phenylketonuria

phenylketonuria什么意思,phenylketonuria翻译

基本解释

n.: 【医】苯酮尿
网络: 苯酮尿症；苯丙酮尿症；苯丙酮酸尿症

英汉解释

• 【医学】苯酮尿

• 费林氏病

• 苯丙酮酸尿症

例句

• 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。

• Conclusion: The special bone changes in phenylketonuria were important X-ray signs suggestive of phenylketonuria .

  结论：苯丙酮尿症特异性的骨骼改变是诊断苯丙酮尿症的重要X线征。

• 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。

• 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

• Identification of novel mutations in the phenylalanine hydroxylase gene of classical phenylketonuria

  经典型苯丙酮尿症苯丙氨酸羟化酶基因的新突变鉴定

• Research on Fluorescence Detection System for Neonatal Phenylketonuria Screening

  新生儿苯丙酮尿症荧光筛查系统的研究