Chiara Reale

Mitochondrial dysfunction in Parkinson disease: evidence in mutant PARK2 fibroblasts

Maria Clara Zanellati, Valentina Monti, Chiara Barzaghi et al. · Frontiers in Genetics · 2015 · 70 citations · Full text

Frequency and phenotypic spectrum of <i>KMT2B</i> dystonia in childhood: A single‐center cohort study

Miryam Carecchio, Federica Invernizzi, Paulina González-Latapí et al. · Movement Disorders · 2019 · 69 citations

Novel GNAL mutation with intra-familial clinical heterogeneity: Expanding the phenotype

Miryam Carecchio, Celeste Panteghini, Chiara Reale et al. · Parkinsonism & Related Disorders · 2015 · 44 citations

Disease Heterogeneity, Mendelian Disorder, Genetic Disorder +6

C19orf12 and FA2H Mutations Are Rare in Italian Patients With Neurodegeneration With Brain Iron Accumulation

Celeste Panteghini, Giovanna Zorzi, Paola Venco et al. · Seminars in Pediatric Neurology · 2012 · 41 citations

Neurodegenerative Diseases, Iron Metabolism, Genetics +11

The “Eye-of-the-Tiger” Sign may be Absent in the Early Stages of Classic Pantothenate Kinase Associated Neurodegeneration

Luisa Chiapparini, M. Savoiardo, Stefano D’Arrigo et al. · Neuropediatrics · 2011 · 41 citations