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Alberto Falchetti

Showing results (61-70 of 102) with videos related to

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International Journal of Molecular Sciences|November 13, 2021
Management and Medical Therapy of Mild HypercortisolismVittoria Favero, Arianna Cremaschi, Alberto Falchetti, et al.
Endocrine|February 25, 2021
Early post-natal life stress induces permanent adrenocorticotropin-dependent hypercortisolism in male miceGabriele Campana, Stefano Loizzo, Andrea Fortuna, et al.
Frontiers in Cell and Developmental Biology|August 29, 2022
Update on the pathogenesis and genetics of Paget's disease of boneLuigi Gennari, Domenico Rendina, Daniela Merlotti, et al.
International Journal of Molecular Sciences|January 21, 2022
Pathophysiology of Mild Hypercortisolism: From the Bench to the BedsideVittoria Favero, Arianna Cremaschi, Chiara Parazzoli, et al.
European Journal of Clinical Investigation|July 27, 2010
Genetic aspects of the Paget's disease of bone: concerns on the introduction of DNA-based tests in the clinical practice. Advantages and disadvantages of its applicationAlberto Falchetti, Falchetti Alberto, Francesca Marini, et al.
Clinical Cases in Mineral and Bone Metabolism : the Official Journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases|March 31, 2012
The role of osteoprotegerin (OPG) and estrogen receptor (ER-α) gene polymorphisms in rheumatoid arthritisLaura Masi, Susanna Maddali Bongi, Chiara Angotti, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|January 29, 2003
Analysis of estrogen receptor (ERalpha and ERbeta) and progesterone receptor (PR) polymorphisms in uterine leiomyomasFrancesco Massart, Lucia Becherini, Francesca Marini, et al.
Calcified Tissue International|October 25, 2024
Glycogen Storage Disease Type I and Bone: Clinical and Cellular CharacterizationSilvia Vai, Alberto Falchetti, Sabrina Corbetta, et al.
International Journal of Molecular Sciences|January 28, 2026
Beyond the Genome: Can Epigenetics Forecast Therapeutic Success in Graves' Disease and Thyroid Eye Disease?Jacopo Manso, Dario Sardone, Vincenzo Marotta, et al.
Arthritis Research & Therapy|November 10, 2005
Segregation of a M404V mutation of the p62/sequestosome 1 (p62/SQSTM1) gene with polyostotic Paget's disease of bone in an Italian familyAlberto Falchetti, Marco Di Stefano, Francesca Marini, et al.
Pageof 11

Showing results (61-70 of 102) with videos related to

Sort By:
Pageof 11
International Journal of Molecular Sciences|November 13, 2021
Management and Medical Therapy of Mild HypercortisolismVittoria Favero, Arianna Cremaschi, Alberto Falchetti, et al.
Endocrine|February 25, 2021
Early post-natal life stress induces permanent adrenocorticotropin-dependent hypercortisolism in male miceGabriele Campana, Stefano Loizzo, Andrea Fortuna, et al.
Frontiers in Cell and Developmental Biology|August 29, 2022
Update on the pathogenesis and genetics of Paget's disease of boneLuigi Gennari, Domenico Rendina, Daniela Merlotti, et al.
International Journal of Molecular Sciences|January 21, 2022
Pathophysiology of Mild Hypercortisolism: From the Bench to the BedsideVittoria Favero, Arianna Cremaschi, Chiara Parazzoli, et al.
European Journal of Clinical Investigation|July 27, 2010
Genetic aspects of the Paget's disease of bone: concerns on the introduction of DNA-based tests in the clinical practice. Advantages and disadvantages of its applicationAlberto Falchetti, Falchetti Alberto, Francesca Marini, et al.
Clinical Cases in Mineral and Bone Metabolism : the Official Journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases|March 31, 2012
The role of osteoprotegerin (OPG) and estrogen receptor (ER-α) gene polymorphisms in rheumatoid arthritisLaura Masi, Susanna Maddali Bongi, Chiara Angotti, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|January 29, 2003
Analysis of estrogen receptor (ERalpha and ERbeta) and progesterone receptor (PR) polymorphisms in uterine leiomyomasFrancesco Massart, Lucia Becherini, Francesca Marini, et al.
Calcified Tissue International|October 25, 2024
Glycogen Storage Disease Type I and Bone: Clinical and Cellular CharacterizationSilvia Vai, Alberto Falchetti, Sabrina Corbetta, et al.
International Journal of Molecular Sciences|January 28, 2026
Beyond the Genome: Can Epigenetics Forecast Therapeutic Success in Graves' Disease and Thyroid Eye Disease?Jacopo Manso, Dario Sardone, Vincenzo Marotta, et al.
Arthritis Research & Therapy|November 10, 2005
Segregation of a M404V mutation of the p62/sequestosome 1 (p62/SQSTM1) gene with polyostotic Paget's disease of bone in an Italian familyAlberto Falchetti, Marco Di Stefano, Francesca Marini, et al.
Pageof 11