Giacomo Garone

Highlighting the Dystonic Phenotype Related to <scp><i>GNAO1</i></scp>

Thomas Wirth, Giacomo Garone, Manju A. Kurian et al. · Movement Disorders · 2022 · 58 citations · Full text

Acute ataxia in paediatric emergency departments: a multicentre Italian study

Giacomo Garone, Antonino Reale, Nicola Vanacore et al. · Archives of Disease in Childhood · 2019 · 37 citations

Epilepsy is a possible feature in Williams‐Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region

Francesco Nicita, Giacomo Garone, Alberto Spalice et al. · American Journal of Medical Genetics Part A · 2015 · 36 citations

Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G Mutations

Sabina Barresi, Maria Lisa Dentici, Francesca Manzoni et al. · Pediatric Neurology · 2019 · 34 citations

Mendelian Disorder, Genetic Disorder, Degenerative Disease +5

Diagnostic Yield of a Targeted Next-Generation Sequencing Gene Panel for Pediatric-Onset Movement Disorders: A 3-Year Cohort Study

Federica Graziola, Giacomo Garone, Fabrizia Stregapede et al. · Frontiers in Genetics · 2019 · 32 citations · Full text

Genetics, Genetic Epidemiology, Disease Gene Identification +22