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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

294 related items for PubMed ID: 3270877

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  • 7. [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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  • 10. 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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  • 11. The occurrence of the Leloir pathway in non-pathogenic mycobacteria.
    Szumiło T.
    Acta Microbiol Pol; 1981 Nov 07; 30(4):327-33. PubMed ID: 6179392
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  • 13. Pathophysiology and targets for treatment in hereditary galactosemia: A systematic review of animal and cellular models.
    Haskovic M, Coelho AI, Bierau J, Vanoevelen JM, Steinbusch LKM, Zimmermann LJI, Villamor-Martinez E, Berry GT, Rubio-Gozalbo ME.
    J Inherit Metab Dis; 2020 May 07; 43(3):392-408. PubMed ID: 31808946
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  • 17. Galactosemia caused by generalized uridine diphosphate galactose-4-epimerase deficiency.
    Garibaldi L, Superti-Furga A, Borrone C.
    J Pediatr; 1986 Dec 07; 109(6):1074-5. PubMed ID: 3783336
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  • 18. The fundamental importance of human galactose metabolism: lessons from genetics and biochemistry.
    Petry KG, Reichardt JK.
    Trends Genet; 1998 Mar 07; 14(3):98-102. PubMed ID: 9540406
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  • 19. Perinatal galactose metabolism.
    Kliegman RM, Sparks JW.
    J Pediatr; 1985 Dec 07; 107(6):831-41. PubMed ID: 3906069
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  • 20. Galactose toxicity in animals.
    Lai K, Elsas LJ, Wierenga KJ.
    IUBMB Life; 2009 Nov 07; 61(11):1063-74. PubMed ID: 19859980
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