1.
Malignant phenylketonuria presented with paroxysmal movement disorders:report of one case and review of the literature
以阵发性运动障碍为表现的恶性苯丙酮尿症1例及文献综述
2.
A specific drug to treat PKU: sapropterin dihydrochloride
治疗苯丙酮尿症特异性药物二盐酸沙丙蝶呤
3.
EVALUATION OF THERAPEUTIC EFFECT AND SCREENING FOR CONGENITAL HY-POTHYROIDISM(CH)AND PHENYLETONURIA(PKU)IN NEONATES
新生儿先天性甲状腺功能低下症和苯丙酮尿症的筛查与疗效评估
4.
The Initial MR Study of Brain Lesions in Chidlren with Phenylketonuria;
苯丙酮尿症儿童脑部病变MR初步研究
5.
Design of Phenylketonuria Fluorescence Detection Optical System
苯丙酮尿症荧光检测光学系统的设计
6.
Study on Phe cut-off point of neonatal phenylketonuria screening in Daqing.
大庆地区新生儿苯丙酮尿症苯丙氨酸筛查切值的研究
7.
Research on Fluorescence Detection System for Neonatal Phenylketonuria Screening;
新生儿苯丙酮尿症（PKU）荧光筛查系统的研究
8.
A Phenylketonuria Detecting System Constituted by Biosensor;
利用生物传感器组建苯丙酮尿症检测系统
9.
Determination and analysis of trace elements for phenylketonuria infant in Changchun
长春地区苯丙酮尿症患儿微量元素检测分析
10.
Newborn Phenylketonuria in Hebei Province:An analysis of screening results from 2000 to 2008
2000—2008年河北省新生儿苯丙酮尿症筛查结果分析
11.
Delayed Brain Myelination in Children with Phenylketonuria Complicated with Epilepsia
苯丙酮尿症并癫患儿脑髓鞘病变的意义
12.
phenylpyruvic oligophrenia
苯丙酮尿性智力发育不全
13.
imbecillitas phenylpyruvica
智力发育不全性苯丙酮尿
14.
Study on incidence and type of phenylketonuria and congenital hypothyroidism in newborn in Jiangmen city
江门地区新生儿先天性甲状腺功能减低症与苯丙酮尿症发病现状分析与研究
15.
Phenylketonuria is a condition in which phenylalanine to tyrosine conversion is diminished because the enzyme phenylalanine hydroxylaze is deficient.
苯丙酮酸尿症是一种由于苯丙氨酸羟化酶缺乏，苯丙氨酸转变成酪氨酸的过程被削弱的
16.
"Tyrosine: One of the amino acids, not essential for humans unless they have the hereditary disorder phenylketonuria. "
酪氨酸 :一种氨基酸,对人体不是必需的,除非它们含有苯丙酮尿症。
17.
Mental and Motor Development as Well as Temperament and Behavior in Children with Phenylketonuria;
苯丙酮尿症儿童智力和运动发育及气质行为研究
18.
Use of new methods of rapid genotyping the model mice for phenylketonuria
快速鉴定苯丙酮尿症模型小鼠基因型的新方法应用