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Annals of Neurology|August 2, 2018
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotypeEdwin Jabbari, John Woodside, Manuela M X Tan, et al.
Neurobiology of Aging|February 12, 2015
The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositisQiang Gang, Conceicao Bettencourt, Pedro M Machado, et al.
The New England Journal of Medicine|November 15, 2013
A novel prion disease associated with diarrhea and autonomic neuropathySimon Mead, Sonia Gandhi, Jon Beck, et al.
Imaging Neuroscience (Cambridge, Mass.)|May 29, 2026
Fast segmentation with the NextBrain histological atlasOula Puonti, Jackson Nolan, Robert Dicamillo, et al.
JAMA Neurology|October 9, 2013
COX10 mutations resulting in complex multisystem mitochondrial disease that remains stable into adulthoodRobert D S Pitceathly, Jan-Willem Taanman, Shamima Rahman, et al.
Brain : a Journal of Neurology|July 15, 2011
A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathiesTammaryn Lashley, Jonathan D Rohrer, Rina Bandopadhyay, et al.
Science Translational Medicine|March 25, 2016
Targeting protein homeostasis in sporadic inclusion body myositisMhoriam Ahmed, Pedro M Machado, Adrian Miller, et al.
Neurology|August 31, 2012
Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth diseaseRobert D S Pitceathly, Sinéad M Murphy, Ellen Cottenie, et al.
Neuropathology and Applied Neurobiology|July 30, 2022
Pathological substrate of memory impairment in multiple system atrophyYasuo Miki, Kunikazu Tanji, Kana Shinnai, et al.
Neurology. Genetics|May 17, 2017
Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial diseaseEnrico Bugiardini, Olivia V Poole, Andreea Manole, et al.
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