Hasil Pencarian - Caterina Cacace
- Menampilkan 1 - 2 hasil dari 2
-
1
A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report oleh Loredana De Pasquale, Petronilla Meo, Francesco Fulia, Antonio Anania, Valerio Meli, Antonina Mondello, Maria Tindara Raimondo, Viviana Tulino, Maria Sole Coletta, Caterina Cacace
Diterbitkan 2022-09-01Dapatkan teks lengkap
Artikel -
2
Congenital emphysematous lung disease associated with a novel Filamin A mutation. Case report and literature review oleh Gloria Pelizzo, Mirella Collura, Aurora Puglisi, Maria Pia Pappalardo, Emanuele Agolini, Antonio Novelli, Maria Piccione, Caterina Cacace, Rossana Bussani, Giovanni Corsello, Valeria Calcaterra
Diterbitkan 2019-03-01Dapatkan teks lengkap
Artikel