Author:
G�ttler F.,Lou H.,Lykkelund C.,Niederwieser A.
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Reference26 articles.
1. Bartholom� K, Lutz P, Bickel H (1975) Determination of phenylalanine hydroxylase activity in patients with phenylketonuria and hyperphenylalaninemia. Pediatr Res 9:899?903
2. Bickel H (1980) Phenylketonuria: Past, present, future. J Inherited Metab Dis 3:123?132
3. Blaskovics ME, Shaw KNF (1971) Hyperphenylalaninemia: Method for differential diagnosis. In: Bickel H, Hudson FP, Woolf L (eds) Phenylketonunia and some other inborn errors of amino acid metabolism. Georg Thieme Verlag, Stuttgart, pp 98?102
4. Curtius H-Ch, Niederwieser A, Viscontini M, Otten A, Schaub J, Scheibenreiter S, Schmidt H (1979) Atypical phenylketonuria due to tetrahydrobiopterin deficiency, diagnosis and treatment with tetrahydrobiopterin, dihydrobiopterin and sepiapterin. Clin Chim Acta 93:251?262
5. Clow C, Scriver CR, Davies E (1969) Results of mass screning for hyperaminoacidemias in the newborn infant. Am J Dis Child 117:48?53
Cited by
18 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