TOSCHI, BENEDETTA Statistiche
TOSCHI, BENEDETTA
Mostra
records
Risultati 1 - 3 di 3 (tempo di esecuzione: 0.007 secondi).
An Ultra-Rare Mixed Phenotype with Combined AP-4 and ERF Mutations: The First Report in a Pediatric Patient and a Literature Review
2024-01-01 Orsini, A.; Santangelo, A.; Carmignani, A.; Camporeale, A.; Massart, F.; Tyutyusheva, N.; Peroni, D.; Foiadelli, T.; Ferretti, A.; Toschi, B.; Romano, S.; Bonuccelli, A.
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
The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion
2024-01-01 Baroncelli, G. I.; Carlucci, G.; Freri, E.; Giuca, M. R.; Guarnieri, V.; Navarra, G.; Toschi, B.; Mora, S.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
An Ultra-Rare Mixed Phenotype with Combined AP-4 and ERF Mutations: The First Report in a Pediatric Patient and a Literature Review | 1-gen-2024 | Orsini, A.; Santangelo, A.; Carmignani, A.; Camporeale, A.; Massart, F.; Tyutyusheva, N.; Peroni, D.; Foiadelli, T.; Ferretti, A.; Toschi, B.; Romano, S.; Bonuccelli, A. | |
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 | |
The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion | 1-gen-2024 | Baroncelli, G. I.; Carlucci, G.; Freri, E.; Giuca, M. R.; Guarnieri, V.; Navarra, G.; Toschi, B.; Mora, S. |