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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

118 related items for PubMed ID: 4193693

  • 21.
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  • 23. Prenatal diagnosis and family studies in a case of propionicacidaemia.
    Gompertz D, Goodey PA, Thom H, Russell G, Johnston AW, Mellor DH, MacLean MW, Ferguson-Smith ME, Ferguson-Smith MA.
    Clin Genet; 1975 Oct; 8(4):244-50. PubMed ID: 1183068
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  • 24. Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.
    Burri BJ, Sweetman L, Nyhan WL.
    J Clin Invest; 1981 Dec; 68(6):1491-5. PubMed ID: 6798072
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  • 27. Evaluation of cofactor responsiveness.
    Leonard JV, Daish P.
    J Inherit Metab Dis; 1985 Dec; 8 Suppl 1():17-9. PubMed ID: 3930836
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  • 28. Defective biotin absorption in multiple carboxylase deficiency.
    Munnich A, Saudubray JM, Carré G, Coudé FX, Ogier H, Charpentier C, Frézal J.
    Lancet; 1981 Aug 01; 2(8240):263. PubMed ID: 6114319
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  • 29. Propionicacidemia (ketotic hyperglycinemia): dietary treatment resulting in normal growth and development.
    Brandt IK, Hsia YE, Clement DH, Provence SA.
    Pediatrics; 1974 Mar 01; 53(3):391-5. PubMed ID: 4815259
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  • 31. Biotin-responsive multiple carboxylase deficiency of infantile onset.
    Packman S, Sweetman L, Yoshino M, Baker H, Cowan M.
    J Pediatr; 1981 Sep 01; 99(3):421-3. PubMed ID: 7264799
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  • 32. Excretion of propionylglycine in propionic acidaemia.
    Rasmussen K, Ando T, Nyhan WL, Hull D, Cottom D, Donnell G, Wadlington W, Kilroy AW.
    Clin Sci; 1972 Jun 01; 42(6):665-71. PubMed ID: 5033805
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  • 33. Biotinidase deficiency in juvenile multiple carboxylase deficiency.
    Thoene J, Wolf B.
    Lancet; 1983 Aug 13; 2(8346):398. PubMed ID: 6135890
    [No Abstract] [Full Text] [Related]

  • 34. An inherited disorder of isoleucine catabolism causing accumulation of alpha-methylacetoacetate and alpha-methyl-beta -hydroxybutyrate, and intermittent metabolic acidosis.
    Daum RS, Scriver CR, Mamer OA, Delvin E, Lamm P, Goldman H.
    Pediatr Res; 1973 Mar 13; 7(3):149-60. PubMed ID: 4690360
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  • 35. Biotin in clinical medicine--a review.
    Roth KS.
    Am J Clin Nutr; 1981 Sep 13; 34(9):1967-74. PubMed ID: 6116428
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  • 36. Multiple biotin-dependent carboxylase deficiencies associated with defects in T-cell and B-cell immunity.
    Cowan MJ, Wara DW, Packman S, Ammann AJ, Yoshino M, Sweetman L, Nyhan W.
    Lancet; 1979 Jul 21; 2(8134):115-8. PubMed ID: 88554
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  • 37. Intermittent ataxia and immunodeficiency with multiple carboxylase deficiencies: a biotin-responsive disorder.
    Sander JE, Malamud N, Cowan MJ, Packman S, Amman AJ, Wara DW.
    Ann Neurol; 1980 Nov 21; 8(5):544-7. PubMed ID: 7436398
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  • 39. Alopecia and periorificial dermatitis in biotin-responsive multiple carboxylase deficiency.
    Williams ML, Packman S, Cowan MJ.
    J Am Acad Dermatol; 1983 Jul 21; 9(1):97-103. PubMed ID: 6886110
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  • 40. Serum and urinary biotin levels during treatment of holocarboxylase synthetase deficiency.
    Roth KS, Allan L, Yang W, Foreman JW, Dakshinamurti K.
    Clin Chim Acta; 1981 Feb 05; 109(3):337-40. PubMed ID: 7226522
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