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BMJ Case Reports|July 17, 2012
Bilateral posterior cerebral artery infarctionDavinia Ryan, Sinead M Murphy, Michael J HennesseyNeuromuscular Disorders : NMD|December 3, 2014
A novel MYH7 Leu1453pro mutation resulting in Laing distal myopathy in an Irish familyStela Lefter, Orla Hardiman, Russell L McLaughlin, et al.Neuromuscular Disorders : NMD|November 7, 2016
Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 geneAlexander M Rossor, Jasper M Morrow, James M Polke, et al.Journal of the Peripheral Nervous System : JPNS|January 14, 2015
A pilot study of proximal strength training in Charcot-Marie-Tooth diseaseGita M Ramdharry, Alexander Pollard, Cheryl Anderson, et al.Journal of Neuromuscular Diseases|April 21, 2020
Chronic Progressive External Ophthalmoplegia due to a Rare de novo m.12334G>A MT-TL2 Mitochondrial DNA Variant1Luke O'Donnell, Emma L Blakely, Karen Baty, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 2, 2012
Comprehensive analysis of the TRPV4 gene in a large series of inherited neuropathies and controlsKatherine A Fawcett, Sinead M Murphy, James M Polke, et al.Journal of Neurology|June 3, 2015
Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and IrelandBoglarka Bansagi, Thalia Antoniadi, Sarah Burton-Jones, et al.European Journal of Neurology|September 27, 2023
Late-onset Tay-Sachs disease presenting with a neuromuscular phenotype-a case seriesSarah Fullam, Zara Togher, Alan Power, et al.Irish Journal of Medical Science|January 8, 2018
Aciclovir-induced acute kidney injury in patients with 'suspected viral encephalitis' encountered on a liaison neurology servicePetya Bogdanova-Mihaylova, David Burke, John P O'Dwyer, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 12, 2012
Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testingSinead M Murphy, Matilde Laura, Katherine Fawcett, et al.Pageof 2