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Movement Disorders : Official Journal of the Movement Disorder Society
|
February 7, 2014
Heterogeneity in primary dystonia: lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites
Rachel Saunders-Pullman, Tania Fuchs, Marta San Luciano, et al.
Parkinsonism & Related Disorders
|
October 26, 2021
The commercial genetic testing landscape for Parkinson's disease
Lola Cook, Jeanine Schulze, Jennifer Verbrugge, et al.
Neuroscience Letters
|
April 25, 2006
Increased frequency of the LRRK2 G2019S mutation in an elderly Ashkenazi Jewish population is not associated with dementia
Rachel Saunders-Pullman, Richard B Lipton, Geetha Senthil, et al.
Clinical Parkinsonism & Related Disorders
|
June 7, 2021
Differences in performance on English and Hebrew versions of the MoCA in Parkinson's patients
Yaqian Xu, Anat Mirelman, Rachel Saunders-Pullman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 27, 2018
Increased substantia nigra echogenicity in LRRK2 family members without mutations
Mariel Pullman, Roberto Ortega, Amanda Glickman, et al.
Parkinsonism & Related Disorders
|
July 25, 2018
Digitized spiral analysis may be a potential biomarker for brachial dystonia
Jeffrey Ratliff, Roberto A Ortega, Hwai Yin Ooi, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
December 10, 2019
LRRK2 and GBA Variants Exert Distinct Influences on Parkinson's Disease-Specific Metabolic Networks
Katharina A Schindlbeck, An Vo, Nha Nguyen, et al.
Muscle & Nerve
|
April 26, 2017
Finger extension weakness and downbeat nystagmus motor neuron disease syndrome: A novel motor neuron disorder?
Aline Delva, Nimish Thakore, Erik P Pioro, et al.
Journal of Sleep Medicine
|
October 1, 2025
More Than Rapid Eye Movement Sleep Behavior Disorder: Sleep Differences in Parkinson's Disease LRRK2 and GBA Genotypes
Adina Wise, Deborah Raymond, Mengxi Yang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 20, 2010
Clinical expression of LRRK2 G2019S mutations in the elderly
Marta San Luciano, Richard B Lipton, Cuiling Wang, et al.
Page
of 14
Search research articles
Search
Showing results (41-50 of 133) with videos related to
Sort By:
Page
of 14
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 7, 2014
Heterogeneity in primary dystonia: lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites
Rachel Saunders-Pullman, Tania Fuchs, Marta San Luciano, et al.
Parkinsonism & Related Disorders
|
October 26, 2021
The commercial genetic testing landscape for Parkinson's disease
Lola Cook, Jeanine Schulze, Jennifer Verbrugge, et al.
Neuroscience Letters
|
April 25, 2006
Increased frequency of the LRRK2 G2019S mutation in an elderly Ashkenazi Jewish population is not associated with dementia
Rachel Saunders-Pullman, Richard B Lipton, Geetha Senthil, et al.
Clinical Parkinsonism & Related Disorders
|
June 7, 2021
Differences in performance on English and Hebrew versions of the MoCA in Parkinson's patients
Yaqian Xu, Anat Mirelman, Rachel Saunders-Pullman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 27, 2018
Increased substantia nigra echogenicity in LRRK2 family members without mutations
Mariel Pullman, Roberto Ortega, Amanda Glickman, et al.
Parkinsonism & Related Disorders
|
July 25, 2018
Digitized spiral analysis may be a potential biomarker for brachial dystonia
Jeffrey Ratliff, Roberto A Ortega, Hwai Yin Ooi, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
December 10, 2019
LRRK2 and GBA Variants Exert Distinct Influences on Parkinson's Disease-Specific Metabolic Networks
Katharina A Schindlbeck, An Vo, Nha Nguyen, et al.
Muscle & Nerve
|
April 26, 2017
Finger extension weakness and downbeat nystagmus motor neuron disease syndrome: A novel motor neuron disorder?
Aline Delva, Nimish Thakore, Erik P Pioro, et al.
Journal of Sleep Medicine
|
October 1, 2025
More Than Rapid Eye Movement Sleep Behavior Disorder: Sleep Differences in Parkinson's Disease LRRK2 and GBA Genotypes
Adina Wise, Deborah Raymond, Mengxi Yang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 20, 2010
Clinical expression of LRRK2 G2019S mutations in the elderly
Marta San Luciano, Richard B Lipton, Cuiling Wang, et al.
Page
of 14