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IEEE Transactions on Neural Systems and Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology Society|July 7, 2025
Evaluating Muscle Fatigue With Non-Invasive Approaches: A Review of Methods, Metrics, and ImplicationsRoberto F Pitzalis, Beatrice Lagomarsino, Indya Ceroni, et al.Pediatric Clinics of North America|May 16, 2024
Strengthening Pediatric and Public Health Collaboration to Protect Children's Health During a PandemicZanah K Francis, Elizabeth M Dufort, Bernadette A Albanese, et al.Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2003
Role of the dopamine D5 receptor (DRD5) as a susceptibility gene for cervical dystoniaF Brancati, E M Valente, M Castori, et al.Proceedings of the National Academy of Sciences of the United States of America|June 3, 2025
Reciprocal projections between the globus pallidus externa and cortex span motor and nonmotor regionsEmily A Ferenczi, Wengang Wang, Anushka Biswas, et al.Brain : a Journal of Neurology|May 29, 2000
The impact of deep brain stimulation on executive function in Parkinson's diseaseM Jahanshahi, C M Ardouin, R G Brown, et al.Plos One|March 2, 2023
Community exposures among Colorado adults who tested positive for SARS-CoV-2 -A case-control study, March-December 2021Alice E White, Amanda D Tran, Michelle R Torok, et al.Journal of Neuro-Oncology|November 18, 2005
Phase II trial of temozolomide in children with recurrent high-grade gliomaA Ruggiero, G Cefalo, M L Garré, et al.Journal of Neuroengineering and Rehabilitation|July 5, 2025
Wristful thinking: exploring the effects of robotic rehabilitation and cross-education for persons with multiple sclerosisKailynn Mannella, Giulia A Albanese, Valentina Massone, et al.Frontiers in Robotics and AI|April 19, 2024
Robotic systems for upper-limb rehabilitation in multiple sclerosis: a SWOT analysis and the synergies with virtual and augmented environmentsGiulia A Albanese, Anna Bucchieri, Jessica Podda, et al.Neuroscience Letters|October 26, 1999
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian casesV Bonifati, M Joosse, D J Nicholl, et al.Pageof 52