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Journal Abstract Search

184 related items for PubMed ID: 22093430

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  • 2. 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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  • 5. 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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  • 6. 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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  • 7. 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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  • 8. 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 29; 54(8):732-7. PubMed ID: 21340161
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  • 9. The Missense Alteration A5T of the Thyroid Peroxidase Gene is Pathogenic and Associated with Mild Congenital Hypothyroidism.
    Cangül H, Demir K, Babayiğit HÖ, Abacı A, Böber E.
    J Clin Res Pediatr Endocrinol; 2015 Sep 29; 7(3):238-41. PubMed ID: 26831560
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  • 12. Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect.
    Bougacha-Elleuch N, Charfi N, Miled N, Bouhajja H, Belguith N, Mnif M, Jaurge P, Chikhrouhou N, Ayadi H, Hachicha M, Abid M.
    Eur J Pediatr; 2015 Nov 29; 174(11):1491-501. PubMed ID: 25968604
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  • 16. Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene.
    Belforte FS, Miras MB, Olcese MC, Sobrero G, Testa G, Muñoz L, Gruñeiro-Papendieck L, Chiesa A, González-Sarmiento R, Targovnik HM, Rivolta CM.
    Clin Endocrinol (Oxf); 2012 Apr 29; 76(4):568-76. PubMed ID: 21981063
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  • 17. A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient.
    Sriphrapradang C, Thewjitcharoen Y, Chanprasertyothin S, Nakasatien S, Himathongkam T, Trachoo O.
    J Clin Res Pediatr Endocrinol; 2016 Jun 05; 8(2):241-5. PubMed ID: 26761947
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  • 18. 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 05; 37(1):124-8. PubMed ID: 20963560
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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 Feb 05; 15(6):909-13. PubMed ID: 26406404
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