Carmelo Amato

6q Terminal Deletion Syndrome Associated with a Distinctive EEG and Clinical Pattern: A Report of Five Cases

Maurizio Elia, Pasquale Striano, Marco Fichera et al. · Epilepsia · 2006 · 50 citations · Full text

An atypical patient with Cowden syndrome and PTEN gene mutation presenting with cortical malformation and focal epilepsy

Maurizio Elia, Carmelo Amato, Maria Bottitta et al. · Brain and Development · 2012 · 43 citations

Focal Epilepsy, Pten Gene Mutation, Cowden Syndrome +1

A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy

Luigi Vetri, Mirella Vinci, Carmelo Amato et al. · European Journal of Medical Genetics · 2020 · 35 citations

Heterozygous Mutation, Epileptic Encephalopathy, Genetic Disorder +9

Nervous system involvement in Degos disease.

Carmelo Amato, Raffaele Ferri, Maurizio Elia et al. · PubMed · 2005 · 27 citations · Full text

Quantitative MRI Harmonization to Maximize Clinical Impact: The RIN–Neuroimaging Network

Anna Nigri, Stefania Ferraro, Claudia A. M. Gandini Wheeler‐Kingshott et al. · Frontiers in Neurology · 2022 · 27 citations · Full text

Neurogenomics, Quality Controls, Statistical Power +19