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PUBMED FOR HANDHELDS

Journal Abstract Search


159 related items for PubMed ID: 9590058

  • 1.
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  • 2. [Glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)].
    Hayasaka K, Ikeda H.
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):332-5. PubMed ID: 9590060
    [No Abstract] [Full Text] [Related]

  • 3. Inborn errors of isoleucine degradation: a review.
    Korman SH.
    Mol Genet Metab; 2006 Dec; 89(4):289-99. PubMed ID: 16950638
    [Abstract] [Full Text] [Related]

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  • 5. [3-Hydroxyisobutyryl-CoA deacylase deficiency].
    Yoshida I.
    Ryoikibetsu Shokogun Shirizu; 1998 Dec; (18 Pt 1):314-6. PubMed ID: 9590055
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  • 9. [Isovaleric acidemia].
    Yoshida I.
    Ryoikibetsu Shokogun Shirizu; 1998 Dec; (18 Pt 1):280-3. PubMed ID: 9590047
    [No Abstract] [Full Text] [Related]

  • 10. [Glutaric aciduria type I: an organic acidemia without acidosis with severe movement disorders].
    Prats Viñas J.
    Neurologia; 2001 Oct; 16(8):337-41. PubMed ID: 11738010
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  • 15. [2,4-Dienoyl-CoA reductase deficiency].
    Kimura M, Yamaguchi S.
    Ryoikibetsu Shokogun Shirizu; 1998 Oct; (18 Pt 1):411-3. PubMed ID: 9590086
    [No Abstract] [Full Text] [Related]

  • 16. [Aciduria, glutaric (type 1)].
    Yamaguchi S.
    Ryoikibetsu Shokogun Shirizu; 2001 Oct; (33):106-7. PubMed ID: 11462353
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  • 19. [2-Ketoadipic dehydrogenase deficiency (2-ketoadipic acidemia)].
    Hayasaka K.
    Ryoikibetsu Shokogun Shirizu; 1998 Oct; (18 Pt 1):336-7. PubMed ID: 9590061
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