Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Genetics(clinical),General Medicine
Reference61 articles.
1. Scriver C, Kaufmann S. The metabolic and molecular basis of inherited disease. In: Hill M-G, editor. Hyperphenylalaninemia: Phenylalanine Hydroxylase Deficiency; 2001. p. 1667–724.
2. Bickel H, Gerrard J, Hickmans E. Influence of phenylalanine intake on phenylketonuria. Lancet. 1953;265(6790):812–3.
3. Guthrie R, Susi A. A simple phenylalanine method for detecting phenylketonuria in large populations in newborn infants. Pediatrics. 1963;32:338–43.
4. Robertson LV, McStravick N, Ripley S, Weetch E, Donald S, Adam S, et al. Body mass index in adult patients with diet-treated phenylketonuria. J Hum Nutr Diet. 2013;26(s1):1–6.
5. Hennermann JB, Roloff S, Gellermann J, Vollmer I, Windt E, Vetter B, et al. Chronic kidney disease in adolescent and adult patients with phenylketonuria. J Inherit Metab Dis. 2013;36(5):747–56.
Cited by
38 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