Biotin-responsive multiple carboxylase deficiency of infantile onset
- 1 September 1981
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 99 (3) , 421-423
- https://doi.org/10.1016/s0022-3476(81)80334-4
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Biotin-Responsive Carboxylase Deficiency Associated with Subnormal Plasma and Urinary BiotinNew England Journal of Medicine, 1981
- Intermittent ataxia and immunodeficiency with multiple carboxylase deficiencies: A biotin‐responsive disorderAnnals of Neurology, 1980
- Holocarboxylase synthetase deficiency: A biotin-responsive organic acidemiaThe Journal of Pediatrics, 1980
- Biotin-response OrganicaciduriaJournal of Clinical Investigation, 1979
- MULTIPLE BIOTIN-DEPENDENT CARBOXYLASE DEFICIENCIES ASSOCIATED WITH DEFECTS IN T-CELL AND B-CELL IMMUNITYThe Lancet, 1979
- BIOTIN-RESPONSIVE ALOPECIA AND DEVELOPMENTAL REGRESSIONThe Lancet, 1979
- Propionyl-CoA Carboxylase Deficiency in a Patient with Biotin-responsive 3-MethylcrotonylglycinuriaPediatric Research, 1977
- Deficiency of propionyl-CoA carboxylase and methylcrotonyl-CoA carboxylase in a patient with methylcrotonylglycinuriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1977
- BIOTIN-RESPONSIVE β-METHYLCROTONYLGLYCINURIAThe Lancet, 1971
- A new assay method for biotin in blood, serum, urine, and tissuesAnalytical Biochemistry, 1962