Showing results (21-30 of 29) with videos related to
Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Acta Neuropathologica|December 24, 2017
Synapse loss in the prefrontal cortex is associated with cognitive decline in amyotrophic lateral sclerosisChristopher M Henstridge, Dimitrios I Sideris, Emily Carroll, et al.Journal of Neurology|December 14, 2022
Genotype-phenotype characterisation of long survivors with motor neuron disease in ScotlandDanielle J Leighton, Morad Ansari, Judith Newton, et al.The Lancet. Neurology|September 22, 2024
Safety and efficacy of memantine and trazodone versus placebo for motor neuron disease (MND SMART): stage two interim analysis from the first cycle of a phase 3, multiarm, multistage, randomised, adaptive platform trialSuvankar Pal, Jeremy Chataway, Robert Swingler, et al.The Lancet. Neurology|October 11, 2014
Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling studyAmmar Al-Chalabi, Andrea Calvo, Adriano Chio, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 21, 2019
Clinical audit research and evaluation of motor neuron disease (CARE-MND): a national electronic platform for prospective, longitudinal monitoring of MND in ScotlandDanielle Leighton, Judith Newton, Shuna Colville, et al.Brain Communications|December 13, 2021
Clinical trials in amyotrophic lateral sclerosis: a systematic review and perspectiveCharis Wong, Maria Stavrou, Elizabeth Elliott, et al.BMJ Open|February 1, 2023
Systematic, comprehensive, evidence-based approach to identify neuroprotective interventions for motor neuron disease: using systematic reviews to inform expert consensusCharis Wong, Jenna M Gregory, Jing Liao, et al.Human Mutation|April 23, 2013
ANO5 gene analysis in a large cohort of patients with anoctaminopathy: confirmation of male prevalence and high occurrence of the common exon 5 gene mutationAnna Sarkozy, Debbie Hicks, Judith Hudson, et al.Nature Genetics|July 26, 2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosisWouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.Pageof 3