Serena Galosi

<i>GNAO1</i> encephalopathy

Federica Rachele Danti, Serena Galosi, Marta Romani et al. · Neurology Genetics · 2017 · 102 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

<i>Caenorhabditis elegans</i> provides an efficient drug screening platform for <i>GNAO1</i> -related disorders and highlights the potential role of caffeine in controlling dyskinesia

Martina Di Rocco, Serena Galosi, Enrico Lanza et al. · Human Molecular Genetics · 2021 · 40 citations · Full text

<i>De novo DHDDS</i> variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus

Serena Galosi, Ban H. Edani, Simone Martinelli et al. · Brain · 2021 · 39 citations · Full text

Delineating the neurological phenotype in children with defects in the <scp><i>ECHS1</i></scp> or <scp><i>HIBCH</i></scp> gene

Laura Martí‐Sánchez, Heidy Baide‐Mairena, Anna Marcé‐Grau et al. · Journal of Inherited Metabolic Disease · 2020 · 38 citations