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Plos One|June 4, 2011
Role of IL-1 beta in the development of human T(H)17 cells: lesson from NLPR3 mutated patientsDenise Lasigliè, Elisabetta Traggiai, Silvia Federici, et al.Neuropediatrics|April 10, 2018
Epileptic Encephalopathy in Adams-Oliver Syndrome Associated to a New DOCK6 Mutation: A Peculiar Behavioral PhenotypeLivia Pisciotta, Valeria Capra, Andrea Accogli, et al.Neurocase|November 9, 2021
An eleven-year history of Vanishing White Matter Disease in an adult patient with no cognitive decline and <i>EIF2B5</i> mutations. A case reportLucia Trevisan, Matteo Grazzini, Annalia Cianflone, et al.European Journal of Medical Genetics|September 19, 2022
Abnormal course of the corticospinal tracts in KIF5C-related encephalopathyAlessandro Naim, Andrea Accogli, Elisabetta Amadori, et al.Journal of Genetics|June 13, 2020
Psychiatric features and variable neurodevelopment outcome in four females with IQSEC2 spectrum disorderAndrea Accogli, G Eric Jarvis, Alessandra Schiavetto, et al.Journal of Child Neurology|October 17, 2019
Heterozygous Missense Pathogenic Variants Within the Second Spectrin Repeat of SPTBN2 Lead to Infantile-Onset Cerebellar AtaxiaAndrea Accogli, Judith St-Onge, Nassima Addour-Boudrahem, et al.Journal of Child Neurology|November 30, 2018
Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare Neurodegenerative DiseaseAndrea Accogli, Kether Guerrero, Maria Daniela D'Agostino, et al.Birth Defects Research|May 28, 2020
Sinus pericranii, skull defects, and structural brain anomalies in TRAF7-related disorderAndrea Accogli, Marcello Scala, Marco Pavanello, et al.European Journal of Human Genetics : EJHG|May 18, 2017
Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type I reveals candidate genes for cranio-facial developmentElisa Merello, Lorenzo Tattini, Alberto Magi, et al.Brain & Development|April 24, 2022
De novo POLR2A p.(Ile457Thr) variant associated with early-onset encephalopathy and cerebellar atrophy: expanding the phenotypic spectrumThea Giacomini, Marcello Scala, Giulia Nobile, et al.Pageof 11