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Brain : a Journal of Neurology|March 8, 2023
Multiomics and machine-learning identify novel transcriptional and mutational signatures in amyotrophic lateral sclerosisAlberto Catanese, Sandeep Rajkumar, Daniel Sommer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 10, 2008
Ablation of proliferating microglia does not affect motor neuron degeneration in amyotrophic lateral sclerosis caused by mutant superoxide dismutaseGenevíève Gowing, Thomas Philips, Bart Van Wijmeersch, et al.
Nature Reviews. Disease Primers|October 6, 2017
Amyotrophic lateral sclerosisOrla Hardiman, Ammar Al-Chalabi, Adriano Chio, et al.
Neuron|December 14, 2011
ELP3 controls active zone morphology by acetylating the ELKS family member BruchpilotKatarzyna Miśkiewicz, Liya E Jose, André Bento-Abreu, et al.
Nature Reviews. Disease Primers|October 21, 2017
Amyotrophic lateral sclerosisOrla Hardiman, Ammar Al-Chalabi, Adriano Chio, et al.
Life Science Alliance|February 28, 2019
FUS (fused in sarcoma) is a component of the cellular response to topoisomerase I-induced DNA breakage and transcriptional stressMaria Isabel Martinez-Macias, Duncan Aq Moore, Ryan L Green, et al.
Brain Communications|July 6, 2026
Value of synaptic proteins as biomarkers in amyotrophic lateral sclerosisFrederik Hobin, Shreyasee Das, Charlotte Lambrechts, et al.
Cell Reports|February 28, 2019
Mutations in the Glycosyltransferase Domain of GLT8D1 Are Associated with Familial Amyotrophic Lateral SclerosisJohnathan Cooper-Knock, Tobias Moll, Tennore Ramesh, et al.
Neurology|May 19, 2025
Primary Lateral Sclerosis: Implications for Diagnostic Criteria From a Natural History Study in the NetherlandsBálint S de Vries, Eva Maria Johanna de Boer, Frans Brugman, et al.
Frontiers in Neurology|October 14, 2022
Tauroursodeoxycholic acid in patients with amyotrophic lateral sclerosis: The TUDCA-ALS trial protocolAlberto Albanese, Albert Christian Ludolph, Christopher J McDermott, et al.
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