Neonatal hyperphenylalaninemia presumably caused by guanosine triphosphate-cyclohydrolase deficiency
- 30 June 1985
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 106 (6) , 954-956
- https://doi.org/10.1016/s0022-3476(85)80251-1
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
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- Guanosine triphosphate cyclohydrolase activity in rat tissuesBiochemical Journal, 1984
- Blood spots on Guthrie cards can be used for inherited tetrahydrobiopterin deficiency screening in hyperphenylalaninaemic infants.Archives of Disease in Childhood, 1984
- Hepatic phenylalanine hydroxylase activity in hyperphenylalaninaemiaJournal of Inherited Metabolic Disease, 1981
- Diagnosis of variants of hyperphenylalaninemia by determination of pterins in urineClinica Chimica Acta; International Journal of Clinical Chemistry, 1981