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   congenital hypothyroidism 的翻译结果: 查询用时:0.01秒
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congenital hypothyroidism     
相关语句
  先天性甲状腺功能低下症
     Screening for congenital hypothyroidism in neonates of Zhejiang Province during 1999-2004
     浙江省1999-2004年新生儿先天性甲状腺功能低下症筛查分析
短句来源
     M. Results NHI were determined averaged 5.6(from 3.0~8.0) in 4 patients with Congenital Hypothyroidism.
     结果  4例先天性甲状腺功能低下症患儿 NHI分值平均 5 .6 (范围 3.8~ 8.0 ) ;
短句来源
     Interview and Observation of 57 Cases With Congenital Hypothyroidism
     先天性甲状腺功能低下症57例随访观察
短句来源
     Screening for congenital hypothyroidism and phenylketonuria in newborn
     新生儿先天性甲状腺功能低下症和苯丙酮尿症筛查
短句来源
     Analysis on the results of congenital hypothyroidism screening in the newborn infants of Chongqing
     重庆市新生儿先天性甲状腺功能低下症的筛查结果分析
短句来源
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  先天性甲状腺功能低下
     Objective To summarize the results of neonatal screening for congenital hypothyroidism(CH),phenylketonuria(PKU) and glucose 6 phosphate dehydrogenase (G 6 PD)deficiency for ten years in Guangzhou.
     目的 总结近10 年来广州市新生儿筛查先天性甲状腺功能低下( CH) 、苯丙酮尿症( PKU) 及葡萄糖6磷酸脱氢酶( G6PD) 缺陷的结果。
短句来源
     Screening for congenital hypothyroidism in neonates of Zhejiang Province during 1999-2004
     浙江省1999-2004年新生儿先天性甲状腺功能低下症筛查分析
短句来源
     M. Results NHI were determined averaged 5.6(from 3.0~8.0) in 4 patients with Congenital Hypothyroidism.
     结果  4例先天性甲状腺功能低下症患儿 NHI分值平均 5 .6 (范围 3.8~ 8.0 ) ;
短句来源
     Interview and Observation of 57 Cases With Congenital Hypothyroidism
     先天性甲状腺功能低下症57例随访观察
短句来源
     Screening for congenital hypothyroidism and phenylketonuria in newborn
     新生儿先天性甲状腺功能低下症和苯丙酮尿症筛查
短句来源
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  先天性甲状腺功能减退症
     The Investigation of T354P, G395R Human Sodium/Iodide Symporter Gene Mutation in Congenital Hypothyroidism
     婴幼儿先天性甲状腺功能减退症患者人钠/碘转运体基因354、395位点突变的研究
短句来源
     Neonatal screening and clinical analysis for congenital hypothyroidism
     新生儿先天性甲状腺功能减退症的筛查及临床分析
短句来源
     A study on TSH receptor gene mutations in one child with congenital hypothyroidism and analysis of the pedigree
     TSH受体基因突变致先天性甲状腺功能减退症一例及其家系分析
短句来源
     Objective To study the relationship of the T354P,G395R mutation of human sodium/iodide symporter gene and congenital hypothyroidism in Linyi.
     目的 探讨临沂地区先天性甲状腺功能减退症患儿在人钠/碘转运体基因T354P、G395R位点是否存在突变。
短句来源
     Investigation of the relationship between G395R mutation of human sodium/iodide symporter and congenital hypothyroidism
     人钠/碘转运体基因G395R与先天性甲状腺功能减退症相关
短句来源
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  先天性甲低
     THE APPLICATION OF ROC CURVE IN NEONATAL CONGENITAL HYPOTHYROIDISM SCREENING
     ROC曲线在新生儿先天性甲低筛查中的应用
短句来源
     Results:As result of the screening of the newborns region of Yangzhou from July of 2002 to December of 2004,there were 106 prescreening positive cases and 20 final diagnosis ones,and that the incidence rate of congenital hypothyroidism was 0.07% while the retest rate 0.38% and the recall rate 98%.
     结果:新生儿筛查结果显示,初筛阳性病例106例,确诊20例,先天性甲低的发病率为0.07%,复检率为0.38%,召回率为98.00%。
短句来源
     [Methods]Dissociation-Enhanced Lanthanide Fluoroimmunoassay(DELFIA)was used to detect TSH,then the accuracy of different critical values of TSH were evaluated according to receiver operating characterics curve(ROC)in neonatal congenital hypothyroidism screening.
     [方法]采用时间分辨镧系荧光免疫(DELFIA)技术进行TSH的检测,应用ROC曲线对我省新生儿先天性甲低(CH)筛查中TSH的不同临界值进行评价。
短句来源
     Results:(1) Among the 21 infants,8 showed normal thyroid function,11 showed hyperthyrotropinemia,2 cases had congenital hypothyroidism,which showed significant differences from those born by healthy mothers.
     结果:21例婴儿中甲状腺功能正常8例,高TSH血症11例,先天性甲低2例,与同期健康母亲的新生儿相比差异有显著性(P<0.01);
短句来源
     Detection of serum TGII in congenital hypothyroidism
     先天性甲低患儿血清TGII的测定
短句来源
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  congenital hypothyroidism
Treatment and follow-up of children with transient congenital hypothyroidism
      
Objective: To study the clinical therapy and prognosis in children with transient congenital hypothyroidism (CH).
      
Such differences in RORα mRNA expression may play a role in the behavioral alterations resulting from congenital hypothyroidism.
      
Technetium 99m pertechnetate thyroid scans were performed on 57 infants referred for evaluation of suspected congenital hypothyroidism.
      
There are diverse etiologies of congenital hypothyroidism.
      
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