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The Journal of Clinical Endocrinology and Metabolism|May 15, 2022
Long-term Efficacy and Safety of Rifampin in the Treatment of a Patient Carrying a CYP24A1 Loss-of-Function VariantAlessandro Brancatella, Daniele Cappellani, Martin Kaufmann, et al.
The Journal of Endocrinology|May 14, 2011
Cardiac extrinsic apoptotic pathway is silent in young but activated in elder mice overexpressing bovine GH: interplay with the intrinsic pathwayFausto Bogazzi, Dania Russo, Francesco Raggi, et al.
Frontiers in Oncology|September 3, 2024
Persistent primary hyperparathyroidism caused by an ectopic adenoma in the piriform sinus: case report and review of the literatureChiara Sardella, Veronica Seccia, Massimo Giambalvo, et al.
Journal of Endocrinological Investigation|June 1, 2026
Clinical and genetic insights into Autosomal Dominant Hypocalcemia type 1: a single-center case series including genotype-phenotype correlations, pregnancy outcomes, and novel CASR variantsSimone Della Valentina, Laura Pierotti, Chiara Sardella, et al.
Endocrinology|August 6, 2013
Growth hormone is necessary for the p53-mediated, obesity-induced insulin resistance in male C57BL/6J x CBA miceFausto Bogazzi, Francesco Raggi, Dania Russo, et al.
Clinical Endocrinology|January 5, 2007
Abnormal expression of PPAR gamma isoforms in the subcutaneous adipose tissue of patients with Cushing's diseaseFausto Bogazzi, Federica Ultimieri, Francesco Raggi, et al.
Clinical Endocrinology|December 14, 2005
Apoptosis is reduced in the colonic mucosa of patients with acromegalyFausto Bogazzi, Dania Russo, Maria Teresa Locci, et al.
Clinical Endocrinology|March 26, 2014
The beneficial effect of acromegaly control on blood pressure values in normotensive patientsChiara Sardella, Claudio Urbani, Martina Lombardi, et al.
Frontiers in Endocrinology|July 24, 2023
Cutaneous lesions and other non-endocrine manifestations of Multiple Endocrine Neoplasia type 1 syndromeLaura Pierotti, Elena Pardi, Elisa Dinoi, et al.
Frontiers in Endocrinology|August 25, 2022
Case report: Early-onset osteoporosis in a patient carrying a novel heterozygous variant of the WNT1 geneMaria Cristina Campopiano, Antonella Fogli, Angela Michelucci, et al.
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