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Neurology|February 11, 2021
Association of Mitochondrial DNA Genomic Variation With Risk of Pick DiseaseRebecca R Valentino, Michael G Heckman, Patrick W Johnson, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|January 27, 2021
Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophyAnna I Wernick, Ronald L Walton, Alexandra I Soto-Beasley, et al.
European Journal of Neurology|July 14, 2011
Death-associated protein kinase 1 variation and Parkinson's diseaseJ C Dachsel, C Wider, C Vilariño-Güell, et al.
Neurology|September 6, 2019
Progressive supranuclear palsy is not associated with neurogenic orthostatic hypotensionJay A van Gerpen, Rana Hanna Al-Shaikh, Philip W Tipton, et al.
The Lancet. Neurology|March 25, 2017
Serotonin and dopamine transporter PET changes in the premotor phase of LRRK2 parkinsonism: cross-sectional studiesDaryl J Wile, Pankaj A Agarwal, Michael Schulzer, et al.
Molecular Genetics & Genomic Medicine|June 18, 2014
A rare sequence variant in intron 1 of THAP1 is associated with primary dystoniaSatya R Vemula, Jianfeng Xiao, Yu Zhao, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2009
GCH1 in early-onset Parkinson's diseaseStephanie A Cobb, Christian Wider, Owen A Ross, et al.
Neurogenetics|April 7, 2010
LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
BMC Medical Genetics|March 17, 2009
High-throughput mutational analysis of TOR1A in primary dystoniaJianfeng Xiao, Robert W Bastian, Joel S Perlmutter, et al.
Neuron|November 16, 2004
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathologyAlexander Zimprich, Saskia Biskup, Petra Leitner, et al.
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