Zhao D - Search Results

1

Genetic testing of PAX8 mutations associated with thyroid dysgenesis in Chinese congenital hypothyroidism patients.

Li M, Wang F, Wang X, Zang Y, Liu W, Wang F, Zhang L, Tang Q, Liu S, Zhao D. Li M, et al. Among authors: zhao d. Endokrynol Pol. 2020;71(2):153-159. doi: 10.5603/EP.a2020.0004. Epub 2020 Feb 25. Endokrynol Pol. 2020. PMID: 32096550 Free article.

2

Newborn screening for congenital hypothyroidism in Henan province, China.

Zhao DH, Shen Y, Gong JM, Meng Y, Su L, Zhang X. Zhao DH, et al. Clin Chim Acta. 2016 Jan 15;452:58-60. doi: 10.1016/j.cca.2015.10.030. Epub 2015 Oct 29. Clin Chim Acta. 2016. PMID: 26522654

3

Chinese expert brief consensus on newborn screening of inherited metabolic disorders during the novel coronavirus infection epidemic.

Liu S, Wang D, Wan K, Liu H, Zhang D, Yang J, Yuan Z, He X, Wang J, Ou M, Zhu W, Qu Y, Zhao D, Wang W, Liu S, Gu M, Huang S, Wang Z, Zou L. Liu S, et al. Among authors: zhao d. Ann Transl Med. 2020 Apr;8(7):429. doi: 10.21037/atm.2020.03.60. Ann Transl Med. 2020. PMID: 32395473 Free PMC article. Review.

4

Dual Oxidase System Genes Defects in Children With Congenital Hypothyroidism.

Wang F, Xiaole L, Ma R, Zhao D, Liu S. Wang F, et al. Among authors: zhao d. Endocrinology. 2021 Aug 1;162(8):bqab043. doi: 10.1210/endocr/bqab043. Endocrinology. 2021. PMID: 33631011

5

Molecular and clinical characteristics of congenital hypothyroidism in a large cohort study based on comprehensive thyroid transcription factor mutation screening in Henan.

Li L, Jia C, Li X, Wang F, Wang Y, Chen Y, Liu S, Zhao D. Li L, et al. Among authors: zhao d. Clin Chim Acta. 2021 Jul;518:162-169. doi: 10.1016/j.cca.2021.03.015. Epub 2021 Mar 24. Clin Chim Acta. 2021. PMID: 33773966

6

Genetic analysis of iodide transporter and recycling (NIS, PDS, SLC26A7, IYD) in patients with congenital hypothyroidism.

Li M, Li X, Wang F, Ren Y, Zhang X, Wang J, Shen L, Zhao D, ShiguoLiu. Li M, et al. Among authors: zhao d. Gene. 2022 May 25;824:146402. doi: 10.1016/j.gene.2022.146402. Epub 2022 Mar 8. Gene. 2022. PMID: 35276235 No abstract available.

7

Mutation screening of eight genes and comparison of the clinical data in a Chinese cohort with congenital hypothyroidism.

Li L, Li X, Wang X, Han M, Zhao D, Wang F, Liu S. Li L, et al. Among authors: zhao d. Endocrine. 2023 Jan;79(1):125-134. doi: 10.1007/s12020-022-03188-4. Epub 2022 Sep 20. Endocrine. 2023. PMID: 36125728

8

JAG1 Variants Confer Genetic Susceptibility to Thyroid Dysgenesis and Thyroid Dyshormonogenesis in 813 Congenital Hypothyroidism in China.

Li M, Wang X, Wang F, Wang F, Zhao D, Liu S. Li M, et al. Among authors: zhao d. Int J Gen Med. 2024 Mar 7;17:885-894. doi: 10.2147/IJGM.S445557. eCollection 2024. Int J Gen Med. 2024. PMID: 38468821 Free PMC article.

9

[Screening and group distribute regularity of congenital hypothyroidism of neonatal in Henan province].

Wang J, Wang BZ, Zhang Z, Hu YL, Zhao DH, Su L, Meng Y. Wang J, et al. Zhonghua Liu Xing Bing Xue Za Zhi. 2006 Sep;27(9):825-6. Zhonghua Liu Xing Bing Xue Za Zhi. 2006. PMID: 17299975 Chinese. No abstract available.

10

Risk factors for neurodevelopmental deficits in congenital hypothyroidism after early substitution treatment.

Huo K, Zhang Z, Zhao D, Li H, Wang J, Wang X, Feng H, Wang X, Zhu C. Huo K, et al. Among authors: zhao d. Endocr J. 2011;58(5):355-61. doi: 10.1507/endocrj.k10e-384. Epub 2011 Apr 5. Endocr J. 2011. PMID: 21467693 Free article.

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