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Journal Abstract Search

97 related items for PubMed ID: 9814507

  • 1.
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  • 2. Minimally invasive follicular thyroid carcinoma developed in dyshormonogenetic multinodular goiter due to thyroid peroxidase gene mutation.
    Chertok Shacham E, Ishay A, Irit E, Pohlenz J, Tenenbaum-Rakover Y.
    Thyroid; 2012 May; 22(5):542-6. PubMed ID: 22435912
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  • 3. Congenital primary hypothyroidism with subsequent adenomatous goiter in a Turkish patient caused by a homozygous 10-bp deletion in the thyroid peroxidase (TPO) gene.
    Pfarr N, Musholt TJ, Musholt PB, Brzezinska R, Pohlenz J.
    Clin Endocrinol (Oxf); 2006 May; 64(5):514-8. PubMed ID: 16649969
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  • 4. Aggressive metastatic follicular thyroid carcinoma with anaplastic transformation arising from a long-standing goiter in a patient with Pendred's syndrome.
    Camargo R, Limbert E, Gillam M, Henriques MM, Fernandes C, Catarino AL, Soares J, Alves VA, Kopp P, Medeiros-Neto G.
    Thyroid; 2001 Oct; 11(10):981-8. PubMed ID: 11716048
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  • 5. Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter.
    Abramowicz MJ, Targovnik HM, Varela V, Cochaux P, Krawiec L, Pisarev MA, Propato FV, Juvenal G, Chester HA, Vassart G.
    J Clin Invest; 1992 Oct; 90(4):1200-4. PubMed ID: 1401057
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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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  • 9. Defective organification of iodide causing congenital goitrous hypothyroidism.
    Ishikawa N, Eguchi K, Ohmori T, Momotani N, Nagayama Y, Hosoya T, Oguchi H, Mimura T, Kimura S, Nagataki S, Ito K.
    J Clin Endocrinol Metab; 1996 Jan; 81(1):376-83. PubMed ID: 8550781
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  • 10. Clinical case seminar: metastatic follicular thyroid carcinoma arising from congenital goiter as a result of a novel splice donor site mutation in the thyroglobulin gene.
    Alzahrani AS, Baitei EY, Zou M, Shi Y.
    J Clin Endocrinol Metab; 2006 Mar; 91(3):740-6. PubMed ID: 16403815
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  • 11. 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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  • 12. Clinical and molecular genetics studies in Pendred's syndrome.
    Billerbeck AE, Cavaliere H, Goldberg AC, Kalil J, Medeiros-Neto G.
    Thyroid; 1994 Jun; 4(3):279-84. PubMed ID: 7833664
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  • 14. 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 Jun; 12():671659. PubMed ID: 34220711
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  • 16. Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: power and limits of homozygosity mapping.
    Pannain S, Weiss RE, Jackson CE, Dian D, Beck JC, Sheffield VC, Cox N, Refetoff S.
    J Clin Endocrinol Metab; 1999 Mar; 84(3):1061-71. PubMed ID: 10084596
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  • 17. Congenital goiter and the development of metastatic follicular carcinoma with evidence for a leak of nonhormonal iodide: clinical, pathological, kinetic, and biochemical studies and a review of the literature.
    Cooper DS, Axelrod L, DeGroot LJ, Vickery AL, Maloof F.
    J Clin Endocrinol Metab; 1981 Feb; 52(2):294-306. PubMed ID: 7462393
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  • 20. Linkage of familial euthyroid goiter to the multinodular goiter-1 locus and exclusion of the candidate genes thyroglobulin, thyroperoxidase, and Na+/I- symporter.
    Neumann S, Willgerodt H, Ackermann F, Reske A, Jung M, Reis A, Paschke R.
    J Clin Endocrinol Metab; 1999 Oct; 84(10):3750-6. PubMed ID: 10523025
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