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Journal Abstract Search

134 related items for PubMed ID: 9590063

  • 21. [Mevalonic aciduria].
    Yoshida I.
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):305-9. PubMed ID: 9590053
    [No Abstract] [Full Text] [Related]

  • 22. Lipoamide dehydrogenase activity in lymphocytes.
    Berger I, Elpeleg ON, Saada A.
    Clin Chim Acta; 1996 Dec 30; 256(2):197-201. PubMed ID: 9027430
    [Abstract] [Full Text] [Related]

  • 23. A novel mutation in the dihydrolipoamide dehydrogenase E3 subunit gene (DLD) resulting in an atypical form of alpha-ketoglutarate dehydrogenase deficiency.
    Odièvre MH, Chretien D, Munnich A, Robinson BH, Dumoulin R, Masmoudi S, Kadhom N, Rötig A, Rustin P, Bonnefont JP.
    Hum Mutat; 2005 Mar 30; 25(3):323-4. PubMed ID: 15712224
    [Abstract] [Full Text] [Related]

  • 24. [Cytosolic acetoacetyl-CoA thiolase deficiency].
    Song XQ, Fukao T.
    Ryoikibetsu Shokogun Shirizu; 1998 Mar 30; (18 Pt 1):359-61. PubMed ID: 9590069
    [No Abstract] [Full Text] [Related]

  • 25. [D-2-hydroxyglutaric aciduria].
    Takayanagi M, Ogawa A.
    Ryoikibetsu Shokogun Shirizu; 1998 Mar 30; (18 Pt 1):389-91. PubMed ID: 9590078
    [No Abstract] [Full Text] [Related]

  • 26. [Trimethylaminuria].
    Yamaguchi S.
    Ryoikibetsu Shokogun Shirizu; 1998 Mar 30; (19 Pt 2):673-5. PubMed ID: 9645164
    [No Abstract] [Full Text] [Related]

  • 27. [Inherited metabolic diseases associated with West syndrome].
    Wada K, Sakuragawa N.
    Ryoikibetsu Shokogun Shirizu; 2002 Mar 30; (37 Pt 6):283-7. PubMed ID: 12483882
    [No Abstract] [Full Text] [Related]

  • 28. [Congenital enterokinase deficiency].
    Igarashi J, Shimizu T, Yamashiro Y.
    Ryoikibetsu Shokogun Shirizu; 1998 Mar 30; (19 Pt 2):661. PubMed ID: 9645159
    [No Abstract] [Full Text] [Related]

  • 29. A decrease in glycine cleavage activity in the liver of a patient with dihydrolipoyl dehydrogenase deficiency.
    Yoshino M, Koga Y, Yamashita F.
    J Inherit Metab Dis; 1986 Mar 30; 9(4):399-400. PubMed ID: 3104678
    [No Abstract] [Full Text] [Related]

  • 30. [Congenital hyaluronidase deficiency].
    Ohashi T.
    Ryoikibetsu Shokogun Shirizu; 1998 Mar 30; (19 Pt 2):453-4. PubMed ID: 9645107
    [No Abstract] [Full Text] [Related]

  • 31. Preclinical diagnosis and carrier detection in ataxia associated with abnormalities of lipoamide dehydrogenase.
    Kark RA, Rodriguez-Budelli M, Perlman S, Gulley WF, Torok K.
    Neurology; 1980 May 30; 30(5):502-8. PubMed ID: 6892725
    [Abstract] [Full Text] [Related]

  • 32. Clinical correlations of partial deficiency of lipoamide dehydrogenase.
    Kark RA, Rodriguez-Budelli MM.
    Neurology; 1979 Jul 30; 29(7):1006-13. PubMed ID: 572926
    [Abstract] [Full Text] [Related]

  • 33. [Organic acidemia, inborn errors of metabolism].
    Yamaguchi S.
    Ryoikibetsu Shokogun Shirizu; 2000 Jul 30; (29 Pt 4):398-409. PubMed ID: 11031982
    [No Abstract] [Full Text] [Related]

  • 34. Transcription factor GCN4 for control of amino acid biosynthesis also regulates the expression of the gene for lipoamide dehydrogenase.
    Zaman Z, Bowman SB, Kornfeld GD, Brown AJ, Dawes IW.
    Biochem J; 1999 Jun 15; 340 ( Pt 3)(Pt 3):855-62. PubMed ID: 10359673
    [Abstract] [Full Text] [Related]

  • 35. [Genetic injuries in 2 families with congenital methemoglobinemia caused by diaphorase I deficiency].
    Pedrinazzi RC, Della Cella G, Famularo L, Cerruti Mainardi P, Borrone C.
    Minerva Pediatr; 1969 May 05; 21(18):800-4. PubMed ID: 5404915
    [No Abstract] [Full Text] [Related]

  • 36. [Recessive congenital methemoglobinemia. Clinical and laboratory study of one case].
    Hermabessiere C, Poisson C, Leveque B, Leroux A, Kaplan JC.
    Ann Pediatr (Paris); 1976 Sep 05; 23(8-9):509-13. PubMed ID: 16104185
    [No Abstract] [Full Text] [Related]

  • 37. [Dihydropyrimidine dehydrogenase deficiency].
    Kouwaki M, Wada Y.
    Ryoikibetsu Shokogun Shirizu; 1998 Sep 05; (18 Pt 1):490-3. PubMed ID: 9590110
    [No Abstract] [Full Text] [Related]

  • 38. [Vitamin dependency syndrome].
    Kuroda Y, Naito E, Ito M.
    Ryoikibetsu Shokogun Shirizu; 2000 Sep 05; (29 Pt 4):437-43. PubMed ID: 11031989
    [No Abstract] [Full Text] [Related]

  • 39. [Very long-chain (and long-chain) acyl-CoA dehydrogenase deficiency].
    Yamaguchi S.
    Ryoikibetsu Shokogun Shirizu; 1998 Sep 05; (18 Pt 1):407-10. PubMed ID: 9590085
    [No Abstract] [Full Text] [Related]

  • 40. [3 beta-hydroxy-delta 5-C27-steroid-oxidoreductase/isomerase deficiency].
    Kamimura R, Maeda Y, Setoguchi T.
    Ryoikibetsu Shokogun Shirizu; 1998 Sep 05; (19 Pt 2):279-81. PubMed ID: 9645061
    [No Abstract] [Full Text] [Related]

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