Marianna Fantin

Oestrogens ameliorate mitochondrial dysfunction in Leber’s hereditary optic neuropathy

Carla Giordano, Monica Montopoli, Elena Perli et al. · Brain · 2010 · 242 citations · Full text

Ocular Disease, Mitochondrial Dysfunction, Genetics +20

Formation and Antitumor Activity of PNU-159682, A Major Metabolite of Nemorubicin in Human Liver Microsomes

Luigi Quintieri, Cristina Geroni, Marianna Fantin et al. · Clinical Cancer Research · 2005 · 70 citations

Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with <i>CYP7B1</i> mutations

Alessia Arnoldi, Claudia Crimella, Erika Tenderini et al. · Clinical Genetics · 2011 · 44 citations

Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study

Andrea Martinuzzi, Domenico Montanaro, Marinela Vavla et al. · PLoS ONE · 2016 · 42 citations · Full text

Functional and Structural Brain Damage in Friedreich's Ataxia

Marinela Vavla, Filippo Arrigoni, Andrea Nordio et al. · Frontiers in Neurology · 2018 · 37 citations · Full text