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Journal Abstract Search

265 related items for PubMed ID: 28867693

  • 1. Mild thyroid peroxidase deficiency caused by TPO mutations with residual activity: Correlation between clinical phenotypes and enzymatic activity.
    Narumi S, Fox LA, Fukudome K, Sakaguchi Z, Sugisawa C, Abe K, Kameyama K, Hasegawa T.
    Endocr J; 2017 Nov 29; 64(11):1087-1097. PubMed ID: 28867693
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  • 2. The TPO mutation screening and genotype-phenotype analysis in 230 Chinese patients with congenital hypothyroidism.
    Zhang RJ, Sun F, Chen F, Fang Y, Yan CY, Zhang CR, Ying YX, Wang Z, Zhang CX, Wu FY, Han B, Liang J, Zhao SX, Song HD.
    Mol Cell Endocrinol; 2020 Apr 15; 506():110761. PubMed ID: 32088313
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  • 6. Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism.
    Fu C, Xie B, Zhang S, Wang J, Luo S, Zheng H, Su J, Hu X, Chen R, Fan X, Luo J, Gu X, Chen S.
    BMJ Open; 2016 May 12; 6(5):e010719. PubMed ID: 27173810
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  • 7. Iodide handling disorders (NIS, TPO, TG, IYD).
    Targovnik HM, Citterio CE, Rivolta CM.
    Best Pract Res Clin Endocrinol Metab; 2017 Mar 12; 31(2):195-212. PubMed ID: 28648508
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  • 8. Screening and Functional Analysis of TPO Gene Mutations in a Cohort of Chinese Patients With Congenital Hypothyroidism.
    Wang H, Wang W, Chen X, Shi H, Shi Y, Ding G.
    Front Endocrinol (Lausanne); 2021 Mar 12; 12():774941. PubMed ID: 35002963
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  • 9. Identification and characterization of novel PAX8 mutations in Congenital Hypothyroidism(CH) in a Chinese population.
    Liu S, Wang X, Zou H, Ge Y, Wang F, Wang Y, Yan S, Xia H, Xing M.
    Oncotarget; 2017 Jan 31; 8(5):8707-8716. PubMed ID: 28060725
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  • 10. Case Report: Functional Analysis and Neuropsychological Evaluation of Dyshormonogenetic Fetal Goiter in Siblings Caused by Novel Compound Hyterozygous TPO Gene Mutations.
    Rodrigues TMB, Silva MMDC, Freitas MM, Duarte ZMC, Frutuoso VS, Rodrigues MT, Rubio IGS.
    Front Endocrinol (Lausanne); 2021 Jan 31; 12():671659. PubMed ID: 34220711
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  • 11. Novel genetic variants in the TPO gene cause congenital hypothyroidism.
    Ma SG, Qiu YL, Zhu H, Liu H, Li Q, Ji CM.
    Scand J Clin Lab Invest; 2015 Jan 31; 75(8):633-7. PubMed ID: 26174974
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  • 13. Compound heterozygous mutations (p.T561M and c.2422delT) in the TPO gene associated with congenital hypothyroidism.
    Ma SG, Zheng X, Qiu YL, Guo ML, Shao XJ.
    J Pediatr Endocrinol Metab; 2016 May 01; 29(5):567-70. PubMed ID: 27135621
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  • 15. Genetic Screening and Functional Analysis of Thyroid Peroxidase Variants in Chinese Patients with Congenital Hypothyroidism.
    Zhang HY, Wu FY, Li XS, Zhang CX, Tu PH, Yang RM, Liu XY, Cui RJ, Yang L, Wu CY, Zhang RJ, Fang Y, Sun F, Liang J, Cheng F, Song HD, Zhao SX.
    Horm Res Paediatr; 2024 May 01; 97(4):353-364. PubMed ID: 37703865
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  • 16. Analysis of TPO gene in Turkish children with iodide organification defect: identification of a novel mutation.
    Turkkahraman D, Alper OM, Pehlivanoglu S, Aydin F, Yildiz A, Luleci G, Akcurin S, Bircan I.
    Endocrine; 2010 Feb 01; 37(1):124-8. PubMed ID: 20963560
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  • 18. Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect.
    Neves SC, Mezalira PR, Dias VM, Chagas AJ, Viana M, Targovnik H, Knobel M, Medeiros-Neto G, Rubio IG.
    Arq Bras Endocrinol Metabol; 2010 Nov 01; 54(8):732-7. PubMed ID: 21340161
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  • 19. TPO gene mutations associated with thyroid carcinoma: Case report and literature review.
    Zhu H, Peng YG, Ma SG, Liu H.
    Cancer Biomark; 2015 Nov 01; 15(6):909-13. PubMed ID: 26406404
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  • 20. Frequency of Mutations in the TPO Gene in Patients with Congenital Hypothyroidism Due to Dyshormonogenesis in Chile.
    Arteaga-Jacobo MC, Roco-Videla Á, Villota Arcos C, González-Hormazábal P, Gonzalo-Castro V, Pérez-Flores MV.
    Medicina (Kaunas); 2024 Jul 16; 60(7):. PubMed ID: 39064575
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