The management of phenylketonuria in childhood requires a multidisciplinary approach across the hospital community interface.
儿童苯丙酮尿症的管理需要多学科的协作。Study on brain delayed myelination and blood phenylalanine of patients with phenylketonuria.
苯丙酮尿症患儿脑髓鞘发育延迟与血苯丙氨酸浓度关系的研究。Objective To design a new type of fluorescence detection optical system for dedicated neonatal PKU screening.
目的：设计一套专用于新生儿苯丙酮尿症（PKU）筛查的新型荧光检测光学系统。will be soaked with cold water, using benzene acetone or 4 carbon gently wipe amination, and then detergent, water wash.
将用冷水浸泡，用苯丙酮或四氨化碳轻轻擦拭，然后再洗涤，清水洗净。Phenylketonuria (PKU) is one kinds of autosomal recessive disease caused by phenylalanine hydroxylase(PAH) gene mutation.
苯丙酮尿症是由于苯丙氨酸羟化酶基因突变引起的常染色体隐性遗传病。A study of phenylketonuria heterozygotes screening in married population of Tianjin area
天津地区已婚群体苯丙酮尿症杂合子筛查Correlation of Conventional Magnetic Resonance Imaging and Clinical Biochemistry of Brain Lesion in Children with Phenylketonuria
苯丙酮尿症儿童脑部磁共振成像与临床生化的相关性Comparison of serum amino acid content before and after controlling pathogenetic condition in patients with phenylketonuria
苯丙酮尿症患者病情控制前后血清氨基酸含量比较Determination of blood contents of calcium and trace elements in children with phenylketonuria on a low phenylalanine diet
饮食治疗苯丙酮尿症患儿全血钙及微量元素水平分析