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BMJ Case Reports|June 21, 2011
A novel phenotype of sporadic Creutzfeldt-Jakob diseaseG Giaccone, Giuseppe Di Fede, Michela Mangieri, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 15, 2020
Cortical network dysfunction revealed by magnetoencephalography in carriers of spinocerebellar ataxia 1 or 2 mutationElisa Visani, Caterina Mariotti, Lorenzo Nanetti, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 17, 2013
Substantia nigra in Parkinson's disease: a multimodal MRI comparison between early and advanced stages of the diseaseDomenico Aquino, Valeria Contarino, Alberto Albanese, et al.Brain : a Journal of Neurology|October 28, 2005
SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2Claudia Cagnoli, Caterina Mariotti, Franco Taroni, et al.Neuroimage. Clinical|March 15, 2026
Pediatric anti-NMDAR encephalitis: Neuroradiological presentation, cognitive outcome and volumetric MRI analysisFabio M Doniselli, Anna Paola Savoldi, João Ramos, et al.Journal of Neuro-Oncology|April 25, 2007
Loss of heterozygosity studies in extracranial metastatic meningiomasCaroline Regna Gladin, Ettore Salsano, Francesca Menghi, et al.Frontiers in Neurology|January 1, 2021
Progression of Cerebellar Atrophy in Spinocerebellar Ataxia Type 2 Gene Carriers: A Longitudinal MRI Study in Preclinical and Early Disease StagesAnna Nigri, Lidia Sarro, Alessia Mongelli, et al.Journal of Neurology|October 16, 2007
Spinocerebellar ataxia type 17 (SCA17): oculomotor phenotype and clinical characterization of 15 Italian patientsCaterina Mariotti, Dario Alpini, Roberto Fancellu, et al.Brain Pathology (Zurich, Switzerland)|December 21, 2016
Alzheimer neuropathology without frontotemporal lobar degeneration hallmarks (TAR DNA-binding protein 43 inclusions) in missense progranulin mutation Cys139ArgVeronica Redaelli, Giacomina Rossi, Emanuela Maderna, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 16, 2025
Implications of the glymphatic system in the diagnostic and surgical workup of normal pressure hydrocephalusMorgan Broggi, Edoardo M Barbieri, Alessandro Gans, et al.Pageof 8