CASSIO, ALESSANDRA
CASSIO, ALESSANDRA
DIPARTIMENTO DI SCIENZE MEDICHE E CHIRURGICHE
A. Cassio; Alessandra Cassio; Cassio A
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
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.
Congenital Hypothyroidism: A 2020-2021 Consensus Guidelines Update-An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology
2021 van Trotsenburg AS, Stoupa A, Léger J, Rohrer TR, Peters C, Fugazzola L, Cassio A, Heinrichs C, Beauloye V, Pohlenz J, Rodien P, Coutant R, Szinnai G, Murray P, Bartès B, Luton D, Salerno M, De Sanctis L, Vigone MC, Krude H, Persani L, Polak M.
Molecular screening of PROKR2 gene in girls with idiopathic central precocious puberty
2021 Aiello F, Cirillo G, Cassio A, Di Mase R, Tornese G, Umano GR, Miraglia Del Giudice E, Grandone A.
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| A Case of Acrodermatitis Dysmetabolica in a Child Affected by Citrullinemia Type I: When Early Diagnosis and Timely Treatment Are Not Enough | Bruni L.; Cassio A.; Di Natale V.; Baronio F.; Ortolano R.; Pession A.; Piraccini B.M.; Neri I. | 2023-01-01 | CHILDREN | - | 1.01 Articolo in rivista | - |
| Auxological and endocrine findings in narcolepsy type 1: seventeen-year follow-up from a pediatric endocrinology center | Casale S.; Assirelli V.; Pizza F.; Balsamo A.; Gennari M.; Pession A.; Plazzi G.; Cassio A. | 2023-01-01 | FRONTIERS IN ENDOCRINOLOGY | - | 1.01 Articolo in rivista | fendo-14-1037398.pdf |
| 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 | Candela, Egidio; Zagariello, Michele; Di Natale, Valeria; Ortolano, Rita; Righetti, Francesca; As...sirelli, Valentina; Biasucci, Giacomo; Cassio, Alessandra; Pession, Andrea; Baronio, Federico | 2023-01-01 | CHILDREN | - | 1.01 Articolo in rivista | children-10-00396.pdf |
| Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism | 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 | 2023-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | s40618-022-01915-2.pdf; 40618.zip |
| A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotype | Palumbo, S; Cirillo, G; Sanchez, G; Aiello, F; Fachin, A; Baldo, F; Pellegrin, M C; Cassio, A; Sa...lerno, M; Maghnie, M; Faienza, M F; Wasniewska, M; Fintini, D; Giacomozzi, C; Ciccone, S; Miraglia Del Giudice, E; Tornese, G; Grandone, A | 2022-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
| Child Neurology: A Case Series of Heterogeneous Neuropsychiatric Symptoms and Outcome in Very Early-Onset Narcolepsy Type 1 | Veneruso M.; Pizza F.; Finotti E.; Amore G.; Vandi S.; Filardi M.; Antelmi E.; Nobili L.; Cassio ...A.; Pession A.; Plazzi G. | 2022-01-01 | NEUROLOGY | - | 1.01 Articolo in rivista | - |
| Effect of initial levothyroxine dose on neurodevelopmental and growth outcomes in children with congenital hypothyroidism | Esposito, Andrea; Vigone, Maria Cristina; Polizzi, Miriam; Wasniewska, Malgorzata Gabriela; Cassi...o, Alessandra; Mussa, Alessandro; Gastaldi, Roberto; Di Mase, Raffaella; Vincenzi, Gaia; Pozzi, Clara; Peroni, Elena; Bravaccio, Carmela; Capalbo, Donatella; Bruzzese, Dario; Salerno, Mariacarolina | 2022-01-01 | FRONTIERS IN ENDOCRINOLOGY | - | 1.01 Articolo in rivista | fendo-13-923448.pdf |
| 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 | Barberi, C; Di Natale, V; Assirelli, V; Bernardini, L; Candela, E; Cassio, A | 2022-01-01 | FRONTIERS IN ENDOCRINOLOGY | - | 1.01 Articolo in rivista | fendo-13-1032914.pdf |
| Isolated childhood growth hormone deficiency: a 30-year experience on final height and a new prediction model | Lonero, Antonella; Giotta, Massimo; Guerrini, Giulia; Calcaterra, Valeria; Galazzi, Elena; Iughet...ti, 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 | 2022-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
