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Journal Abstract Search

251 related items for PubMed ID: 232826

  • 1. [Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)].
    Brivet M, Moatti N, Lemonnier A.
    Ann Biol Clin (Paris); 1979; 37(5):259-70. PubMed ID: 232826
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  • 4. [Double heterozygosity (transferase-/epimerase-defect) and galactosemia cataract].
    Heyne K, Shin YS, Schwinger E.
    Monatsschr Kinderheilkd; 1988 Dec; 136(12):828-30. PubMed ID: 2853298
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  • 6. [Tests for galactose metabolism].
    Ohya N.
    Nihon Rinsho; 1997 Mar; 55 Suppl 1():244-7. PubMed ID: 9097598
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  • 11. Inexplicable infantile cataracts and partial maternal galactose disorder.
    Brivet M, Abadie V, Soni T, Cheron G, Dufier JL.
    Arch Dis Child; 1986 May; 61(5):445-8. PubMed ID: 3013103
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  • 13. [Congenital disorders of galactose metabolism].
    Sitzmann FC, Kaloud H.
    Med Klin; 1975 Mar 21; 70(12):491-8. PubMed ID: 165390
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  • 15. Galactosaemia: a new severe variant due to uridine diphosphate galactose-4-epimerase deficiency.
    Holton JB, Gillett MG, MacFaul R, Young R.
    Arch Dis Child; 1981 Nov 21; 56(11):885-7. PubMed ID: 7305435
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  • 16. [Galactosemia].
    Ohtake A, Amemiya S.
    Nihon Rinsho; 2006 Sep 28; Suppl 3():215-9. PubMed ID: 17022534
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  • 18. Structure and function of enzymes of the Leloir pathway for galactose metabolism.
    Holden HM, Rayment I, Thoden JB.
    J Biol Chem; 2003 Nov 07; 278(45):43885-8. PubMed ID: 12923184
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  • 20. [Galactosemia].
    Owada M.
    Tanpakushitsu Kakusan Koso; 1988 Apr 07; 33(5):647-51. PubMed ID: 3270877
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