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Journal of Neurology|September 28, 2024
Exploiting the role of CSF NfL, CHIT1, and miR-181b as potential diagnostic and prognostic biomarkers for ALSDelia Gagliardi, Mafalda Rizzuti, Pegah Masrori, et al.
Nature Communications|December 21, 2025
Targeted antisense oligonucleotide treatment rescues developmental alterations in spinal muscular atrophy organoidsIrene Faravelli, Paola Rinchetti, Monica Tambalo, et al.
American Journal of Human Genetics|January 29, 2013
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instabilityDario Ronchi, Alessio Di Fonzo, Weiqiang Lin, et al.
Neurology|May 9, 2014
Lower motor neuron disease with respiratory failure caused by a novel MAPT mutationAlessio Di Fonzo, Dario Ronchi, Francesca Gallia, et al.
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