[1] |
JIANG Xiang, XU Ai-jing, TANG Fang, JIA Xue-fang, TANG Cheng-fang, CHEN Qian-yu, ZHENG Rui-dan, LIU Ji-lian, HUANG Yong-lan.
Application of auto regressive integrated moving average model in predicting the incidence of congenital hypothyroidism in Guangzhou
[J]. Chinese Journal of Child Health Care, 2021, 29(4): 425-429.
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[2] |
ZHANG Xue-mei, XIE Bang-gui, CHEN Xiao-bing, PAN Cai-qin, LU Yu-zhu, LI Jun-ke, CHEN Qiu-ning.
Analysis of the influencing factors for congenital hypothyroidism in 45 infants
[J]. Chinese Journal of Child Health Care, 2021, 29(11): 1233-1236.
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[3] |
WANG Li-wen, NI Min, LIU Su-na, JIA Chen-lu, LUO Chun-wei, ZHAO De-hua.
Evaluation of the performance of genetic screening processor and setting the cut-off values in screening for congenital hypothyroidism in newborns
[J]. journal1, 2019, 27(10): 1147-1150.
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[4] |
YANG Ying, GAO Zhen-yan, YAN Chong-huai.
Research advances on soluble transferrin receptor for diagnosing iron deficiency in children
[J]. journal1, 2018, 26(9): 969-972.
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[5] |
LONG Wei, YANG Yu-qi, ZHOU Wen-bai,GUO Fang,ZHOU Hong,ZHANG Bin, LIU Jian-bing, YU Bin.
Effect of hypothyroidism in pregnancy on thyroid stimulating hormone of heel blood in neonates
[J]. journal1, 2018, 26(8): 839-842.
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[6] |
LIU Hong-li,LI Feng-xia.
Treatment and follow-up results of neonatal diseases screening in Shaanxi province from 2010 to 2016
[J]. journal1, 2018, 26(11): 1221-1223.
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[7] |
YANG Cheng-yu, LIU Yu-na, LIU Wen-miao, LIU Shi-guo, YI Ming-ji, YAN Sheng-li.
Study on nicotinamide nucleotide transhydrogenase gene mutation in Shandong Han patients with congenital hypothyroidism
[J]. journal1, 2018, 26(1): 11-14.
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[8] |
SONG Dong-po,LI Wen-jie.
Research on metabolic disorder of maple syrup urine disease
[J]. journal1, 2017, 25(2): 143-146.
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[9] |
YANG Ru-lai,TONG Fan,XU Yan-hua,ZHAO Zheng-yan.
Clinical analysis about 2 789cases of congenital hypothyroidism
[J]. journal1, 2017, 25(11): 1094-1097.
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[10] |
WANG Wei,ZHANG Xiao-yan,YUAN Shuai,HE Fa-lin,ZHONG Kun,WANG Zhi-guo.
External quality survey on quality indicators of neonatal screening for inherited metabolic diseases in China
[J]. journal1, 2017, 25(11): 1182-1185.
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[11] |
HAN Wen-xiu,ZANG Hong-wei,ZANG Yu-cui,YI Ming-ji,YAN Sheng-li,LIU Shi-guo,GE Yin-lin..
Screening of double oxide enzyme mutations in patients with congenital hypothyroidism.
[J]. journal1, 2016, 24(8): 795-799.
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[12] |
LIU Hong-li,LI Feng-xia,SHI Qiao-wei,ZHU Chang-qiong..
Screening and treatment of congenital hypothyroidism.
[J]. journal1, 2016, 24(11): 1219-1221.
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[13] |
YANG Xiao-yan,LI Rui-ling,ZHANG Mei,CAO Chun-hong,YOU Jia.
Analysis of neonatal congenital hypothyroidism and phenylketonuria screening and therapy in Xi'an from 2008 to 2013
[J]. journal1, 2015, 23(4): 427-429.
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[14] |
HUANG Sai-jun,SU Xi,YU Hong,WU Cui-ling,SUN Ya-lian.
Comparative study on visual and anditory continuous performance test in children with congenital hypothyroidism.
[J]. journal1, 2015, 23(11): 1134-1137.
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[15] |
LIU Lu,LI Hui-chao,CHAI Jian,SHAO Hui-ying,YI Ming-ji,CHEN Pei-jie,LIU Shi-guo,YAN Sheng-li.
Study on DUOXA2 gene mutation in patients with congenital hypothyroidism and goiter.
[J]. journal1, 2015, 23(1): 7-10.
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