These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 6135890)

  • 1. Biotinidase deficiency in juvenile multiple carboxylase deficiency.
    Thoene J; Wolf B
    Lancet; 1983 Aug; 2(8346):398. PubMed ID: 6135890
    [No Abstract]   [Full Text] [Related]  

  • 2. Deficient liver biotinidase activity in multiple carboxylase deficiency.
    Gaudry M; Munnich A; Saudubray JM; Ogier H; Mitchell G; Marsac C; Causse M; Marquet A; Frezal J
    Lancet; 1983 Aug; 2(8346):397. PubMed ID: 6135889
    [No Abstract]   [Full Text] [Related]  

  • 3. 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; 7 Suppl 2():123-5. PubMed ID: 6434862
    [No Abstract]   [Full Text] [Related]  

  • 4. Clinical and biochemical findings on a child with multiple biotin-responsive carboxylase deficiencies.
    Narisawa K; Arai N; Igarashi Y; Satoh T; Tada K; Hirooka Y
    J Inherit Metab Dis; 1982; 5(2):67-8. PubMed ID: 6133032
    [No Abstract]   [Full Text] [Related]  

  • 5. Biotinidase deficiency.
    Wolf B; Heard GS; McVoy JR; Grier RE
    Ann N Y Acad Sci; 1985; 447():252-62. PubMed ID: 3925856
    [No Abstract]   [Full Text] [Related]  

  • 6. Enzyme studies in biotin-responsive disorders.
    Bartlett K; Ghneim HK; Stirk HJ; Wastell H
    J Inherit Metab Dis; 1985; 8 Suppl 1():46-52. PubMed ID: 2864473
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic variation in biotinidase deficiency.
    Wolf B; Grier RE; Allen RJ; Goodman SI; Kien CL; Parker WD; Howell DM; Hurst DL
    J Pediatr; 1983 Aug; 103(2):233-7. PubMed ID: 6875714
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Biotin-responsive multiple carboxylase deficiency and immunodeficiency.
    Williams ML
    Curr Probl Dermatol; 1989; 18():89-92. PubMed ID: 2663376
    [No Abstract]   [Full Text] [Related]  

  • 9. Enzyme studies in combined carboxylase deficiency.
    Bartlett K; Ghneim HK; Stirk JH; Wastell HJ; Sherratt HS; Leonard JV
    Ann N Y Acad Sci; 1985; 447():235-51. PubMed ID: 2861780
    [No Abstract]   [Full Text] [Related]  

  • 10. Deficient biotinidase activity in late-onset multiple carboxylase deficiency.
    Wolf B; Grier RE; Parker WD; Goodman SI; Allen RJ
    N Engl J Med; 1983 Jan; 308(3):161. PubMed ID: 6848914
    [No Abstract]   [Full Text] [Related]  

  • 11. A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria.
    Bartlett K; Ng H; Leonard JV
    Clin Chim Acta; 1980 Jan; 100(2):183-6. PubMed ID: 6766095
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 144(1):21-6. PubMed ID: 3926500
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Biotinidase deficiency associated with renal loss of biocytin and biotin.
    Baumgartner ER; Suormala T; Wick H; Bausch J; Bonjour JP
    Ann N Y Acad Sci; 1985; 447():272-87. PubMed ID: 3925858
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multiple carboxylase deficiency.
    Nyhan WL
    Int J Biochem; 1988; 20(4):363-70. PubMed ID: 3284772
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Biotin-responsive multiple carboxylase deficiency of infantile onset.
    Packman S; Sweetman L; Yoshino M; Baker H; Cowan M
    J Pediatr; 1981 Sep; 99(3):421-3. PubMed ID: 7264799
    [No Abstract]   [Full Text] [Related]  

  • 17. Inborn errors of biotin metabolism.
    Nyhan WL
    Arch Dermatol; 1987 Dec; 123(12):1696-1698a. PubMed ID: 3318710
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A bioassay for determining biotinidase activity and for discriminating biocytin from biotin using holocarboxylase synthetase-deficient cultured fibroblasts.
    Weiner DL; Grier RE; Wolf B
    J Inherit Metab Dis; 1985; 8 Suppl 2():101-2. PubMed ID: 3930849
    [No Abstract]   [Full Text] [Related]  

  • 19. Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiency.
    Wolf B; Grier RE; Allen RJ; Goodman SI; Kien CL
    Clin Chim Acta; 1983 Jul; 131(3):273-81. PubMed ID: 6883721
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Inborn errors of biotin metabolism. Clinical and laboratory features of eight cases.
    Coşkun T; Tokatli A; Ozalp I
    Turk J Pediatr; 1994; 36(4):267-78. PubMed ID: 7825232
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.