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Journal Abstract Search

132 related items for PubMed ID: 165390

  • 1. [Congenital disorders of galactose metabolism].
    Sitzmann FC, Kaloud H.
    Med Klin; 1975 Mar 21; 70(12):491-8. PubMed ID: 165390
    [No Abstract] [Full Text] [Related]

  • 2. [Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)].
    Brivet M, Moatti N, Lemonnier A.
    Ann Biol Clin (Paris); 1979 Mar 21; 37(5):259-70. PubMed ID: 232826
    [Abstract] [Full Text] [Related]

  • 3. [Screening of newborns for inborn errors of galactose metabolism. Methods and results].
    Gitzelmann R.
    Monatsschr Kinderheilkd (1902); 1976 Sep 21; 129(9):654-7. PubMed ID: 185513
    [Abstract] [Full Text] [Related]

  • 4. [Gene frequency of hereditary galactosemia with reference to the Duarte variant].
    Kaloud H, Sitzmann FC.
    Z Kinderheilkd; 1972 Sep 21; 113(3):205-14. PubMed ID: 4674437
    [No Abstract] [Full Text] [Related]

  • 5. Newborn screening for galactosemia and other galactose metabolic defects.
    Levy HL, Hammersen G.
    J Pediatr; 1978 Jun 21; 92(6):871-7. PubMed ID: 660351
    [No Abstract] [Full Text] [Related]

  • 6. Screening for galactosemia. Studies of the gene frequencies for galactosemia and the Duarte variant.
    Beutler E.
    Isr J Med Sci; 1973 Jun 21; 9(9):1323-9. PubMed ID: 4149512
    [No Abstract] [Full Text] [Related]

  • 7. Maternal enzymes of galactose metabolism and the "inexplicable" infantile cataract.
    Harley JD, Mutton P, Irvine S, Gupta JD.
    Lancet; 1974 Aug 03; 2(7875):259-61. PubMed ID: 4136146
    [No Abstract] [Full Text] [Related]

  • 8. [Galactose-1-phosphate uridyltransferase deficiency].
    Okano Y, Isshiki G.
    Ryoikibetsu Shokogun Shirizu; 1998 Aug 03; (18 Pt 1):15-21. PubMed ID: 9589977
    [No Abstract] [Full Text] [Related]

  • 9. [Clinical and morphological findings in during galactosemia].
    Roschlau G, Hinkel GK, Gottschalk B.
    Monatsschr Kinderheilkd (1902); 1969 Jan 03; 117(1):7-13. PubMed ID: 5407995
    [No Abstract] [Full Text] [Related]

  • 10. Normal pregnancy and childbirth in a galactosemic woman.
    Tedesco TA, Morrow G, Mellman WJ.
    J Pediatr; 1972 Dec 03; 81(6):1159-61. PubMed ID: 4674573
    [No Abstract] [Full Text] [Related]

  • 11. A patient with hereditary galactokinase deficiency.
    Dahlqvist A, Gamstorp I, Madsen H.
    Acta Paediatr Scand; 1970 Nov 03; 59(6):669-75. PubMed ID: 5482251
    [No Abstract] [Full Text] [Related]

  • 12. Galactosaemia and the problem of galactose toxicity.
    Schwarz V.
    Biochem Soc Trans; 1975 Nov 03; 3(2):234-8. PubMed ID: 165990
    [No Abstract] [Full Text] [Related]

  • 13. Galactose metabolism of the red cell.
    Ng WG.
    Exp Eye Res; 1971 May 03; 11(3):402-14. PubMed ID: 4942259
    [No Abstract] [Full Text] [Related]

  • 14. [Gene frequencies of both forms of galactosaemia in the western Hungarian province of Vas (author's transl)].
    Sitzmann FC, Istvan L, Teubl I, Kaloud H, Cholnoky P.
    Wien Klin Wochenschr; 1978 Jan 06; 90(1):16-20. PubMed ID: 204112
    [Abstract] [Full Text] [Related]

  • 15. [Diagnosis and therapy of 6 hereditary, to mental-deficiency-leading, metabolic disorders. 2].
    Menne F, Enzenauer J, Matz D.
    Med Klin; 1976 Apr 30; 71(18):779-85. PubMed ID: 178988
    [No Abstract] [Full Text] [Related]

  • 16. [Early diagnosis of congenital disorders].
    Méhes K.
    Orv Hetil; 1978 Jul 23; 119(30):1819-23. PubMed ID: 353640
    [No Abstract] [Full Text] [Related]

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  • 19. [Galactosemia].
    Grodzka Z, Zbieg-Sendecka E.
    Probl Med Wieku Rozwoj; 1979 Jul 23; 8():70-6. PubMed ID: 263529
    [Abstract] [Full Text] [Related]

  • 20. [Double heterozygosity (transferase-/epimerase-defect) and galactosemia cataract].
    Heyne K, Shin YS, Schwinger E.
    Monatsschr Kinderheilkd; 1988 Dec 23; 136(12):828-30. PubMed ID: 2853298
    [Abstract] [Full Text] [Related]

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