Zobrazeno 1 - 10
of 111
pro vyhledávání: '"Tal Krasovsky"'
Publikováno v:
Journal of NeuroEngineering and Rehabilitation, Vol 21, Iss 1, Pp 1-15 (2024)
Abstract Background Hybrid models that integrate both in-person and remote health services are increasingly recognized as a promising approach. Nevertheless, research that defines and characterizes these models in children and young people is scarce
Externí odkaz:
https://doaj.org/article/b7f15fa08eed45f680d2ec98a5da9e4f
Publikováno v:
Journal of NeuroEngineering and Rehabilitation, Vol 21, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/5e37735cdbe34f2cbc1cc745fcc5fca4
Autor:
Tal Krasovsky, Benedetta Heimler, Or Koren, Noam Galor, Sharon Hassin-Baer, Gabi Zeilig, Meir Plotnik
Publikováno v:
IEEE Transactions on Neural Systems and Rehabilitation Engineering, Vol 31, Pp 798-805 (2023)
Freezing of Gait (FOG) is among the most debilitating symptoms of Parkinson’s Disease (PD), characterized by a sudden inability to generate effective stepping. In preparation for the development of a real-time FOG prediction and intervention device
Externí odkaz:
https://doaj.org/article/14aa130dbd8c4f0588d5ab099825b725
Autor:
Shiri Embon-Magal, Tal Krasovsky, Israel Doron, Kfir Asraf, Iris Haimov, Efrat Gil, Maayan Agmon
Publikováno v:
BMC Geriatrics, Vol 22, Iss 1, Pp 1-10 (2022)
Abstract Background Cognition and motor skills are interrelated throughout the aging process and often show simultaneous deterioration among older adults with cognitive impairment. Co-dependent training has the potential to ameliorate both domains; h
Externí odkaz:
https://doaj.org/article/da961c116f914f579e1d6e9ea422a116
Publikováno v:
Journal of NeuroEngineering and Rehabilitation, Vol 17, Iss 1, Pp 1-8 (2020)
Abstract This article is inspired by a pseudo Oxford-style debate, which was held in Tel Aviv University, Israel at the International Conference on Virtual Rehabilitation (ICVR) 2019, which is the official conference of the International Society for
Externí odkaz:
https://doaj.org/article/f0d7684129544145b652a9c4951291fc
Publikováno v:
Frontiers in Human Neuroscience, Vol 16 (2022)
Persons with Parkinson’s disease (PwP) are advised to use compensatory strategies such as external cues or cognitive movement strategies to overcome gait disturbances. It is suggested that external cues involve the processing of sensory stimulation
Externí odkaz:
https://doaj.org/article/9875c55cc1c04153bf6d2ab6f0275611
Publikováno v:
Journal of NeuroEngineering and Rehabilitation, Vol 18, Iss 1, Pp 1-12 (2021)
Abstract Background Persistent postural-perceptual dizziness (PPPD) is a condition characterized by chronic subjective dizziness and exacerbated by visual stimuli or upright movement. Typical balance tests do not replicate the environments known to i
Externí odkaz:
https://doaj.org/article/96690d334cd643edac8d2d36db435222
Autor:
Rachel Proffitt, Stephanie Glegg, Tal Krasovsky, Belinda Lange, Danielle Levac, Anat V. Lubetzky, Wendy A. Powell, Maxime T. Robert
Publikováno v:
Frontiers in Virtual Reality, Vol 2 (2021)
Externí odkaz:
https://doaj.org/article/01ef3c5ed8044b0686967982f0794a68
Publikováno v:
Gait & Posture. 98:96-100
Children with ADHD show deficits in executive function, as well as motor symptoms such as difficulties in gross and fine motor skills and gait stability. Texting while walking is becoming increasingly common and is a significant health risk among peo
Autor:
Elad Jacoby, Omer Bar-Yosef, Noah Gruber, Einat Lahav, Nira Varda-Bloom, Yoav Bolkier, Diana Bar, Moriya Ben-Yakir Blumkin, Sharon Barak, Etzyona Eisenstein, Jaana Ahonniska-Assa, Tamar Silberg, Tal Krasovsky, Orly Bar, Neta Erez, Bella Bielorai, Hana Golan, Benjamin Dekel, Michal J. Besser, Gat Pozner, Hanan Khoury, Alan Jacobs, John Campbell, Eli Herskovitz, Noa Sher, Natalie Yivgi-Ohana, Yair Anikster, Amos Toren
Publikováno v:
Science translational medicine. 14(676)
Patients with single large-scale mitochondrial DNA (mtDNA) deletion syndromes (SLSMDs) usually present with multisystemic disease, either as Pearson syndrome in early childhood or as Kearns-Sayre syndrome later in life. No disease-modifying therapies