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Neurogenetics|September 18, 2009
Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosisJanine Kirby, Emily F Goodall, William Smith, et al.
Blood Cells, Molecules & Diseases|January 28, 2003
Neuroferritinopathy: a window on the role of iron in neurodegenerationDouglas E Crompton, Patrick F Chinnery, Constanze Fey, et al.
The European Journal of Neuroscience|May 9, 2018
Proteomic and cellular localisation studies suggest non-tight junction cytoplasmic and nuclear roles for occludin in astrocytesSarah V Morgan, Claire J Garwood, Luke Jennings, et al.
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.
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.
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.
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