Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Roberto Gastaldi"'
Autor:
Giuseppa Patti, Federica Malerba, Maria Grazia Calevo, Maurizio Schiavone, Marco Scaglione, Emilio Casalini, Silvia Russo, Daniela Fava, Marta Bassi, Flavia Napoli, Anna Elsa Maria Allegri, Giuseppe D’Annunzio, Roberto Gastaldi, Mohamad Maghnie, Natascia Di Iorgi
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/2157d110a282474c99eb73597a384b3f
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:
Giuseppa Patti, Federica Malerba, Maria Grazia Calevo, Maurizio Schiavone, Marco Scaglione, Emilio Casalini, Silvia Russo, Daniela Fava, Marta Bassi, Flavia Napoli, Anna Elsa Maria Allegri, Giuseppe D’Annunzio, Roberto Gastaldi, Mohamad Maghnie, Natascia Di Iorgi
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
ContextData on pubertal timing in Silver Russell syndrome (SRS) are limited.Design and methodsRetrospective observational study including twenty-three SRS patients [11p15 loss of methylation, (11p15 LOM, n=10) and maternal uniparental disomy of chrom
Externí odkaz:
https://doaj.org/article/6d3d40a3253d447497bb22f2eb81f286
Autor:
Ivan Ivanovski, Olivera Djuric, Serena Broccoli, Stefano Giuseppe Caraffi, Patrizia Accorsi, Margaret P. Adam, Kristina Avela, Magdalena Badura-Stronka, Allan Bayat, Jill Clayton-Smith, Isabella Cocco, Duccio Maria Cordelli, Goran Cuturilo, Veronica Di Pisa, Juliette Dupont Garcia, Roberto Gastaldi, Lucio Giordano, Andrea Guala, Christina Hoei-Hansen, Mie Inaba, Alessandro Iodice, Jens Erik Klint Nielsen, Vladimir Kuburovic, Brissia Lazalde-Medina, Baris Malbora, Seiji Mizuno, Oana Moldovan, Rikke S. Møller, Petra Muschke, Valeria Otelli, Chiara Pantaleoni, Carmelo Piscopo, Maria Luisa Poch-Olive, Igor Prpic, Purificación Marín Reina, Federico Raviglione, Emilia Ricci, Emanuela Scarano, Graziella Simonte, Robert Smigiel, George Tanteles, Luigi Tarani, Aurelien Trimouille, Elvis Terci Valera, Samantha Schrier Vergano, Karin Writzl, Bert Callewaert, Salvatore Savasta, Maria Elisabeth Street, Lorenzo Iughetti, Sergio Bernasconi, Paolo Giorgi Rossi, Livia Garavelli
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Abstract Background Mowat–Wilson syndrome (MWS; OMIM #235730) is a genetic condition caused by heterozygous mutations or deletions of the ZEB2 gene. It is characterized by moderate-severe intellectual disability, epilepsy, Hirschsprung disease and
Externí odkaz:
https://doaj.org/article/80124a98602c4794863224c650289c08
Autor:
Angelo Florio, Riccardo Papa, Roberta Caorsi, Alessandro Consolaro, Roberto Gastaldi, Marco Gattorno, Paolo Picco
Publikováno v:
Italian Journal of Pediatrics, Vol 45, Iss 1, Pp 1-3 (2019)
Abstract Heterozygous mutations of the ACAN gene have been associated with a broad spectrum of non-lethal skeletal dysplasias, called Aggrecanopathies. We report a case of a child with severe inflammatory elbow involvement mimicking septic arthritis
Externí odkaz:
https://doaj.org/article/23d7151bef134996b5d8fa77ab79cdb0
Autor:
Giorgio Radetti, Mariacarolina Salerno, Chiara Guzzetti, Marco Cappa, Andrea Corrias, Alessandra Cassio, Graziano Cesaretti, Roberto Gastaldi, Mario Rotondi, Fiorenzo Lupi, Antonio Fanolla, Giovanna Weber, Sandro Loche
Publikováno v:
Endocrine Connections, Vol 6, Iss 4, Pp 206-212 (2017)
Objective: Thyroid function may recover in patients with Hashimoto’s thyroiditis (HT). Design: To investigate thyroid function and the need to resume l-thyroxine treatment after its discontinuation. Setting: Nine Italian pediatric endocrinology c
Externí odkaz:
https://doaj.org/article/0d7ee91149314ccdb5724f0c4e4c5f75
Autor:
Maria Cristina Vigone, Alessandra Cassio, Graziano Cesaretti, Carlo Corbetta, Roberto Gastaldi, Mariacarolina Salerno, Vera Stoppioni, Massimo Tonacchera, Giovanna Weber, Antonella Olivieri
Publikováno v:
L'Endocrinologo. 23:33-39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2094e9593efb128c24d0890bf559454
https://doi.org/10.1007/s40619-021-01010-3
https://doi.org/10.1007/s40619-021-01010-3
Publikováno v:
L'Endocrinologo. 22:293-297
SommarioLo iodio viene assunto esclusivamente attraverso gli alimenti e rappresenta un componente essenziale per la sintesi degli ormoni tiroidei. Una carenza iodica misconosciuta da inadeguato apporto dietetico che si instaura nei primi anni di vita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30d2e15ecb6fbaa22879580d9ea09cc4
https://doi.org/10.1007/s40619-021-00924-2
https://doi.org/10.1007/s40619-021-00924-2
Autor:
Luisa De Sanctis, Maria Cristina Vigone, Paola Borgia, Gerdi Tuli, Giovanni Battista Ferrero, Jessica Munarin, Roberto Gastaldi, Diana Carli, Alessandro Mussa, Marco Abbate
Publikováno v:
Endocrine
Purpose To report the incidence of 4–12% of differentiated thyroid cancer (DTC) and up to 50% of benign thyroid nodular disease and to describe nodular thyroid disease in a multicentre pediatric population with PTEN mutations. Methods: Retrospectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6334b4453b8f931844d5c1f193b9a173
https://doi.org/10.1007/s12020-021-02805-y
https://doi.org/10.1007/s12020-021-02805-y
Autor:
Daniela Fava, Andrea Calandrino, Maria Grazia Calevo, Anna Elsa Maria Allegri, Flavia Napoli, Roberto Gastaldi, Giuseppa Patti, Emilio Casalini, Marta Bassi, Andrea Accogli, Abdel Razaq Ahmad A Alyasin, Antonia Ramaglia, Andrea Rossi, Mohamad Maghnie, Giovanni Morana, Natascia Di Iorgi
Publikováno v:
The Journal of clinical endocrinology and metabolism. 107(10)
Context The etiology of central precocious puberty (CPP) includes a spectrum of conditions. Girls younger than age 6 years with CPP should undergo cranial magnetic resonance imaging (MRI), but it remains controversial whether all girls who develop CP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::398e3108c26f4bdc76c69b82d2c3235f
https://pubmed.ncbi.nlm.nih.gov/35881919
https://pubmed.ncbi.nlm.nih.gov/35881919