Biotin-related abnormalities in human metabolism

This publication has 13 references indexed in Scilit:

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  The Journal of Pediatrics, 1983
• Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.
  Journal of Clinical Investigation, 1981
• Biotin-Responsive Carboxylase Deficiency Associated with Subnormal Plasma and Urinary Biotin
  New England Journal of Medicine, 1981
• Deficient acetyl CoA carboxylase activity in multiple carboxylase deficiency
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1981
• Serum and urinary biotin levels during treatment of holocarboxylase synthetase deficiency
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1981
• A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1980
• Biotin-response Organicaciduria
  Journal of Clinical Investigation, 1979
• MULTIPLE BIOTIN-DEPENDENT CARBOXYLASE DEFICIENCIES ASSOCIATED WITH DEFECTS IN T-CELL AND B-CELL IMMUNITY
  The Lancet, 1979
• Deficiency of propionyl-CoA carboxylase and methylcrotonyl-CoA carboxylase in a patient with methylcrotonylglycinuria
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1977
• BIOTIN-RESPONSIVE β-METHYLCROTONYLGLYCINURIA
  The Lancet, 1971