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Journal Abstract Search

223 related items for PubMed ID: 3920902

  • 1. Heterogeneity of holocarboxylase synthetase in patients with biotin-responsive multiple carboxylase deficiency.
    Burri BJ, Sweetman L, Nyhan WL.
    Am J Hum Genet; 1985 Mar; 37(2):326-37. PubMed ID: 3920902
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  • 6. Enzyme studies in combined carboxylase deficiency.
    Bartlett K, Ghneim HK, Stirk JH, Wastell HJ, Sherratt HS, Leonard JV.
    Ann N Y Acad Sci; 1985 Mar; 447():235-51. PubMed ID: 2861780
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  • 8. Enzyme studies in biotin-responsive disorders.
    Bartlett K, Ghneim HK, Stirk HJ, Wastell H.
    J Inherit Metab Dis; 1985 Mar; 8 Suppl 1():46-52. PubMed ID: 2864473
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  • 10. Acetyl CoA carboxylase in cultured fibroblasts: differential biotin dependence in the two types of biotin-responsive multiple carboxylase deficiency.
    Packman S, Caswell N, Gonzalez-Rios MC, Kadlecek T, Cann H, Rassin D, McKay C.
    Am J Hum Genet; 1984 Jan; 36(1):80-92. PubMed ID: 6141728
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  • 11. Biotin-responsive multiple carboxylase deficiency (MCD): deficient biotinidase activity associated with renal loss of biotin.
    Baumgartner ER, Suormala T, Wick H, Bonjour JP.
    J Inherit Metab Dis; 1984 Jan; 7 Suppl 2():123-5. PubMed ID: 6434862
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  • 12. Biotin holocarboxylase synthetase deficiency.
    Sweetman L, Burri BJ, Nyhan WL.
    Ann N Y Acad Sci; 1985 Jan; 447():288-96. PubMed ID: 3860175
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  • 18. Fatty-acid-responsive alopecia in multiple carboxylase deficiency.
    Munnich A, Saudubray JM, Coude FX, Charpentier C, Saurat JH, Frezal J.
    Lancet; 1980 May 17; 1(8177):1080-1. PubMed ID: 6103410
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  • 19. Intestinal absorption and renal excretion of biotin in patients with biotinidase deficiency.
    Suormala T, Wick H, Bonjour JP, Baumgartner ER.
    Eur J Pediatr; 1985 May 17; 144(1):21-6. PubMed ID: 3926500
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