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Luca Persani

Showing results (161-170 of 321) with videos related to

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Human Molecular Genetics|August 7, 2015
A new variant in signal peptide of the human luteinizing hormone receptor (LHCGR) affects receptor biogenesis causing leydig cell hypoplasiaValeria Vezzoli, Paolo Duminuco, Alessandra Vottero, et al.
Plos One|August 11, 2012
Blood cell mitochondrial DNA content and premature ovarian agingMarco Bonomi, Edgardo Somigliana, Chiara Cacciatore, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|February 1, 2026
Response to the Letter to the Editor: "Hypertensive Hypercortisolism: What Does 1.14 μg/dL Really Mean?"Antonio Musolino, Vittoria Favero, Grzegorz Bilo, et al.
Plos Biology|August 19, 2009
Persistent cAMP-signals triggered by internalized G-protein-coupled receptorsDavide Calebiro, Viacheslav O Nikolaev, Maria Cristina Gagliani, et al.
Molecular Endocrinology (Baltimore, Md.)|August 5, 2006
Selective modulation of protein kinase A I and II reveals distinct roles in thyroid cell gene expression and growthDavide Calebiro, Tiziana de Filippis, Simona Lucchi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 11, 2012
Difficult treatment of consumptive hypothyroidism in a child with massive parotid hemangiomaMaria Cristina Vigone, Francesca Cortinovis, Sarah Rabbiosi, et al.
Journal of the Endocrine Society|July 24, 2020
Defining Nonfunctioning Adrenal Adenomas on the Basis of the Occurrence of Hypocortisolism after AdrenalectomyCristina Eller-Vainicher, Valentina Morelli, Carmen Aresta, et al.
European Journal of Endocrinology|May 12, 2012
MEN1-related hyperparathyroidism: response to cinacalcet and its relationship with the calcium-sensing receptor gene variant Arg990GlyMarcello Filopanti, Uberta Verga, Federica Ermetici, et al.
Thyroid : Official Journal of the American Thyroid Association|July 30, 2025
Variable Diagnoses in Cases Referred for Discordant Thyroid Function Tests: Focus on Lymphoproliferative DisordersAntonio Musolino, Giacomo Fabio Antonio Grifoni, Simone Rodolfi, et al.
Human Molecular Genetics|November 1, 2016
Impaired protein stability and nuclear localization of NOBOX variants associated with premature ovarian insufficiencyIlaria Ferrari, Justine Bouilly, Isabelle Beau, et al.
Pageof 33

Showing results (161-170 of 321) with videos related to

Sort By:
Pageof 33
Human Molecular Genetics|August 7, 2015
A new variant in signal peptide of the human luteinizing hormone receptor (LHCGR) affects receptor biogenesis causing leydig cell hypoplasiaValeria Vezzoli, Paolo Duminuco, Alessandra Vottero, et al.
Plos One|August 11, 2012
Blood cell mitochondrial DNA content and premature ovarian agingMarco Bonomi, Edgardo Somigliana, Chiara Cacciatore, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|February 1, 2026
Response to the Letter to the Editor: "Hypertensive Hypercortisolism: What Does 1.14 μg/dL Really Mean?"Antonio Musolino, Vittoria Favero, Grzegorz Bilo, et al.
Plos Biology|August 19, 2009
Persistent cAMP-signals triggered by internalized G-protein-coupled receptorsDavide Calebiro, Viacheslav O Nikolaev, Maria Cristina Gagliani, et al.
Molecular Endocrinology (Baltimore, Md.)|August 5, 2006
Selective modulation of protein kinase A I and II reveals distinct roles in thyroid cell gene expression and growthDavide Calebiro, Tiziana de Filippis, Simona Lucchi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 11, 2012
Difficult treatment of consumptive hypothyroidism in a child with massive parotid hemangiomaMaria Cristina Vigone, Francesca Cortinovis, Sarah Rabbiosi, et al.
Journal of the Endocrine Society|July 24, 2020
Defining Nonfunctioning Adrenal Adenomas on the Basis of the Occurrence of Hypocortisolism after AdrenalectomyCristina Eller-Vainicher, Valentina Morelli, Carmen Aresta, et al.
European Journal of Endocrinology|May 12, 2012
MEN1-related hyperparathyroidism: response to cinacalcet and its relationship with the calcium-sensing receptor gene variant Arg990GlyMarcello Filopanti, Uberta Verga, Federica Ermetici, et al.
Thyroid : Official Journal of the American Thyroid Association|July 30, 2025
Variable Diagnoses in Cases Referred for Discordant Thyroid Function Tests: Focus on Lymphoproliferative DisordersAntonio Musolino, Giacomo Fabio Antonio Grifoni, Simone Rodolfi, et al.
Human Molecular Genetics|November 1, 2016
Impaired protein stability and nuclear localization of NOBOX variants associated with premature ovarian insufficiencyIlaria Ferrari, Justine Bouilly, Isabelle Beau, et al.
Pageof 33