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Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 16, 2017
A novel PMCA3 mutation in an ataxic patient with hypomorphic phosphomannomutase 2 (PMM2) heterozygote mutations: Biochemical characterization of the pump defectMattia Vicario, Tito Calì, Domenico Cieri, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 24, 2016
Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxiaLorena Travaglini, Marta Nardella, Emanuele Bellacchio, et al.Cancers|June 25, 2020
Circulating miRNAs in Small Extracellular Vesicles Secreted by a Human Melanoma Xenograft in Mouse BrainsLoredana Guglielmi, Marta Nardella, Carla Musa, et al.Oncotarget|October 7, 2015
Down-regulation of the Lamin A/C in neuroblastoma triggers the expansion of tumor initiating cellsMarta Nardella, Loredana Guglielmi, Carla Musa, et al.Journal of Neurology|July 15, 2019
Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variantsFrancesco Nicita, Fabrizia Stregapede, Alessandra Tessa, et al.Pageof 2