GIUSTI, FRANCESCA
GIUSTI, FRANCESCA
Scienze Biomediche, Sperimentali e Cliniche 'Mario Serio'
[Left laparoscopic adrenalectomy for pheochromocytoma in MEN 2B: case report].
2011 T. Bargellini; G. Cantelli; A. Bruscino; A. Falchetti; F. Giusti; M. L. Brandi; A. Valeri
A heterozygous frameshift mutation in exon 1 of CDKN1B gene in a patient affected by MEN4 syndrome.
2014 Tonelli F;Giudici F;Giusti F;Marini F;Cianferotti L;Nesi G;Brandi ML
A New Fgf23 Gene Polymorphism: Possible Role In the Pathogenesis of the Development of Extraskeletal Calcifications?
2013 G. Marcucci;L. Masi;F. Giusti;L. Cavalli;F. Franceschelli;G. Leoncini;C. Fossi;M. L. Brandi
A novel germline inactivating mutation in the CASR gene in an Italian kindred affected by familial hypocalciuric hypercalcemia.
2012 A. Falchetti; A. Gozzini; A. Terranegra; L. Soldati; G. Vezzoli; G. Leoncini; F. Giusti; F. Franceschelli; L. Masi; A. Tanini; L. Cavalli; M.L. Brandi
A NOVEL TISSUE-NONSPECIFIC ISOENZYME OF ALKALINE PHOSPHATASE (TNSALP) MUTATION IN ADULT PATIENT WITH LOW BONE MASS AND MUSCULOSKELETAL SYMPTOMS
2018 Masi, L; Franceschelli, F; Leoncini, G; Cioppi, F; Ottanelli, S; Marcucci, G; Giusti, F; Brandi, ML
ALPL genotypes in patients with atypical femur fractures or other biochemical and clinical signs of hypophosphatasia
2022 Francesca Marini, Laura Masi, Francesca Giusti, Luisella Cianferotti, Federica Cioppi, Gemma Marcucci, Simone Ciuffi, Emmanuel Biver, Giuseppe Toro, Giovanni Iolascon, Teresa Iantomasi, and Maria Luisa Brandi
Association between vitamin D and bisphenol A levels in an elderly Italian population: results from the InCHIANTI study
2022 Maria Luisa Brandi , Stefania Bandinelli, Teresa Iantomasi, Francesca Giusti, Eleonora Talluri, Giovanna Sini, Fabrizio Nannipieri, Santina Battaglia, Riccardo Giusti, Colin Gerard Egan, Luigi Ferrucci
Association of vitamin D and bisphenol A levels with cardiovascular risk in an elderly Italian population: results from the InCHIANTI study
2024 Maria Luisa Brandi; Francesca Marini; Simone Parri; Stefania Bandinelli; Teresa Iantomasi; Francesca Giusti; Eleonora Talluri; Giovanna Sini; Fabrizio Nannipieri; Santina Battaglia; Giovanni Tripepi; Colin Gerard Egan; Luigi Ferrucci
Blomstrand’s chondrodysplasia
2015 Giusti, Francesca; Cianferotti, Luisella; Masi, Laura; Brandi, Maria Luisa
Calcifediol: mechanisms of action
2023 Simone Donati, Gaia Palmini, Cinzia Aurilia, Irene Falsetti, Francesca Marini, Francesca Giusti, Teresa Iantomasi, Maria Luisa Brandi
Calcifediol: Why, When, How Much?
2023 Donati, Simone; Marini, Francesca; Giusti, Francesca; Palmini, Gaia; Aurilia, Cinzia; Falsetti, Irene; Iantomasi, Teresa; Brandi, Maria Luisa
CALCIFICATIONS IN DERMATOMYOSITIS: A CLINICAL CASE WITH AN ALTERATION OF PHOSPHATE HOMEOSTASIS, CARRIER OF A NEW FGF23 GENE MUTATION
2017 Masi, L; Marcucci, G; Giusti, F; Fossi, C; Franceschelli, F; Leoncini, G; Cioppi, F; Cianferotti, L; Brandi, L
Calcium Intake in Bone Health: A Focus on Calcium-Rich Mineral Waters
2018 Vannucci L, Fossi C, Quattrini S, Guasti L, Pampaloni B, Gronchi G, Giusti F, Romagnoli C, Cianferotti L, Marcucci G, Brandi ML
Calcolosi renale recidivante: una nnuova mutazione del gene codificante il recettore del calcio( CASR)
2012 E.Colli; L.Masi; G. Leoncini; F. Cioppi; S. Ottanelli; F. Giusti; G. Marcucci; C. Fossi; A. Tanini; M.L. Brandi
Carcinoma mammario e osteoporosi: risultati preliminari di uno studio fiorentino
2013 Giusti F; Ottanelli S; Masi L; Cioppi F; Marini F; Fossi C; Signorini C; Ramon D; De Luca Cardillo C; Simoncini R; Brandi M L
Characterization of a novel CDC73 gene mutation in a hyperparathyrodism-jaw tumor patient affected by parathyroid carcinoma in the absence of somatic loss of heterozygosity.
