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Alberto Brusati

Showing results (11-20 of 18) with videos related to

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Frontiers in Genetics|December 26, 2022
Analysis of miRNA rare variants in amyotrophic lateral sclerosis and <i>in silico</i> prediction of their biological effectsAlberto Brusati, Antonia Ratti, Viviana Pensato, et al.
Frontiers in Aging Neuroscience|February 23, 2023
Association of the risk factor <i>UNC13A</i> with survival and upper motor neuron involvement in amyotrophic lateral sclerosisArianna Manini, Valeria Casiraghi, Alberto Brusati, et al.
Brain Communications|September 24, 2024
Investigating the prevalence of <i>MFN2</i> mutations in amyotrophic lateral sclerosis: insights from an Italian cohortElena Abati, Delia Gagliardi, Arianna Manini, et al.
Clinical Epigenetics|August 20, 2024
Epigenetic patterns, accelerated biological aging, and enhanced epigenetic drift detected 6 months following COVID-19 infection: insights from a genome-wide DNA methylation studyLuciano Calzari, Davide Fernando Dragani, Lucia Zanotti, 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.
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Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Frontiers in Genetics|December 26, 2022
Analysis of miRNA rare variants in amyotrophic lateral sclerosis and <i>in silico</i> prediction of their biological effectsAlberto Brusati, Antonia Ratti, Viviana Pensato, et al.
Frontiers in Aging Neuroscience|February 23, 2023
Association of the risk factor <i>UNC13A</i> with survival and upper motor neuron involvement in amyotrophic lateral sclerosisArianna Manini, Valeria Casiraghi, Alberto Brusati, et al.
Brain Communications|September 24, 2024
Investigating the prevalence of <i>MFN2</i> mutations in amyotrophic lateral sclerosis: insights from an Italian cohortElena Abati, Delia Gagliardi, Arianna Manini, et al.
Clinical Epigenetics|August 20, 2024
Epigenetic patterns, accelerated biological aging, and enhanced epigenetic drift detected 6 months following COVID-19 infection: insights from a genome-wide DNA methylation studyLuciano Calzari, Davide Fernando Dragani, Lucia Zanotti, 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.
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