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Journal Abstract Search


74 related items for PubMed ID: 1450458

  • 1. Prenatal diagnosis of congenital nephrotic syndrome of Finnish type.
    Srsnová K, Bencat M, Srsen S, Miháliková J, Slávik P, Svihrová V.
    Funct Dev Morphol; 1992; 2(2):133-4. PubMed ID: 1450458
    [No Abstract] [Full Text] [Related]

  • 2. Heredity in the congenital nephrotic syndrome. A genetic study of 57 finnish FAMILIES WITH A REVIEW OF REPORTED CASES.
    Norio R.
    Ann Paediatr Fenn; 1966; 12():Suppl 27:1-94. PubMed ID: 5915041
    [No Abstract] [Full Text] [Related]

  • 3. [Congenital nephrotic syndrome - Finnish type].
    Mihatsch MJ, Rapola J.
    Verh Dtsch Ges Pathol; 1982; 66():307-11. PubMed ID: 7184252
    [No Abstract] [Full Text] [Related]

  • 4. Prenatal diagnosis of congenital nephrotic syndrome of non Finnish type.
    Braga S, Zimmermann A, Oetliker O.
    Prog Clin Biol Res; 1989; 305():199-203. PubMed ID: 2762353
    [No Abstract] [Full Text] [Related]

  • 5. 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; 16(3):207-13. PubMed ID: 8710773
    [Abstract] [Full Text] [Related]

  • 6. Congenital nephrotic syndrome: clinico-pathological heterogeneity and prenatal diagnosis.
    Schneller M, Braga SE, Moser H, Zimmermann A, Oetliker O.
    Clin Nephrol; 1983 May; 19(5):243-9. PubMed ID: 6851264
    [Abstract] [Full Text] [Related]

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  • 8. Early detection of congenital nephrotic syndrome of finnish type by the neonatal hypothyroid screening program.
    Lison M, Sack J, Katznelson D.
    Int J Pediatr Nephrol; 1983 Mar; 4(1):61. PubMed ID: 6853043
    [No Abstract] [Full Text] [Related]

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  • 10. [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; 33(2):153-6. PubMed ID: 2410560
    [Abstract] [Full Text] [Related]

  • 11. Amniotic alpha-fetoprotein in the prenatal diagnosis of congenital nephrotic syndrome of the Finnish type.
    Morris J, Ellwood D, Kennedy D, Knight J.
    Prenat Diagn; 1995 May; 15(5):482-5. PubMed ID: 7543998
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  • 13. [The Finnish-type congenital nephrotic syndrome. Comments on 2 cases].
    Sabău I, Potencz E.
    Rev Pediatr Obstet Ginecol Pediatr; 1989 May; 38(1):79-86. PubMed ID: 2505364
    [Abstract] [Full Text] [Related]

  • 14. 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]

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  • 16. [Prenatal diagnosis of a fetus affected with Finnish type congenital nephrotic syndrome].
    Chu Y, Hou Q, Wu D, Lou G, Yang K, Guo L, Qi N, Duan X, Wang W, Qin L, Liao S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct 10; 36(10):1022-1024. PubMed ID: 31598951
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  • 18. [Finnish nephrosis, a rare diagnosis in genetic counseling].
    Theile U, Schulte-Wissermann H, Becker K, Schofer O.
    Verh Dtsch Ges Pathol; 1982 Oct 10; 66():312-5. PubMed ID: 7184253
    [No Abstract] [Full Text] [Related]

  • 19. [Hydramnios with alpha fetoprotein increase: congenital nephrotic syndrome].
    Larbre F, Guibaud S, Guibaud P, Parchoux B, Chopard P, Kossmann JC, Dumont M.
    Pediatrie; 1979 Oct 10; 34(7):731-5. PubMed ID: 93268
    [No Abstract] [Full Text] [Related]

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