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Parkinsonism & Related Disorders|August 30, 2008
Dopamine beta-hydroxylase -1021C>T association and Parkinson's diseaseOwen A Ross, Michael G Heckman, Alexandra I Soto, et al.
Acta Neuropathologica Communications|December 8, 2020
MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical featuresRebecca R Valentino, Shunsuke Koga, Ronald L Walton, et al.
Parkinsonism & Related Disorders|July 8, 2022
PLA2G6-associated neurodegeneration in four different populations-case series and literature reviewRana Hanna Al-Shaikh, Lukasz M Milanowski, Vikram V Holla, et al.
Acta Neuropathologica|October 15, 2013
Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degenerationNaomi Kouri, Yari Carlomagno, Matthew Baker, et al.
Neuroimage. Clinical|October 8, 2021
Connectivity correlates to predict essential tremor deep brain stimulation outcome: Evidence for a common treatment pathwayErik H Middlebrooks, Lela Okromelidze, Joshua K Wong, et al.
American Journal of Human Genetics|December 24, 2003
The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing intervalAlexander Zimprich, Bertram Müller-Myhsok, Matthew Farrer, et al.
Parkinsonism & Related Disorders|September 16, 2008
Genetic variation of Omi/HtrA2 and Parkinson's diseaseOwen A Ross, Alexandra I Soto, Carles Vilariño-Güell, et al.
Neurology|December 16, 2011
Cerebrospinal fluid amyloid β and tau in LRRK2 mutation carriersJ O Aasly, M Shi, V Sossi, et al.
Parkinsonism & Related Disorders|September 2, 2009
LINGO1 rs9652490 is associated with essential tremor and Parkinson diseaseCarles Vilariño-Güell, Owen A Ross, Christian Wider, et al.
Neurobiology of Aging|April 2, 2014
Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson's diseaseBarbara Shannon, Alexandra Soto-Ortolaza, Sruti Rayaprolu, et al.
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