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Neuroscience Letters|May 2, 2018
Multiple system atrophy and CAG repeat length: A genetic screening of polyglutamine disease genes in Italian patientsAlessia Mongelli, Lidia Sarro, Elena Rizzo, et al.
Brain Communications|September 25, 2025
Impact of age on neurofilament light chain in Friedreich ataxia: a 1-year longitudinal studySara Petrillo, Alessia Mongelli, Anna Castaldo, et al.
International Journal of Molecular Sciences|March 11, 2023
Epigenetic Signatures in Arterial Hypertension: Focus on the MicrovasculatureAlessandro Mengozzi, Sarah Costantino, Alessia Mongelli, et al.
La Radiologia Medica|July 2, 2024
Tracking longitudinal thalamic volume changes during early stages of SCA1 and SCA2Marina Grisoli, Anna Nigri, Jean Paul Medina Carrion, 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.
Journal of Proteome Research|June 18, 2025
Correlation Networks To Uncover Changes in Protein Relationships in Spinocerebellar Ataxia Type 2 and Cerebellar Multiple System AtrophyAurelia Morabito, Giulia De Simone, Stefania Magri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 16, 2020
Frequency and distribution of polyQ disease intermediate-length repeat alleles in healthy Italian populationAlessia Mongelli, Stefania Magri, Elena Salvatore, et al.
Human Genomics|May 22, 2024
An RNA-seq study in Friedreich ataxia patients identified hsa-miR-148a-3p as a putative prognostic biomarker of the diseaseChiara Vancheri, Andrea Quatrana, Elena Morini, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 22, 2025
Neuromagnetic responses to multimodal stimuli in Friedreich's ataxiaElisa Visani, Laura Canafoglia, Lorenzo Nanetti, 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.
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