Sfoglia per Rivista ORPHANET JOURNAL OF RARE DISEASES
Mostrati risultati da 1 a 3 di 3
Clinical and genetic characterization of Chanarin-Dorfman Syndrome patients: first report of large deletions in the ABHD5 gene
2010-01-01 Redaelli, C.; Coleman, Ra; Moro, Laura; Dacou Voutetakis, C.; Elsayed, Sm; Prati, D.; Colli, A.; Mela, D.; Colombo, R.; Tavian, D.
Invasive meningococcal disease in three siblings with hereditary deficiency of the 8(th) component of complement: evidence for the importance of an early diagnosis
2016-01-01 Dellepiane, Rosa Maria; Dell'Era, Laura; Pavesi, Paola; Macor, Paolo; Giordano, Mara; De Maso, Luca; Pietrogrande, Maria Cristina; Cugno, Massimo
Variables affecting pricing of orphan drugs: the Italian case
2021-01-01 Jommi, Claudio; Listorti, Elisabetta; Villa, Federico; Ghislandi, Simone; Genazzani, Armando; Cangini, Agnese; Trotta, Francesco
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Clinical and genetic characterization of Chanarin-Dorfman Syndrome patients: first report of large deletions in the ABHD5 gene | 1-gen-2010 | Redaelli, C.; Coleman, Ra; Moro, Laura; Dacou Voutetakis, C.; Elsayed, Sm; Prati, D.; Colli, A.; Mela, D.; Colombo, R.; Tavian, D. | |
| Invasive meningococcal disease in three siblings with hereditary deficiency of the 8(th) component of complement: evidence for the importance of an early diagnosis | 1-gen-2016 | Dellepiane, Rosa Maria; Dell'Era, Laura; Pavesi, Paola; Macor, Paolo; Giordano, Mara; De Maso, Luca; Pietrogrande, Maria Cristina; Cugno, Massimo | |
| Variables affecting pricing of orphan drugs: the Italian case | 1-gen-2021 | Jommi, Claudio; Listorti, Elisabetta; Villa, Federico; Ghislandi, Simone; Genazzani, Armando; Cangini, Agnese; Trotta, Francesco |
Mostrati risultati da 1 a 3 di 3
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