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Rachel Saunders-Pullman

Showing results (41-50 of 133) with videos related to

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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-MennonitesRachel Saunders-Pullman, Tania Fuchs, Marta San Luciano, et al.
Parkinsonism & Related Disorders|October 26, 2021
The commercial genetic testing landscape for Parkinson's diseaseLola 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 dementiaRachel 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 patientsYaqian 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 mutationsMariel Pullman, Roberto Ortega, Amanda Glickman, 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.
Cerebral Cortex (New York, N.Y. : 1991)|December 10, 2019
LRRK2 and GBA Variants Exert Distinct Influences on Parkinson's Disease-Specific Metabolic NetworksKatharina 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 GenotypesAdina 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 elderlyMarta San Luciano, Richard B Lipton, Cuiling Wang, et al.
Pageof 14

Showing results (41-50 of 133) with videos related to

Sort By:
Pageof 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-MennonitesRachel Saunders-Pullman, Tania Fuchs, Marta San Luciano, et al.
Parkinsonism & Related Disorders|October 26, 2021
The commercial genetic testing landscape for Parkinson's diseaseLola 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 dementiaRachel 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 patientsYaqian 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 mutationsMariel Pullman, Roberto Ortega, Amanda Glickman, 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.
Cerebral Cortex (New York, N.Y. : 1991)|December 10, 2019
LRRK2 and GBA Variants Exert Distinct Influences on Parkinson's Disease-Specific Metabolic NetworksKatharina 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 GenotypesAdina 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 elderlyMarta San Luciano, Richard B Lipton, Cuiling Wang, et al.
Pageof 14