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Journal Abstract Search

94 related items for PubMed ID: 9590043

  • 1. [N5-methyltetrahydrofolate: homocysteine methyltransferase deficiency].
    Yoshino M.
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):267-8. PubMed ID: 9590043
    [No Abstract] [Full Text] [Related]

  • 2. [Inherited disorders of cobalamin metabolism].
    Sato K.
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):215-8. PubMed ID: 9645046
    [No Abstract] [Full Text] [Related]

  • 3. [Methylmalonic acidemia].
    Kawakami C, Tamai H.
    Ryoikibetsu Shokogun Shirizu; 2000; (32):358-61. PubMed ID: 11212744
    [No Abstract] [Full Text] [Related]

  • 4. [Isolated methylmalonyl-CoA mutase deficiency].
    Yoshino M.
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):269-72. PubMed ID: 9590044
    [No Abstract] [Full Text] [Related]

  • 5. Intractable Epilepsy due to MTR Deficiency: Importance of Homocysteine Analysis.
    Komulainen-Ebrahim J, Saastamoinen E, Rahikkala E, Helander H, Hinttala R, Risteli L, Rantala H, Uusimaa J.
    Neuropediatrics; 2017 Dec; 48(6):467-472. PubMed ID: 28666289
    [No Abstract] [Full Text] [Related]

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  • 7. Methionine synthase deficiency: a rare cause of adult-onset leukoencephalopathy.
    Outteryck O, de Sèze J, Stojkovic T, Cuisset JM, Dobbelaere D, Delalande S, Lacour A, Cabaret M, Lepoutre AC, Deramecourt V, Zéphir H, Fowler B, Vermersch P.
    Neurology; 2012 Jul 24; 79(4):386-8. PubMed ID: 22786600
    [No Abstract] [Full Text] [Related]

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  • 10. [Defects in adenosylcobalamin biosynthesis].
    Yoshino M.
    Ryoikibetsu Shokogun Shirizu; 1998 Jul 24; (18 Pt 1):273-5. PubMed ID: 9590045
    [No Abstract] [Full Text] [Related]

  • 11. [Lipoamide dehydrogenase deficiency].
    Ito M, Matsuda J.
    Ryoikibetsu Shokogun Shirizu; 1998 Jul 24; (18 Pt 1):341-2. PubMed ID: 9590063
    [No Abstract] [Full Text] [Related]

  • 12. [Pyruvate decarboxylase deficiency].
    Saijo T, Kuroda Y.
    Ryoikibetsu Shokogun Shirizu; 1998 Jul 24; (18 Pt 1):338-40. PubMed ID: 9590062
    [No Abstract] [Full Text] [Related]

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  • 14. [Inborn errors of catecholamine metabolism].
    Suzuki T.
    Ryoikibetsu Shokogun Shirizu; 1998 Jul 24; (19 Pt 2):640-4. PubMed ID: 9645154
    [No Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis for methylmalonic acidemia and inborn errors of vitamin B12 metabolism and transport.
    Morel CF, Watkins D, Scott P, Rinaldo P, Rosenblatt DS.
    Mol Genet Metab; 2005 Jul 24; 86(1-2):160-71. PubMed ID: 16150626
    [Abstract] [Full Text] [Related]

  • 16. [Adenosine triphosphate: glycerol 3-phosphotransferase deficiency].
    Yoshida I.
    Ryoikibetsu Shokogun Shirizu; 1998 Jul 24; (18 Pt 1):376-9. PubMed ID: 9590075
    [No Abstract] [Full Text] [Related]

  • 17. [Succinyl-CoA: 3-ketoacid CoA transferase deficiency].
    Fukao T.
    Ryoikibetsu Shokogun Shirizu; 1998 Jul 24; (18 Pt 1):355-8. PubMed ID: 9590068
    [No Abstract] [Full Text] [Related]

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