Author:
Niederwieser A.,Ponzone A.,Curtius H. -Ch.
Subject
Genetics(clinical),Genetics
Reference40 articles.
1. Arai, N., Narisawa, K., Hayakawa, H. and Tada, K. Hyperphenylalaninaemia due to dihydropteridine reductase deficiency: Diagnosis by enzyme assay on dried blood spots.Pediatrics 98 (1982) 426–430
2. Bartholomé, K. A new molecular defect in phenylketonuria.Lancet II (1974) 1980
3. Bartholomé, K. and Byrd, D. J.l-Dopa and 5-hydroxytryptophan therapy in phenylketonuria with normal phenylalanine hydroxylase activity.Lancet II (1975) 1042
4. Blau, N., Joller, P., Atares, M., Cardesa-Garcia, J. and Niederwieser, A. Increase of GTP cyclohydrolase I activity in mononuclear blood cells by stimulation: Detection of heterozygotes of GTP cyclohydrolase I deficiency.Clin. Chim. Acta (In press) (1985)
5. Blau, N. and Niederwieser, A. GTP-cyclohydrolase I assay in human and rat liver using high-performance liquid chromatography of neopterin phosphates and guanine nucleotides.Analyt. Biochem. 128 (1983) 446–452
Cited by
43 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献