1.
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
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.
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
4.
"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。
5.
phenylpyruvic oligophrenia
苯丙酮尿性智力发育不全
6.
imbecillitas phenylpyruvica
智力发育不全性苯丙酮尿
7.
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
8.
Design of Phenylketonuria Fluorescence Detection Optical System
苯丙酮尿症荧光检测光学系统的设计
9.
Roles of prephenate dehydrogenase and p-hydroxyphenylpyruvate reductase involved in isoflavonoid biosynthesis in cell suspension cultures of Pueraria lobata
预苯酸脱氢酶和对羟基苯丙酮酸还原酶与野葛异黄酮的生物合成
10.
ANALYSIS OF PHE, PPA AND BENZALHYDANTOIN BY= HIGH PERFORMANCE CAPILLARY ELECTROPHORESIS
高效毛细管电泳法分析苯丙氨酸苯丙酮酸和亚苄基海因
11.
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
12.
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
13.
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
14.
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
15.
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
16.
Cyclic Voltammetry Determination of Uric Acid at a L-Phenylalanine Modified Electrode
尿酸在聚L-苯丙氨酸修饰电极上的伏安测定
17.
Reactions of Acylthiobenzothiazole with Ethyl Acetoacetate, Diethyl Malonate and Pentane-2, 4-dione
酰硫基苯并噻唑与丁酮酸乙酯、丙二酸二乙酯及戊二酮的反应
18.
Catalytic synthesis of butanone 1,2-propanediol ketal over H_3PW_6Mo_6O_(40)/PAn;
磷钨钼杂多酸掺杂聚苯胺催化合成丁酮1,2—丙二醇缩酮