2023
DOI: 10.1016/j.nbd.2023.106056
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Peripheral nerve injury elicits microstructural and neurochemical changes in the striatum and substantia nigra of a DYT-TOR1A mouse model with dystonia-like movements

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Cited by 5 publications
(7 citation statements)
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“…Their high sensitivity has recently been shown to facilitate clinical trials, genotype predictions and continuous monitoring in neurological disorders [24,42,55]. Moreover, our framework may bridge methodological gaps between clinical and experimental neuroscience, which has already widely adapted computer vision for phenotyping animal models of dystonia [15][16][17]. We envisage the proposed tool to strengthen translational and precision medicine approaches in modern neurology.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Their high sensitivity has recently been shown to facilitate clinical trials, genotype predictions and continuous monitoring in neurological disorders [24,42,55]. Moreover, our framework may bridge methodological gaps between clinical and experimental neuroscience, which has already widely adapted computer vision for phenotyping animal models of dystonia [15][16][17]. We envisage the proposed tool to strengthen translational and precision medicine approaches in modern neurology.…”
Section: Discussionmentioning
confidence: 99%
“…These kinematic features aimed to quantify clinically relevant observations in dystonia that are commonly noted but seldom quantified in clinical settings, such as movement overflow to other bodyparts as well as action-induced changes of dystonia, both resulting in asymmetrical or abnormal movement trajectories, dystonic tremor[14] and the complexity of dystonia characterised by the involvement of multiple axes in phasic or tonic movements and movement predictability over time. The features were partially harmonised with kinematic features recently reported to be relevant to dystonia phenotype and genetics in rodent models of dystonia [15, 16] as well as the characterisation of brain dynamics more broadly [37, 38]. The derived features primarily included correlations, symmetries, oscillatory and entropy-related characteristics, which are further described below.…”
Section: Methodsmentioning
confidence: 99%
“…Their high sensitivity has recently been shown to facilitate clinical trials, genotype predictions and continuous monitoring in neurological disorders 25,38,56 . Moreover, our framework may bridge methodological gaps between clinical and experimental neuroscience, which has already widely adapted computer vision for phenotyping animal models of dystonia [15][16][17] . We envisage the proposed tool to strengthen translational and precision medicine approaches in modern neurology.…”
Section: Discussionmentioning
confidence: 99%
“…These kinematic features aimed to quantify clinically relevant observations in dystonia that are commonly noted but seldom quantified in clinical settings, such as movement overflow to other bodyparts as well as action-induced changes of dystonia, both resulting in asymmetrical or abnormal movement trajectories, dystonic tremor 14 and the complexity of dystonia characterised by the involvement of multiple axes in phasic or tonic movements and movement predictability over time. The features were partially harmonised with kinematic features recently reported to be relevant to dystonia phenotype and genetics in rodent models of dystonia 15 , 16 as well as the characterisation of brain dynamics more broadly 59 , 60 .…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation