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Pediatric Dermatology|August 2, 2021
Perinatal-lethal Gaucher disease presenting with blueberry muffin lesionsFrancesco Maria Rosanio, Ida D'Acunzo, Filomena Mozzillo, et al.
American Journal of Medical Genetics. Part A|February 7, 2014
17p13.1 microdeletion: genetic and clinical findings in a new patient with epilepsy and comparison with literatureLucio Giordano, Filippo Palestra, Maria Grazia Giuffrida, et al.
Developmental Medicine and Child Neurology|September 11, 2020
Cognitive improvement after cochlear implantation in deaf children with associated disabilitiesSerena Micheletti, Patrizia Accorsi, Lucio Giordano, et al.
Developmental Medicine and Child Neurology|September 8, 2015
The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathyElena Cellini, Aglaia Vignoli, Tiziana Pisano, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|December 16, 2014
Non-epileptic myoclonic attacks in infancy: three casesAglaia Vignoli, Lucio Giordano, Daniela Guerra, et al.
Pediatric Neurology|February 4, 2014
Setleis syndrome: genetic and clinical findings in a new case with epilepsyLucio Giordano, Robert J Desnick, Anna Molinaro, et al.
Seizure|December 17, 2019
Infantile spasms followed by childhood absence epilepsy: A case seriesLucio Giordano, Renato Tambucci, Isabella Emanuela Cocco, et al.
Seizure|June 24, 2014
Panayiotopoulos syndrome with convulsive status epilepticus at the onset: a long-term studyAlberto Verrotti, Marianna Sebastiani, Lucio Giordano, et al.
Sleep Medicine|September 10, 2025
Sleep disorders in children with neurodevelopmental disorders: Comparative actigraphy and questionnaire assessment in ASD, ADHD, and controlsSara Pinghini, Lucio Giordano, Francesca Banditelli, et al.
Epilepsia Open|October 16, 2023
Electroclinical features and phenotypic differences in adenylosuccinate lyase deficiency: Long-term follow-up of seven patients from four families and appraisal of the literatureGianni Cutillo, Silvia Masnada, Gaetan Lesca, et al.
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