VARIANT FORMS OF PHENYLKETONURIA
- 5 June 1976
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 307 (7971) , 1236-1237
- https://doi.org/10.1016/s0140-6736(76)92179-6
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- BIOPTERIN DERIVATIVES IN ATYPICAL PHENYLKETONURIAThe Lancet, 1976
- Determination of Phenylalanine Hydroxylase Activity in Patients with Phenylketonuria and HyperphenylalaninemiaPediatric Research, 1975
- TETRAHYDROBIOPTERIN TREATMENT OF VARIANT FORM OF PHENYLKETONURIAThe Lancet, 1975
- L-DOPA AND 5-HYDROXYTRYPTOPHAN THERAPY IN PHENYLKETONURIA WITH NORMAL PHENYLALANINE-HYDROXYLASE ACTIVITYThe Lancet, 1975
- Phenylketonuria Due to a Deficiency of Dihydropteridine ReductaseNew England Journal of Medicine, 1975
- NEW VARIANT OF PHENYLKETONURIA WITH PROGRESSIVE NEUROLOGICAL ILLNESS UNRESPONSIVE TO PHENYLALANINE RESTRICTIONThe Lancet, 1975
- A NEW MOLECULAR DEFECT IN PHENYLKETONURIAThe Lancet, 1974
- Subacute Necrotizing Encephalomyelopathy (Leigh's Disease): a Consideration of Clinical Features and EtiologyDevelopmental Medicine and Child Neurology, 1972
- A disease in infants resembling chronic Wernicke's encephalopathyThe Journal of Pediatrics, 1954
- SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY IN AN INFANTJournal of Neurology, Neurosurgery & Psychiatry, 1951