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Neurology|April 19, 2013
Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosisAshley Cannon, Shinsuke Fujioka, Nicola J Rutherford, et al.
The European Respiratory Journal|October 20, 2006
Chest CT screening of asbestos-exposed workers: lung lesions and incidental findingsT Vierikko, R Järvenpää, T Autti, et al.
BMC Medical Genetics|March 20, 2012
Polymorphic genes of detoxification and mitochondrial enzymes and risk for progressive supranuclear palsy: a case control studyLisa F Potts, Alex C Cambon, Owen A Ross, et al.
Parkinsonism & Related Disorders|April 3, 2007
Lack of evidence for association of Parkin promoter polymorphism (PRKN-258) with increased risk of Parkinson's diseaseOwen A Ross, Kristoffer Haugarvoll, Jeremy T Stone, et al.
Neurocase|April 27, 2021
Underlying pathology identified after 20 years of disease course in two cases of slowly progressive frontotemporal dementia syndromesFatma Ozlem Hokelekli, Jennifer L Whitwell, Mary M Machulda, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
VPS35 and DNAJC13 disease-causing variants in essential tremorAlex Rajput, Jay P Ross, Cecily Q Bernales, et al.
Parkinsonism & Related Disorders|December 10, 2023
Genetics of Parkinson's disease heterogeneity: A genome-wide association study of clinical subtypesJarosław Dulski, Ryan J Uitti, Alexandra Beasley, et al.
Parkinsonism & Related Disorders|April 13, 2011
Human leukocyte antigen variation and Parkinson's diseaseAndreas Puschmann, Christophe Verbeeck, Michael G Heckman, et al.
Acta Neuropathologica Communications|September 18, 2020
Associations of mitochondrial genomic variation with corticobasal degeneration, progressive supranuclear palsy, and neuropathological tau measuresRebecca R Valentino, Nikoleta Tamvaka, Michael G Heckman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 19, 2007
ELAVL4, PARK10, and the CeltsKristoffer Haugarvoll, Mathias Toft, Owen A Ross, et al.
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