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Current Opinion in Neurology|August 28, 2014
Recent advances in bulbar syndromes: genetic causes and disease mechanismsAndreea Manole, Pietro Fratta, Henry HouldenSeminars in Cell & Developmental Biology|May 28, 2019
Cytoplasmic functions of TDP-43 and FUS and their role in ALSNicol Birsa, Matthew Peter Bentham, Pietro FrattaAnnual Review of Genomics and Human Genetics|April 21, 2026
Cryptic Splicing in ALS: From Driving Disease Progression to Unlocking Novel TherapeuticsSara Emad El-Agamy, Francesca Mattedi, Pietro FrattaThe Journal of Pathology|March 28, 2022
Markers of cognitive resilience and a framework for investigating clinical heterogeneity in ALS†Puja R Mehta, Tammaryn Lashley, Pietro Fratta, et al.Trends in Neurosciences|November 21, 2019
Travelling Together: A Unifying Pathomechanism for ALSPietro Fratta, Nicol Birsa, Andrew P Tosolini, et al.Frontiers in Neuroscience|March 3, 2020
The Overlapping Genetics of Amyotrophic Lateral Sclerosis and Frontotemporal DementiaYevgeniya A Abramzon, Pietro Fratta, Bryan J Traynor, et al.Neuropathology and Applied Neurobiology|January 22, 2022
HnRNP K mislocalisation in neurons of the dentate nucleus is a novel neuropathological feature of neurodegenerative disease and ageingRahul Sidhu, Ariana Gatt, Pietro Fratta, et al.Frontiers in Genetics|December 17, 2020
A Comparison of Low Read Depth QuantSeq 3' Sequencing to Total RNA-Seq in FUS Mutant MiceSeth Jarvis, Nicol Birsa, Maria Secrier, et al.Molecular Neurodegeneration|March 16, 2023
The era of cryptic exons: implications for ALS-FTDPuja R Mehta, Anna-Leigh Brown, Michael E Ward, et al.Acta Neuropathologica|August 5, 2020
The role of hnRNPs in frontotemporal dementia and amyotrophic lateral sclerosisAlexander Bampton, Lauren M Gittings, Pietro Fratta, et al.Pageof 12