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Volumn 75, Issue 3, 1996, Pages 245-246

Familial hypothyroidism with autosomal dominant inheritance

Author keywords

Non goitrous hypothyroidism; Thyroid stimulating hormone unresponsiveness

Indexed keywords

THYROTROPIN;

EID: 0029828429     PISSN: 00039888     EISSN: 14682044     Source Type: Journal    
DOI: 10.1136/adc.75.3.245     Document Type: Article
Times cited : (13)

References (10)
  • 1
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    • (1992) Williams Textbook of Endocrinology , pp. 357-487
    • Reed-Larsen, P.1    Ingbar, S.H.2
  • 2
    • 0014425946 scopus 로고
    • Congenital hypothyroidism with impaired thyroid response to thyrotropin
    • Stanbury JB, Rocmans P, Buhler UK, Ochi Y. Congenital hypothyroidism with impaired thyroid response to thyrotropin. N Engl J Med 1968; 279: 1132-6.
    • (1968) N Engl J Med , vol.279 , pp. 1132-1136
    • Stanbury, J.B.1    Rocmans, P.2    Buhler, U.K.3    Ochi, Y.4
  • 3
    • 0018967019 scopus 로고
    • Congenital hypothyroidism associated with thyrotropin unresponsiveness and thyroid cell membrane alterations
    • Codaccioni JL, Carayon P, Michel-Bechet M, et al. Congenital hypothyroidism associated with thyrotropin unresponsiveness and thyroid cell membrane alterations. J Clin Endocrinol Metab 1980; 50: 932-7.
    • (1980) J Clin Endocrinol Metab , vol.50 , pp. 932-937
    • Codaccioni, J.L.1    Carayon, P.2    Michel-Bechet, M.3
  • 4
    • 0018677930 scopus 로고
    • Impaired cyclic-AMP response to thyrotropin in congenital hypothyroidism with thyroglobulin deficiency
    • Medeiros-Neto GA, Knobel M, Bronstein MD, et al. Impaired cyclic-AMP response to thyrotropin in congenital hypothyroidism with thyroglobulin deficiency. Acta Endocrinol 1979; 92: 62-79.
    • (1979) Acta Endocrinol , vol.92 , pp. 62-79
    • Medeiros-Neto, G.A.1    Knobel, M.2    Bronstein, M.D.3
  • 7
    • 0021344637 scopus 로고
    • Evaluation of the rat thyroid strain FRTL-5 as an in vitro bioassay system for thyrotropin
    • Bidey SP, Chiovato L, Day A, et al. Evaluation of the rat thyroid strain FRTL-5 as an in vitro bioassay system for thyrotropin. J Endocrinol 1984; 101: 269-76.
    • (1984) J Endocrinol , vol.101 , pp. 269-276
    • Bidey, S.P.1    Chiovato, L.2    Day, A.3
  • 8
    • 0019829793 scopus 로고
    • Hereditary congenital non-goiterous hypothyroidism
    • White CW, Wiedermann BL, Rebecca TK, et al. Hereditary congenital non-goiterous hypothyroidism. Am J Dis Child 1981; 135: 568-9.
    • (1981) Am J Dis Child , vol.135 , pp. 568-569
    • White, C.W.1    Wiedermann, B.L.2    Rebecca, T.K.3
  • 9
    • 0028888593 scopus 로고
    • Brief report: Resistance to thyrotropin caused by mutations in the thyrotropin receptor gene
    • Sunthornthepvarakul T, Gottschalk ME, Hayashi Y, et al. Brief report: resistance to thyrotropin caused by mutations in the thyrotropin receptor gene. N Engl J Med 1995; 332: 155-60.
    • (1995) N Engl J Med , vol.332 , pp. 155-160
    • Sunthornthepvarakul, T.1    Gottschalk, M.E.2    Hayashi, Y.3
  • 10
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    • Assignment of the human thyroid stimulating hormone receptor (TSHR) gene to chromosome 14q31
    • Rousseau-Merck MF, Misrachi M, Lossfelt H, et al. Assignment of the human thyroid stimulating hormone receptor (TSHR) gene to chromosome 14q31. Genomics 1990; 8: 233-6.
    • (1990) Genomics , vol.8 , pp. 233-236
    • Rousseau-Merck, M.F.1    Misrachi, M.2    Lossfelt, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.