Sfoglia per Autore
The complex interactions amongst serotonin, insulin, leptin and glycolipid metabolic parameters in human obesity
2022-01-01 Marazziti, D.; Betti, L.; Baroni, S.; Palego, L.; Mucci, F.; Carpita, B.; Cremone, I. M.; Santini, F.; Fabbrini, L.; Pelosini, C.; Marsili, A.; Massimetti, E.; Giannaccini, G.; Dell'Osso, L.
Post-acute cardiac complications following SARS-CoV-2 infection in partial lipodystrophy due to LMNA gene p.R349W mutation
2022-01-01 Ceccarini, G; Gilio, D; Magno, S; Pelosini, C; Leverone, M; Miceli, C; Barison, A; Fabiani, I; Emdin, M; Santini, F
Circulating Levels of MiRNAs From 320 Family in Subjects With Lipodystrophy: Disclosing Novel Signatures of the Disease
2022-01-01 Dattilo, Alessia; Ceccarini, Giovanni; Scabia, Gaia; Magno, Silvia; Quintino, Lara; Pelosini, Caterina; Salvetti, Guido; Cusano, Roberto; Massidda, Matteo; Montanelli, Lucia; Gilio, Donatella; Gatti, Gianluca; Giacomina, Alessandro; Costa, Mario; Santini, Ferruccio; Maffei, Margherita
Effect of burosumab treatment on phosphate metabolism and bone health in patients with X-linked hypophosphatemic rickets (XLH). Preliminary data within an Italian sample
2022-01-01 Baroncelli, Giampiero; Comberiati, Pasquale; Rita Sessa, Maria; Pelosini, Caterina; Grandone, Anna; Camodeca, Rosanna; Emma, Francesco
Oxidative and DNA damage in obese patients undergoing bariatric surgery: A one-year follow-up study
2023-01-01 Chiaramonte, Anna; Testi, Serena; Pelosini, Caterina; Micheli, Consuelo; Falaschi, Aurora; Ceccarini, Giovanni; Santini, Ferruccio; Scarpato, Roberto
A new mutation in the CAVIN1/PTRF gene in two siblings with congenital generalized lipodystrophy type 4: case reports and review of the literature
2023-01-01 Mancioppi, Valentina; Daffara, Tommaso; Romanisio, Martina; Ceccarini, Giovanni; Pelosini, Caterina; Santini, Ferruccio; Bellone, Simonetta; Mellone, Simona; Baricich, Alessio; Rabbone, Ivana; Aimaretti, Gianluca; Akinci, Baris; Giordano, Mara; Prodam, Flavia
Intact FGF23 concentration in healthy infants, children, and adolescents, and diagnostic usefulness in patients with X-linked hypophosphatemic rickets
2024-01-01 Baroncelli, G I; Sessa, M R; Pelosini, C; Bertelloni, S; Michelucci, A; Toschi, B; Piaggi, P; Peroni, D; Comberiati, P
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| The complex interactions amongst serotonin, insulin, leptin and glycolipid metabolic parameters in human obesity | 1-gen-2022 | Marazziti, D.; Betti, L.; Baroni, S.; Palego, L.; Mucci, F.; Carpita, B.; Cremone, I. M.; Santini, F.; Fabbrini, L.; Pelosini, C.; Marsili, A.; Massimetti, E.; Giannaccini, G.; Dell'Osso, L. | |
| Post-acute cardiac complications following SARS-CoV-2 infection in partial lipodystrophy due to LMNA gene p.R349W mutation | 1-gen-2022 | Ceccarini, G; Gilio, D; Magno, S; Pelosini, C; Leverone, M; Miceli, C; Barison, A; Fabiani, I; Emdin, M; Santini, F | |
| Circulating Levels of MiRNAs From 320 Family in Subjects With Lipodystrophy: Disclosing Novel Signatures of the Disease | 1-gen-2022 | Dattilo, Alessia; Ceccarini, Giovanni; Scabia, Gaia; Magno, Silvia; Quintino, Lara; Pelosini, Caterina; Salvetti, Guido; Cusano, Roberto; Massidda, Matteo; Montanelli, Lucia; Gilio, Donatella; Gatti, Gianluca; Giacomina, Alessandro; Costa, Mario; Santini, Ferruccio; Maffei, Margherita | |
| Effect of burosumab treatment on phosphate metabolism and bone health in patients with X-linked hypophosphatemic rickets (XLH). Preliminary data within an Italian sample | 1-gen-2022 | Baroncelli, Giampiero; Comberiati, Pasquale; Rita Sessa, Maria; Pelosini, Caterina; Grandone, Anna; Camodeca, Rosanna; Emma, Francesco | |
| Oxidative and DNA damage in obese patients undergoing bariatric surgery: A one-year follow-up study | 1-gen-2023 | Chiaramonte, Anna; Testi, Serena; Pelosini, Caterina; Micheli, Consuelo; Falaschi, Aurora; Ceccarini, Giovanni; Santini, Ferruccio; Scarpato, Roberto | |
| A new mutation in the CAVIN1/PTRF gene in two siblings with congenital generalized lipodystrophy type 4: case reports and review of the literature | 1-gen-2023 | Mancioppi, Valentina; Daffara, Tommaso; Romanisio, Martina; Ceccarini, Giovanni; Pelosini, Caterina; Santini, Ferruccio; Bellone, Simonetta; Mellone, Simona; Baricich, Alessio; Rabbone, Ivana; Aimaretti, Gianluca; Akinci, Baris; Giordano, Mara; Prodam, Flavia | |
| Intact FGF23 concentration in healthy infants, children, and adolescents, and diagnostic usefulness in patients with X-linked hypophosphatemic rickets | 1-gen-2024 | Baroncelli, G I; Sessa, M R; Pelosini, C; Bertelloni, S; Michelucci, A; Toschi, B; Piaggi, P; Peroni, D; Comberiati, P |
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