139 related articles for article (PubMed ID: 36740391)
1. [Genetic mutation profiles for children with congenital hypothyroidism in Fujian province].
Cheng F; Su YQ; Wang XR; Wu FY; Sun F; Fang Y; Zhang RJ; Zhao SX; Song HD
Zhonghua Yi Xue Za Zhi; 2023 Feb; 103(5):336-343. PubMed ID: 36740391
[No Abstract] [Full Text] [Related]
2. Analysis of Mutation Spectra of 28 Pathogenic Genes Associated With Congenital Hypothyroidism in the Chinese Han Population.
Huang M; Lu X; Dong G; Li J; Chen C; Yu Q; Li M; Su Y
Front Endocrinol (Lausanne); 2021; 12():695426. PubMed ID: 34276565
[TBL] [Abstract][Full Text] [Related]
3.
Peters C; Nicholas AK; Schoenmakers E; Lyons G; Langham S; Serra EG; Sebire NJ; Muzza M; Fugazzola L; Schoenmakers N
Thyroid; 2019 Jun; 29(6):790-801. PubMed ID: 31044655
[No Abstract] [Full Text] [Related]
4. The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes.
Sun F; Zhang JX; Yang CY; Gao GQ; Zhu WB; Han B; Zhang LL; Wan YY; Ye XP; Ma YR; Zhang MM; Yang L; Zhang QY; Liu W; Guo CC; Chen G; Zhao SX; Song KY; Song HD
Eur J Endocrinol; 2018 Jun; 178(6):623-633. PubMed ID: 29650690
[TBL] [Abstract][Full Text] [Related]
5. Mutation spectrum analysis of 29 causative genes in 43 Chinese patients with congenital hypothyroidism.
Wang H; Kong X; Pei Y; Cui X; Zhu Y; He Z; Wang Y; Zhang L; Zhuo L; Chen C; Yan X
Mol Med Rep; 2020 Jul; 22(1):297-309. PubMed ID: 32319661
[TBL] [Abstract][Full Text] [Related]
6. Genetic Evaluation of Congenital Hypothyroidism with Gland
Shin JH; Kim HY; Kim YM; Lee H; Bae MH; Park KH; Lee SM; Kwak MJ
Ann Clin Lab Sci; 2021 Jan; 51(1):73-81. PubMed ID: 33653783
[TBL] [Abstract][Full Text] [Related]
7. Gene mutations in children with permanent congenital hypothyroidism in Yunnan, China.
Gong Y; Zhang Y; Liu F; Zhu B; Zhou X; Chan Y; Li S; Li L
Zhejiang Da Xue Xue Bao Yi Xue Ban; 2022 Jun; 51(3):306-313. PubMed ID: 36207832
[TBL] [Abstract][Full Text] [Related]
8.
Wang F; Zang Y; Li M; Liu W; Wang Y; Yu X; Li H; Wang F; Liu S
Front Endocrinol (Lausanne); 2020; 11():237. PubMed ID: 32425884
[No Abstract] [Full Text] [Related]
9. Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis.
Molina MF; Papendieck P; Sobrero G; Balbi VA; Belforte FS; Martínez EB; Adrover E; Olcese MC; Chiesa A; Miras MB; González VG; Pio MG; González-Sarmiento R; Targovnik HM; Rivolta CM
Endocrine; 2022 Jun; 77(1):86-101. PubMed ID: 35507000
[TBL] [Abstract][Full Text] [Related]
10. [Genetic analysis of TPO, DUOX2 and DUOXA2 genes in children with permanent congenital hypothyroidism suspected dyshormonogenesis].
Huang YL; Tan MY; Jiang X; Li B; Chen QY; Jia XF; Tang CF; Liu JL; Liu L
Zhonghua Er Ke Za Zhi; 2017 Mar; 55(3):210-214. PubMed ID: 28273705
[No Abstract] [Full Text] [Related]
11. Newborn screening and single nucleotide variation profiling of TSHR, TPO, TG and DUOX2 candidate genes for congenital hypothyroidism.
Kollati Y; Akella RRD; Naushad SM; Borkar D; Thalla M; Nagalingam S; Lingappa L; Patel RK; Reddy GB; Dirisala VR
Mol Biol Rep; 2020 Oct; 47(10):7467-7475. PubMed ID: 32930933
[TBL] [Abstract][Full Text] [Related]
12. Clinical and genetic investigation of 136 Japanese patients with congenital hypothyroidism.
Tanaka T; Aoyama K; Suzuki A; Saitoh S; Mizuno H
J Pediatr Endocrinol Metab; 2020 May; 33(6):691-701. PubMed ID: 32469330
[TBL] [Abstract][Full Text] [Related]
13. Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism.
Bruellman RJ; Watanabe Y; Ebrhim RS; Creech MK; Abdullah MA; Dumitrescu AM; Refetoff S; Weiss RE
J Clin Endocrinol Metab; 2020 May; 105(5):1564-72. PubMed ID: 31867598
[TBL] [Abstract][Full Text] [Related]
14. Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7.
Acar S; Gürsoy S; Arslan G; Nalbantoğlu Ö; Hazan F; Köprülü Ö; Özkaya B; Özkan B
J Endocrinol Invest; 2022 Apr; 45(4):773-786. PubMed ID: 34780050
[TBL] [Abstract][Full Text] [Related]
15. Clinical, biochemical characteristics and genotype-phenotype analysis of congenital hypothyroidism diagnosed by newborn screening in China.
Zhang T; Shen Y; Xu Y; Wu D; Chen C; Yang R
Clin Chim Acta; 2023 Jul; 547():117459. PubMed ID: 37390946
[TBL] [Abstract][Full Text] [Related]
16. Heterozygous Mutations of the DUOXA2 and DUOX2 Genes in Dizygotic Twins with Congenital Hypothyroidism.
Yang LX; Ma SG; Qiu YL; Zheng X
Clin Lab; 2016; 62(5):849-54. PubMed ID: 27349010
[TBL] [Abstract][Full Text] [Related]
17. DUOX2 Mutations Are Associated With Congenital Hypothyroidism With Ectopic Thyroid Gland.
Kizys MML; Louzada RA; Mitne-Neto M; Jara JR; Furuzawa GK; de Carvalho DP; Dias-da-Silva MR; Nesi-França S; Dupuy C; Maciel RMB
J Clin Endocrinol Metab; 2017 Nov; 102(11):4060-4071. PubMed ID: 28666341
[TBL] [Abstract][Full Text] [Related]
18. Genetics of primary congenital hypothyroidism-a review.
Kostopoulou E; Miliordos K; Spiliotis B
Hormones (Athens); 2021 Jun; 20(2):225-236. PubMed ID: 33400193
[TBL] [Abstract][Full Text] [Related]
19. Targeted next-generation sequencing of thirteen causative genes in Chinese patients with congenital hypothyroidism.
Long W; Lu G; Zhou W; Yang Y; Zhang B; Zhou H; Jiang L; Yu B
Endocr J; 2018 Oct; 65(10):1019-1028. PubMed ID: 30022773
[TBL] [Abstract][Full Text] [Related]
20. DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population.
Park KJ; Park HK; Kim YJ; Lee KR; Park JH; Park JH; Park HD; Lee SY; Kim JW
Ann Lab Med; 2016 Mar; 36(2):145-53. PubMed ID: 26709262
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]