Author:
Takahashi T.,Kodama S.,Nishio H.,Takumi T.,Matsuo T.,Hase Y.,Sawada Y.
Subject
Genetics(clinical),Genetics
Reference18 articles.
1. Arai, N., Narisawa, K., Hayakawa, H. and Tada, K. Hyperphenylalaninaemia due to dihydropteridine reductase deficiency; diagnosis by enzyme assay on dried blood spot.Pediatrics 70 (1982) 205–214
2. Curtius, H.-Ch., Wang, M. and Niederwisser, A. X. Screening of newborn with hyperphenylalaninaemia for tetrahydrobiopterin. In Naruse, H. and Irie, M. (eds.)Neonatal Screening, Excerpta Medica, Amsterdam, 1983, pp. 191–200
3. Dhondt, J. L., Largilliue, C., Ardouin, P., Farriaux, J. P. and Dautrevaux, M. Diagnosis of variants of hyperphenyl-alaninaemia by determination of pterins in urine.Clin. Chim. Acta 110 (1981) 205–214
4. Dhondt, J. L., Ardouin, P., Hayte, J. M. and Farriaux, J. P. Developmental aspects of pteridine metabolism and relationships with phenylalanine metabolism.Clin. Chim. Acta 116 (1981) 143–152
5. Dhondt, J. L. Tetrahydrobiopterin deficiencies. Preliminary analysis from an international survey.J. Pediatr. 104 (1984) 501–508
Cited by
10 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