| 释义 |
phen·yl·ke·to·nur·i·a 英ˌfenəlˌkiːtnˈʊəriːə, -ˈjʊər-, ˌfiːnəl-美ˌfɛnəlˌkitņˈʊriə, -ˈjʊr-, ˌfinəl-AHDfĕn'əl-kēt'n-‹rʹē-ə, -y‹rʹ-, fē'nəl- 高COCA¹⁰¹¹³⁵BNC³⁹³⁸⁴iWeb⁵⁰²¹⁶
基本英英记法近义反义例句
n.医苯丙酮尿症一种先天性代谢异常形容词phenylketonuric
Noun:
a genetic disorder of metabolism; lack of the enzyme needed to turn phenylalanine into tyrosine results in an accumulation of phenylalanine in the body fluids which causes various degrees of mental deficiency词根记忆phen-苯-yl基ket-酮-on量ur-尿-ia病⇒n.医苯丙酮尿症一种先天性代谢异常近义词 PKU苯酮尿症=phenyl…
Borsi Batki suffers from phenylketonuria(PKU, a metabolic disorder that if undetected, can lead to problems with brain development, progressive mental retardation, brain damage and seizures.
她患有苯丙酮酸尿症，这是一种先天性代谢异常病，会影响大脑发育、损伤脑部神经和损害智力。 www.china.org.cn
It suggested a potential neuroprotective action of BDNF in prevention and treatment of brain injury in the patients with phenylketonuria.
BDNF对治疗苯丙酮尿症脑损伤可能具有潜在的应用价值。 d.wanfangdata.com.cn
Objective: To explore effective dietary regimens in treating phenylketonuria PKU after summing up20 years practice in652 patients.
目的总结20年对652例苯丙酮尿症患儿进行低苯丙氨酸饮食治疗经验，探讨有效的饮食控制方案。 cnki
The comparison of ABR changes at the beginning of therapy against congenital hypothyroidism and phenylketonuria and later could serve as an objective criteria for follow-up of therapeutic efficiency.
先天性甲状腺功能低下及苯丙酮尿症的治疗早晚的 ABR对比观察，可作为疗效随访和追踪观察的客观指标。 cnki
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。 cpgn
As phenylalanine dehydrogenase is used to determine the concentration of plasma phenylalanine for monitoring of phenylketonuria and synthesize L- amino acids, it is drawing more and more attention.
苯丙氨酸脱氢酶因在临床上可用作苯丙酮尿症的检测用酶，工业上可用于合成手性氨基酸而越来越受到关注。 dictall
Conclusion It is invaluable for improving the quality of people for us to strength the screening of neonates, and do our best to let all of neonates be screened for phenylketonuria.
结论加大新生儿筛查力度，动员全社会关心和支持这项工作，让所有孩子一出生就接受苯丙酮尿症的筛查，这对提高我国出生人口素质有极其重要的意义。 cnki
Objective To make a further understanding of MRI manifestations of the brain in maternal phenylketonuria MPKU offspring.
目的提高对母亲苯丙酮尿症 MPKU后代脑 MRI表现的认识。 cnki
Objective To describe the incidence of congenital hypothyroidism CH and phenylketonuria PKUin Maanshan city.
目的：报告先天性甲状腺功能低下症 CH和苯丙酮尿症 PKU的患病率。 dictall
Objective To establish a simple, accurate and rapid method for screening of the mutant genes in phenylketonuria PKU.
目的建立一种简便、准确和快速的筛查苯丙酮尿症 PKU突变基因的方法。 cnki
Objective To explore the incidence and distribution features of neonatal phenylketonuria PKU and congenital hypothyroidism CH in Lianyungang area.
目的探讨连云港地区新生儿先天性甲状腺功能减退症 CH及苯丙酮尿症 PKU发病及分布特征。 cnki
Objective To identify the mutations of the phenylalanine hydroxylase gene in Yunnan so as to enhance the gene diagnosis of classical phenylketonuria PKU in that south western province of China.
目的研究云南苯丙氨酸羟化酶基因点突变分布概况，以提高该地区苯丙酮尿症 PKU的基因诊断率。 cnki
Objective:To study the mutations of phenylalanine hydroxylase PAH gene in phenylketonuria PKU patients.
目的：探讨苯丙酮尿症 PKU患者 PAH基因突变特点。 http://dict.cnki.net
Take the gene mutation that causes phenylketonuria, or PKU. People with the disease can't break down the amino acid phenylalanine, a problem that can lead to severe cognitive damage.
提取能导致苯丙酮尿症 PKU的基因突变。患这种病的人不能分解氨基酸苯丙氨酸，这会导致严重的认知损坏。 yeeyan
This method is suited for identifying errors of amino acid metabolism and phenylketonuria in particular.
是筛查氨基酸代谢病尤其筛查苯丙酮尿症的准确而简便的方法。 cnki
To develop a fluorescent MGB probe real time PCR platform for detection the mutation of phenylalanine hydroxylase gene in patients with phenylketonuria.
探讨荧光 MGB探针实时 PCR技术检测经典型苯丙酮尿症的基因突变。 cnki
To explore the morbidity of Congenital hypothyroidism CH and phenylketonuria PKU among newborn in Heze city.
了解菏泽市新生儿甲状腺功能低下症 CH与苯丙酮尿症 PKU发病率。 dictall
To understand the prevalence of thyroid hypofunction CH and phenylketonuria PKU among newborn in Penglai in order to find and treat them in time.
为了解蓬莱市新生儿甲状腺功能低下 CH和苯丙酮尿症 PKU的发病情况，以便早期发现、及时治疗。 dictall
Tragically, their daughter Carol was born in 1920 with a genetic birth defect called phenylketonuria, which led to mental impairment.
不幸的是，1920年赛珍珠的女儿卡罗出生时患有一种叫做苯丙酮酸尿症的先天基因缺陷症，导致智力受损。 yeeyan
Urine sample of the normal children and children patients with phenylketonuria or neuroblastoma were analysed by two methods.
并对正常儿、苯丙酮尿症患儿、神经母细胞瘤患儿的尿标本进行了两种方法的对比研究。 cnki |