2019 Ciuffi S, Cianferotti L, Nesi G, Luzi E, Marini F, Giusti F, Zonefrati R, Gronchi G, Perigli G, Brandi ML
Cinacalcet therapy in patients affected by primary hyperparathyroidism associated to Multiple Endocrine Neoplasia Syndrome type 1 (MEN1)
2016 Giusti, F; Cianferotti, L; Gronchi, G; Cioppi, F; Masi, L; Faggiano, A; Colao, A; Ferolla, P; Brandi, Ml.
Circulating MicroRNAs as Biomarkers of Osteoporosis and Fragility Fractures
2022 Simone Ciuffi, Francesca Marini, Caterina Fossi, Simone Donati, Francesca Giusti, Annalisa Botta, Laura Masi, Giancarlo Isaia, Claudio Marcocci, Silvia Migliaccio, Salvatore Minisola, Ranuccio Nuti, Umberto Tarantino, Teresa Iantomasi, Maria Luisa Brandi
Clinical guidelines for the prevention and treatment of osteoporosis: summary statements and recommendations from the Italian Society for Orthopaedics and Traumatology
2017 Tarantino, Umberto; Iolascon, Giovanni; Cianferotti, Luisella; Masi, Laura; Marcucci, Gemma; Giusti, Francesca; Marini, Francesca; Parri, Simone; Feola, Maurizio; Rao, Cecilia; Piccirilli, Eleonora; Zanetti, Emanuela Basilici; Cittadini, Noemi; Alvaro, Rosaria; Moretti, Antimo; Calafiore, Dario; Toro, Giuseppe; Gimigliano, Francesca; Resmini, Giuseppina; Brandi, Maria Luisa
Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease.
2013 O. M. E;M. R. Visconti;N. Alonso;S. Wani;K. Goodman;W. D. Fraser;L. Gennari;D. Merlotti;F. Gianfrancesco;T. Esposito;D. Rendina;M. d. Stefano;G. Isaia;M. L. Brandi;F. Giusti;J. D. Pino-Montes;L. Corral-Gudino;R. Gonzalez-Sarmiento;L. Ward;S. L. Rea;T. Ratajczak;J. P. Walsh;S. H. Ralston
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| [Left laparoscopic adrenalectomy for pheochromocytoma in MEN 2B: case report]. | 2011 | T. Bargellini; G. Cantelli; A. Bruscino; A. Falchetti; F. Giusti; M. L. Brandi; A. Valeri | |
| A heterozygous frameshift mutation in exon 1 of CDKN1B gene in a patient affected by MEN4 syndrome. | 2014 | Tonelli F;Giudici F;Giusti F;Marini F;Cianferotti L;Nesi G;Brandi ML | |
| A New Fgf23 Gene Polymorphism: Possible Role In the Pathogenesis of the Development of Extraskeletal Calcifications? | 2013 | G. Marcucci;L. Masi;F. Giusti;L. Cavalli;F. Franceschelli;G. Leoncini;C. Fossi;M. L. Brandi | |
| A novel germline inactivating mutation in the CASR gene in an Italian kindred affected by familial hypocalciuric hypercalcemia. | 2012 | A. Falchetti; A. Gozzini; A. Terranegra; L. Soldati; G. Vezzoli; G. Leoncini; F. Giusti; F. Franceschelli; L. Masi; A. Tanini; L. Cavalli; M.L. Brandi | |
| A NOVEL TISSUE-NONSPECIFIC ISOENZYME OF ALKALINE PHOSPHATASE (TNSALP) MUTATION IN ADULT PATIENT WITH LOW BONE MASS AND MUSCULOSKELETAL SYMPTOMS | 2018 | Masi, L; Franceschelli, F; Leoncini, G; Cioppi, F; Ottanelli, S; Marcucci, G; Giusti, F; Brandi, ML | |
| ALPL genotypes in patients with atypical femur fractures or other biochemical and clinical signs of hypophosphatasia | 2022 | Francesca Marini, Laura Masi, Francesca Giusti, Luisella Cianferotti, Federica Cioppi, Gemma Marcucci, Simone Ciuffi, Emmanuel Biver, Giuseppe Toro, Giovanni Iolascon, Teresa Iantomasi, and Maria Luisa Brandi | |
| Association between vitamin D and bisphenol A levels in an elderly Italian population: results from the InCHIANTI study | 2022 | Maria Luisa Brandi , Stefania Bandinelli, Teresa Iantomasi, Francesca Giusti, Eleonora Talluri, Giovanna Sini, Fabrizio Nannipieri, Santina Battaglia, Riccardo Giusti, Colin Gerard Egan, Luigi Ferrucci | |
