238 related articles for article (PubMed ID: 30154845)
1. Mutational Spectrum Analysis of Seven Genes Associated with Thyroid Dyshormonogenesis.
Chen X; Kong X; Zhu J; Zhang T; Li Y; Ding G; Wang H
Int J Endocrinol; 2018; 2018():8986475. PubMed ID: 30154845
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ.
Nicholas AK; Serra EG; Cangul H; Alyaarubi S; Ullah I; Schoenmakers E; Deeb A; Habeb AM; Almaghamsi M; Peters C; Nathwani N; Aycan Z; Saglam H; Bober E; Dattani M; Shenoy S; Murray PG; Babiker A; Willemsen R; Thankamony A; Lyons G; Irwin R; Padidela R; Tharian K; Davies JH; Puthi V; Park SM; Massoud AF; Gregory JW; Albanese A; Pease-Gevers E; Martin H; Brugger K; Maher ER; Chatterjee VK; Anderson CA; Schoenmakers N
J Clin Endocrinol Metab; 2016 Dec; 101(12):4521-4531. PubMed ID: 27525530
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. Molecular basis of thyroid dyshormonogenesis: genetic screening in population-based Japanese patients.
Narumi S; Muroya K; Asakura Y; Aachi M; Hasegawa T
J Clin Endocrinol Metab; 2011 Nov; 96(11):E1838-42. PubMed ID: 21900383
[TBL] [Abstract][Full Text] [Related]
7. Targeted Next-Generation Sequencing for Congenital Hypothyroidism With Positive Neonatal TSH Screening.
Yamaguchi T; Nakamura A; Nakayama K; Hishimura N; Morikawa S; Ishizu K; Tajima T
J Clin Endocrinol Metab; 2020 Aug; 105(8):. PubMed ID: 32459320
[TBL] [Abstract][Full Text] [Related]
8. DUOX2 variants are a frequent cause of congenital primary hypothyroidism in Thai patients.
Sorapipatcharoen K; Tim-Aroon T; Mahachoklertwattana P; Chantratita W; Iemwimangsa N; Sensorn I; Panthan B; Jiaranai P; Noojarern S; Khlairit P; Pongratanakul S; Suprasongsin C; Korwutthikulrangsri M; Sriphrapradang C; Poomthavorn P
Endocr Connect; 2020 Nov; 9(11):1121-1134. PubMed ID: 33310921
[TBL] [Abstract][Full Text] [Related]
9. 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]
10.
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]
11. 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]
12. Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis.
Zou M; Alzahrani AS; Al-Odaib A; Alqahtani MA; Babiker O; Al-Rijjal RA; BinEssa HA; Kattan WE; Al-Enezi AF; Al Qarni A; Al-Faham MSA; Baitei EY; Alsagheir A; Meyer BF; Shi Y
J Clin Endocrinol Metab; 2018 May; 103(5):1889-1898. PubMed ID: 29546359
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Genetic and Phenotypic Characteristics of Congenital Hypothyroidism in a Chinese Cohort.
Long W; Guo F; Yao R; Wang Y; Wang H; Yu B; Xue P
Front Endocrinol (Lausanne); 2021; 12():705773. PubMed ID: 34539567
[TBL] [Abstract][Full Text] [Related]
16. Case Report: Expanding the Digenic Variants Involved in Thyroid Hormone Synthesis-10 New Cases of Congenital Hypothyroidism and a Literature Review.
Yang R; Lu Y; Yang C; Wu X; Feng J; Zhu L; Shu Q; Jiang P
Front Genet; 2021; 12():694683. PubMed ID: 34456971
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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
Endocrine; 2023 Jan; 79(1):125-134. PubMed ID: 36125728
[TBL] [Abstract][Full Text] [Related]
19. [Genetic analysis for 5 congenital hypothyroidism patients due to dyshormonogenesis].
Fu CY; Zhang SJ; Luo SY; Wang J; Yang Q; Xie BB; Chen SK
Zhonghua Er Ke Za Zhi; 2016 Jun; 54(6):433-6. PubMed ID: 27256230
[TBL] [Abstract][Full Text] [Related]
20. Clinical genetics of defects in thyroid hormone synthesis.
Kwak MJ
Ann Pediatr Endocrinol Metab; 2018 Dec; 23(4):169-175. PubMed ID: 30599477
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]