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Volumn 34, Issue 4, 2000, Pages 189-193

Autoimmune thyroiditis with severe hypothyroidism resistant to the treatment with high peroral doses of thyroxine: Case report

Author keywords

Autoimmune thyroiditis; Hypothyroidism; Thyroxine pseudomalabsorption

Indexed keywords

THYROTROPIN; THYROXINE;

EID: 0034569509     PISSN: 12100668     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (12)

References (10)
  • 1
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    • Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin causing profound hypoplasia of the thyroid gland
    • ABRAMOWICS MJ, DUPREZ L, PARMA J, VASSART G, HEINRICHS C: Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin causing profound hypoplasia of the thyroid gland. J Clin Invest 99, 3018-3024, 1997
    • (1997) J Clin Invest , vol.99 , pp. 3018-3024
    • Abramowics, M.J.1    Duprez, L.2    Parma, J.3    Vassart, G.4    Heinrichs, C.5
  • 3
    • 0030983833 scopus 로고    scopus 로고
    • Mutations of the human thyrotropin receptor gene causng thyroid hypoplasisa and persistant congenutal hypothyroidism
    • BIEBERMAN H, SCHONEBERG T, KRUDE H, SCHUKTZ G, GUDERMAN T, GRUTERS A: Mutations of the human thyrotropin receptor gene causng thyroid hypoplasisa and persistant congenutal hypothyroidism. J Clin Endocrinol Metab 82, 3471-3480, 1997
    • (1997) J Clin Endocrinol Metab , vol.82 , pp. 3471-3480
    • Bieberman, H.1    Schoneberg, T.2    Krude, H.3    Schuktz, G.4    Guderman, T.5    Gruters, A.6
  • 4
    • 0030989828 scopus 로고    scopus 로고
    • Two novel mutations in the thyrotropin (TSH) receptor gene in a child with resistance to TSH
    • CLIFTON-BLIGH RG, GREGORY JW, LUDGATE M et al.: Two novel mutations in the thyrotropin (TSH) receptor gene in a child with resistance to TSH. J Clin Endocrinol Metab 82, 1094-1100, 1997
    • (1997) J Clin Endocrinol Metab , vol.82 , pp. 1094-1100
    • Clifton-Bligh, R.G.1    Gregory, J.W.2    Ludgate, M.3
  • 5
    • 10544240361 scopus 로고    scopus 로고
    • Four families with loss of function mutations of the thyrotropin receptor
    • DE Roux N, MISRAHI M, BRAUNER Pet al.: Four families with loss of function mutations of the thyrotropin receptor. J Clin Endocrinol Metab 81, 4229-4235, 1996
    • (1996) J Clin Endocrinol Metab , vol.81 , pp. 4229-4235
    • De Roux, N.1    Misrahi, M.2    Brauner, P.3
  • 6
    • 0031755047 scopus 로고    scopus 로고
    • Apparent congenital athyreosis contrasting with normal plasma thyroglobulin levels and associated with inactivating mutations in the thyrotropin receptor gene: Are athyreosis and ectopic thyroid distinct entities?
    • GAGNE N, PARMA J, DEAL C, VASSART G, VAN VLIET G: Apparent congenital athyreosis contrasting with normal plasma thyroglobulin levels and associated with inactivating mutations in the thyrotropin receptor gene: are athyreosis and ectopic thyroid distinct entities? J Clin Endocrinol Metab 83, 1771-1775, 1998
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 1771-1775
    • Gagne, N.1    Parma, J.2    Deal, C.3    Vassart, G.4    Van Vliet, G.5
  • 8
    • 0014425946 scopus 로고
    • Congenital hypothyroidism with impaired thyroid response to thyrotropin
    • STANBURY JB, ROCMANS F, BUHLER UK, OCHI Y: Congenital hypothyroidism with impaired thyroid response to thyrotropin. N Eng J Med 21, 1132-1136, 1968
    • (1968) N Eng J Med , vol.21 , pp. 1132-1136
    • Stanbury, J.B.1    Rocmans, F.2    Buhler, U.K.3    Ochi, Y.4
  • 9
    • 0028888593 scopus 로고
    • Resistance to thyrotropin caused by mutations in the thyrotropin-receptor gene
    • SUNTHORNTHEPVARAKUL T, GOTTSCHALK ME, HAYASHI Y, REFETOFF S: resistance to thyrotropin caused by mutations in the thyrotropin-receptor gene. N Eng J Med 332, 156-160, 1995
    • (1995) N Eng J Med , vol.332 , pp. 156-160
    • Sunthornthepvarakul, T.1    Gottschalk, M.E.2    Hayashi, Y.3    Refetoff, S.4
  • 10
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    • 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, AGRETI P, PINCHERA A, ROSELLINI V, PERRI A, COLLECCHI P, VITTI P, CHIOVATO L: Congenital hypothyroidism with impaired thyroid response to thyrotropin (TSH) and absent circulating thyroglobulin: Evidence for a new inactivating mutation of the TSh receptor gene. J Clin Endocrinol Metab 85, 1001-1008, 2000
    • (2000) J Clin Endocrinol Metab , vol.85 , pp. 1001-1008
    • Tonacchera, M.1    Agreti, P.2    Pinchera, A.3    Rosellini, V.4    Perri, A.5    Collecchi, P.6    Vitti, P.7    Chiovato, L.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.