1. Null ABCA3 in humans: Large homozygous ABCA3 deletion, correlation to clinical–pathological findings. Issue 3 (14th January 2014) Authors: Carrera, Paola; Ferrari, Maurizio; Presi, Silvia; Ventura, Luisa; Vergani, Barbara; Lucchini, Valeria; Cogo, Paola E.; Carnielli, Virgilio P.; Somaschini, Marco; Tagliabue, Paolo Journal: Pediatric pulmonology Issue: Volume 49:Issue 3(2014:Mar.) Page Start: E116 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1. Issue 9 (24th July 2018) Authors: Ripolone, Michela; Lucchini, Valeria; Ronchi, Dario; Fagiolari, Gigliola; Bordoni, Andreina; Fortunato, Francesco; Mondello, Stefania; Bonato, Sara; Meregalli, Mirella; Torrente, Yvan; Corti, Stefania; Comi, Giacomo P.; Moggio, Maurizio; Sciacco, Monica Journal: Journal of neuroscience research Issue: Volume 96:Issue 9(2018) Page Start: 1576 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