Author:
Arturi F.,Chiefari E.,Tumino S.,Russo D.,Squatrito S.,Chazenbalk G.,Persani L.,Rapoport B.,Filetti S.
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference28 articles.
1. Thomas J.L., Leclere J., Hartemann P. eaet al. Familial hyperthyroidism without evidence of autoimmunity. Acta Endocrinol. (Copenh.) 1982, 100: 512–518.
2. Leclere J., Bene M.C., Aubert V. et al. Clinical consequences of activating germline mutations of TSH receptor, the concept of toxic hyperplasia. Horm. Res. 1997, 47: 158–162.
3. Duprez L., Parma J., Van Sande J., et al. Germline mutations in non-autoimmune the thyrotropin receptor gene cause autosomal dominant hyperthyroidism. Nat. Genet. 1994, 7: 396–401.
4. Tonacchera M., Van Sande J., Cetani F., et al. Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia. J. Clin. Endocrinol. Metab. 1996, 81: 547–554.
5. Schwab K.O., Sohlemann P., Gerlich M., et al. Mutations of the TSH receptor as cause of congenital hyperthyroidism. Exp. Clin. Endocrinol. Diabetes 1996, 104: (4) 124–128.
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