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Journal Abstract Search

155 related items for PubMed ID: 99939

  • 1. Biochemical studies on the iodine organification defect of Pendred's syndrome.
    Niepomniszcze H, Coleoni AH, Degrossi OJ, Scavini LM, Curutchet HP.
    Acta Endocrinol (Copenh); 1978 Sep; 89(1):70-9. PubMed ID: 99939
    [No Abstract] [Full Text] [Related]

  • 2. Normal peroxidase activity in Pendred's syndrome.
    Burrow GN, Spaulding SW, Alexander NM, Bower BF.
    J Clin Endocrinol Metab; 1973 Mar; 36(3):522-30. PubMed ID: 4346605
    [No Abstract] [Full Text] [Related]

  • 3. Thyroidal iodoproteins in Pendred's syndrome.
    Medeiros-Neto GA, Nicolau W, Kieffer J, Cintra AB.
    J Clin Endocrinol Metab; 1968 Aug; 28(8):1205-13. PubMed ID: 4970955
    [No Abstract] [Full Text] [Related]

  • 4. Peroxidase deficiency in familial goiter with iodide organification defect.
    Hagen GA, Niepomniszcze H, Haibach H, Bigazzi M, Hati R, Rapoport B, Jimenez C, DeGroot LJ, Frawley TF.
    N Engl J Med; 1971 Dec 16; 285(25):1394-8. PubMed ID: 4330593
    [No Abstract] [Full Text] [Related]

  • 5. 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 16; 6(1):27-39. PubMed ID: 844215
    [Abstract] [Full Text] [Related]

  • 6. Management of goitre in Pendred's syndrome.
    al-Jaberi TM, Hussein AD, Heis HA.
    Br J Surg; 1994 Oct 16; 81(10):1511. PubMed ID: 7820488
    [No Abstract] [Full Text] [Related]

  • 7. Thyroidal iodopriteins in Pendred's syndrome.
    Desai KB, Mehta MN, Patel MC, Ramanna L, Ganatra RD.
    J Endocrinol; 1974 Nov 16; 63(2):409-10. PubMed ID: 4443702
    [No Abstract] [Full Text] [Related]

  • 8. The concentration of peroxidase in normal and adenomatous human thyroid tissue with special reference to patients with Pendred's syndrome.
    Ljunggren JG, Lindström H, Hjern B.
    Acta Endocrinol (Copenh); 1973 Feb 16; 72(2):272-8. PubMed ID: 4739179
    [No Abstract] [Full Text] [Related]

  • 9. Dyshormonogenetic goitre.
    Barsano CP, De Groot LJ.
    Clin Endocrinol Metab; 1979 Mar 16; 8(1):145-65. PubMed ID: 371867
    [No Abstract] [Full Text] [Related]

  • 10. 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 16; 42(2):319-29. PubMed ID: 1262432
    [Abstract] [Full Text] [Related]

  • 11. Abnormal H2O2 supply in the thyroid of a patient with goiter and iodine organification defect.
    Niepomniszcze H, Targovnik HM, Gluzman BE, Curutchet P.
    J Clin Endocrinol Metab; 1987 Aug 16; 65(2):344-8. PubMed ID: 3597712
    [Abstract] [Full Text] [Related]

  • 12. Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome.
    Gausden E, Armour JA, Coyle B, Coffey R, Hochberg Z, Pembrey M, Britton KE, Grossman A, Reardon W, Trembath R.
    Clin Endocrinol (Oxf); 1996 Apr 16; 44(4):441-6. PubMed ID: 8706311
    [Abstract] [Full Text] [Related]

  • 13. Studies on the thyroidal defect in an atypical form of Pendred's syndrome.
    Cave WT, Dunn JT.
    J Clin Endocrinol Metab; 1975 Sep 16; 41(3):590-9. PubMed ID: 1159063
    [Abstract] [Full Text] [Related]

  • 14. Thyroid function in patients with Pendred's syndrome.
    Friis J, Johnsen T, Feldt-Rasmussen U, Bech K, Friis T.
    J Endocrinol Invest; 1988 Feb 16; 11(2):97-101. PubMed ID: 3361085
    [Abstract] [Full Text] [Related]

  • 15. Deficient cytochrome b5 reductase activity in nontoxic goiter with iodide organification defect.
    Kusakabe T.
    Metabolism; 1975 Oct 16; 24(10):1103-13. PubMed ID: 1165726
    [Abstract] [Full Text] [Related]

  • 16. Dissociation of thyrotropin-dependent enzyme activities, reduced iodide transport, and preserved iodide organification in nonfunctioning thyroid adenoma and multinodular goiter.
    Masini-Repiso AM, Cabanillas AM, Bonaterra M, Coleoni AH.
    J Clin Endocrinol Metab; 1994 Jul 16; 79(1):39-44. PubMed ID: 8027249
    [Abstract] [Full Text] [Related]

  • 17. Increased peroxidase activity in Pendred's syndrome with hypothyroidism.
    Yamamoto M, Saito S, Sakurada T, Yoshida K, Yoshinaga K.
    Tohoku J Exp Med; 1976 Jun 16; 119(2):103-13. PubMed ID: 951708
    [Abstract] [Full Text] [Related]

  • 18. Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification.
    Sheffield VC, Kraiem Z, Beck JC, Nishimura D, Stone EM, Salameh M, Sadeh O, Glaser B.
    Nat Genet; 1996 Apr 16; 12(4):424-6. PubMed ID: 8630498
    [Abstract] [Full Text] [Related]

  • 19. Monoamine oxidase activity of the thyroid glands in thyroid disease.
    Hidaka H, Nagatsu T, Nagasaka A, Ishizuki Y.
    Clin Chim Acta; 1969 Mar 16; 23(3):383-6. PubMed ID: 5794475
    [No Abstract] [Full Text] [Related]

  • 20. Congenital goiter with hypothyroidism and iodo-serum albumin replacing thyroglobulin.
    Lissitzky S, Codaccioni JL, Bismuth J, Depieds R.
    J Clin Endocrinol Metab; 1967 Feb 16; 27(2):185-96. PubMed ID: 4163612
    [No Abstract] [Full Text] [Related]

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