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Journal Abstract Search

144 related items for PubMed ID: 23329183

  • 1. Mutations of the thyroid peroxidase gene in Chinese siblings with congenital goitrous hypothyroidism.
    Ma SG, Wu XJ, Liu H, Xu W, He L.
    Arq Bras Endocrinol Metabol; 2012 Dec; 56(9):614-7. PubMed ID: 23329183
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  • 5. Congenital goitrous primary hypothyroidism in two German families caused by novel thyroid peroxidase (TPO) gene mutations.
    Altmann K, Hermanns P, Mühlenberg R, Fricke-Otto S, Wentzell R, Pohlenz J.
    Exp Clin Endocrinol Diabetes; 2013 Jun; 121(6):343-6. PubMed ID: 23512414
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  • 6. Two novel mutations in the thyroid peroxidase gene with goitrous hypothyroidism.
    Tajima T, Tsubaki J, Fujieda K.
    Endocr J; 2005 Oct; 52(5):643-5. PubMed ID: 16284446
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  • 7. Goitrous congenital hypothyroidism and hearing impairment associated with mutations in the TPO and SLC26A4/PDS genes.
    Pfarr N, Borck G, Turk A, Napiontek U, Keilmann A, Müller-Forell W, Kopp P, Pohlenz J.
    J Clin Endocrinol Metab; 2006 Jul; 91(7):2678-81. PubMed ID: 16684826
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  • 8. Prevalence of c.2268dup and detection of two novel alterations, c.670_672del and c.1186C>T, in the TPO gene in a cohort of Malaysian-Chinese with thyroid dyshormonogenesis.
    Lee CC, Harun F, Jalaludin MY, Heh CH, Othman R, Junit SM.
    BMJ Open; 2015 Jan 05; 5(1):e006121. PubMed ID: 25564141
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  • 9. Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect.
    Nascimento AC, Guedes DR, Santos CS, Knobel M, Rubio IG, Medeiros-Neto G.
    Thyroid; 2003 Dec 05; 13(12):1145-51. PubMed ID: 14751036
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  • 10. 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 Dec 05; 75(8):633-7. PubMed ID: 26174974
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  • 11. Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism.
    Umeki K, Kotani T, Kawano J, Suganuma T, Yamamoto I, Aratake Y, Furujo M, Ichiba Y.
    Eur J Endocrinol; 2002 Apr 05; 146(4):491-8. PubMed ID: 11916616
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  • 14. Two compound heterozygous mutations (c.215delA/c.2422T-->C and c.387delC/c.1159G-->A) in the thyroid peroxidase gene responsible for congenital goitre and iodide organification defect.
    Rivolta CM, Louis-Tisserand M, Varela V, Gruñeiro-Papendieck L, Chiesa A, González-Sarmiento R, Targovnik HM.
    Clin Endocrinol (Oxf); 2007 Aug 05; 67(2):238-46. PubMed ID: 17547680
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  • 15. A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect.
    Santos CL, Bikker H, Rego KG, Nascimento AC, Tambascia M, De Vijlder JJ, Medeiros-Neto G.
    Clin Endocrinol (Oxf); 1999 Aug 05; 51(2):165-72. PubMed ID: 10468986
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  • 16. TPO gene mutations associated with thyroid carcinoma: Case report and literature review.
    Zhu H, Peng YG, Ma SG, Liu H.
    Cancer Biomark; 2015 Aug 05; 15(6):909-13. PubMed ID: 26406404
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  • 20. 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 05; 76(4):568-76. PubMed ID: 21981063
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