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Acta Neuropathologica Communications|June 5, 2020
Transcriptional profiling of multiple system atrophy cerebellar tissue highlights differences between the parkinsonian and cerebellar sub-types of the diseaseIgnazio S Piras, Christiane Bleul, Isabelle Schrauwen, et al.
Neuromuscular Disorders : NMD|August 20, 2020
Results of an open label feasibility study of sodium valproate in people with McArdle diseaseRenata S Scalco, Mads Stemmerik, Nicoline Løkken, et al.
Neurobiology of Aging|October 14, 2014
Analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonismLucia V Schottlaender, James M Polke, Helen Ling, et al.
Lancet (London, England)|February 1, 2005
A common LRRK2 mutation in idiopathic Parkinson's diseaseWilliam P Gilks, Patrick M Abou-Sleiman, Sonia Gandhi, et al.
Acta Neuropathologica|September 3, 2013
Globular glial tauopathies (GGT): consensus recommendationsZeshan Ahmed, Eileen H Bigio, Herbert Budka, et al.
Annals of Neurology|December 24, 2016
Proteomics of rimmed vacuoles define new risk allele in inclusion body myositisAnne-Katrin Güttsches, Stefen Brady, Kathryn Krause, et al.
Brain : a Journal of Neurology|July 24, 2003
Neurofilament inclusion body disease: a new proteinopathy?Keith A Josephs, Janice L Holton, Martin N Rossor, et al.
European Journal of Nuclear Medicine and Molecular Imaging|August 10, 2018
Disease-related patterns of in vivo pathology in Corticobasal syndromeFlavia Niccolini, Heather Wilson, Stephanie Hirschbichler, et al.
Neurocase|August 17, 2018
Pathological correlates of white matter hyperintensities in a case of progranulin mutation associated frontotemporal dementiaIone O C Woollacott, Martina Bocchetta, Carole H Sudre, et al.
JAMA Neurology|March 6, 2013
Parkin disease: a clinicopathologic entity?Karen M Doherty, Laura Silveira-Moriyama, Laura Parkkinen, et al.
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