Literature DB >> 27510867

[Consensus statement on diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency].

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Abstract

Entities:  

Year:  2016        PMID： 27510867     DOI： 10.3760/cma.j.issn.0578-1310.2016.08.003

Source DB:  PubMed          Journal:  Zhonghua Er Ke Za Zhi        ISSN： 0578-1310


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  3 in total

1.  Analysis of the Screening Results for Congenital Adrenal Hyperplasia Involving 7.85 Million Newborns in China: A Systematic Review and Meta-Analysis.

Authors:  Zhuoguang Li; Lianjing Huang; Caiqi Du; Cai Zhang; Mini Zhang; Yan Liang; Xiaoping Luo
Journal:  Front Endocrinol (Lausanne)       Date:  2021-04-23       Impact factor: 5.555

2.  Neonatal Screening and Genotype-Phenotype Correlation of 21-Hydroxylase Deficiency in the Chinese Population.

Authors:  Xin Wang; Yanyun Wang; Dingyuan Ma; Zhilei Zhang; Yahong Li; Peiying Yang; Yun Sun; Tao Jiang
Journal:  Front Genet       Date:  2021-01-22       Impact factor: 4.599

3.  Clinical applications of genetic analysis and liquid chromatography tandem-mass spectrometry in rare types of congenital adrenal hyperplasia.

Authors:  Zhuoguang Li; Yan Liang; Caiqi Du; Xiao Yu; Ling Hou; Wei Wu; Yanqing Ying; Xiaoping Luo
Journal:  BMC Endocr Disord       Date:  2021-11-25       Impact factor: 2.763
  3 in total

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