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Journal Abstract Search

141 related items for PubMed ID: 7355662

  • 1. Congenital goitre due to "thyroid peroxidase-iodinase defect".
    Niepomniszcze H, Coleoni AH, Targovnik HM, Iorcansky S, Degrossi OJ.
    Acta Endocrinol (Copenh); 1980 Jan; 93(1):25-31. PubMed ID: 7355662
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  • 2. Thyroid iodine organification defects: a case with lack of thyroglobulin iodination and a case without any peroxidase activity.
    Pommier J, Tourniaire J, Rahmoun B, Déme D, Pallo D, Bornet H, Nunez J.
    J Clin Endocrinol Metab; 1976 Feb; 42(2):319-29. PubMed ID: 1262432
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  • 3. Familial goitre with partial iodine organification defect, lack of thyroglobulin, and high levels of thyroid peroxidase.
    Niepomniszcze H, Medeiros-Neto GA, Refetoff S, Degroot LJ, Fang VS.
    Clin Endocrinol (Oxf); 1977 Jan; 6(1):27-39. PubMed ID: 844215
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  • 4. Differentiation of two abnormalities in thyroid peroxidase causing organification defect and goitrous hypothyroidism.
    Niepomniszcze H, Rosenbloom AL, Degroot LJ, Shimaoka K, Refetoff S, Yamamoto K.
    Metabolism; 1975 Jan; 24(1):57-67. PubMed ID: 162974
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  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Congenital goitre and hypothyroidism with impaired iodide organification and high thyroid peroxidase concentration.
    Medeiros-Neto GA, Nakashima T, Taurog A, Knobel M, Simonetti JP, Mattar E.
    Clin Endocrinol (Oxf); 1979 Jan; 11(2):123-39. PubMed ID: 487612
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  • 7. Deficient thyroid peroxidase causing organification defect and goitrous hypothyroidism.
    Medeiros-Neto GA, Knobel M, Yamamoto K, Cavaliere H, Kallas W.
    J Endocrinol Invest; 1979 Jan; 2(4):353-7. PubMed ID: 231615
    [No Abstract] [Full Text] [Related]

  • 8. Thyroid peroxidase in dyshormonogenetic goiters with organification and thyroglobulin defects.
    de Carvalho DP, Rego KG, Rosenthal D.
    Thyroid; 1994 Jan; 4(4):421-6. PubMed ID: 7711505
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  • 9. Association of peroxidase enzyme defect and low thyroglobulin content in a case of endemic cretinism.
    Ait Hammou N, Abdelmoumene N, Benmiloud M.
    J Endocrinol Invest; 1985 Jun; 8(3):257-62. PubMed ID: 4031389
    [Abstract] [Full Text] [Related]

  • 10. 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; 51(2):165-72. PubMed ID: 10468986
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  • 14. Characterization of human thyroid peroxidase purified by monoclonal antibody-assisted chromatography.
    Ohtaki S, Kotani T, Nakamura Y.
    J Clin Endocrinol Metab; 1986 Sep; 63(3):570-6. PubMed ID: 3016020
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  • 16. Mechanism of simultaneous iodination and coupling catalyzed by thyroid peroxidase.
    Taurog A, Dorris ML, Doerge DR.
    Arch Biochem Biophys; 1996 Jun 01; 330(1):24-32. PubMed ID: 8651700
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  • 17. 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 01; 13(12):1145-51. PubMed ID: 14751036
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  • 19. 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 01; 64(5):514-8. PubMed ID: 16649969
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  • 20. Improved assay method for activity of thyroid peroxidase-catalysed coupling of iodotyrosine residues of thyroglobulin utilizing h.p.l.c. for analysis of iodothyronines.
    Ohmori T, Tarutani O, Hosoya T.
    Biochem J; 1989 Aug 15; 262(1):209-14. PubMed ID: 2818564
    [Abstract] [Full Text] [Related]

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