CASSIO, ALESSANDRA
CASSIO, ALESSANDRA
DIPARTIMENTO DI SCIENZE MEDICHE E CHIRURGICHE
A. Cassio; Alessandra Cassio; Cassio A
46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features
2019 Federico Baronio, Rita Ortolano, Soara Menabò, Alessandra Cassio, Lilia Baldazzi, Valeria Di Natale, Giacomo Tonti, Benedetta Vestrucci, Antonio Balsamo
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.
A Frequent Oligogenic Involvement in Congenital Hypothyroidism
2017 de Filippis, Tiziana; Gelmini, Giulia; Paraboschi, Elvezia; Vigone, Maria Cristina; Di Frenna, Marianna; Marelli, Federica; Bonomi, Marco; Cassio, Alessandra; Larizza, Daniela; Moro, Mirella; Radetti, Giorgio; Salerno, Mariacarolina; Ardissino, Diego; Weber, Giovanna; Gentilini, Davide; Guizzardi, Fabiana; Duga, Stefano; Persani, Luca
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism
2005 Balsamo A.; Antelli A.; Baldazzi L.; Baronio F.; Lazareva D.; Cassio A.; Cicognani A.
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
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.
Active and total ghrelin concentrations in the newborn
2005 Pirazzoli P; Lanari M; Zucchini S; Gennari M; Pagotto U; De Iasio R; Pasquali R; Cassio A; Cicognani A; Cacciari E.
Acute suppurative thyroiditis in childhood: spontaneous closure of sinus pyriform fistola may occur even very early.
2007 Wasniewska M; Vigone MC; Cappa M; Cassio A; Scognamillo R; Aversa T; Rubino M; De Luca F.
Acute suppurative thyroiditis: prevalence and natural history in an Italian pediatric population
2006 M Wasniewska; C Vigone; M Cappa; A Cassio; R Scognamillo; T Aversa; F De Luca
Adolescents with severe obesity show a higher cardiovascular (CV) risk than those with type 1 diabetes: a study with skin advanced glycation end products and intima media thickness evaluation. Acta Diabetol. 2020 Nov;57(11):1297-1305. doi: 10.1007/s00592-020-01537-1. Epub 2020 Jun 5. PMID: 32504306
2020 Zucchini S, Fabi M, Maltoni G, Zioutas M, Trevisani V, Di Natale V, Cassio A, Pession A.
Analysis of the TSHR gene in patients with isolated hyperthyrotropinemia
2005 M. Bal;L. Barp;A. Cassio;L. Baldazzi;S. Salardi;L. Lugaresi;A. Cicognani
Autoimmune polyglandular syndrome type III after haploidentical hematopoietic stem cell transplantation in a child with acute myeloid leukemia.
2012 Kleinschmidt K;Martoni A;Masetti R;Cassio A;Prete A;Pession A
Autoimmune-Polyendocrinopathy-Candidiasis-Ectodermal- Dystrophy (APECED) in Calabria: clinical, immunological and genetic patterns.
2012 Betterle C.; Ghizzoni L.; Cassio A.; Baronio F.; Cervato S.; Garelli S.; Barbi E.; Tonini G.
AutoimmunePolyendocrinopathyCandidiasisEctodermalDystrophy Syndrome(APECED) clinical and molecular features in three patients from southernItaly.
2008 F.Baronio;A Cassio; G.Tonini; E.Faleschini; M.Gallucci; C.Betterle; ; A .Cicognani
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.
Behavioural and emotional aspects in children with early-treated congenital hypothyroidism
2005 L. Nardi;A. Cassio;N. Bisacchi ;E. De Cristofaro;M. Bal;D. Lazareva;F. D'Alberton;A. Cicognani
Beta-ketothiolase (T2) deficiency detected with newborn screening (NBS)
2012 I.Bettocchi; F.Baronio; A.Martini; M.Bal; A.Marsigli; A.Cassio
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.
Carnitine longitudinal pattern in preterm infants <1800 g body weight: a case–control study