| Isolated childhood growth hormone deficiency: a 30-year experience on final height and a new prediction model | Lonero, Antonella; Giotta, Massimo; Guerrini, Giulia; Calcaterra, Valeria; Galazzi, Elena; Iughet...ti, 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 | 2022-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
| Management of Childhood-onset Craniopharyngioma in Italy: A Multicenter, 7-Year Follow-up Study of 145 Patients | Zucchini, Stefano; Di Iorgi, Natascia; Pozzobon, Gabriella; Pedicelli, Stefania; Parpagnoli, Mari...a; 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 | 2022-01-01 | THE JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | - | 1.01 Articolo in rivista | - |
| Management of Childhood-onset Craniopharyngioma in Italy: A Multicenter, 7-Year Follow-up Study of 145 Patients | Zucchini, Stefano; Di Iorgi, Natascia; Pozzobon, Gabriella; Pedicelli, Stefania; Parpagnoli, Mari...a; 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 | 2022-01-01 | THE JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | - | 1.01 Articolo in rivista | - |
| Rare PHEX intron variant causes complete and severe phenotype in a family with hypophosphatemic rickets: a case report | Aiello, Francesca; Pasquali, Daniela; Baronio, Federico; Cassio, Alessandra; Rossi, Cesare; Di Fr...aia, Rosa; Carotenuto, Raffaela; Digitale, Lucia; Festa, Adalgisa; Luongo, Caterina; Maltoni, Giulio; Schiano di Cola, Roberta; Del Giudice, Emanuele Miraglia; Grandone, Anna | 2022-01-01 | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | - | 1.01 Articolo in rivista | - |
| Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism | 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 | 2022-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
| 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 | Baccelli, F; Ortolano, R; Conti, F; Soncini, E; Baronio, F; Masetti, R; Ferrari, S; Cassio, A; Pe...ssion, A | 2022-01-01 | CLINICAL IMMUNOLOGY | - | 1.01 Articolo in rivista | - |
| Treatment of congenital hypothyroidism: comparison between L-thyroxine oral solution and tablet formulations up to 3 years of age | 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. | 2022-01-01 | EUROPEAN JOURNAL OF ENDOCRINOLOGY | - | 1.01 Articolo in rivista | - |
| A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder. | Graziano C, Despang P, Palombo F, Severi G, Posar A, Cassio A, Pippucci T, Isidori F, Matthes J, ...Bonora E. | 2021-01-01 | JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS | - | 1.01 Articolo in rivista | s10803-020-04551-y.pdf; 231308c7-61b5-43e5-befd-365842d292a9.pdf |
| Biological clock and heredity in pubertal timing: what is new? | Barbieri F, Inzaghi E, Caruso Nicoletti M, Cassio A, Grandone A, DE Sanctis L, Bizzarri C. | 2021-01-01 | MINERVA PEDIATRICS | - | 1.01 Articolo in rivista | - |
| Congenital Hypothyroidism: A 2020-2021 Consensus Guidelines Update-An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology | van Trotsenburg AS, Stoupa A, Léger J, Rohrer TR, Peters C, Fugazzola L, Cassio A, Heinrichs C, B...eauloye V, Pohlenz J, Rodien P, Coutant R, Szinnai G, Murray P, Bartès B, Luton D, Salerno M, De Sanctis L, Vigone MC, Krude H, Persani L, Polak M. | 2021-01-01 | THYROID | - | 1.01 Articolo in rivista | Congenital Hypothyroidism.pdf |
| Molecular screening of PROKR2 gene in girls with idiopathic central precocious puberty | Aiello F, Cirillo G, Cassio A, Di Mase R, Tornese G, Umano GR, Miraglia Del Giudice E, Grandone A. | 2021-01-01 | THE ITALIAN JOURNAL OF PEDIATRICS | - | 1.01 Articolo in rivista | IJP2021.pdf |