Full text
PDFPage 242

Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Cutler P. Arginase deficiency and phenylketonuria. J Neurol Neurosurg Psychiatry. 1986 Sep;49(9):1090–1090. doi: 10.1136/jnnp.49.9.1090. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Govaerts L., Bakkeren J., Monnens L., Maas J., Trijbels F., Kleijer W. Disturbed very long chain (C24-C26) fatty acid pattern in fibroblasts of patients with Zellweger's syndrome. J Inherit Metab Dis. 1985;8(1):5–8. doi: 10.1007/BF01805473. [DOI] [PubMed] [Google Scholar]
- Howells D. W., Smith I., Hyland K. Estimation of tetrahydrobiopterin and other pterins in cerebrospinal fluid using reversed-phase high-performance liquid chromatography with electrochemical and fluorescence detection. J Chromatogr. 1986 Sep 5;381(2):285–294. doi: 10.1016/s0378-4347(00)83594-x. [DOI] [PubMed] [Google Scholar]
- Hyland K., Smith I., Clayton P. T., Leonard J. V. Impaired neurotransmitter amine metabolism in arginase deficiency. J Neurol Neurosurg Psychiatry. 1985 Nov;48(11):1188–1189. doi: 10.1136/jnnp.48.11.1188-a. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Leeming R. J., Barford P. A., Blair J. A., Smith I. Blood spots on Guthrie cards can be used for inherited tetrahydrobiopterin deficiency screening in hyperphenylalaninaemic infants. Arch Dis Child. 1984 Jan;59(1):58–61. doi: 10.1136/adc.59.1.58. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Milstien S., Kaufman S., Summer G. K. Hyperphenylalaninemia due to dihydropteridine reductase deficiency: diagnosis by measurement of oxidized and reduced pterins in urine. Pediatrics. 1980 Apr;65(4):806–810. [PubMed] [Google Scholar]
- Smith I., Leeming R. J., Cavanagh N. P., Hyland K. Neurological aspects of biopterin metabolism. Arch Dis Child. 1986 Feb;61(2):130–137. doi: 10.1136/adc.61.2.130. [DOI] [PMC free article] [PubMed] [Google Scholar]
