TYUTYUSHEVA, NINA Statistiche
TYUTYUSHEVA, NINA
DIPARTIMENTO DI MEDICINA CLINICA E SPERIMENTALE
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.
Serum levels of adiponectin differentiate generalized lipodystrophies from anorexia nervosa
2024-01-01 Ceccarini, G; Pelosini, C; Paoli, M; Tyutyusheva, N; Magno, S; Gilio, D; Palladino, L; Sessa, M R; Bertelloni, S; Santini, F
Complete Androgen Insensitivity Syndrome: From Bench to Bed
2021-01-01 Tyutyusheva, N; Mancini, I; Baroncelli, Gi; D'Elios, S; Peroni, D; Meriggiola, Mc; Bertelloni, S.
Disorders of sexual development with XY karyotype and female phenotype: clinical findings and genetic background in a cohort from a single centre
2021-01-01 Costagliola, G; Cosci, O di Coscio M; Masini, B; Baldinotti, F; Caligo, Ma; Tyutyusheva, N; Sessa, Mr; Peroni, D; Bertelloni, S.
Disorders/Differences of Sex Development Presenting in the Newborn With 46,XY Karyotype.
2021-01-01 Bertelloni, S; Tyutyusheva, N; Valiani, M; D'Alberton, F; Baldinotti, F; Caligo, Ma; Baroncelli, Gi; Peroni, D
Management of patients with X-linked hypophosphatemic rickets during Covid-19 pandemic lockdown.
2021-01-01 Baroncelli, Gi; Bertelloni, S; Cosci, M; Tyutyusheva, N; D'Elios, S; Peroni, D
17β-hydroxysteroid dehydrogenase type 3 deficiency: female sex assignment and follow-up
2020-01-01 Faienza, Mf; Baldinotti, F; Marrocco, G; Tyutyusheva, N; Peroni, D; Baroncelli, Gi; Bertelloni, 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. | |
| Serum levels of adiponectin differentiate generalized lipodystrophies from anorexia nervosa | 1-gen-2024 | Ceccarini, G; Pelosini, C; Paoli, M; Tyutyusheva, N; Magno, S; Gilio, D; Palladino, L; Sessa, M R; Bertelloni, S; Santini, F | |
| Complete Androgen Insensitivity Syndrome: From Bench to Bed | 1-gen-2021 | Tyutyusheva, N; Mancini, I; Baroncelli, Gi; D'Elios, S; Peroni, D; Meriggiola, Mc; Bertelloni, S. | |
| Disorders of sexual development with XY karyotype and female phenotype: clinical findings and genetic background in a cohort from a single centre | 1-gen-2021 | Costagliola, G; Cosci, O di Coscio M; Masini, B; Baldinotti, F; Caligo, Ma; Tyutyusheva, N; Sessa, Mr; Peroni, D; Bertelloni, S. | |
| Disorders/Differences of Sex Development Presenting in the Newborn With 46,XY Karyotype. | 1-gen-2021 | Bertelloni, S; Tyutyusheva, N; Valiani, M; D'Alberton, F; Baldinotti, F; Caligo, Ma; Baroncelli, Gi; Peroni, D | |
| Management of patients with X-linked hypophosphatemic rickets during Covid-19 pandemic lockdown. | 1-gen-2021 | Baroncelli, Gi; Bertelloni, S; Cosci, M; Tyutyusheva, N; D'Elios, S; Peroni, D | |
| 17β-hydroxysteroid dehydrogenase type 3 deficiency: female sex assignment and follow-up | 1-gen-2020 | Faienza, Mf; Baldinotti, F; Marrocco, G; Tyutyusheva, N; Peroni, D; Baroncelli, Gi; Bertelloni, S. |