272 related articles for article (PubMed ID: 28666341)
1. 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]
2.
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]
3. Identification and analyzes of DUOX2 mutations in two familial congenital hypothyroidism cases.
Li L; Liu W; Zhang L; Wang F; Wang F; Gu M; Wang X; Liu S
Endocrine; 2021 Apr; 72(1):147-156. PubMed ID: 32803677
[TBL] [Abstract][Full Text] [Related]
4. Conformation of the N-Terminal Ectodomain Elicits Different Effects on DUOX Function: A Potential Impact on Congenital Hypothyroidism Caused by a H
Louzada RA; Corre R; Ameziane-El-Hassani R; Hecht F; Cazarin J; Buffet C; Carvalho DP; Dupuy C
Thyroid; 2018 Aug; 28(8):1052-1062. PubMed ID: 29845893
[TBL] [Abstract][Full Text] [Related]
5.
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]
6. 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]
7. 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]
8. 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]
9. DUOX Defects and Their Roles in Congenital Hypothyroidism.
De Deken X; Miot F
Methods Mol Biol; 2019; 1982():667-693. PubMed ID: 31172499
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis.
Kühnen P; Turan S; Fröhler S; Güran T; Abali S; Biebermann H; Bereket A; Grüters A; Chen W; Krude H
J Clin Endocrinol Metab; 2014 Jan; 99(1):E169-76. PubMed ID: 24248179
[TBL] [Abstract][Full Text] [Related]
12. Clinical and genetic investigation in patients with permanent congenital hypothyroidism.
Zhou L; Liu S; Long W; Wang LL; Yu B
Clin Chim Acta; 2023 Jan; 539():1-6. PubMed ID: 36423704
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. Compound Heterozygous Mutations in the DUOX2/DUOXA2 Genes Cause Congenital Hypothyroidism.
Zheng X; Ma SG; Guo ML; Qiu YL; Yang LX
Yonsei Med J; 2017 Jul; 58(4):888-890. PubMed ID: 28541007
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. New phenotypes in thyroid dyshormonogenesis: hypothyroidism due to DUOX2 mutations.
Moreno JC; Visser TJ
Endocr Dev; 2007; 10():99-117. PubMed ID: 17684392
[TBL] [Abstract][Full Text] [Related]
17. Correlation of DUOX2 residual enzymatic activity with phenotype in congenital hypothyroidism caused by biallelic DUOX2 defects.
Sun F; Zhang RJ; Cheng F; Fang Y; Yang RM; Ye XP; Han B; Zhao SX; Dong M; Song HD
Clin Genet; 2021 Dec; 100(6):713-721. PubMed ID: 34564849
[TBL] [Abstract][Full Text] [Related]
18. [Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases].
Enacán RE; Masnata ME; Belforte F; Papendieck P; Olcese MC; Siffo S; Gruñeiro-Papendieck L; Targovnik H; Rivolta CM; Chiesa AE
Arch Argent Pediatr; 2017 Jun; 115(3):e162-e165. PubMed ID: 28504502
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]