Vitamin-responsive genetic disease
Open Access
- 1 January 1974
- journal article
- inborn errors-of-metabolism
- Published by BMJ in Journal of Clinical Pathology
- Vol. 27 (Suppl 8) , 38-47
- https://doi.org/10.1136/jcp.27.suppl_8.38
Abstract
No abstract availableThis publication has 45 references indexed in Scilit:
- Coenzyme dissociation, a possible determinant of short half-life of inducible enzymes in mammalian liverBiochemical and Biophysical Research Communications, 1973
- Combined vitamin responsiveness in homocystinuriaThe Journal of Pediatrics, 1972
- Homocystinuria associated with decreased methylenetetrahydrofolate reductase activityBiochemical and Biophysical Research Communications, 1972
- Defective metabolism of vitamin B12 in fibroblasts from children with methylmalonicaciduriaBiochemical and Biophysical Research Communications, 1971
- Homocystinuria with methylmalonic aciduria: Two cases in a sibshipBiochemical Medicine, 1970
- BIOTIN-RESPONSIVE PROPIONICACIDÆMIAThe Lancet, 1970
- Cystathioninemia: A benign genetic conditionThe Journal of Pediatrics, 1970
- Thiamine-responsive megaloblastic anemiaThe Journal of Pediatrics, 1969
- Vitamin B6 Dependent Xanthurenic AciduriaThe Tohoku Journal of Experimental Medicine, 1967
- Cystathioninuria: Study of an infant withnormal mentality, thrombocytopenia, and renal calculiThe Journal of Pediatrics, 1966