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Christopher D Stephen

Showing results (51-60 of 66) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
Eye Tracking during Passage Reading Supports Precise Oculomotor Assessment in AtaxiasBrandon Oubre, Faye Yang, Anna C Luddy, et al.
Frontiers in Neurology|July 5, 2021
Gait Difficulties and Postural Instability in AdrenoleukodystrophyNeha P Godbole, Reza Sadjadi, Madeline A DeBono, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences|August 12, 2020
A Review and Expert Opinion on the Neuropsychiatric Assessment of Motor Functional Neurological DisordersDavid L Perez, Selma Aybek, Stoyan Popkirov, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Functional Connectivity Predictors and Mechanisms of Symptom Change in Functional Neurological DisorderChristiana Westlin, Cristina Bleier, Andrew J Guthrie, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|October 30, 2025
Functional Connectivity Gradients Reveal Altered Hierarchical Cortical Organization in Functional Neurological DisorderChristiana Westlin, Andrew J Guthrie, Cristina Bleier, et al.
Medrxiv : the Preprint Server for Health Sciences|June 12, 2025
Functional Connectivity Gradients Reveal Altered Hierarchical Cortical Organization in Functional Neurological DisorderChristiana Westlin, Andrew J Guthrie, Cristina Bleier, et al.
Movement Disorders Clinical Practice|January 23, 2024
Gerstmann-Sträussler-Scheinker Disease Presenting as Late-Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with NeuropathologyChristopher D Stephen, Claudio Melo de Gusmao, Sharan R Srinivasan, et al.
International Journal of Molecular Sciences|July 24, 2021
Neither a Novel Tau Proteinopathy nor an Expansion of a Phenotype: Reappraising Clinicopathology-Based NosologyLuca Marsili, Jennifer Sharma, Alberto J Espay, et al.
Human Molecular Genetics|September 22, 2017
Mutations in TGM6 induce the unfolded protein response in SCA35Debasmita Tripathy, Beatrice Vignoli, Nandini Ramesh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 19, 2025
Unravelling the Global Tapestry of Genetic Ataxias: Epidemiology and Genetic Testing ApproachesMalco Rossi, Christopher D Stephen, Joana Damásio, et al.
Pageof 7

Showing results (51-60 of 66) with videos related to

Sort By:
Pageof 7
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
Eye Tracking during Passage Reading Supports Precise Oculomotor Assessment in AtaxiasBrandon Oubre, Faye Yang, Anna C Luddy, et al.
Frontiers in Neurology|July 5, 2021
Gait Difficulties and Postural Instability in AdrenoleukodystrophyNeha P Godbole, Reza Sadjadi, Madeline A DeBono, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences|August 12, 2020
A Review and Expert Opinion on the Neuropsychiatric Assessment of Motor Functional Neurological DisordersDavid L Perez, Selma Aybek, Stoyan Popkirov, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Functional Connectivity Predictors and Mechanisms of Symptom Change in Functional Neurological DisorderChristiana Westlin, Cristina Bleier, Andrew J Guthrie, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|October 30, 2025
Functional Connectivity Gradients Reveal Altered Hierarchical Cortical Organization in Functional Neurological DisorderChristiana Westlin, Andrew J Guthrie, Cristina Bleier, et al.
Medrxiv : the Preprint Server for Health Sciences|June 12, 2025
Functional Connectivity Gradients Reveal Altered Hierarchical Cortical Organization in Functional Neurological DisorderChristiana Westlin, Andrew J Guthrie, Cristina Bleier, et al.
Movement Disorders Clinical Practice|January 23, 2024
Gerstmann-Sträussler-Scheinker Disease Presenting as Late-Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with NeuropathologyChristopher D Stephen, Claudio Melo de Gusmao, Sharan R Srinivasan, et al.
International Journal of Molecular Sciences|July 24, 2021
Neither a Novel Tau Proteinopathy nor an Expansion of a Phenotype: Reappraising Clinicopathology-Based NosologyLuca Marsili, Jennifer Sharma, Alberto J Espay, et al.
Human Molecular Genetics|September 22, 2017
Mutations in TGM6 induce the unfolded protein response in SCA35Debasmita Tripathy, Beatrice Vignoli, Nandini Ramesh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 19, 2025
Unravelling the Global Tapestry of Genetic Ataxias: Epidemiology and Genetic Testing ApproachesMalco Rossi, Christopher D Stephen, Joana Damásio, et al.
Pageof 7