Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Raffaella Di Mase"'
Autor:
Donatella Capalbo, Andrea Esposito, Valeria Gaeta, Paola Lorello, Sara Vasaturo, Raffaella Di Mase, Mariacarolina Salerno
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Primary adrenal insufficiency (PAI) is a rare medical condition, characterized by a deficiency in adrenal hormones. Although rare, PAI is a life-threatening disease requiring prompt recognition and treatment. However, symptoms of PAI are often non-sp
Externí odkaz:
https://doaj.org/article/403190e2ae104495b3ff04e8531b9cc5
Autor:
Octavio Rivera Romero, Hyun Wook Chae, Maria Felicia Faienza, Edoardo Vergani, Chong Kun Cheon, Raffaella Di Mase, Francesco Frasca, Hae Sang Lee, Claudia Giavoli, Jihyun Kim, Antonella Klain, Jung Eun Moon, Maria Laura Iezzi, James Yeh, Antonio Aversa, Young-Jun Rhie, Ekaterina Koledova
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionTo analyse the perspectives of healthcare professionals (HCPs) regarding the acceptance of digital health solutions for growth hormone (GH) deficiency care. This study identified factors impacting HCPs’ intent to use and recommend digit
Externí odkaz:
https://doaj.org/article/d39198b264284160b7bbac5088f8dee9
Autor:
Andrea Esposito, Maria Cristina Vigone, Miriam Polizzi, Malgorzata Gabriela Wasniewska, Alessandra Cassio, Alessandro Mussa, Roberto Gastaldi, Raffaella Di Mase, Gaia Vincenzi, Clara Pozzi, Elena Peroni, Carmela Bravaccio, Donatella Capalbo, Dario Bruzzese, Mariacarolina Salerno
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
ObjectivesWe designed a multicentre open prospective randomized trial to evaluate the risk-benefit profile of two different initial treatment schemes with levothyroxine (L-T4), 10-12.5 μg/kg/day vs 12.6-15 μg/kg/day, on growth and neurodevelopmenta
Externí odkaz:
https://doaj.org/article/ffce6b27a165420787fa8276e3309eb1
Autor:
Francesca Aiello, Grazia Cirillo, Alessandra Cassio, Raffaella Di Mase, Gianluca Tornese, Giuseppina R. Umano, Emanuele Miraglia del Giudice, Anna Grandone
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-5 (2021)
Abstract Background Prokineticin receptor 2 (PROKR2) loss of function mutations have been described as cause of hypogonadotropic hypogonadism. In 2017, a first case of central precocious puberty (CPP) caused by PROKR2 heterozygous gain of function mu
Externí odkaz:
https://doaj.org/article/5c3e0a88af17406facfef84ad10a6185
Autor:
Lucia De Martino, Donatella Capalbo, Nicola Improda, Paola Lorello, Carla Ungaro, Raffaella Di Mase, Emilia Cirillo, Claudio Pignata, Mariacarolina Salerno
Publikováno v:
Frontiers in Pediatrics, Vol 4 (2016)
Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy (APECED), formerly known as Autoimmune Polyendocrine Syndrome type 1 (APS-1), is a paradigm of a monogenic autoimmune disease caused by mutations of a gene, named autoimmune regulator (AI
Externí odkaz:
https://doaj.org/article/62dffb5bac194b0da6bb71fb503ffa61
Autor:
Donatella Capalbo, Lucia De Martino, Giuliana Giardino, Raffaella Di Mase, Iolanda Di Donato, Giancarlo Parenti, Pietro Vajro, Claudio Pignata, Mariacarolina Salerno
Publikováno v:
International Journal of Endocrinology, Vol 2012 (2012)
Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED) is a rare autosomal recessive disease, caused by mutations of a single gene named autoimmune regulator gene (AIRE) which results in a failure of T cell tolerance within the thymu
Externí odkaz:
https://doaj.org/article/49f2d52131a24a7cbcfd0dc363b543df
Publikováno v:
L'Endocrinologo. 23:74-76
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43a9bbbef40fe9a3bcd03c9110cc3702
https://doi.org/10.1007/s40619-022-01114-4
https://doi.org/10.1007/s40619-022-01114-4
Autor:
Daniela Driul, Stefano Tumini, Carlo Efisio Marras, Valentino Cherubini, Natascia Di Iorgi, Stefano Cianfarani, Stefania Pedicelli, Lorenzo Genitori, Mino Zucchelli, Malgorzata Wasniewska, Giovanna Giudica, Marco Vindigni, Cristina Partenope, Chiara Guzzetti, Maria Parpagnoli, Stefano Zucchini, Lorenzo Iughetti, Maria Laura Iezzi, Alessandro Consales, Rachele Menardi, Sandro Loche, Irene Rutigliano, Patrizia Bruzzi, Federico Baronio, Francesco Zenga, Mariafelicia Faienza, Tommaso Aversa, Marco Crocco, Gerdi Tuli, P Matarazzo, Raffaella Di Mase, Mohamad Maghnie, Beatrice Nardini, Claudia Milanaccio, Pietro Mortini, Cristina Baldoli, Graziamaria Ubertini, Anna Grandone, Mariacarolina Salerno, Gabriella Pozzobon, Alessandra Cassio
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 107:e1020-e1031
Context Nationwide data on children diagnosed with craniopharyngioma (CP) are not available in Italy. Objective This work aimed to identify patients’ characteristics, type of surgical approach, complications and recurrences, number of pituitary def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b5e90dab1ede08c7aa5dad17288a2be
https://doi.org/10.1210/clinem/dgab784
https://doi.org/10.1210/clinem/dgab784
Autor:
Maria Cristina Vigone, Rita Ortolano, Gaia Vincenzi, Clara Pozzi, Micol Ratti, Valentina Assirelli, Sofia Vissani, Paolo Cavarzere, Alessandro Mussa, Roberto Gastaldi, Raffaella Di Mase, Mariacarolina Salerno, Maria Elisabeth Street, Jessica Trombatore, Giovanna Weber, Alessandra Cassio
Publikováno v:
European journal of endocrinology. 186(1)
Objective Oral solution and tablet formulations of levothyroxine (L-T4) are both used in the treatment of congenital hypothyroidism (CH). However, few studies and with a limited follow-up period have been published comparing these two formulations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3d7f1f88a5da4c273f30e67d8d7b17c
https://pubmed.ncbi.nlm.nih.gov/34714772
https://pubmed.ncbi.nlm.nih.gov/34714772
Autor:
Gianluca Tornese, Giuseppina Rosaria Umano, Emanuele Miraglia del Giudice, Francesca Aiello, Raffaella Di Mase, Alessandra Cassio, Anna Grandone, Grazia Cirillo
Publikováno v:
Italian Journal of Pediatrics
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-5 (2021)
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-5 (2021)
Background Prokineticin receptor 2 (PROKR2) loss of function mutations have been described as cause of hypogonadotropic hypogonadism. In 2017, a first case of central precocious puberty (CPP) caused by PROKR2 heterozygous gain of function mutation wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2c4d6ec909fb2cc1caab5248ad90430
https://hdl.handle.net/11585/796308
https://hdl.handle.net/11585/796308
