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Acta Neuropathologica Communications|August 25, 2022
Co-deposition of SOD1, TDP-43 and p62 proteinopathies in ALS: evidence for multifaceted pathways underlying neurodegenerationBenjamin G Trist, Jennifer A Fifita, Alison Hogan, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|January 13, 2015
BrainNet Europe's Code of Conduct for brain bankingNatasja M Klioueva, Marleen C Rademaker, David T Dexter, et al.
Neuromuscular Disorders : NMD|July 14, 2010
Congenital muscular dystrophy, myasthenic symptoms and epidermolysis bullosa simplex (EBS) associated with mutations in the PLEC1 gene encoding plectinKatharine Forrest, Jemima E Mellerio, Stephanie Robb, et al.
Anticancer Research|December 16, 2014
Expression of the chondroitin sulphate proteoglycan, NG2, in paediatric brain tumorsSamantha C Higgins, Anna J Bolteus, Laura K Donovan, et al.
Archives of Neurology|September 15, 2005
Magnetic resonance imaging signatures of tissue pathology in frontotemporal dementiaJennifer L Whitwell, Keith A Josephs, Martin N Rossor, et al.
Journal of Neuropathology and Experimental Neurology|December 13, 2016
Tubular Aggregates and Cylindrical Spirals Have Distinct Immunohistochemical SignaturesStefen Brady, Estelle G Healy, Qiang Gang, et al.
Acta Neuropathologica Communications|February 27, 2016
Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTDMichael Niblock, Bradley N Smith, Youn-Bok Lee, et al.
Genome Biology|June 19, 2012
Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and bloodMatthew N Davies, Manuela Volta, Ruth Pidsley, et al.
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