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Journal Abstract Search

134 related items for PubMed ID: 9590063

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

  • 2. Biochemical and molecular diagnosis of lipoamide dehydrogenase deficiency in a North American Ashkenazi Jewish family.
    Sansaricq C, Pardo S, Balwani M, Grace M, Raymond K.
    J Inherit Metab Dis; 2006 Feb; 29(1):203-4. PubMed ID: 16601893
    [Abstract] [Full Text] [Related]

  • 3. Lipoamide dehydrogenase deficiency in Ashkenazi Jews: an insertion mutation in the mitochondrial leader sequence.
    Elpeleg ON, Shaag A, Glustein JZ, Anikster Y, Joseph A, Saada A.
    Hum Mutat; 1997 Feb; 10(3):256-7. PubMed ID: 9298831
    [No Abstract] [Full Text] [Related]

  • 4. Lipoamide dehydrogenase deficiency: a new cause for recurrent myoglobinuria.
    Elpeleg ON, Saada AB, Shaag A, Glustein JZ, Ruitenbeek W, Tein I, Halevy J.
    Muscle Nerve; 1997 Feb; 20(2):238-40. PubMed ID: 9040667
    [No Abstract] [Full Text] [Related]

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

  • 9. [Fumarase deficiency].
    Miyabayashi S.
    Ryoikibetsu Shokogun Shirizu; 1998 Feb; (18 Pt 1):351-4. PubMed ID: 9590067
    [No Abstract] [Full Text] [Related]

  • 10. [Mitochondrial acetoacetyl-CoA thiolase deficiency].
    Fukao T.
    Ryoikibetsu Shokogun Shirizu; 1998 Feb; (18 Pt 1):310-3. PubMed ID: 9590054
    [No Abstract] [Full Text] [Related]

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

  • 12. Lipoamide dehydrogenase deficiency due to a novel mutation in the interface domain.
    Shany E, Saada A, Landau D, Shaag A, Hershkovitz E, Elpeleg ON.
    Biochem Biophys Res Commun; 1999 Aug 19; 262(1):163-6. PubMed ID: 10448086
    [Abstract] [Full Text] [Related]

  • 13. Molecular basis of lipoamide dehydrogenase deficiency in Ashkenazi Jews.
    Shaag A, Saada A, Berger I, Mandel H, Joseph A, Feigenbaum A, Elpeleg ON.
    Am J Med Genet; 1999 Jan 15; 82(2):177-82. PubMed ID: 9934985
    [Abstract] [Full Text] [Related]

  • 14. Novel mutations in a boy with dihydrolipoamide dehydrogenase deficiency.
    Cerna L, Wenchich L, Hansiková H, Kmoch S, Peskova K, Chrastina P, Brynda J, Zeman J.
    Med Sci Monit; 2001 Jan 15; 7(6):1319-25. PubMed ID: 11687750
    [Abstract] [Full Text] [Related]

  • 15. [N5-methyltetrahydrofolate: homocysteine methyltransferase deficiency].
    Yoshino M.
    Ryoikibetsu Shokogun Shirizu; 1998 Jan 15; (18 Pt 1):267-8. PubMed ID: 9590043
    [No Abstract] [Full Text] [Related]

  • 16. Lipoamide dehydrogenase deficiency.
    Robinson BH, Sherwood WG, Kahler S, O'Flynn ME, Nadler H.
    N Engl J Med; 1981 Jan 01; 304(1):53-4. PubMed ID: 6893619
    [No Abstract] [Full Text] [Related]

  • 17. [Cholinesterase deficiency].
    Hada T.
    Ryoikibetsu Shokogun Shirizu; 1998 Jan 01; (19 Pt 2):649-52. PubMed ID: 9645156
    [No Abstract] [Full Text] [Related]

  • 18. [Inborn errors of catecholamine metabolism].
    Suzuki T.
    Ryoikibetsu Shokogun Shirizu; 1998 Jan 01; (19 Pt 2):640-4. PubMed ID: 9645154
    [No Abstract] [Full Text] [Related]

  • 19. [Isovaleric acidemia].
    Yoshida I.
    Ryoikibetsu Shokogun Shirizu; 1998 Jan 01; (18 Pt 1):280-3. PubMed ID: 9590047
    [No Abstract] [Full Text] [Related]

  • 20. Lipoamide dehydrogenase deficiency: a newly discovered cause of acute hepatitis in adults.
    Barak N, Huminer D, Segal T, Ben Ari Z, Halevy J, Tur-Kaspa R.
    J Hepatol; 1998 Sep 01; 29(3):482-4. PubMed ID: 9764998
    [Abstract] [Full Text] [Related]

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