Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Mariacarolina Salerno"'
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
Autor:
Martin O. Savage, Donatella Capalbo, Vivian Hwa, Helen L Storr, Avinaash Maharaj, Sumana Chatterjee, Mariacarolina Salerno, Katharina Schilbach, Stefania Palumbo, Claudio Pignata, Emanuele Miraglia del Giudice, Louise A. Metherell, Grazia Cirillo, Emily Cottrell, Anna Grandone, Jack Williams, Martin Bidlingmaier, Adalgisa Festa
Publikováno v:
The Journal of Clinical Endocrinology and Metabolism
Context Severe forms of growth hormone insensitivity (GHI) are characterized by extreme short stature, dysmorphism, and metabolic anomalies. Objective This work aims to identify the genetic cause of growth failure in 3 “classical” GHI individuals
Autor:
Mariacarolina Salerno, Giuseppa Patti, Mohamad Maghnie, Sara Azzolini, Silvia Longhi, Alessandra di Lascio, Gianni Russo, Corrado Betterle, Giusy Ferro, Carla Bizzarri, Marco Cappa, Giorgio Radetti, Marianna Rita Stancampiano, Mariella Valenzise, Donatella Capalbo, Cristina Moracas, Antonio Balsamo, Nella Augusta Greggio, Malgorzata Wasniewska, Federico Baronio
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 106:762-773
Context Primary adrenal insufficiency (PAI) is a rare and potentially life-threatening condition that is poorly characterized in children. Objective To describe causes, presentation, auxological outcome, frequency of adrenal crisis and mortality of a
Autor:
Carmela Bravaccio, Raffaella Di Mase, Miriam Polizzi, Nicola Improda, Mariacarolina Salerno, Donatella Capalbo, Andrea Esposito, Sara Alfano
Background Long-term consequences of mild subclinical hypothyroidism (SH) in children are still unclear, and the need for levothyroxine (L-T4) supplementation remains controversial. We designed a 2-year, case-control, prospective study of a cohort of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5d92e032bf23c3c0260910860086d0d
http://hdl.handle.net/11588/811375
http://hdl.handle.net/11588/811375
Autor:
Francesco Giallauria, Flavia Barbieri, Di Mase R, Nicola Improda, Di Pietro E, Donatella Capalbo, Antonio Rapacciuolo, Mariacarolina Salerno, Carlo Vigorito
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 102:4080-4088
Context Growth hormone deficiency (GHD) in children may be associated with early cardiovascular risk factors and alterations in left ventricular (LV) structure and function; data on cardiopulmonary functional capacity are lacking. Objectives Aim of t
Autor:
Rita Marabese, Claudio Bardelli, Luigi Tiradani, Michela Godi, Gianni Bona, Mara Giordano, Simona Mellone, Patricia Momigliano-Richiardi, Simonetta Bellone, Flavia Prodam, Mariacarolina Salerno, Antonella Petri
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 97:E1791-E1797
Context: Mutations within the PROP1 gene represent one of the main causes of familial combined pituitary hormone deficiency (CPHD). However, most of the cases are sporadic with an unknown genetic cause. Objective: The aim of this study was the search
Autor:
Sabrina Corbetta, Patrizia Porazzi, Mariacarolina Salerno, Paolo Prontera, Gabriella Nebbia, Natascia Tiso, Mohamad Maghnie, Roberto Gastaldi, Giovanna Weber, Daniela Frizziero, Laura Fugazzola, Luana Mandarà, Roberta Biffanti, Federica Marelli, Giorgio Radetti, Maria Cristina Vigone, Luca Persani, Tiziana de Filippis
Publikováno v:
Europe PubMed Central
CONTEXT: The pathogenesis of congenital hypothyroidism (CH) is still largely unexplained. We previously reported that perturbations of the Notch pathway and knockdown of the ligand jagged1 cause a hypothyroid phenotype in the zebrafish. Heterozygous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c503b84fc2252c736abc88a8c8b591cd
http://hdl.handle.net/11567/876561
http://hdl.handle.net/11567/876561
Autor:
Mariacarolina Salerno, Luigi Saccà, Ugo Oliviero, Vincenzo Guardasole, Donatella Capalbo, Teresa Lettiero, Lavinia Saldamarco, Antonio Lucariello, Dario Maria Mattiacci, Antonio Cittadini
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 93:2486-2491
Context: Congenital hypothyroidism (CH) is the most prevalent endocrine disorder in the newborn and is routinely treated with life-long levothyroxine replacement therapy. Although several studies have demonstrated that such therapy may impact on the
Autor:
Donatella Capalbo, Amato De Paulis, Andrea Salzano, Maria Alessio, Antonio Cittadini, Nicola Improda, Mariacarolina Salerno, Michele Arcopinto, Andrea Lenzi, Andrea M. Isidori, Alberto M. Marra
Context: Patients with classic congenital adrenal hyperplasia (CAH) are treated with lifelong glucocorticoids (GCs). Cardiovascular and metabolic effects of such therapy in adolescents have never been quantified. Objective: Our objective was to inves
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2047b4ab4736fb5e15d0a38f9bdfe7ed
https://hdl.handle.net/11588/614301
https://hdl.handle.net/11588/614301
Autor:
Mariacarolina Salerno, Annamaria Colao, Salvatore Di Maio, Francesca Rota, Stefano Spiezia, Gaetano Lombardi, Carolina Di Somma, Antonella Klain
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 90:2659-2665
We prospectively investigated the risk of early atherosclerosis, by classical cardiovascular risk factors and intima-media thickness (IMT) at the common carotid arteries, in 23 adolescents diagnosed as GH deficient (GHD) during childhood and in 23 he