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Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2003
Anatamopathological spectrum of tauopathiesTamas Revesz, Janice L HoltonCurrent Opinion in Rheumatology|December 4, 2004
Is it really myositis? A consideration of the differential diagnosisNiranjanan Nirmalananthan, Janice L Holton, Michael G HannaNeuropathology and Applied Neurobiology|July 28, 2021
Neurodegenerative movement disorders: An epigenetics perspective and promise for the futureMegha Murthy, Yun Yung Cheng, Janice L Holton, et al.Muscle & Nerve|September 17, 2011
Clinical and pathological heterogeneity in late-onset partial merosin deficiencySanjeev Rajakulendran, Matt Parton, Janice L Holton, et al.Acta Neuropathologica|July 2, 2011
Neuropathology underlying clinical variability in patients with synucleinopathiesGlenda M Halliday, Janice L Holton, Tamas Revesz, et al.JAMA Neurology|May 1, 2018
A Histologic Study of the Circadian System in Parkinson Disease, Multiple System Atrophy, and Progressive Supranuclear PalsyEduardo De Pablo-Fernández, Robert Courtney, Thomas T Warner, et al.Nature Reviews. Neuroscience|September 5, 2008
Research in motion: the enigma of Parkinson's disease pathology spreadPatrik Brundin, Jia-Yi Li, Janice L Holton, et al.Brain Pathology (Zurich, Switzerland)|September 22, 2012
Identification and quantification of oligodendrocyte precursor cells in multiple system atrophy, progressive supranuclear palsy and Parkinson's diseaseZeshan Ahmed, Yasmine T Asi, Andrew J Lees, et al.Journal of Child Neurology|August 12, 2006
Case of X-linked myopathy with excessive autophagyGabriel Chow, Clare E Beesley, Keith Robson, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2007
Pure akinesia with gait freezing: a third clinical phenotype of progressive supranuclear palsyDavid R Williams, Janice L Holton, Kate Strand, et al.Pageof 17