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Journal Abstract Search

153 related items for PubMed ID: 4162599

  • 1.
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  • 2. THE POSSIBLE OCCURRENCE OF TWO INBORN ERRORS OF IODINE METABOLISM IN ONE PATIENT.
    WIENER JD, LINDEBOOM GA.
    Acta Endocrinol (Copenh); 1964 Nov; 47():385-401. PubMed ID: 14225837
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  • 5. THYROID FUNCTION IN A GOITER ENDEMIC. V. MECHANISM OF THYROID FAILURE IN THE UELE ENDEMIC CRETINS.
    DUMONT JE, ERMANS AM, BASTENIE PA.
    J Clin Endocrinol Metab; 1963 Sep; 23():847-60. PubMed ID: 14064130
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  • 6. Thyroglobulin defect in a human congenital goiter.
    Riesco G, Bernal J, Sanchez-Franco F.
    J Clin Endocrinol Metab; 1974 Jan; 38(1):33-41. PubMed ID: 4203525
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  • 7. [Thyroid hormonosynthesis disorders due to iodotyrosine-dehalogenase deficiency. Value of the D.I.T. test for the detection of heterozygotes].
    Rochiccioli P, Dutau G.
    Arch Fr Pediatr; 1974 Jan; 31(1):25-36. PubMed ID: 4135480
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  • 8. The hormone synthesis of hyperfunctioning thyroid nodules in euthyroid patients.
    Agerbaek H.
    Acta Endocrinol (Copenh); 1974 Sep; 77(1):53-63. PubMed ID: 4137272
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  • 9. A novel compound heterozygous mutation in the thyroglobulin gene resulting in congenital goitrous hypothyroidism with high serum triiodothyronine levels.
    Kitanaka S, Takeda A, Sato U, Miki Y, Hishinuma A, Ieiri T, Igarashi T.
    J Hum Genet; 2006 Sep; 51(4):379-382. PubMed ID: 16477365
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  • 10. Mild familial goitrous hypothyroidism associated with prolonged 131-iodine retention: possible defect in thyroglobulin synthesis.
    McKenna TJ, Loughlin T, Ohman M, Schneider A, Towers R.
    J Endocrinol Invest; 1989 Apr; 12(4):229-34. PubMed ID: 2745934
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  • 12. [Clinical and chromosomal studies in a congenital hypothyroidism caused by thyroxin synthesis disorders and middle ear hearing disorders (Pendred- or goiter-deafness syndrome)].
    Kitlak W, Gebert P.
    Arch Kinderheilkd; 1968 Apr; 177(2):170-83. PubMed ID: 5723894
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  • 15. [IOSINE-TYROSYL COUPLING DEFECT IN CONGENITAL HYPOTHYROIDISM WITH GOITER].
    RICCABONA G.
    Klin Med Osterr Z Wiss Prakt Med; 1964 Apr; 19():151-4. PubMed ID: 14201635
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  • 16. [SPORADIC GOITER IN AN ADULT WITH HYPOTHYROIDISM. LARGE EXCESS OF MONO-IODOTYROSINE AND ABSENCE OF IODOTHYRONINES IN THYROGLOBULIN].
    CODACCIONI JL, BOYER J, BISMUTH J, GASCARD E, VAGUE J.
    Ann Endocrinol (Paris); 1963 Apr; 24():582-7. PubMed ID: 14051312
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  • 19. [A study of 2 congenital hypothyroid goiters in siblings: identification of a genetic abnormality in thyroid hormonogenesis marked by the absence of thyroglobulin and by the iodination of unsuitable proteins rich in iodohistidine and deficient in thyroxine].
    Savoie JC, Massin JP, Sizonenko PC, Job JC.
    Ann Endocrinol (Paris); 1973 Apr; 34(5):539-48. PubMed ID: 4136284
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  • 20. Congenital goiter with iodoalbumin replacing thyroglobulin and defect of deiodination of iodotyrosines. Serum origin of the thyroid iodoalbumin.
    Lissitzky S, Bismuth J, Codaccioni JL, Cartouzou G.
    J Clin Endocrinol Metab; 1968 Dec; 28(12):1797-806. PubMed ID: 4972509
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