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Volumn 154, Issue 6, 2009, Pages

Autonomous Thyroid Adenoma: Only an Adulthood Disease?

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; GUANINE NUCLEOTIDE BINDING PROTEIN; THYROTROPIN RECEPTOR;

EID: 65549170359     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpeds.2008.12.019     Document Type: Article
Times cited : (21)

References (12)
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    • (1973) Mayo Clin Proc , vol.48 , pp. 273-275
    • Popma, B.H.1    Cloutier, M.D.2    Hayles, A.B.3
  • 2
    • 58149403808 scopus 로고
    • Suppression of pituitary TSH in a child with a hyperfunctioning thyroid nodule
    • Granoff A.B., and Hershman J.M. Suppression of pituitary TSH in a child with a hyperfunctioning thyroid nodule. J Pediatr 90 (1977) 83-85
    • (1977) J Pediatr , vol.90 , pp. 83-85
    • Granoff, A.B.1    Hershman, J.M.2
  • 4
    • 0030830146 scopus 로고    scopus 로고
    • Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (serine281→isoleucine) in the extracellular domain of the thyrotropin receptor
    • Kopp P., Muirhead S., Jourdain N., Gu W.X., Jameson J.L., and Rodd C. Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (serine281→isoleucine) in the extracellular domain of the thyrotropin receptor. J Clin Invest 100 (1997) 1634-1639
    • (1997) J Clin Invest , vol.100 , pp. 1634-1639
    • Kopp, P.1    Muirhead, S.2    Jourdain, N.3    Gu, W.X.4    Jameson, J.L.5    Rodd, C.6
  • 5
    • 0025818413 scopus 로고
    • Solitary polyclonal autonomous thyroid nodule: a rare cause of childhood hyperthyroidism
    • Namba H., Ross J.L., Goodman D., and Fagin J.A. Solitary polyclonal autonomous thyroid nodule: a rare cause of childhood hyperthyroidism. J Clin Endocrinol Metab 72 (1991) 1108-1112
    • (1991) J Clin Endocrinol Metab , vol.72 , pp. 1108-1112
    • Namba, H.1    Ross, J.L.2    Goodman, D.3    Fagin, J.A.4
  • 6
    • 0038745922 scopus 로고    scopus 로고
    • A new heterozygous mutation (L338N) in the human Gsalpha (GNAS1) gene as a cause for congenital hypothyroidism in Albright's hereditary osteodystrophy
    • Pohlenz J., Ahrens W., and Hiort O. A new heterozygous mutation (L338N) in the human Gsalpha (GNAS1) gene as a cause for congenital hypothyroidism in Albright's hereditary osteodystrophy. Eur J Endocrinol 148 (2003) 463-468
    • (2003) Eur J Endocrinol , vol.148 , pp. 463-468
    • Pohlenz, J.1    Ahrens, W.2    Hiort, O.3
  • 7
    • 0030710212 scopus 로고    scopus 로고
    • Somatic mutations in the thyrotropin receptor gene and not in the Gs alpha protein gene in 31 toxic thyroid nodules
    • Fuhrer D., Holzapfel H.P., Wonerow P., Scherbaum W.A., and Paschke R. Somatic mutations in the thyrotropin receptor gene and not in the Gs alpha protein gene in 31 toxic thyroid nodules. J Clin Endocrinol Metab 82 (1997) 3885-3891
    • (1997) J Clin Endocrinol Metab , vol.82 , pp. 3885-3891
    • Fuhrer, D.1    Holzapfel, H.P.2    Wonerow, P.3    Scherbaum, W.A.4    Paschke, R.5
  • 10
    • 0028040908 scopus 로고
    • Novel mutations of thyrotropin receptor gene in thyroid hyperfunctioning adenomas. Rapid identification by fine needle aspiration biopsy
    • Porcellini A., Ciullo I., Laviola L., Amabile G., Fenzi G., and Avvedimento V.E. Novel mutations of thyrotropin receptor gene in thyroid hyperfunctioning adenomas. Rapid identification by fine needle aspiration biopsy. J Clin Endocrinol Metab 79 (1994) 657-661
    • (1994) J Clin Endocrinol Metab , vol.79 , pp. 657-661
    • Porcellini, A.1    Ciullo, I.2    Laviola, L.3    Amabile, G.4    Fenzi, G.5    Avvedimento, V.E.6
  • 11
    • 8544221172 scopus 로고    scopus 로고
    • Diversity and prevalence of somatic mutations in the thyrotropin receptor and Gs alpha genes as a cause of toxic thyroid adenomas
    • Parma J., Duprez L., Van Sande J., Hermans J., Rocmans P., Van Vliet G., et al. Diversity and prevalence of somatic mutations in the thyrotropin receptor and Gs alpha genes as a cause of toxic thyroid adenomas. J Clin Endocrinol Metab 82 (1997) 2695-2701
    • (1997) J Clin Endocrinol Metab , vol.82 , pp. 2695-2701
    • Parma, J.1    Duprez, L.2    Van Sande, J.3    Hermans, J.4    Rocmans, P.5    Van Vliet, G.6
  • 12
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    • Activating thyrotropin receptor mutations in histologically heterogeneous hyperfunctioning nodules of multinodular goiter
    • Tonacchera M., Vitti P., Agretti P., Giulianetti B., Mazzi B., Cavaliere R., et al. Activating thyrotropin receptor mutations in histologically heterogeneous hyperfunctioning nodules of multinodular goiter. Thyroid 8 (1998) 559-564
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.