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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 4, 2020
Concurrent sodium channelopathies and amyotrophic lateral sclerosis supports shared pathogenesisJohn P Franklin, Johnathan Cooper-Knock, Aravindhan Baheerathan, et al.
Neuropathology and Applied Neurobiology|October 17, 2014
Invited review: decoding the pathophysiological mechanisms that underlie RNA dysregulation in neurodegenerative disorders: a review of the current state of the artMatthew J Walsh, Johnathan Cooper-Knock, Jennifer E Dodd, et al.
Neurology|October 11, 2013
C9ORF72 transcription in a frontotemporal dementia case with two expanded allelesJohnathan Cooper-Knock, Adrian Higginbottom, Natalie Connor-Robson, et al.
The Journal of Pathology|May 12, 2020
Oligodendrocyte pathology exceeds axonal pathology in white matter in human amyotrophic lateral sclerosisAlejandro Lorente Pons, Adrian Higginbottom, Johnathan Cooper-Knock, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|May 14, 2011
Early diagnosis of Horner syndrome using topical apraclonidineJohnathan Cooper-Knock, Irene Pepper, Timothy Hodgson, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|August 26, 2015
Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALSJoanna J Bury, J Robin Highley, Johnathan Cooper-Knock, et al.
BMC Medicine|January 20, 2021
The gut microbiome: a key player in the complexity of amyotrophic lateral sclerosis (ALS)Sarah L Boddy, Ilaria Giovannelli, Matilde Sassani, et al.
Acta Neuropathologica|May 7, 2015
Antisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathyJohnathan Cooper-Knock, Adrian Higginbottom, Matthew J Stopford, et al.
Brain : a Journal of Neurology|November 18, 2021
A review of Mendelian randomization in amyotrophic lateral sclerosisThomas H Julian, Sarah Boddy, Mahjabin Islam, et al.
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