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Journal of Endocrinological Investigation|January 1, 1995
Mild iodine deficiency during fetal/neonatal life and neuropsychological impairment in TuscanyF A Aghini Lombardi, A Pinchera, L Antonangeli, et al.
Journal of Endocrinological Investigation|April 1, 1996
Transfection with the cDNA of the human thyrotropin receptor of a poorly differentiated rat thyroid cell line (FRT)R Elisei, A Pinchera, L Chiovato, et al.
Thyroid : Official Journal of the American Thyroid Association|November 18, 2000
Sporadic nonautoimmune congenital hyperthyroidism due to a strong activating mutation of the thyrotropin receptor geneM Tonacchera, P Agretti, V Rosellini, et al.
Surgery|December 1, 1996
Surgical treatment of Graves' disease: subtotal or total thyroidectomy?P Miccoli, P Vitti, T Rago, et al.
Thyroid : Official Journal of the American Thyroid Association|June 1, 1997
Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequent cause of congenital hypothyroidism (CH) with thyroid dysgenesisP Lapi, P E Macchia, L Chiovato, et al.
The Journal of Clinical Endocrinology and Metabolism|June 14, 2000
Activating thyrotropin receptor mutations are present in nonadenomatous hyperfunctioning nodules of toxic or autonomous multinodular goiterM Tonacchera, P Agretti, L Chiovato, et al.
Endocrinology and Metabolism Clinics of North America|June 30, 2000
The genetics of Hashimoto's diseaseG Barbesino, L Chiovato
European Journal of Endocrinology|January 1, 1996
Study of serum 3,5,3'-triiodothyronine sulfate concentration in patients with systemic non-thyroidal illnessF Santini, L Chiovato, L Bartalena, et al.
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