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Stroke|December 26, 2008
Microarray RNA expression analysis of cerebral white matter lesions reveals changes in multiple functional pathwaysJulie E Simpson, Ola Hosny, Stephen B Wharton, et al.
Neuropathology and Applied Neurobiology|May 29, 2020
Neuropathological and biochemical investigation of Hereditary Ferritinopathy cases with ferritin light chain mutation: Prominent protein aggregation in the absence of major mitochondrial or oxidative stressM Kurzawa-Akanbi, M Keogh, E Tsefou, et al.
Brain Pathology (Zurich, Switzerland)|December 18, 2020
Heterogeneity of cellular inflammatory responses in ageing white matter and relationship to Alzheimer's and small vessel disease pathologiesRachel Waller, Ruth Narramore, Julie E Simpson, et al.
Annals of Clinical and Translational Neurology|September 25, 2015
Genome-wide association study of neocortical Lewy-related pathologyTerhi Peuralinna, Liisa Myllykangas, Minna Oinas, et al.
Plos One|March 31, 2010
Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS)Laura E Cox, Laura Ferraiuolo, Emily F Goodall, et al.
Neuropathology and Applied Neurobiology|November 10, 2007
Microglial activation in white matter lesions and nonlesional white matter of ageing brainsJ E Simpson, P G Ince, C E Higham, et al.
Nature Genetics|July 5, 2001
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseA R Curtis, C Fey, C M Morris, et al.
Brain : a Journal of Neurology|February 28, 2012
Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72Johnathan Cooper-Knock, Christopher Hewitt, J Robin Highley, et al.
The Lancet. Neurology|February 19, 2013
Controversies and priorities in amyotrophic lateral sclerosisMartin R Turner, Orla Hardiman, Michael Benatar, et al.
Annals of Neurology|May 1, 2007
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutationsIan R A Mackenzie, Eileen H Bigio, Paul G Ince, et al.
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