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Journal Abstract Search

172 related items for PubMed ID: 9097598

  • 1. [Tests for galactose metabolism].
    Ohya N.
    Nihon Rinsho; 1997 Mar; 55 Suppl 1():244-7. PubMed ID: 9097598
    [No Abstract] [Full Text] [Related]

  • 2. On the screening for inborn errors of galactose metabolism.
    Vaca G, Sànchez-Corona J, Olivares N, Medina C, Ibarra B, Cantú JM.
    Ann Genet; 1983 Mar; 26(3):191-2. PubMed ID: 6606384
    [Abstract] [Full Text] [Related]

  • 3. [Galactosemia].
    Ohtake A, Amemiya S.
    Nihon Rinsho; 2006 Sep 28; Suppl 3():215-9. PubMed ID: 17022534
    [No Abstract] [Full Text] [Related]

  • 4. Molecular basis of disorders of human galactose metabolism: past, present, and future.
    Novelli G, Reichardt JK.
    Mol Genet Metab; 2000 Sep 28; 71(1-2):62-5. PubMed ID: 11001796
    [Abstract] [Full Text] [Related]

  • 5. [Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)].
    Brivet M, Moatti N, Lemonnier A.
    Ann Biol Clin (Paris); 1979 Sep 28; 37(5):259-70. PubMed ID: 232826
    [Abstract] [Full Text] [Related]

  • 6. [Galactosemia].
    Grodzka Z, Zbieg-Sendecka E.
    Probl Med Wieku Rozwoj; 1979 Sep 28; 8():70-6. PubMed ID: 263529
    [Abstract] [Full Text] [Related]

  • 7. 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
    [No Abstract] [Full Text] [Related]

  • 8. Diagnosis of inherited disorders of galactose metabolism.
    Cuthbert C, Klapper H, Elsas L.
    Curr Protoc Hum Genet; 2008 Jan 07; Chapter 17():Unit 17.5. PubMed ID: 18428423
    [Abstract] [Full Text] [Related]

  • 9. Perinatal galactose metabolism.
    Kliegman RM, Sparks JW.
    J Pediatr; 1985 Dec 07; 107(6):831-41. PubMed ID: 3906069
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  • 11. [Double heterozygosity (transferase-/epimerase-defect) and galactosemia cataract].
    Heyne K, Shin YS, Schwinger E.
    Monatsschr Kinderheilkd; 1988 Dec 07; 136(12):828-30. PubMed ID: 2853298
    [Abstract] [Full Text] [Related]

  • 12. Rare cases of galactose metabolic disorders: identification of more than two mutations per patient.
    Schulpis KH, Thodi G, Chatzidaki M, Iakovou K, Molou E, Dotsikas Y, Loukas YL.
    J Pediatr Endocrinol Metab; 2017 Oct 26; 30(10):1119-1120. PubMed ID: 28902631
    [No Abstract] [Full Text] [Related]

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  • 14. [The diagnosis of galactosemia: screening or clinical diagnosis?].
    Derksen-Lubsen G.
    Ned Tijdschr Geneeskd; 1980 Jul 26; 124(30):1250-6. PubMed ID: 7412896
    [No Abstract] [Full Text] [Related]

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  • 20. [Identification of inborn errors of galactose metabolism in patients with cataracts].
    Vaca-Pacheco G, Medina C, García-Cruz D, Sánchez-Corona J, Chávez-Anaya E, Jaimes C, Hernández-Córdova A.
    Arch Invest Med (Mex); 1990 Jul 26; 21(2):127-32. PubMed ID: 2103700
    [Abstract] [Full Text] [Related]

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