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164 related items for PubMed ID: 2745934
1. 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 [Abstract] [Full Text] [Related]
2. The effect of oral administration of iodine to patients with goiter and hypothyroidism due to defective synthesis of thyroglobulin. Vono J, Lima N, Knobel M, Medeiros-Neto G. Thyroid; 1996 Feb; 6(1):11-5. PubMed ID: 8777378 [Abstract] [Full Text] [Related]
3. Low levels of thyroglobulin messenger ribonucleic acid in congenital goitrous hypothyroidism with defective thyroglobulin synthesis. Targovnik H, Propato F, Varela V, Wajchenberg B, Knobel M, D'Abronzo HF, Medeiros-Neto G. J Clin Endocrinol Metab; 1989 Dec; 69(6):1137-47. PubMed ID: 2584351 [Abstract] [Full Text] [Related]
5. 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 Jun; 11(2):123-39. PubMed ID: 487612 [Abstract] [Full Text] [Related]
6. Differential levels of thyroid peroxidase and thyroglobulin messenger ribonucleic acids in congenital goiter with defective thyroglobulin synthesis. Targovnik HM, Varela V, Juvenal GJ, Propato F, Chester HA, Krawiec L, Frechtel G, Moran DH, Perinetti HA, Pisarev MA. J Endocrinol Invest; 1990 Nov; 13(10):797-806. PubMed ID: 2096156 [Abstract] [Full Text] [Related]
7. 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 [Abstract] [Full Text] [Related]
8. Congenital hypothyroidism with impaired thyroid response to thyrotropin (TSH) and absent circulating thyroglobulin: evidence for a new inactivating mutation of the TSH receptor gene. Tonacchera M, Agretti P, Pinchera A, Rosellini V, Perri A, Collecchi P, Vitti P, Chiovato L. J Clin Endocrinol Metab; 2000 Mar; 85(3):1001-8. PubMed ID: 10720030 [Abstract] [Full Text] [Related]
9. Evaluation and characterization of the hyt/hyt hypothyroid mouse. II. Abnormalities of TSH and the thyroid gland. Stein SA, Shanklin DR, Krulich L, Roth MG, Chubb CM, Adams PM. Neuroendocrinology; 1989 May; 49(5):509-19. PubMed ID: 2725843 [Abstract] [Full Text] [Related]
10. Studies on mono- and diiodohistidine. II. Congenital goitrous hypothyroidism with thyroglobulin defect and iodohistidine-rich iodoalbumin production. Savoie JC, Massin JP, Savoie F. J Clin Invest; 1973 Jan; 52(1):116-25. PubMed ID: 4629905 [Abstract] [Full Text] [Related]
11. Dissociated thyroxine, triiodothyronine and reverse triiodothyronine levels in patients with familial goitre due to iodide organification defects. Chan V, Wang C, Yeung RT. Clin Endocrinol (Oxf); 1979 Sep; 11(3):257-65. PubMed ID: 509742 [Abstract] [Full Text] [Related]
12. [Thyroid hormones and thyroid-stimulating hormone in patients with chronic heart failure--relationship between primary hypothyroidism with iodine organification defect and chronic heart failure]. Matsumura K, Nakase E, Kawai I, Saito T, Kikkawa N, Haiyama T. Kaku Igaku; 1995 Mar; 32(3):241-51. PubMed ID: 7739154 [Abstract] [Full Text] [Related]
13. A patient with Pendred syndrome whose goiter progressed with normal serum thyrotropin and iodine organification. Asakura Y, Narumi S, Muroya K, Fujita K, Aida N, Hasagawa T, Adachi M. Am J Med Genet A; 2010 Jul; 152A(7):1793-7. PubMed ID: 20583162 [Abstract] [Full Text] [Related]
14. Studies on the thyroidal defect in an atypical form of Pendred's syndrome. Cave WT, Dunn JT. J Clin Endocrinol Metab; 1975 Sep; 41(3):590-9. PubMed ID: 1159063 [Abstract] [Full Text] [Related]
15. Clinical and laboratory features of children and adolescents with congenital hypothyroidism due to dyshormonogenesis in southern Brazil. Ramos JC, Lacerda Filho Ld, DeMartini Ade A, Silveira RB, Pereira RM, Sandrini Neto R, França SN. Arq Bras Endocrinol Metabol; 2012 Apr; 56(3):201-8. PubMed ID: 22666737 [Abstract] [Full Text] [Related]
17. 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 [Abstract] [Full Text] [Related]
18. Concentration of plasma thyroglobulin and urinary excretion of iodinated material in the diagnosis of thyroid disorders in congenital hypothyroidism. Gons MH, Kok JH, Tegelaers WH, de Vijlder JJ. Acta Endocrinol (Copenh); 1983 Sep; 104(1):27-34. PubMed ID: 6624362 [Abstract] [Full Text] [Related]
19. Goitrous hypothyroidism due to iodide-trapping defect. Saito K, Yamamoto K, Yoshida S, Manabe S, Suzuki M, Takai T, Saito T, Kuzuya T, Moriyama S. J Clin Endocrinol Metab; 1981 Dec; 53(6):1267-72. PubMed ID: 6271803 [Abstract] [Full Text] [Related]
20. [Thyroid hormone profiles in goitrous and non-goitrous subjects seen in an endemic goiter area of the Central African Republic]. Biassoni P, Ravera G, Garibaldi C, Barbera F, Villa G. Boll Soc Ital Biol Sper; 1991 Aug; 67(8):795-802. PubMed ID: 1809308 [Abstract] [Full Text] [Related] Page: [Next] [New Search]