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- 苯丙酮尿癥（PKU）Phenylketonuria
- 湖南省新生兒先天性甲狀腺功能減低癥和苯丙酮尿癥的篩查分析Neonatal Screening Analysis for Congenital Hypothyroidism and Phenylketonuria in Human Province
- 經(jīng)典型苯丙酮尿癥classic phenylketonuria
- 苯丙酮尿癥患兒腦髓鞘發(fā)育延遲與血苯丙氨酸濃度關(guān)系的研究。Study on brain delayed myelination and blood phenylalanine of patients with phenylketonuria.
- 新生兒篩查能使苯丙酮尿癥患兒得到早期診斷和治療,防止智力低下的發(fā)生,Newborn screening can let PKU patients get early diagnosis and treatment and also avoid abnormal intelligence development.
- 新生兒苯丙酮尿癥熒光篩查系統的研究Research on Fluorescence Detection System for Neonatal Phenylketonuria Screening
- β-芐基-α-苯丙酮酸β-Benzyl-α-phenylpyruvic acid
- 對羥基苯丙酮酸還原酶p- hydroxyphenylpyruvate reductase
- 氨基酸尿癥aminoaciduria
- 先天性戊糖尿癥congenital pentosuria
- 苯丙酮尿phenylketonuria
- 苯丙酮酸性精神幼稚癥[醫] phenylpyruvic imbecility
- 少尿癥oliguria
- 苯丙酮酸尿phenylketonuria
- 病毒尿癥viruria
- 苯丙酮尿Ⅱ型phenylketonuria Ⅱ
- 糖尿癥melituria
- 苯丙酮尿Ⅲ型phenylketonuria Ⅲ
- 氯尿癥chloriduria
- 母體苯丙酮尿maternal phenylketonuria
