CASSIO, ALESSANDRA
CASSIO, ALESSANDRA
DIMEC - DIPARTIMENTO DI SCIENZE MEDICHE E CHIRURGICHE
A. Cassio; Alessandra Cassio; Cassio A
Comparison between Liquid and Tablet Formulations in the Treatment of Congenital Hypothyroidism up to 3 Years of Age: The First Italian Study
2024 Ortolano, Rita; Cantarelli, Erika; Baronio, Federico; Assirelli, Valentina; Candela, Egidio; Mastrangelo, Carla; Vissani, Sofia; Alqaisi, Randa S.; Lanari, Marcello; Cassio, Alessandra
A Case of Acrodermatitis Dysmetabolica in a Child Affected by Citrullinemia Type I: When Early Diagnosis and Timely Treatment Are Not Enough
2023 Bruni L.; Cassio A.; Di Natale V.; Baronio F.; Ortolano R.; Pession A.; Piraccini B.M.; Neri I.
Auxological and endocrine findings in narcolepsy type 1: seventeen-year follow-up from a pediatric endocrinology center
2023 Casale S.; Assirelli V.; Pizza F.; Balsamo A.; Gennari M.; Pession A.; Plazzi G.; Cassio A.
Cystathionine Beta-Synthase Deficiency: Three Consecutive Cases Detected in 40 Days by Newborn Screening in Emilia Romagna (Italy) and a Comprehensive Review of the Literature
2023 Candela, Egidio; Zagariello, Michele; Di Natale, Valeria; Ortolano, Rita; Righetti, Francesca; Assirelli, Valentina; Biasucci, Giacomo; Cassio, Alessandra; Pession, Andrea; Baronio, Federico
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism
2023 Gentilini, D; Muzza, M; de Filippis, T; Vigone, M C; Weber, G; Calzari, L; Cassio, A; Di Frenna, M; Bartolucci, M; Grassi, E S; Carbone, E; Olivieri, A; Persani, L
Testicular Adrenal Rest Tumors in Congenital Adrenal Hyperplasia: Study of a Cohort of Patients from a Single Italian Center
2023 Ortolano, R.; Cassio, A.; Alqaisi, R. S.; Candela, E.; Di Natale, V.; Assirelli, V.; Bernardini, L.; Bortolamedi, E.; Cantarelli, E.; Corcioni, B.; Renzulli, M.; Balsamo, A.; Baronio, F.
A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotype
2022 Palumbo, S; Cirillo, G; Sanchez, G; Aiello, F; Fachin, A; Baldo, F; Pellegrin, M C; Cassio, A; Salerno, M; Maghnie, M; Faienza, M F; Wasniewska, M; Fintini, D; Giacomozzi, C; Ciccone, S; Miraglia Del Giudice, E; Tornese, G; Grandone, A
Child Neurology: A Case Series of Heterogeneous Neuropsychiatric Symptoms and Outcome in Very Early-Onset Narcolepsy Type 1
2022 Veneruso M.; Pizza F.; Finotti E.; Amore G.; Vandi S.; Filardi M.; Antelmi E.; Nobili L.; Cassio A.; Pession A.; Plazzi G.
