Daniele Galatolo

The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families

Maria Lieto, Vittorio Riso, Daniele Galatolo et al. · European Journal of Neurology · 2019 · 55 citations

Identification of mutations in <i>AP4S1/</i>SPG52 through next generation sequencing in three families

Alessandra Tessa, Roberta Battini, Anna Rubegni et al. · European Journal of Neurology · 2016 · 38 citations

A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findings

Alexandros A. Polymeris, Alessandra Tessa, Katherine K. Anagnostopoulou et al. · Journal of Neurology · 2016 · 29 citations

Pain Disorders, Greek Children, Genetic Findings +4

New pathogenic variants in COQ4 cause ataxia and neurodevelopmental disorder without detectable CoQ10 deficiency in muscle or skin fibroblasts

Serena Mero, Leonardo Salviati, Vincenzo Leuzzi et al. · Journal of Neurology · 2021 · 29 citations

New Pathogenic Variants, Neurobiology Of Disease, Autoimmune Disease +10

NGS in Hereditary Ataxia: When Rare Becomes Frequent

Daniele Galatolo, Giovanna De Michele, Gabriella Silvestri et al. · International Journal of Molecular Sciences · 2021 · 29 citations · Full text