Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Clelia Cipolla"'
Autor:
Barbara Fraccascia, Giorgio Sodero, Lucia Celeste Pane, Elena Malavolta, Caterina Gola, Luigi Pane, Valentina Filomena Paradiso, Lorenzo Nanni, Donato Rigante, Clelia Cipolla
Publikováno v:
Diseases, Vol 12, Iss 10, p 235 (2024)
Background: Complete androgen insensitivity syndrome (CAIS) is a rare disorder of sex development characterized by 46,XY karyotype and testes, yet presenting with a complete female phenotype, which is related to mutations in the androgen receptor (AR
Externí odkaz:
https://doaj.org/article/e643b0852bdc4d7586d1c16559260941
Autor:
Giorgio Sodero, Clelia Cipolla, Laura Martino, Carolina Gentili, Claudia Rendeli, Danilo Buonsenso
Publikováno v:
Children, Vol 11, Iss 7, p 794 (2024)
Purpose The incidence of endocrine sequelae following central nervous system (CNS) infections in pediatric age is not known. We conducted this scoping review to assess the incidence of endocrinological alterations in patients with prior CNS infection
Externí odkaz:
https://doaj.org/article/ea1e06cc152f481799a5fd0d92892aeb
Autor:
Giorgio Sodero, Donato Rigante, Lucia Celeste Pane, Linda Sessa, Ludovica Quarta, Marcello Candelli, Clelia Cipolla
Publikováno v:
Diseases, Vol 12, Iss 6, p 119 (2024)
Background: Individuals with hyperinsulinemia may initially not meet any diagnostic criteria for metabolic syndrome, though displaying a higher risk of cardiovascular complications combined with obesity, diabetes, and hypertension. Aim: The main obje
Externí odkaz:
https://doaj.org/article/63da20b12502457b9f581136c400f936
Autor:
Giorgio Sodero, Lucia Celeste Pane, Elena Malavolta, Giulia Rotunno, Linda Sessa, Barbara Fraccascia, Marcello Candelli, Donato Rigante, Clelia Cipolla
Publikováno v:
Children, Vol 11, Iss 6, p 639 (2024)
Background: A correlation between plasma lipids and timing of pubertal development has been hypothesized, though lipid influence remains unclear in central precocious puberty (CPP). Aim: To assess any possible alterations in the lipid profile and tri
Externí odkaz:
https://doaj.org/article/7b4251d587144b5e8591cd3ec6282ac5
Autor:
Clelia Cipolla, Linda Sessa, Giulia Rotunno, Giorgio Sodero, Francesco Proli, Chiara Veredice, Valentina Giorgio, Chiara Leoni, Jessica Rosati, Domenico Limongelli, Eliza Kuczynska, Elisabetta Sforza, Valentina Trevisan, Donato Rigante, Giuseppe Zampino, Roberta Onesimo
Publikováno v:
Children, Vol 10, Iss 9, p 1451 (2023)
Background: Smith-Magenis syndrome (SMS) is caused by either interstitial deletions in the 17p11.2 region or pathogenic variants in the RAI1 gene and is marked by a distinct set of physical, developmental, neurological, and behavioral features. Hyper
Externí odkaz:
https://doaj.org/article/298308fab9ca46c58a588bcc0e7d8db9
Autor:
Clelia Cipolla, Ilaria Lazzareschi, Antonietta Curatola, Claudia Lasorella, Lucia Celeste Pane, Linda Sessa, Giulia Rotunno, Donato Rigante, Giorgio Sodero
Publikováno v:
Diseases, Vol 11, Iss 3, p 110 (2023)
The aim of this study was to evaluate a potential correlation between results of the oral glucose tolerance test (OGTT) and the auxological/metabolic parameters in a cohort of overweight patients assessed for suspicion of hyperinsulinism. We analyzed
Externí odkaz:
https://doaj.org/article/c5a4ed41175945c0899ded728954fcbf
Autor:
Clelia Cipolla, Giorgio Sodero, Lucia Celeste Pane, Francesco Mariani, Lorenzo Di Sarno, Donato Rigante, Marcello Candelli
Publikováno v:
Biomedicines, Vol 11, Iss 6, p 1678 (2023)
Background—Central precocious puberty (CPP) is characterized by clinical, biochemical, and radiological features similar to those of normal puberty, but CPP occurs before the age of eight in girls and before the age of nine in boys, subsequently le
Externí odkaz:
https://doaj.org/article/ff8d6ee6bdbe4d34b080bb6427852994
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Childhood overweight and obesity are among the major health problems of modern times, especially in Western countries, due to their association with increased cardiovascular and cancer risk in adulthood. Neudesin, a recently discovered peptide secret
Externí odkaz:
https://doaj.org/article/a8f1345314134d79ad72ee8bc5668d8e
Autor:
Roberta Onesimo, Cristina De Rose, Clelia Cipolla, Silvia Della Casa, Chiara Leoni, Annabella Salerni, Daniela Ricci, Giuseppe Zampino
Publikováno v:
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-4 (2020)
Abstract Background Stickler syndrome is a connective tissue disorder with predominantly autosomal dominant inheritance, with ocular, auditory and joint involvement. Thyroid dysfunction was not described as part of alterations in Stickler syndrome an
Externí odkaz:
https://doaj.org/article/a2d384f1f1374d7e924f3555691b5c40
Autor:
Susanna Esposito, Marta Cofini, Donato Rigante, Alberto Leonardi, Laura Lucchetti, Clelia Cipolla, Lucia Lanciotti, Laura Penta
Publikováno v:
Italian Journal of Pediatrics, Vol 44, Iss 1, Pp 1-7 (2018)
Abstract Background Cryptorchidism, the most common male genital abnormality observed in paediatrics, might often be associated with long-term functional consequences and can even reoccur after a successful orchidopexy. Serum markers that identify cr
Externí odkaz:
https://doaj.org/article/f2bb76b87ceb44a19dce33a67358e2bc