Franco Taroni
Fondazione IRCCS Istituto Neurologico Carlo Besta(IT)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Hereditary Neurological Disorders, Metabolism and Genetic Disorders, Neurological diseases and metabolism
Most-Cited Works
- → Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis(2012)594 cited
- → Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS(2014)368 cited
- → Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28(2010)341 cited
- → NEK1 variants confer susceptibility to amyotrophic lateral sclerosis(2016)285 cited
- → The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder(2012)230 cited
- → High frequency ofTARDBPgene mutations in Italian patients with amyotrophic lateral sclerosis(2009)207 cited
- → Alpha-lipoic acid prevents mitochondrial damage and neurotoxicity in experimental chemotherapy neuropathy