- 更多网络例句与丙酮尿相关的网络例句 [注：此内容来源于网络，仅供参考]
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Objective To investigate the mutation characteristics in exon 7 of the PAH gene in phenylketonuria patients in Xinjiang.
目的研究分析新疆地区苯丙酮尿症患者中苯丙氨酸羟化酶基因外显子7的突变特征。
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Neonatal screening ; Congenital hypothyroidism; Phenyl ketonuria; Glucose-6-phosphate dehydrogenase（G6PD） deficiency
新生儿疾病筛查；先天性甲状腺功能低下症；苯丙酮尿症；葡萄糖6-磷酸脱氢酶缺乏症
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Objective:Analysis of screening results of three neonatal diseases to further clarify the incidence of phenyl ketonuria,congenital hypothyroidism and glucose-6-phosphate dehydrogenase(G6PD) deficiency in Hainan Province.
目的：对海南省新生儿疾病筛查情况进行分析，了解海南省新生儿苯丙酮尿症、先天性甲状腺功能低下症、葡萄糖6-磷酸脱氢酶缺乏症(G-6-PDD)的发病率。方法：对出生72h后的7412名新生儿采集足跟血制作血滤纸干标本，PKU筛查采用荧光定量法检测滤纸干血斑中Phe含量；CH筛查采用时间分辨荧光免疫法检测滤干血斑中TSH含量；G6PD缺乏的筛查采用荧光斑点定性试验测定G6PD活性。
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Other trace elements have been observed with phenylketonuria, an inherited metabolic disorder, and kwashiorkor, a severe form of malnutrition that occurs mainly in developing nations.
在苯丙酮尿症和恶性营养不良(一种主要发生在发展中国家的严重营养不良)患者的毛发中，也观察到了其它种微量元素。
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Objective To establish a simple, accurate and rapid method for screening of the mutant genes in phenylketonuria.
目的 建立一种简便、准确和快速的筛查苯丙酮尿症突变基因的方法。
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Objective To observe delayed myelination in delayed treated Phenylketonuria with MRI and changes of IQ before and after treatment.
目的 应用磁共振成像观察苯丙酮尿症治疗延迟患儿治疗前后脑髓鞘发育延迟与智商的关系。
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Because of its phenylalanine content, persons with phenylketonuria must avoid it.
由于内含苯丙氨酸，患有苯丙酮尿症的人必须避免。
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Persons with phenylketonuria do not metabolize phenylalanine properly and must adhere to a diet free of it.
患有苯丙酮尿症的人不能进行苯丙氨酸的正常代谢，必须采取没有苯丙氨酸的饮食方式。
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BH loading tast and urine pterin analysis can be used as differental diagnosis methods for classical PKU and BH deficiency.
血苯丙氨酸浓度在口服BH后无明显变化，尿喋呤谱分析基本正常的患儿诊断为经典型苯丙酮尿症
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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。
- 更多网络解释与丙酮尿相关的网络解释 [注：此内容来源于网络，仅供参考]
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acetonemia,acetonaemia：酮血症,丙酮血症
\\"丙酮体\\",\\"acetone body\\" | \\"酮血症,丙酮血症\\",\\"acetonemia,acetonaemia\\" | \\"丙酮尿症\\",\\"acetonuria\\"
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acetonuria：丙酮尿症
\\"酮血症,丙酮血症\\",\\"acetonemia,acetonaemia\\" | \\"丙酮尿症\\",\\"acetonuria\\" | \\"丙酮基苯香豆素\\",\\"acetonylbenzyl hydroxy coumarin\\"
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acetonuria：丙酮尿
acetonebutanol fermentation 丙酮丁醇发酵 | acetonuria 丙酮尿 | acetophenone 乙酰苯;苯乙酮(增香剂)
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phenyl ketonuria, PKU：苯丙酮尿症
Phenylalanine hydroxylase 苯丙氨酸羟化酶 | phenyl ketonuria,PKU 苯丙酮尿症 | norepinephrine 去甲肾上腺素
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Maple syrup urine disease：枫糖浆尿病
前者为已知某种酶或尚不能肯定的某种酶活性缺乏或降低,如苯丙氨酸羟化酶的缺乏引起苯丙酮尿症;分支氨基酸α-酮酸脱羧酶的缺乏或降低引起枫糖浆尿病(maple syrup urine disease);异戊酰辅酶A脱氢酶缺乏引起的异戊酸血症;胱硫醚合成酶缺乏引起的同型胱氨酸尿症;
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phenylpyruvic oligophrenia：苯丙酮尿性智力发育不全
phenylpropanolamine hydrochloride 盐酸去甲麻黄碱 | phenylpyruvic oligophrenia 苯丙酮尿性智力发育不全 | pheromone 外激素
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phenylpyruvic oligophrenia syndrome：苯丙酮尿白痴综合征
Persistent postpartum amenorrhea-galactorrhea syndrome 持久性产后闭经-乳溢综合征 | phenylpyruvic oligophrenia syndrome 苯丙酮尿白痴综合征 | plica syndrome 滑膜皱襞综合征
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phenylketonuria：苯丙酮尿症
PKU 苯丙酮尿症(phenylketonuria)的缩写,一种遗传病,其症状是尿中出现超出常规水平的苯丙酮酸. 苯丙酮尿症,又称苯酮尿症(phenylketonuria,缩写为PKU)是一种氨基酸代谢缺陷,患者肝脏中缺乏苯丙氨酸羟化酶,使得食物中的苯氨酸无法转化为酪氨酸,
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phenylketonuria,PKU：苯丙酮尿症
苯丙酮尿症(phenylketonuria' PKU)是较常见的氨基酸代谢异常性疾病之一. 本症系因先天性苯丙氨酸羟化酶缺乏,使苯丙氨酸羟化为酪氨酸的过程受阻,造成苯丙氨酸及其代谢产物在体内蓄积,引发一系列神经系统和骨骼结构损害,并在尿中出现大量苯丙氨酸及苯丙酮酸等物质,
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PKU phenylketonuria：苯丙酮尿症
PK pyruvate kinase 丙酮酸激酶 | PKU phenylketonuria 苯丙酮尿症 | pm picometer 微微米