Effect of initial levothyroxine dose on neurodevelopmental and growth outcomes in children with congenital hypothyroidism
2022 Esposito, Andrea; Vigone, Maria Cristina; Polizzi, Miriam; Wasniewska, Malgorzata Gabriela; Cassio, Alessandra; Mussa, Alessandro; Gastaldi, Roberto; Di Mase, Raffaella; Vincenzi, Gaia; Pozzi, Clara; Peroni, Elena; Bravaccio, Carmela; Capalbo, Donatella; Bruzzese, Dario; Salerno, Mariacarolina
Implicating factors in the increase in cases of central precocious puberty (CPP) during the COVID-19 pandemic: Experience of a tertiary centre of pediatric endocrinology and review of the literature
2022 Barberi, C; Di Natale, V; Assirelli, V; Bernardini, L; Candela, E; Cassio, A
Isolated childhood growth hormone deficiency: a 30-year experience on final height and a new prediction model
2022 Lonero, Antonella; Giotta, Massimo; Guerrini, Giulia; Calcaterra, Valeria; Galazzi, Elena; Iughetti, Lorenzo; Cassio, Alessandra; Wasniewska, Gabriela Malgorzata; Mameli, Chiara; Tornese, Gianluca; Salerno, Mariacarolina; Cherubini, Valentino; Caruso Nicoletti, Manuela; Street, Maria Elisabeth; Grandone, Anna; Giacomozzi, Claudio; Faienza, Maria Felicia; Guzzetti, Chiara; Bellone, Simonetta; Parpagnoli, Maria; Musolino, Gianluca; Maggio, Maria Cristina; Bozzola, Mauro; Trerotoli, Paolo; Delvecchio, Maurizio
Isolated childhood growth hormone deficiency: a 30-year experience on final height and a new prediction model
2022 Lonero, Antonella; Giotta, Massimo; Guerrini, Giulia; Calcaterra, Valeria; Galazzi, Elena; Iughetti, Lorenzo; Cassio, Alessandra; Wasniewska, Gabriela Malgorzata; Mameli, Chiara; Tornese, Gianluca; Salerno, Mariacarolina; Cherubini, Valentino; Caruso Nicoletti, Manuela; Street, Maria Elisabeth; Grandone, Anna; Giacomozzi, Claudio; Faienza, Maria Felicia; Guzzetti, Chiara; Bellone, Simonetta; Parpagnoli, Maria; Musolino, Gianluca; Maggio, Maria Cristina; Bozzola, Mauro; Trerotoli, Paolo; Delvecchio, Maurizio
Management of Childhood-onset Craniopharyngioma in Italy: A Multicenter, 7-Year Follow-up Study of 145 Patients
2022 Zucchini, Stefano; Di Iorgi, Natascia; Pozzobon, Gabriella; Pedicelli, Stefania; Parpagnoli, Maria; Driul, Daniela; Matarazzo, Patrizia; Baronio, Federico; Crocco, Marco; Iudica, Giovanna; Partenope, Cristina; Nardini, Beatrice; Ubertini, Graziamaria; Menardi, Rachele; Guzzetti, Chiara; Iughetti, Lorenzo; Aversa, Tommaso; Di Mase, Raffaella; Cassio, Alessandra
Management of Childhood-onset Craniopharyngioma in Italy: A Multicenter, 7-Year Follow-up Study of 145 Patients
2022 Zucchini, Stefano; Di Iorgi, Natascia; Pozzobon, Gabriella; Pedicelli, Stefania; Parpagnoli, Maria; Driul, Daniela; Matarazzo, Patrizia; Baronio, Federico; Crocco, Marco; Iudica, Giovanna; Partenope, Cristina; Nardini, Beatrice; Ubertini, Graziamaria; Menardi, Rachele; Guzzetti, Chiara; Iughetti, Lorenzo; Aversa, Tommaso; Di Mase, Raffaella; Cassio, Alessandra
Rare PHEX intron variant causes complete and severe phenotype in a family with hypophosphatemic rickets: a case report
2022 Aiello, Francesca; Pasquali, Daniela; Baronio, Federico; Cassio, Alessandra; Rossi, Cesare; Di Fraia, Rosa; Carotenuto, Raffaela; Digitale, Lucia; Festa, Adalgisa; Luongo, Caterina; Maltoni, Giulio; Schiano di Cola, Roberta; Del Giudice, Emanuele Miraglia; Grandone, Anna
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism
2022 Gentilini, D; Muzza, M; de Filippis, T; Vigone, M C; Weber, G; Calzari, L; Cassio, A; Di Frenna, M; Bartolucci, M; Grassi, E S; Carbone, E; Olivieri, A; Persani, L
Transplantation to save the life, TSH screening to save the brain: A report and brief literature review of autoimmune thyroid disease after HSCT for severe combined immunodeficiency
2022 Baccelli, F; Ortolano, R; Conti, F; Soncini, E; Baronio, F; Masetti, R; Ferrari, S; Cassio, A; Pession, A
Treatment of congenital hypothyroidism: comparison between L-thyroxine oral solution and tablet formulations up to 3 years of age
2022 Vigone MC, Ortolano R, Vincenzi G, Pozzi C, Ratti M, Assirelli V, Vissani S, Cavarzere P, Mussa A, Gastaldi R, Di Mase R, Salerno M, Street ME, Trombatore J, Weber G, Cassio A.
A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder.
2021 Graziano C, Despang P, Palombo F, Severi G, Posar A, Cassio A, Pippucci T, Isidori F, Matthes J, Bonora E.
Biological clock and heredity in pubertal timing: what is new?
2021 Barbieri F, Inzaghi E, Caruso Nicoletti M, Cassio A, Grandone A, DE Sanctis L, Bizzarri C.