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Annals of Clinical and Translational Neurology|December 16, 2022
Serum levels of glial fibrillary acidic protein in patients with amyotrophic lateral sclerosisFederico Verde, Ilaria Milone, Alessio Maranzano, et al.
Frontiers in Aging Neuroscience|April 3, 2023
Phenotypic correlates of serum neurofilament light chain levels in amyotrophic lateral sclerosisFederico Verde, Ilaria Milone, Eleonora Colombo, et al.
Brain Communications|September 24, 2024
Investigating the prevalence of MFN2 mutations in amyotrophic lateral sclerosis: insights from an Italian cohortElena Abati, Delia Gagliardi, Arianna Manini, et al.
Biomolecules|October 28, 2023
Optical Genome Mapping Enables Detection and Accurate Sizing of RFC1 Repeat ExpansionsStefano Facchini, Natalia Dominik, Arianna Manini, et al.
European Journal of Neurology|June 10, 2024
Association of APOE genotype and cerebrospinal fluid Aβ and tau biomarkers with cognitive and motor phenotype in amyotrophic lateral sclerosisAlessio Maranzano, Federico Verde, Antonella Dubini, et al.
Journal of Neurology|June 19, 2025
Exploring NEK1 genetic variability in Italian amyotrophic lateral sclerosis patientsViviana Pensato, Silvia Peverelli, Cinzia Tiloca, et al.
Annals of Clinical and Translational Neurology|April 25, 2025
KIF5A p.Pro986Leu Risk Variant and Accelerated Progression of Amyotrophic Lateral SclerosisArianna Manini, Rosario Vasta, Alberto Brusati, et al.
Journal of Neurology|August 22, 2025
Whole genome sequencing analysis in primary lateral sclerosis (PLS) patients reveals mutations in neurological diseases-causing genesArianna Manini, Alberto Brusati, Maurizio Grassano, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 6, 2023
Serum Neurofilament Light Chain in Replication Factor Complex Subunit 1 CANVAS and Disease SpectrumIlaria Quartesan, Elisa Vegezzi, Riccardo Currò, et al.
Brain : a Journal of Neurology|July 14, 2023
Normal and pathogenic variation of RFC1 repeat expansions: implications for clinical diagnosisNatalia Dominik, Stefania Magri, Riccardo Currò, et al.
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