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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 12, 2024
Expanding SPG18 clinical spectrum: autosomal dominant mutation causes complicated hereditary spastic paraplegia in a large familyAssunta Trinchillo, Valeria Valente, Marcello Esposito, et al.Clinical Chemistry|September 8, 2011
Motor chip: a comparative genomic hybridization microarray for copy-number mutations in 245 neuromuscular disordersGiulio Piluso, Manuela Dionisi, Francesca Del Vecchio Blanco, et al.Journal of Parkinson'S Disease|February 6, 2014
Genetic screening for the LRRK2 R1441C and G2019S mutations in Parkinsonian patients from CampaniaAnna De Rosa, Giuseppe De Michele, Anna Guacci, et al.Frontiers in Neurology|July 7, 2020
Peripapillary Vessel Density as Early Biomarker in Multiple SclerosisGilda Cennamo, Antonio Carotenuto, Daniela Montorio, et al.Cell Death & Disease|March 9, 2018
Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutationsDominga Fasano, Silvia Parisi, Giovanna Maria Pierantoni, et al.Journal of Neurology|April 14, 2009
Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic studyChiara Criscuolo, Alessandro Filla, Giovanni Coppola, et al.Heliyon|March 5, 2025
Modulation of NCX1 expression in monocytes associates with multiple sclerosis progressionValentina Rubino, Mariarosaria Cammarota, Chiara Criscuolo, et al.Journal of Neurology|December 4, 2025
Novel missense ALDH18A1 variant in a family with autosomal dominant spastic paraplegiaFederica Novarella, Alessandra Tessa, Chiara Criscuolo, et al.Neurology|September 4, 2016
Impulsive-compulsive behaviors in parkin-associated Parkinson diseaseFrancesca Morgante, Alfonso Fasano, Monia Ginevrino, et al.Frontiers in Genetics|June 1, 2022
Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 OverexpressionLaura De Rosa, Dominga Fasano, Lucrezia Zerillo, et al.Pageof 8