| Association of vitamin D and bisphenol A levels with cardiovascular risk in an elderly Italian population: results from the InCHIANTI study | 2024 | Maria Luisa Brandi; Francesca Marini; Simone Parri; Stefania Bandinelli; Teresa Iantomasi; Francesca Giusti; Eleonora Talluri; Giovanna Sini; Fabrizio Nannipieri; Santina Battaglia; Giovanni Tripepi; Colin Gerard Egan; Luigi Ferrucci | |
| Blomstrand’s chondrodysplasia | 2015 | Giusti, Francesca; Cianferotti, Luisella; Masi, Laura; Brandi, Maria Luisa | |
| Calcifediol: mechanisms of action | 2023 | Simone Donati, Gaia Palmini, Cinzia Aurilia, Irene Falsetti, Francesca Marini, Francesca Giusti, Teresa Iantomasi, Maria Luisa Brandi | |
| Calcifediol: Why, When, How Much? | 2023 | Donati, Simone; Marini, Francesca; Giusti, Francesca; Palmini, Gaia; Aurilia, Cinzia; Falsetti, Irene; Iantomasi, Teresa; Brandi, Maria Luisa | |
| CALCIFICATIONS IN DERMATOMYOSITIS: A CLINICAL CASE WITH AN ALTERATION OF PHOSPHATE HOMEOSTASIS, CARRIER OF A NEW FGF23 GENE MUTATION | 2017 | Masi, L; Marcucci, G; Giusti, F; Fossi, C; Franceschelli, F; Leoncini, G; Cioppi, F; Cianferotti, L; Brandi, L | |
| Calcium Intake in Bone Health: A Focus on Calcium-Rich Mineral Waters | 2018 | Vannucci L, Fossi C, Quattrini S, Guasti L, Pampaloni B, Gronchi G, Giusti F, Romagnoli C, Cianferotti L, Marcucci G, Brandi ML | |
| Calcolosi renale recidivante: una nnuova mutazione del gene codificante il recettore del calcio( CASR) | 2012 | E.Colli; L.Masi; G. Leoncini; F. Cioppi; S. Ottanelli; F. Giusti; G. Marcucci; C. Fossi; A. Tanini; M.L. Brandi | |
| Carcinoma mammario e osteoporosi: risultati preliminari di uno studio fiorentino | 2013 | Giusti F; Ottanelli S; Masi L; Cioppi F; Marini F; Fossi C; Signorini C; Ramon D; De Luca Cardillo C; Simoncini R; Brandi M L | |
| Characterization of a novel CDC73 gene mutation in a hyperparathyrodism-jaw tumor patient affected by parathyroid carcinoma in the absence of somatic loss of heterozygosity. | 2019 | Ciuffi S, Cianferotti L, Nesi G, Luzi E, Marini F, Giusti F, Zonefrati R, Gronchi G, Perigli G, Brandi ML | |
| Cinacalcet therapy in patients affected by primary hyperparathyroidism associated to Multiple Endocrine Neoplasia Syndrome type 1 (MEN1) | 2016 | Giusti, F; Cianferotti, L; Gronchi, G; Cioppi, F; Masi, L; Faggiano, A; Colao, A; Ferolla, P; Brandi, Ml. | |
| Circulating MicroRNAs as Biomarkers of Osteoporosis and Fragility Fractures | 2022 | Simone Ciuffi, Francesca Marini, Caterina Fossi, Simone Donati, Francesca Giusti, Annalisa Botta, Laura Masi, Giancarlo Isaia, Claudio Marcocci, Silvia Migliaccio, Salvatore Minisola, Ranuccio Nuti, Umberto Tarantino, Teresa Iantomasi, Maria Luisa Brandi | |
| Clinical guidelines for the prevention and treatment of osteoporosis: summary statements and recommendations from the Italian Society for Orthopaedics and Traumatology | 2017 | Tarantino, Umberto; Iolascon, Giovanni; Cianferotti, Luisella; Masi, Laura; Marcucci, Gemma; Giusti, Francesca; Marini, Francesca; Parri, Simone; Feola, Maurizio; Rao, Cecilia; Piccirilli, Eleonora; Zanetti, Emanuela Basilici; Cittadini, Noemi; Alvaro, Rosaria; Moretti, Antimo; Calafiore, Dario; Toro, Giuseppe; Gimigliano, Francesca; Resmini, Giuseppina; Brandi, Maria Luisa | |
| Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease. | 2013 | O. M. E;M. R. Visconti;N. Alonso;S. Wani;K. Goodman;W. D. Fraser;L. Gennari;D. Merlotti;F. Gianfrancesco;T. Esposito;D. Rendina;M. d. Stefano;G. Isaia;M. L. Brandi;F. Giusti;J. D. Pino-Montes;L. Corral-Gudino;R. Gonzalez-Sarmiento;L. Ward;S. L. Rea;T. Ratajczak;J. P. Walsh;S. H. Ralston |