Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Marco Pitea"'
Autor:
Giampiero I. Baroncelli, Pasquale Comberiati, Tommaso Aversa, Federico Baronio, Alessandra Cassio, Mariangela Chiarito, Mirna Cosci o di Coscio, Luisa De Sanctis, Natascia Di Iorgi, Maria Felicia Faienza, Danilo Fintini, Roberto Franceschi, Mila Kalapurackal, Silvia Longhi, Michela Mariani, Marco Pitea, Andrea Secco, Daniele Tessaris, Francesco Vierucci, Malgorzata Wasniewska, Giovanna Weber, Stefano Mora
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Rickets results from impaired mineralization of growing bone due to alterations in calcium and phosphate homeostasis. Clinical signs of rickets are related to the age of the patient, the duration of the disease, and the underlying disorder. The most
Externí odkaz:
https://doaj.org/article/4f680e033815480ba82d6dae0a6f7336
Autor:
Patrizia Bruzzi, Silvia Vannelli, Emanuela Scarano, Natascia Di Iorgi, Maria Parpagnoli, MariaCarolina Salerno, Marco Pitea, Maria Elisabeth Street, Andrea Secco, Adolfo Andrea Trettene, Malgorzata Wasniewska, Nicola Corciulo, Gianluca Tornese, Maria Felicia Faienza, Maurizio Delvecchio, Simona Filomena Madeo, Lorenzo Iughetti
Publikováno v:
Endocrine Connections, Vol 12, Iss 7, Pp 1-10 (2023)
Objective: This Italian survey aims to evaluate real-life long-term efficac y and safety of recombinant human growth hormone (rhGH) therapy in children wit h short stature homeobox-containing gene deficiency disorders (SHOX-D) and to id entify potent
Externí odkaz:
https://doaj.org/article/82d6fe2bd57c403b9090fe00f9ba81ab
Autor:
Daniele Tessaris, Elisa Bonino, Giovanna Weber, Malgorzata Wasniewska, Domenico Corica, Marco Pitea, Giuseppe Scirè, Manuela Caruso-Nicoletti, Danilo Fintini, Luisa de Sanctis
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-8 (2021)
Abstract Background Pseudohypoparathyroidism (PHP) represents a heterogeneous group of rare endocrine disorders caused by (epi) genetic abnormalities affecting the GNAS locus. It is mainly characterized by resistance to PTH and TSH, and by peculiar c
Externí odkaz:
https://doaj.org/article/f98a88457a1d43e793f38a10305734c6
Autor:
Stefano Martinelli, Marco Pitea, Italo Francesco Gatelli, Tara Raouf, Graziano Barera, Ottavio Vitelli
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Subcutaneous fat necrosis of the newborn (SCFN) is a panniculitis that develops in fatty areas after fetal or perinatal distress. Prognosis is generally good with complete regression, but it can be complicated by metabolic abnormalities like hypoglyc
Externí odkaz:
https://doaj.org/article/8971473553c24d73830a6ad7d8b3662a
Autor:
Teresa Arcidiacono, Nadia E. Foligno, Elena Brioni, Arianna Bologna, Giovanna Weber, Stefano Mora, Marco Pitea, Corrado Vitale, Giuseppe Vezzoli
Publikováno v:
Journal of Clinical Medicine; Volume 12; Issue 8; Pages: 2906
Burosumab is a monoclonal anti-FGF23 antibody used to treat patients with X-linked hypophosphatemic rickets (XLH). Its effect on serum phosphate and physical performance was compared in patients during a 6-month treatment with burosumab. Eight adult
Publikováno v:
L'Endocrinologo. 23:633-634
Publikováno v:
L'Endocrinologo. 23:647-648
Publikováno v:
L'Endocrinologo. 21:485-487
Autor:
Marco Pitea, Giuseppe Scirè, Danilo Fintini, Malgorzata Wasniewska, M. Caruso-Nicoletti, Luisa de Sanctis, Daniele Tessaris, Giovanna Weber, Domenico Corica, Elisa Bonino
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-8 (2021)
Italian Journal of Pediatrics
Italian Journal of Pediatrics
Background Pseudohypoparathyroidism (PHP) represents a heterogeneous group of rare endocrine disorders caused by (epi) genetic abnormalities affecting the GNAS locus. It is mainly characterized by resistance to PTH and TSH, and by peculiar clinical f
COVID‐19 infection in a paucisymptomatic infant: Raising the index of suspicion in epidemic settings
Autor:
Gianni Russo, Marco Pitea, Alessio Priolo, Daniele Canarutto, Graziano Barera, Maria Cristina Vigone
Publikováno v:
Pediatric Pulmonology
Few children have been reported to have been affected by novel coronavirus disease 2019 (COVID‐19); it is unclear whether children are less likely to be infected or rather display fewer symptoms. We present the case of a 32‐day‐old boy infected