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Concurrent sodium channelopathies and amyotrophic lateral sclerosis supports shared pathogenesis.
Franklin JP, Cooper-Knock J, Baheerathan A, Moll T, Männikkö R, Heverin M, Hardiman O, Shaw PJ, Hanna MG. Franklin JP, et al. Among authors: hardiman o. Amyotroph Lateral Scler Frontotemporal Degener. 2020 Nov;21(7-8):627-630. doi: 10.1080/21678421.2020.1786128. Epub 2020 Jul 3. Amyotroph Lateral Scler Frontotemporal Degener. 2020. PMID: 32619119 Free article.
Physical decline and quality of life in amyotrophic lateral sclerosis.
Hardiman O, Hickey A, O'Donerty LJ. Hardiman O, et al. Among authors: o donerty lj. Amyotroph Lateral Scler Other Motor Neuron Disord. 2004 Dec;5(4):230-4. doi: 10.1080/226-14660820410021294. Amyotroph Lateral Scler Other Motor Neuron Disord. 2004. PMID: 15799552 Review. No abstract available.
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.
Greenway MJ, Andersen PM, Russ C, Ennis S, Cashman S, Donaghy C, Patterson V, Swingler R, Kieran D, Prehn J, Morrison KE, Green A, Acharya KR, Brown RH Jr, Hardiman O. Greenway MJ, et al. Among authors: hardiman o. Nat Genet. 2006 Apr;38(4):411-3. doi: 10.1038/ng1742. Epub 2006 Feb 26. Nat Genet. 2006. PMID: 16501576
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B).
Parkinson N, Ince PG, Smith MO, Highley R, Skibinski G, Andersen PM, Morrison KE, Pall HS, Hardiman O, Collinge J, Shaw PJ, Fisher EM; MRC Proteomics in ALS Study; FReJA Consortium. Parkinson N, et al. Among authors: hardiman o. Neurology. 2006 Sep 26;67(6):1074-7. doi: 10.1212/01.wnl.0000231510.89311.8b. Epub 2006 Jun 28. Neurology. 2006. PMID: 16807408
492 results