Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Gregorio Guabello"'
Autor:
Sabrina Corbetta, Laura Gianotti, Elena Castellano, Silvia Carrara, Francesca Raineri, Elisabetta Munari, Gregorio Guabello, Elisa Cairoli, Iacopo Chiodini, Luca Giovanelli, Laura Pierotti, Elisa Dinoi, Simone Della Valentina, Filomena Cetani
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
PurposeThe current primary hyperparathyroidism (PHPT) presents as a mild disease. We explored skeletal phenotypes in postmenopausal women affected by PHPT, focusing on fracture prevalence.MethodsPHPT women were retrospectively evaluated at four Itali
Externí odkaz:
https://doaj.org/article/4dcb7794e3684de8b68b9c955222e66f
Autor:
Luigia Cinque, Flavia Pugliese, Antonio Stefano Salcuni, Domenico Trombetta, Claudia Battista, Tommaso Biagini, Bartolomeo Augello, Grazia Nardella, Francesco Conti, Sabrina Corbetta, Rita Fischetto, Thomas Foiadelli, Agostino Gaudio, Cosimo Giannini, Enrico Grosso, Gregorio Guabello, Stefania Massuras, Andrea Palermo, Luisa Politano, Francesca Pigliaru, Rosaria Maddalena Ruggeri, Emanuela Scarano, Piera Vicchio, Salvatore Cannavò, Mauro Celli, Francesco Petrizzelli, Mario Mastroianno, Marco Castori, Alfredo Scillitani, Vito Guarnieri
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionHypophosphatasia (HPP) is a rare genetic disease caused by inactivating variants of the ALPL gene. Few data are available on the clinical presentation in Italy and/or on Italian HPP surveys.MethodsThere were 30 suspected HPP patients recr
Externí odkaz:
https://doaj.org/article/0354a004b69343bd97c812b9b831c063
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Hypercalciuria may represent a challenge during the workup for osteoporosis management. The present study aimed: (1) to describe the phenotype associated with hypercalciuria in vitamin D-sufficient (serum 25 hydroxyvitamin D (25OHD) > 20 ng/ml) patie
Externí odkaz:
https://doaj.org/article/2b5b0be019a946d19f8cec4b217837f7
Autor:
Giulia Carosi, Gregorio Guabello, Matteo Longhi, Federica Grifoni, Elena Passeri, Sabrina Corbetta
Publikováno v:
Mediators of Inflammation, Vol 2020 (2020)
Purpose. Systemic mastocytosis (SM) is characterized by a clonal proliferation of neoplastic mast cells (MCs) in one or more extracutaneous organs including the bone marrow (BM). SM is often associated with osteoporosis (OP) and fractures. Hypertrypt
Externí odkaz:
https://doaj.org/article/a25a6a12f729460daef8d0251572a0ce
Autor:
Sabrina Corbetta, Laura Gianotti, Elena Castellano, Francesca Raineri, Elisabetta Munari, Gregorio Guabello, Laura Pierotti, Elisa Dinoi, Simone Della Valentina, Filomena Cetani
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e35e1eeee34002e7afe3a2b78913181
https://doi.org/10.1530/endoabs.90.oc8.6
https://doi.org/10.1530/endoabs.90.oc8.6
Autor:
Vito Guarnieri, Matteo Longhi, Chiara Verdelli, F. Sileri, Sabrina Corbetta, Gregorio Guabello, Rita Indirli, G. Dito
Publikováno v:
Journal of Endocrinological Investigation
Purpose The study aimed to define the clinical, biochemical and genetic features of adult patients with osteopenia/osteoporosis and/or bone fragility and low serum alkaline phosphatase (sALP). Methods Twenty-two patients with at least two sALP values
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5b996f04a0d2011febf0e2515c06c52
http://europepmc.org/articles/PMC8741696
http://europepmc.org/articles/PMC8741696
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98f13a8b658efb308a09953ebe86ac21
https://doi.org/10.1530/endoabs.81.p306
https://doi.org/10.1530/endoabs.81.p306
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1504090b14d93686cfaab561aba1e385
https://doi.org/10.1530/endoabs.81.ep162
https://doi.org/10.1530/endoabs.81.ep162
Publikováno v:
Journal of Clinical Densitometry. 23:690-694
Background: Melorheostosis is a rare sporadic sclerosing bone dysplasia, which commonly affects appendicular skeleton with bone hyperostosis and soft tissues sclerosis; fragility fractures are rare in melorheostotic patients. We investigated bone fea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::762a5101fb42736fac067ae8ad46d28e
https://doi.org/10.1016/j.jocd.2020.01.002
https://doi.org/10.1016/j.jocd.2020.01.002
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42b426cb677c0dc658da8810e0cef3b1
https://doi.org/10.1530/endoabs.73.aep131
https://doi.org/10.1530/endoabs.73.aep131