BAGATTINI, BRUNELLA Statistiche
BAGATTINI, BRUNELLA
DIPARTIMENTO DI MEDICINA CLINICA E SPERIMENTALE
Clinical Course of Congenital Hypothyroidism With Gland In Situ and Necessity of L-Thyroxine Therapy After Re-evaluation
2024-01-01 Pignata, Luisa; Bagattini, Brunella; Di Cosmo, Caterina; Agretti, Patrizia; De Marco, Giuseppina; Ferrarini, Eleonora; Montanelli, Lucia; Tonacchera, Massimo
Late-onset dyshormonogenic goitrous hypothyroidism due to a homozygous mutation of the SLC26A7 gene: a case report
2024-01-01 Sciarroni, Elisabetta; Montanelli, Lucia; Di Cosmo, Caterina; Bagattini, Brunella; Comi, Simone; Pignata, Luisa; Brancatella, Alessandro; De Marco, Giuseppina; Ferrarini, Eleonora; Nencetti, Chiara; Sessa, Maria Rita; Latrofa, Francesco; Santini, Ferruccio; Tonacchera, Massimo; Agretti, Patrizia
Thyroid autoimmunity in different phenotypes of polycystic ovary syndrome: a single-center experience
2024-01-01 Benelli, E.; Marradi, M.; Sciarroni, E.; Di Cosmo, C.; Bagattini, B.; Del Ghianda, S.; Simoncini, T.; Fruzzetti, F.; Tonacchera, M.; Fiore, E.
Thyroid Function Rather Than Thyroid Antibodies Affects Pregnancy and Perinatal Outcomes: Results of a Prospective Study
2022-01-01 Orsolini, F; Gianetti, E; Terrenzio, C; Montanelli, L; Benelli, E; Bagattini, B; Fiore, E; Tonacchera, M
Effect of aging on clinical features and metabolic complications of women with polycystic ovary syndrome
2021-01-01 Falcetta, P; Benelli, E; Molinaro, A; Di Cosmo, C; Bagattini, B; Del Ghianda, S; Salvetti, G; Fiore, E; Pucci, E; Fruzzetti, F; Tonacchera, M.
Gene expression profile in functioning and non-functioning nodules of autonomous multinodular goiter from an area of iodine deficiency: unexpected common characteristics between the two entities
2021-01-01 Agretti, P; De Marco, G; Ferrarini, E; Di Cosmo, C; Montanelli, L; Bagattini, B; Chiovato, L; Tonacchera, M.
The Role of Nuclear Medicine in the Clinical Management of Benign Thyroid Disorders, Part 2: Nodular Goiter, Hypothyroidism, and Subacute Thyroiditis
2021-01-01 Mariani, G; Tonacchera, M; Grosso, M; Fiore, E; Falcetta, P; Montanelli, L; Bagattini, B; Vitti, P; Strauss, Hw.
Functional Characterization of Four Mutations of the Calcium Sensing Receptor Gene Identified in Patients with Familial Hypocalciuric Hypercalcemia Type 1
2020-01-01 Cetani, Giusy; F, (Cetani; Filomena)(, 1 ); Borsari, Simona; S, (Borsari; Simona)(, 2 ); Pardi, ; E, (Pardi; Elena)(, 2 ); Biagioni, ; T, (Biagioni; Tommaso)(, 2 ); Bagattini, Brunella; B, (Bagattini; Brunella)(, 2 ); Saponaro, Federica; F, (Saponaro; Federica)(, 2 ); Marcocci, Claudio; C, (Marcocci; Claudio)(, 2 )
Familial hypocalciuric hypercalcemia associated with a novel homozygous loss-of-function mutation, E671D, of the calcium-sensing receptor gene
2014-01-01 Cetani, F; Borsari, S; Pardi, E; Bagattini, B; Saponaro, F; Marcocci, C
The different requirement of L-T4therapy in congenital athyreosis compared with adult-acquired hypothyroidism suggests a persisting thyroid hormone resistance at the hypothalamic-pituitary level
2014-01-01 Bagattini, Brunella; Di Cosmo, Caterina; Montanelli, Lucia; Piaggi, Paolo; Ciampi, Mariella; Agretti, Patrizia; De Marco, Giuseppina; Vitti, Paolo; Tonacchera, Massimo
Congenital hypothyroidism caused by a novel homozygous mutation in the thyroglobulin gene.
