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Rachel Saunders-Pullman

Showing results (121-130 of 133) with videos related to

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Annals of Neurology|January 5, 2022
Parkinson Disease and Subthalamic Nucleus Deep Brain Stimulation: Cognitive Effects in GBA Mutation CarriersGian Pal, Graziella Mangone, Emily J Hill, et al.
European Journal of Neurology|July 23, 2021
Predictive modeling of spread in adult-onset isolated dystonia: Key properties and effect of tremor inclusionMeng Wang, Tolulope Sajobi, Francesca Morgante, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 6, 2014
Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participantsRoy N Alcalay, Jan Aasly, Daniela Berg, et al.
Nature Aging|January 10, 2022
Dysregulation of mitochondrial and proteolysosomal genes in Parkinson's disease myeloid cellsElisa Navarro, Evan Udine, Katia de Paiva Lopes, et al.
Science Translational Medicine|August 17, 2018
Finding useful biomarkers for Parkinson's diseaseAlice S Chen-Plotkin, Roger Albin, Roy Alcalay, et al.
Movement Disorders Clinical Practice|October 11, 2025
Segmental and Multifocal Isolated Dystonias: Similarities and DifferencesHyder A Jinnah, Vittorio Velucci, Daniele Belvisi, et al.
Neurology|October 13, 2020
Dystonia and Tremor: A Cross-Sectional Study of the Dystonia Coalition CohortAasef G Shaikh, Sinem Balta Beylergil, Laura Scorr, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 19, 2013
Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutationsRoy N Alcalay, Anat Mirelman, Rachel Saunders-Pullman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 28, 2021
A Multi-center Genome-wide Association Study of Cervical DystoniaYan V Sun, Chengchen Li, Qin Hui, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 17, 2024
Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association StudiesBjörn-Hergen Laabs, Katja Lohmann, Eva-Juliane Vollstedt, et al.
Pageof 14

Showing results (121-130 of 133) with videos related to

Sort By:
Pageof 14
Annals of Neurology|January 5, 2022
Parkinson Disease and Subthalamic Nucleus Deep Brain Stimulation: Cognitive Effects in GBA Mutation CarriersGian Pal, Graziella Mangone, Emily J Hill, et al.
European Journal of Neurology|July 23, 2021
Predictive modeling of spread in adult-onset isolated dystonia: Key properties and effect of tremor inclusionMeng Wang, Tolulope Sajobi, Francesca Morgante, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 6, 2014
Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participantsRoy N Alcalay, Jan Aasly, Daniela Berg, et al.
Nature Aging|January 10, 2022
Dysregulation of mitochondrial and proteolysosomal genes in Parkinson's disease myeloid cellsElisa Navarro, Evan Udine, Katia de Paiva Lopes, et al.
Science Translational Medicine|August 17, 2018
Finding useful biomarkers for Parkinson's diseaseAlice S Chen-Plotkin, Roger Albin, Roy Alcalay, et al.
Movement Disorders Clinical Practice|October 11, 2025
Segmental and Multifocal Isolated Dystonias: Similarities and DifferencesHyder A Jinnah, Vittorio Velucci, Daniele Belvisi, et al.
Neurology|October 13, 2020
Dystonia and Tremor: A Cross-Sectional Study of the Dystonia Coalition CohortAasef G Shaikh, Sinem Balta Beylergil, Laura Scorr, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 19, 2013
Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutationsRoy N Alcalay, Anat Mirelman, Rachel Saunders-Pullman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 28, 2021
A Multi-center Genome-wide Association Study of Cervical DystoniaYan V Sun, Chengchen Li, Qin Hui, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 17, 2024
Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association StudiesBjörn-Hergen Laabs, Katja Lohmann, Eva-Juliane Vollstedt, et al.
Pageof 14