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L Persani

Showing results (51-60 of 99) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Evaluation of the adequacy of levothyroxine replacement therapy in patients with central hypothyroidismE Ferretti, L Persani, M L Jaffrain-Rea, et al.
Journal of Endocrinological Investigation|November 1, 1991
Patterns of gastrin secretion in patients with nonfunctioning pituitary adenomasL Persani, P Beck-Peccoz, M Quatrini, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1994
Evidence for the secretion of thyrotropin with enhanced bioactivity in syndromes of thyroid hormone resistanceL Persani, C Asteria, M Tonacchera, et al.
The Journal of Clinical Endocrinology and Metabolism|July 5, 2003
Monoallelic expression of mutant thyroid peroxidase allele causing total iodide organification defectL Fugazzola, N Cerutti, D Mannavola, et al.
Acta Medica Austriaca|January 1, 1996
Thyrotropin-secreting pituitary tumors in hyper- and hypothyroidismP Beck-Peccoz, L Persani, C Asteria, et al.
The Journal of Clinical Endocrinology and Metabolism|August 18, 2000
Induction of specific phosphodiesterase isoforms by constitutive activation of the cAMP pathway in autonomous thyroid adenomasL Persani, A Lania, L Alberti, et al.
The Journal of Endocrinology|September 1, 2007
Expression and biological effects of bone morphogenetic protein-15 in the hen ovaryS Elis, J Dupont, I Couty, et al.
European Journal of Endocrinology|August 23, 2001
A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidismL Alberti, M C Proverbio, S Costagliola, et al.
Thyroid : Official Journal of the American Thyroid Association|February 12, 1998
Clinical and hormonal outcome after two years of triiodothyroacetic acid treatment in a child with thyroid hormone resistanceG Radetti, L Persani, G Molinaro, et al.
European Journal of Endocrinology|March 29, 2001
Lectin analyses of glycoprotein hormones in patients with congenital disorders of glycosylationM C Ferrari, R Parini, M D Di Rocco, et al.
Pageof 10

Showing results (51-60 of 99) with videos related to

Sort By:
Pageof 10
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Evaluation of the adequacy of levothyroxine replacement therapy in patients with central hypothyroidismE Ferretti, L Persani, M L Jaffrain-Rea, et al.
Journal of Endocrinological Investigation|November 1, 1991
Patterns of gastrin secretion in patients with nonfunctioning pituitary adenomasL Persani, P Beck-Peccoz, M Quatrini, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1994
Evidence for the secretion of thyrotropin with enhanced bioactivity in syndromes of thyroid hormone resistanceL Persani, C Asteria, M Tonacchera, et al.
The Journal of Clinical Endocrinology and Metabolism|July 5, 2003
Monoallelic expression of mutant thyroid peroxidase allele causing total iodide organification defectL Fugazzola, N Cerutti, D Mannavola, et al.
Acta Medica Austriaca|January 1, 1996
Thyrotropin-secreting pituitary tumors in hyper- and hypothyroidismP Beck-Peccoz, L Persani, C Asteria, et al.
The Journal of Clinical Endocrinology and Metabolism|August 18, 2000
Induction of specific phosphodiesterase isoforms by constitutive activation of the cAMP pathway in autonomous thyroid adenomasL Persani, A Lania, L Alberti, et al.
The Journal of Endocrinology|September 1, 2007
Expression and biological effects of bone morphogenetic protein-15 in the hen ovaryS Elis, J Dupont, I Couty, et al.
European Journal of Endocrinology|August 23, 2001
A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidismL Alberti, M C Proverbio, S Costagliola, et al.
Thyroid : Official Journal of the American Thyroid Association|February 12, 1998
Clinical and hormonal outcome after two years of triiodothyroacetic acid treatment in a child with thyroid hormone resistanceG Radetti, L Persani, G Molinaro, et al.
European Journal of Endocrinology|March 29, 2001
Lectin analyses of glycoprotein hormones in patients with congenital disorders of glycosylationM C Ferrari, R Parini, M D Di Rocco, et al.
Pageof 10