2019 Baronio F.; Righi B.; Righetti F.; Bettocchi I.; Ortolano R.; Faldella G.; Rondelli R.; Pession A.; Cassio A.
Central Precocious Puberty: Treatment with Triptorelin 11.25 mg
2012 Elena Chiocca;Eleonora Dati;Giampiero I. Baroncelli;Alessandra Cassio;Malgorzata Wasniewska;Fiorella Galluzzi;Silvia Einaudi;Marco Cappa;Gianni Russo;Silvano Bertelloni
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| 46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features | Federico Baronio, Rita Ortolano, Soara Menabò, Alessandra Cassio, Lilia Baldazzi, Valeria Di Nata...le, Giacomo Tonti, Benedetta Vestrucci, Antonio Balsamo | 2019-01-01 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | - | 1.01 Articolo in rivista | 46,XX DSD.pdf; ijms-20-04605-s001.pdf |
| 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 | - |
| A Frequent Oligogenic Involvement in Congenital Hypothyroidism | de Filippis, Tiziana; Gelmini, Giulia; Paraboschi, Elvezia; Vigone, Maria Cristina; Di Frenna, Ma...rianna; Marelli, Federica; Bonomi, Marco; Cassio, Alessandra; Larizza, Daniela; Moro, Mirella; Radetti, Giorgio; Salerno, Mariacarolina; Ardissino, Diego; Weber, Giovanna; Gentilini, Davide; Guizzardi, Fabiana; Duga, Stefano; Persani, Luca | 2017-01-01 | HUMAN MOLECULAR GENETICS | - | 1.01 Articolo in rivista | - |
| A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism | Balsamo A.; Antelli A.; Baldazzi L.; Baronio F.; Lazareva D.; Cassio A.; Cicognani A. | 2005-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART A | - | 1.01 Articolo in rivista | - |
| 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 | - |
| 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 |
| Active and total ghrelin concentrations in the newborn | Pirazzoli P; Lanari M; Zucchini S; Gennari M; Pagotto U; De Iasio R; Pasquali R; Cassio A; Cicogn...ani A; Cacciari E. | 2005-01-01 | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | - | 1.01 Articolo in rivista | - |
| Acute suppurative thyroiditis in childhood: spontaneous closure of sinus pyriform fistola may occur even very early. | Wasniewska M; Vigone MC; Cappa M; Cassio A; Scognamillo R; Aversa T; Rubino M; De Luca F. | 2007-01-01 | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | - | 1.01 Articolo in rivista | - |
| Acute suppurative thyroiditis: prevalence and natural history in an Italian pediatric population | M Wasniewska; C Vigone; M Cappa; A Cassio; R Scognamillo; T Aversa; F De Luca | 2006-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Adolescents with severe obesity show a higher cardiovascular (CV) risk than those with type 1 diabetes: a study with skin advanced glycation end products and intima media thickness evaluation. Acta Diabetol. 2020 Nov;57(11):1297-1305. doi: 10.1007/s00592-020-01537-1. Epub 2020 Jun 5. PMID: 32504306 | Zucchini S, Fabi M, Maltoni G, Zioutas M, Trevisani V, Di Natale V, Cassio A, Pession A. | 2020-01-01 | ACTA DIABETOLOGICA | - | 1.01 Articolo in rivista | - |
| Analysis of the TSHR gene in patients with isolated hyperthyrotropinemia | M. Bal;L. Barp;A. Cassio;L. Baldazzi;S. Salardi;L. Lugaresi;A. Cicognani | 2005-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Autoimmune polyglandular syndrome type III after haploidentical hematopoietic stem cell transplantation in a child with acute myeloid leukemia. | Kleinschmidt K;Martoni A;Masetti R;Cassio A;Prete A;Pession A | 2012-01-01 | PEDIATRIC BLOOD & CANCER | - | 1.01 Articolo in rivista | - |
| Autoimmune-Polyendocrinopathy-Candidiasis-Ectodermal- Dystrophy (APECED) in Calabria: clinical, immunological and genetic patterns. | Betterle C.; Ghizzoni L.; Cassio A.; Baronio F.; Cervato S.; Garelli S.; Barbi E.; Tonini G. | 2012-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
| AutoimmunePolyendocrinopathyCandidiasisEctodermalDystrophy Syndrome(APECED) clinical and molecular features in three patients from southernItaly. | F.Baronio;A Cassio; G.Tonini; E.Faleschini; M.Gallucci; C.Betterle; ; A .Cicognani | 2008-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| 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 |
| Behavioural and emotional aspects in children with early-treated congenital hypothyroidism | L. Nardi;A. Cassio;N. Bisacchi ;E. De Cristofaro;M. Bal;D. Lazareva;F. D'Alberton;A. Cicognani | 2005-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Beta-ketothiolase (T2) deficiency detected with newborn screening (NBS) | I.Bettocchi; F.Baronio; A.Martini; M.Bal; A.Marsigli; A.Cassio | 2012-01-01 | JOURNAL OF INHERITED METABOLIC DISEASE | - | 4.02 Riassunto (Abstract) | - |
| 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 | - |
| Carnitine longitudinal pattern in preterm infants <1800 g body weight: a case–control study | Baronio F.; Righi B.; Righetti F.; Bettocchi I.; Ortolano R.; Faldella G.; Rondelli R.; Pession A....; Cassio A. | 2019-01-01 | PEDIATRIC RESEARCH | - | 1.01 Articolo in rivista | - |
| Central Precocious Puberty: Treatment with Triptorelin 11.25 mg | Elena Chiocca;Eleonora Dati;Giampiero I. Baroncelli;Alessandra Cassio;Malgorzata Wasniewska;Fiore...lla Galluzzi;Silvia Einaudi;Marco Cappa;Gianni Russo;Silvano Bertelloni | 2012-01-01 | THE SCIENTIFIC WORLD JOURNAL | - | 1.01 Articolo in rivista | Central Precocious Puberty.pdf |