2013-01-01 Agretti, P; DE MARCO, Giuseppina; DI COSMO, CATERINA ANNA GRAZIA; Ferrarini, E; Montanelli, Lucia; Bagattini, Brunella; Vitti, Paolo; Tonacchera, Massimo
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Clinical Course of Congenital Hypothyroidism With Gland In Situ and Necessity of L-Thyroxine Therapy After Re-evaluation | 1-gen-2024 | Pignata, Luisa; Bagattini, Brunella; Di Cosmo, Caterina; Agretti, Patrizia; De Marco, Giuseppina; Ferrarini, Eleonora; Montanelli, Lucia; Tonacchera, Massimo | |
| Late-onset dyshormonogenic goitrous hypothyroidism due to a homozygous mutation of the SLC26A7 gene: a case report | 1-gen-2024 | Sciarroni, Elisabetta; Montanelli, Lucia; Di Cosmo, Caterina; Bagattini, Brunella; Comi, Simone; Pignata, Luisa; Brancatella, Alessandro; De Marco, Giuseppina; Ferrarini, Eleonora; Nencetti, Chiara; Sessa, Maria Rita; Latrofa, Francesco; Santini, Ferruccio; Tonacchera, Massimo; Agretti, Patrizia | |
| Thyroid autoimmunity in different phenotypes of polycystic ovary syndrome: a single-center experience | 1-gen-2024 | Benelli, E.; Marradi, M.; Sciarroni, E.; Di Cosmo, C.; Bagattini, B.; Del Ghianda, S.; Simoncini, T.; Fruzzetti, F.; Tonacchera, M.; Fiore, E. | |
| Thyroid Function Rather Than Thyroid Antibodies Affects Pregnancy and Perinatal Outcomes: Results of a Prospective Study | 1-gen-2022 | Orsolini, F; Gianetti, E; Terrenzio, C; Montanelli, L; Benelli, E; Bagattini, B; Fiore, E; Tonacchera, M | |
| Effect of aging on clinical features and metabolic complications of women with polycystic ovary syndrome | 1-gen-2021 | Falcetta, P; Benelli, E; Molinaro, A; Di Cosmo, C; Bagattini, B; Del Ghianda, S; Salvetti, G; Fiore, E; Pucci, E; Fruzzetti, F; Tonacchera, M. | |
| Gene expression profile in functioning and non-functioning nodules of autonomous multinodular goiter from an area of iodine deficiency: unexpected common characteristics between the two entities | 1-gen-2021 | Agretti, P; De Marco, G; Ferrarini, E; Di Cosmo, C; Montanelli, L; Bagattini, B; Chiovato, L; Tonacchera, M. | |
| The Role of Nuclear Medicine in the Clinical Management of Benign Thyroid Disorders, Part 2: Nodular Goiter, Hypothyroidism, and Subacute Thyroiditis | 1-gen-2021 | Mariani, G; Tonacchera, M; Grosso, M; Fiore, E; Falcetta, P; Montanelli, L; Bagattini, B; Vitti, P; Strauss, Hw. | |
| Functional Characterization of Four Mutations of the Calcium Sensing Receptor Gene Identified in Patients with Familial Hypocalciuric Hypercalcemia Type 1 | 1-gen-2020 | Cetani, Giusy; F, (Cetani; Filomena)(, 1 ); Borsari, Simona; S, (Borsari; Simona)(, 2 ); Pardi, ; E, (Pardi; Elena)(, 2 ); Biagioni, ; T, (Biagioni; Tommaso)(, 2 ); Bagattini, Brunella; B, (Bagattini; Brunella)(, 2 ); Saponaro, Federica; F, (Saponaro; Federica)(, 2 ); Marcocci, Claudio; C, (Marcocci; Claudio)(, 2 ) | |
| Familial hypocalciuric hypercalcemia associated with a novel homozygous loss-of-function mutation, E671D, of the calcium-sensing receptor gene | 1-gen-2014 | Cetani, F; Borsari, S; Pardi, E; Bagattini, B; Saponaro, F; Marcocci, C | |
| The different requirement of L-T4therapy in congenital athyreosis compared with adult-acquired hypothyroidism suggests a persisting thyroid hormone resistance at the hypothalamic-pituitary level | 1-gen-2014 | Bagattini, Brunella; Di Cosmo, Caterina; Montanelli, Lucia; Piaggi, Paolo; Ciampi, Mariella; Agretti, Patrizia; De Marco, Giuseppina; Vitti, Paolo; Tonacchera, Massimo | |
| Congenital hypothyroidism caused by a novel homozygous mutation in the thyroglobulin gene. | 1-gen-2013 | Agretti, P; DE MARCO, Giuseppina; DI COSMO, CATERINA ANNA GRAZIA; Ferrarini, E; Montanelli, Lucia; Bagattini, Brunella; Vitti, Paolo; Tonacchera, Massimo |