 2. [The genetic basis of childhood nephrotic syndrome].
    Maruniak-Chudek I, Niemir ZI, Swietliński J.
    Postepy Hig Med Dosw (Online); 2004; 58():405-15. PubMed ID: 15577748
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  • 4. Genetic forms of nephrotic syndrome: a single-center experience in Brussels.
    Ismaili K, Pawtowski A, Boyer O, Wissing KM, Janssen F, Hall M.
    Pediatr Nephrol; 2009 Feb; 24(2):287-94. PubMed ID: 18709391
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  • 6. [Congenital nephrotic syndrome].
    Hattori M.
    Nihon Rinsho; 2004 Oct; 62(10):1861-6. PubMed ID: 15500131
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  • 10. [Congenital and infantile nephrotic syndrome].
    Niaudet P.
    Nephrol Ther; 2005 Mar; 1(1):63-70. PubMed ID: 16895669
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  • 11. Patients with different or identical genotypes of the WT1 gene present different phenotypes.
    Yang Y, Zhao F, Huang J, Nie X, Yu Z.
    Eur J Pediatr; 2013 Dec; 172(12):1707-8. PubMed ID: 23835859
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  • 13. [Congenital nephrotic syndrome of the Finnish type--key to the mechanisms of proteinuria].
    Holmberg C, Jalanko H.
    Duodecim; 2011 Dec; 127(10):1017-25. PubMed ID: 21696001
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  • 14. Detailed clinical manifestations at onset and prognosis of neonatal-onset Denys-Drash syndrome and congenital nephrotic syndrome of the Finnish type.
    Nishi K, Inoguchi T, Kamei K, Hamada R, Hataya H, Ogura M, Sato M, Yoshioka T, Ogata K, Ito S, Nakanishi K, Nozu K, Hamasaki Y, Ishikura K.
    Clin Exp Nephrol; 2019 Aug; 23(8):1058-1065. PubMed ID: 30963316
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  • 16. Case report: WT1 exon 6 truncation mutation and ambiguous genitalia in a patient with Denys-Drash syndrome.
    Chiang PW, Aliaga S, Travers S, Spector E, Tsai AC.
    Curr Opin Pediatr; 2008 Feb; 20(1):103-6. PubMed ID: 18197048
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  • 18. Two cases of congenital nephrotic syndrome.
    Iitaka K, Motoyama O, Hojo M, Iwanami N, Koshino H, Nakamura S, Moriya S.
    Clin Exp Nephrol; 2004 Jun; 8(2):146-9. PubMed ID: 15235932
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