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JAMA Neurology|July 23, 2019
Lifetime Risk and Heritability of Amyotrophic Lateral SclerosisMarie Ryan, Mark Heverin, Russell L McLaughlin, et al.Human Mutation|March 1, 2013
Using reference databases of genetic variation to evaluate the potential pathogenicity of candidate disease variantsKevin P Kenna, Russell L McLaughlin, Orla Hardiman, et al.Neuromuscular 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.Neurology|February 5, 2017
Genetic testing in ALS: A survey of current practicesAlice Vajda, Russell L McLaughlin, Mark Heverin, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 19, 2016
The selective anatomical vulnerability of ALS: 'disease-defining' and 'disease-defying' brain regionsPeter Bede, Parameswaran M Iyer, Christina Schuster, et al.Nature Communications|September 12, 2020
Dutch population structure across space, time and GWAS designRoss P Byrne, Wouter van Rheenen, , et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 1, 2017
Neuroimaging patterns along the ALS-FTD spectrum: a multiparametric imaging studyTaha Omer, Eoin Finegan, Siobhan Hutchinson, et al.Neurology|November 12, 2013
Basal ganglia involvement in amyotrophic lateral sclerosisPeter Bede, Marwa Elamin, Susan Byrne, et al.Plos Genetics|January 26, 2018
Insular Celtic population structure and genomic footprints of migrationRoss P Byrne, Rui Martiniano, Lara M Cassidy, et al.European Journal of Neurology|May 10, 2025
Progressive Thalamo-Cortical Disconnection in Amyotrophic Lateral Sclerosis Genotypes: Structural Degeneration and Network Dysfunction of Thalamus-Relayed CircuitsMarlene Tahedl, Jana Kleinerova, Mark A Doherty, et al.Pageof 8