ArticleJournal of neurophysiology2020
Temporal but not spatial dysmetria relates to disease severity in FA.
Article in Journal of neurophysiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed, 3 citations in OpenAlex.
- Quantification of Upper Limb Movements in Patients with Hereditary or Idiopathic Ataxia.Cerebellum (London, England) · 2023Article
- Older adults use a motor plan that is detrimental to endpoint control.Scientific reports · 2021Article
- Neurologic outcomes in Friedreich ataxia: Study of a single-site cohort.Neurology. Genetics · 2020Article
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Authors and funding
9 authors at 1 institution in 1 country.
Funding
Abstract
Friedreich's ataxia (FA) is an inherited disease that causes degeneration of the nervous system. Features of FA include proprioceptive and cerebellar deficits leading to impaired muscle coordination and, consequently, dysmetria in force and time of movement. The aim of this study is to characterize dysmetria and its association to disease severity. Also, we examine the neural mechanisms of dysmetria by quantifying the EMG burst area, duration, and time-to-peak of the agonist muscle. Twenty-seven individuals with FA and 13 healthy controls (HCs) performed the modified Functional Ataxia Rating Scale and goal-directed movements with the ankle. Dysmetria was quantified as position and time error during dorsiflexion. FA individuals exhibited greater time but not position error than HCs. Moreover, time error correlated with disease severity and was related to increased agonist EMG burst. Temporal dysmetria is associated to disease severity, likely due to altered activation of the agonist muscle.
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Registered trials
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