377 related articles for article (PubMed ID: 18765513)
1. Transient congenital hypothyroidism caused by biallelic mutations of the dual oxidase 2 gene in Japanese patients detected by a neonatal screening program.
Maruo Y; Takahashi H; Soeda I; Nishikura N; Matsui K; Ota Y; Mimura Y; Mori A; Sato H; Takeuchi Y
J Clin Endocrinol Metab; 2008 Nov; 93(11):4261-7. PubMed ID: 18765513
[TBL] [Abstract][Full Text] [Related]
2. Natural course of congenital hypothyroidism by dual oxidase 2 mutations from the neonatal period through puberty.
Maruo Y; Nagasaki K; Matsui K; Mimura Y; Mori A; Fukami M; Takeuchi Y
Eur J Endocrinol; 2016 Apr; 174(4):453-63. PubMed ID: 26742565
[TBL] [Abstract][Full Text] [Related]
3. Compound heterozygosity for a novel hemizygous missense mutation and a partial deletion affecting the catalytic core of the H2O2-generating enzyme DUOX2 associated with transient congenital hypothyroidism.
Hoste C; Rigutto S; Van Vliet G; Miot F; De Deken X
Hum Mutat; 2010 Apr; 31(4):E1304-19. PubMed ID: 20187165
[TBL] [Abstract][Full Text] [Related]
4. Genotypes and phenotypes of congenital goitre and hypothyroidism caused by mutations in dual oxidase 2 genes.
Wang F; Lu K; Yang Z; Zhang S; Lu W; Zhang L; Liu S; Yan S
Clin Endocrinol (Oxf); 2014 Sep; 81(3):452-7. PubMed ID: 24735383
[TBL] [Abstract][Full Text] [Related]
5. High frequency of DUOX2 mutations in transient or permanent congenital hypothyroidism with eutopic thyroid glands.
Jin HY; Heo SH; Kim YM; Kim GH; Choi JH; Lee BH; Yoo HW
Horm Res Paediatr; 2014; 82(4):252-60. PubMed ID: 25248169
[TBL] [Abstract][Full Text] [Related]
6. High prevalence of DUOX2 mutations in Japanese patients with permanent congenital hypothyroidism or transient hypothyroidism.
Matsuo K; Tanahashi Y; Mukai T; Suzuki S; Tajima T; Azuma H; Fujieda K
J Pediatr Endocrinol Metab; 2016 Jul; 29(7):807-12. PubMed ID: 27166716
[TBL] [Abstract][Full Text] [Related]
7. Congenital hypothyroidism caused by a novel mutation of the dual oxidase 2 (DUOX2) gene.
Yoshizawa-Ogasawara A; Ogikubo S; Satoh M; Narumi S; Hasegawa T
J Pediatr Endocrinol Metab; 2013; 26(1-2):45-52. PubMed ID: 23457309
[TBL] [Abstract][Full Text] [Related]
8. Identification and functional analysis of novel dual oxidase 2 (DUOX2) mutations in children with congenital or subclinical hypothyroidism.
De Marco G; Agretti P; Montanelli L; Di Cosmo C; Bagattini B; De Servi M; Ferrarini E; Dimida A; Freitas Ferreira AC; Molinaro A; Ceccarelli C; Brozzi F; Pinchera A; Vitti P; Tonacchera M
J Clin Endocrinol Metab; 2011 Aug; 96(8):E1335-9. PubMed ID: 21565790
[TBL] [Abstract][Full Text] [Related]
9. Transient congenital hypothyroidism caused by compound heterozygous mutations affecting the NADPH-oxidase domain of DUOX2.
Yoshizawa-Ogasawara A; Abe K; Ogikubo S; Narumi S; Hasegawa T; Satoh M
J Pediatr Endocrinol Metab; 2016 Mar; 29(3):363-71. PubMed ID: 26565538
[TBL] [Abstract][Full Text] [Related]
10. Pseudodominant inheritance in a family with nonautoimmune hypothyroidism due to biallelic DUOX2 mutations.
Abe K; Narumi S; Suwanai AS; Hamajima T; Hasegawa T
Clin Endocrinol (Oxf); 2015 Sep; 83(3):394-8. PubMed ID: 25263060
[TBL] [Abstract][Full Text] [Related]
11. A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism.
Zheng X; Ma SG; Qiu YL; Guo ML; Shao XJ
J Clin Res Pediatr Endocrinol; 2016 Jun; 8(2):224-7. PubMed ID: 26758695
[TBL] [Abstract][Full Text] [Related]
12. Mutation screening of DUOX2 in Chinese patients with congenital hypothyroidism.
Fu C; Zhang S; Su J; Luo S; Zheng H; Wang J; Qin H; Chen Y; Shen Y; Hu X; Fan X; Luo J; Xie B; Chen R; Chen S
J Endocrinol Invest; 2015 Nov; 38(11):1219-24. PubMed ID: 26349762
[TBL] [Abstract][Full Text] [Related]
13. Congenital hypothyroidism, dwarfism, and hearing impairment caused by a missense mutation in the mouse dual oxidase 2 gene, Duox2.
Johnson KR; Marden CC; Ward-Bailey P; Gagnon LH; Bronson RT; Donahue LR
Mol Endocrinol; 2007 Jul; 21(7):1593-602. PubMed ID: 17440044
[TBL] [Abstract][Full Text] [Related]
14. The Prevalence, Clinical, and Molecular Characteristics of Congenital Hypothyroidism Caused by DUOX2 Mutations: A Population-Based Cohort Study in Guangzhou.
Tan M; Huang Y; Jiang X; Li P; Tang C; Jia X; Chen Q; Chen W; Sheng H; Feng Y; Wu D; Liu L
Horm Metab Res; 2016 Sep; 48(9):581-8. PubMed ID: 27557340
[TBL] [Abstract][Full Text] [Related]
15. Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patients.
Fu C; Luo S; Zhang S; Wang J; Zheng H; Yang Q; Xie B; Hu X; Fan X; Luo J; Chen R; Su J; Shen Y; Gu X; Chen S
Clin Chim Acta; 2016 Jul; 458():30-4. PubMed ID: 27108200
[TBL] [Abstract][Full Text] [Related]
16. Persistent mild hypothyroidism associated with novel sequence variants of the DUOX2 gene in two siblings.
Vigone MC; Fugazzola L; Zamproni I; Passoni A; Di Candia S; Chiumello G; Persani L; Weber G
Hum Mutat; 2005 Oct; 26(4):395. PubMed ID: 16134168
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. High prevalence of DUOX2 gene mutations among children with congenital hypothyroidism in central China.
Jiang H; Wu J; Ke S; Hu Y; Fei A; Zhen Y; Yu J; Zhu K
Eur J Med Genet; 2016 Oct; 59(10):526-31. PubMed ID: 27498126
[TBL] [Abstract][Full Text] [Related]
19. Hypothyroidism caused by the combination of two heterozygous mutations: one in the TSH receptor gene the other in the DUOX2 gene.
Satoh M; Aso K; Ogikubo S; Yoshizawa-Ogasawara A; Saji T
J Pediatr Endocrinol Metab; 2015 May; 28(5-6):657-61. PubMed ID: 25928756
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]