Chiara Pisciotta

Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Andrea Cortese, Yi Zhu, Adriana Rebelo et al. · Nature Genetics · 2020 · 170 citations · Full text

Biallelic Mutations, Somatic Variant, Genetic Disorder +9

Functional involvement of central cholinergic circuits and visual hallucinations in Parkinson's disease

Fiore Manganelli, Carmine Vitale, Gabriella Santangelo et al. · Brain · 2009 · 124 citations · Full text

Neuropsychology, Brain Function, Corticobasal Degeneration +22

Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability

Lucio Santoro, Guido J. Breedveld, Fiore Manganelli et al. · Neurogenetics · 2010 · 101 citations · Full text

Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study

Menelaos Pipis, Shawna Feely, James M. Polke et al. · Brain · 2020 · 87 citations · Full text

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