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Movement Disorders : Official Journal of the Movement Disorder Society|February 12, 2011
Substantia nigra hyperechogenicity with LRRK2 G2019S mutationsNorbert Brüggemann, Johann Hagenah, Kaili Stanley, et al.
Parkinsonism & Related Disorders|December 2, 2021
The minimal clinically important change in the motor section of the Burke-Fahn-Marsden Dystonia Rating Scale for generalized dystonia: Results from deep brain stimulationEsther Cubo, Joan Miravite, Sara Calvo, et al.
Statistics in Medicine|June 29, 2017
Estimation of genetic risk function with covariates in the presence of missing genotypesAnnie J Lee, Karen Marder, Roy N Alcalay, et al.
Neuroscience Letters|April 25, 2006
Increased frequency of the LRRK2 G2019S mutation in an elderly Ashkenazi Jewish population is not associated with dementiaRachel Saunders-Pullman, Richard B Lipton, Geetha Senthil, et al.
Parkinsonism & Related Disorders|July 25, 2018
Digitized spiral analysis may be a potential biomarker for brachial dystoniaJeffrey Ratliff, Roberto A Ortega, Hwai Yin Ooi, et al.
Brain Structure & Function|July 13, 2016
A cognitive fMRI study in non-manifesting LRRK2 and GBA carriersNoa Bregman, Avner Thaler, Anat Mirelman, et al.
Clinical Parkinsonism & Related Disorders|June 7, 2021
Differences in performance on English and Hebrew versions of the MoCA in Parkinson's patientsYaqian Xu, Anat Mirelman, Rachel Saunders-Pullman, et al.
Neurology|February 6, 2015
Differential effects of severe vs mild GBA mutations on Parkinson diseaseZiv Gan-Or, Idan Amshalom, Laura L Kilarski, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 13, 2007
Validity of spiral analysis in early Parkinson's diseaseRachel Saunders-Pullman, Carol Derby, Kaili Stanley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 15, 2013
Fall risk and gait in Parkinson's disease: the role of the LRRK2 G2019S mutationAnat Mirelman, Talia Heman, Kira Yasinovsky, et al.
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