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G Fenzi

Showing results (41-50 of 53) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|July 1, 1990
Incidence of antibodies blocking thyrotropin effect in vitro in patients with euthyroid or hypothyroid autoimmune thyroiditisL Chiovato, P Vitti, F Santini, et al.
Hormone Research|January 21, 2000
Power Doppler improves the diagnostic accuracy of color Doppler ultrasonography in cold thyroid nodules: follow-up resultsG Cerbone, S Spiezia, A Colao, et al.
Journal of Endocrinological Investigation|December 30, 1999
Percutaneous ethanol injection under Power Doppler ultrasound assistance in the treatment of autonomously functioning thyroid nodulesG Cerbone, S Spiezia, A Colao, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
Orbital scintigraphy with [111In-diethylenetriamine pentaacetic acid-D-phe1]-octreotide predicts the clinical response to corticosteroid therapy in patients with Graves' ophthalmopathyA Colao, S Lastoria, D Ferone, et al.
Clinical Endocrinology|August 10, 2000
Increased prevalence of thyroid autoimmunity in patients successfully treated for Cushing's diseaseA Colao, R Pivonello, A Faggiano, et al.
Recenti Progressi in Medicina|September 1, 1985
[Iodine-induced hyperthyroidism caused by amiodarone]F Aghini-Lombardi, E Martino, M Lenziardi, et al.
Annali Dell'Istituto Superiore Di Sanita|March 3, 1999
[Widespread endemic goiter and iodine deficiency in the province of Avellino]S Pagliara, E Spagnuolo, A D'Avanzo, et al.
The Journal of Clinical Endocrinology and Metabolism|November 4, 2000
Tyrosines 1015 and 1062 are in vivo autophosphorylation sites in ret and ret-derived oncoproteinsD Salvatore, M V Barone, G Salvatore, 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.
Journal of Endocrinological Investigation|June 23, 2009
Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesisA M Ferrara, L De Sanctis, G Rossi, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
The Journal of Clinical Endocrinology and Metabolism|July 1, 1990
Incidence of antibodies blocking thyrotropin effect in vitro in patients with euthyroid or hypothyroid autoimmune thyroiditisL Chiovato, P Vitti, F Santini, et al.
Hormone Research|January 21, 2000
Power Doppler improves the diagnostic accuracy of color Doppler ultrasonography in cold thyroid nodules: follow-up resultsG Cerbone, S Spiezia, A Colao, et al.
Journal of Endocrinological Investigation|December 30, 1999
Percutaneous ethanol injection under Power Doppler ultrasound assistance in the treatment of autonomously functioning thyroid nodulesG Cerbone, S Spiezia, A Colao, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
Orbital scintigraphy with [111In-diethylenetriamine pentaacetic acid-D-phe1]-octreotide predicts the clinical response to corticosteroid therapy in patients with Graves' ophthalmopathyA Colao, S Lastoria, D Ferone, et al.
Clinical Endocrinology|August 10, 2000
Increased prevalence of thyroid autoimmunity in patients successfully treated for Cushing's diseaseA Colao, R Pivonello, A Faggiano, et al.
Recenti Progressi in Medicina|September 1, 1985
[Iodine-induced hyperthyroidism caused by amiodarone]F Aghini-Lombardi, E Martino, M Lenziardi, et al.
Annali Dell'Istituto Superiore Di Sanita|March 3, 1999
[Widespread endemic goiter and iodine deficiency in the province of Avellino]S Pagliara, E Spagnuolo, A D'Avanzo, et al.
The Journal of Clinical Endocrinology and Metabolism|November 4, 2000
Tyrosines 1015 and 1062 are in vivo autophosphorylation sites in ret and ret-derived oncoproteinsD Salvatore, M V Barone, G Salvatore, 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.
Journal of Endocrinological Investigation|June 23, 2009
Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesisA M Ferrara, L De Sanctis, G Rossi, et al.
Pageof 6