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Sherrington

Showing results (551-560 of 569) with videos related to

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Human Molecular Genetics|July 1, 1996
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrantR Sherrington, S Froelich, S Sorbi, et al.
Physiotherapy|June 20, 2024
Patients', physiotherapists' and other stakeholders' experiences and perceptions about supported home physiotherapy for people with musculoskeletal conditions: a qualitative studyHannah G Withers, Hueiming Liu, Joanne V Glinsky, et al.
Journal of Physiotherapy|March 17, 2024
Remotely delivered physiotherapy is as effective as face-to-face physiotherapy for musculoskeletal conditions (REFORM): a randomised trialHannah G Withers, Joanne V Glinsky, Jackie Chu, et al.
Archives of Physical Medicine and Rehabilitation|March 2, 2026
Was the Motor Training in the SCI-MT Trial delivered by therapists and received by participants according to the protocol? A fidelity analysisMarsha Ben, Joanne V Glinsky, Jackie Chu, et al.
BMJ Open|August 29, 2023
Early and Intensive Motor Training for people with spinal cord injuries (the SCI-MT Trial): protocol of the process evaluationJackie Chu, Joanne V Glinsky, Hueiming Liu, et al.
American Journal of Human Genetics|April 3, 2004
Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic IsolatesRonald G Lafreniere, Marcia L E MacDonald, Marie-Pierre Dube, et al.
BMJ Nutrition, Prevention & Health|January 30, 2025
Promotion of Physical Activity by Health Professionals (PROMOTE-PA): protocol for effectiveness outcomes in a hybrid type I effectiveness-implementation cluster randomised controlled trialJennifer Naomi Baldwin, Kate Purcell, Leanne Hassett, et al.
Human Molecular Genetics|July 1, 1996
Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeatS Igarashi, Y Takiyama, G Cancel, et al.
Clinical Genetics|May 2, 2007
Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populationsY P Goldberg, J MacFarlane, M L MacDonald, et al.
BMC Geriatrics|February 4, 2018
Standard set of health outcome measures for older personsAsangaedem Akpan, Charlotte Roberts, Karen Bandeen-Roche, et al.
Pageof 57

Showing results (551-560 of 569) with videos related to

Sort By:
Pageof 57
Human Molecular Genetics|July 1, 1996
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrantR Sherrington, S Froelich, S Sorbi, et al.
Physiotherapy|June 20, 2024
Patients', physiotherapists' and other stakeholders' experiences and perceptions about supported home physiotherapy for people with musculoskeletal conditions: a qualitative studyHannah G Withers, Hueiming Liu, Joanne V Glinsky, et al.
Journal of Physiotherapy|March 17, 2024
Remotely delivered physiotherapy is as effective as face-to-face physiotherapy for musculoskeletal conditions (REFORM): a randomised trialHannah G Withers, Joanne V Glinsky, Jackie Chu, et al.
Archives of Physical Medicine and Rehabilitation|March 2, 2026
Was the Motor Training in the SCI-MT Trial delivered by therapists and received by participants according to the protocol? A fidelity analysisMarsha Ben, Joanne V Glinsky, Jackie Chu, et al.
BMJ Open|August 29, 2023
Early and Intensive Motor Training for people with spinal cord injuries (the SCI-MT Trial): protocol of the process evaluationJackie Chu, Joanne V Glinsky, Hueiming Liu, et al.
American Journal of Human Genetics|April 3, 2004
Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic IsolatesRonald G Lafreniere, Marcia L E MacDonald, Marie-Pierre Dube, et al.
BMJ Nutrition, Prevention & Health|January 30, 2025
Promotion of Physical Activity by Health Professionals (PROMOTE-PA): protocol for effectiveness outcomes in a hybrid type I effectiveness-implementation cluster randomised controlled trialJennifer Naomi Baldwin, Kate Purcell, Leanne Hassett, et al.
Human Molecular Genetics|July 1, 1996
Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeatS Igarashi, Y Takiyama, G Cancel, et al.
Clinical Genetics|May 2, 2007
Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populationsY P Goldberg, J MacFarlane, M L MacDonald, et al.
BMC Geriatrics|February 4, 2018
Standard set of health outcome measures for older personsAsangaedem Akpan, Charlotte Roberts, Karen Bandeen-Roche, et al.
Pageof 57