Emilia Bellone

Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy

Emilio Di Maria, Massimo Tabaton, Tiziana Vigo et al. · Annals of Neurology · 2000 · 197 citations

Neurological Disorder, Corticobasal Degeneration, Genetics +19

Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy

Emilio Di Maria, Massimo Tabaton, Tiziana Vigo et al. · Annals of Neurology · 2000 · 167 citations

Neurological Disorder, Corticobasal Degeneration, Genetics +25

<i>RFC1</i> expansions are a common cause of idiopathic sensory neuropathy

Riccardo Curró, Alessandro Salvalaggio, Stefano Tozza et al. · Brain · 2021 · 128 citations · Full text

Neurological Disorder, Diagnosis, Neuropathic Pain +22

Charcot‐Marie‐Tooth disease: frequency of genetic subtypes in a Southern Italy population

Fiore Manganelli, Stefano Tozza, Chiara Pisciotta et al. · Journal of the Peripheral Nervous System · 2014 · 78 citations

Genetic Subtypes, Genetics, Genetic Epidemiology +19

A Novel Mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 disease

Emilia Bellone, Emilio Di Maria, S Soriani et al. · Human Mutation · 1999 · 69 citations · Full text

Hereditary Motor, Genetics, Motor Development +26