Phenylketonuria.
Open Access
- 1 March 1971
- journal article
- Published by BMJ in Journal of Medical Genetics
- Vol. 8 (1) , 37-40
- https://doi.org/10.1136/jmg.8.1.37
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Evaluation of Treatment Begun in First Three Months of Life in 184 Cases of PhenylketonuriaArchives of Disease in Childhood, 1970
- CHILDREN OF MOTHERS WITH PHENYLKETONURIAThe Lancet, 1970
- Phenylketonuria and Intelligence: Trimodal Response to Dietary TreatmentNature, 1969
- Diagnosis of Phenylketonuria (Phenylalanine Hydroxylase Deficiency, Temporary and Permanent)BMJ, 1967
- Dietetic treatment of phenylketonuria: a follow-up study.BMJ, 1967
- PHENYLALANINE-HYDROXYLASE ACTIVITY IN HYPERPHENYLALANINÆMIAThe Lancet, 1967
- Legislation and advances in medical knowledge—acceleration or inhibition?The Journal of Pediatrics, 1966
- Megaloblastic Anaemia Complicating Dietary Treatment of Phenylketonuria in InfancyArchives of Disease in Childhood, 1962
- Phenylalanine as Inhibitor of Transport of Amino-Acids in BrainNature, 1961
- Further Experiences in the Treatment of PhenylketonuriaBMJ, 1961