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[PDF] Top 20 A Robust Role for Motor Cortex

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A Robust Role for Motor Cortex

A Robust Role for Motor Cortex

... of motor control (Glees & Cole, 1950; Cole, ...the motor cor- ...ing motor cortical areas surrounding the circumscribed lesions, they were able to evoke movements in the impacted digits and ... See full document

158

The anterior cingulate cortex

The anterior cingulate cortex

... and motor response; in affective tasks such as emotional processing (enhanced activity leads to sadness); in feelings of anxiety, phobia, guilt, pain, embarrassment, deception, humor, trust, and empa- thy; in ... See full document

15

Dopamine in motor cortex is necessary for skill learning and synaptic plasticity.

Dopamine in motor cortex is necessary for skill learning and synaptic plasticity.

... for motor skill ...somatosensory cortex or by associative stimulation of somatosensory cortex and thalamus ...that motor learning is impaired after lesioning relevant regions of somato- ... See full document

10

Brain-derived neurotrophic factor--a major player in stimulation-induced homeostatic metaplasticity of human motor cortex?

Brain-derived neurotrophic factor--a major player in stimulation-induced homeostatic metaplasticity of human motor cortex?

... In addition to manifold genetic factors that regulate the induction of synaptic plasticity, the ‘‘neural state’’ at the time of transcranial conditioning is highly relevant. For instance, changes in attention at the time ... See full document

11

Contribution of the resting-state functional connectivity of the contralesional primary sensorimotor cortex to motor recovery after subcortical stroke.

Contribution of the resting-state functional connectivity of the contralesional primary sensorimotor cortex to motor recovery after subcortical stroke.

... in motor recovery after ...in motor recovery also comes from other contradictory findings obtained by fMRI and TMS studies ...important role in subcortical stroke patients performing complex ... See full document

9

Reinforcement learning of targeted movement in a spiking neuronal model of motor cortex.

Reinforcement learning of targeted movement in a spiking neuronal model of motor cortex.

... Sensorimotor mappings can be thought of as stimulus-response mappings, suggesting reinforcement learning (RL) as a mechanism for learning. The essence of this learning mechanism was summarized over 100 years ago in ... See full document

8

The role of pulse shape in motor cortex transcranial magnetic stimulation using full-sine stimuli.

The role of pulse shape in motor cortex transcranial magnetic stimulation using full-sine stimuli.

... Transcranial magnetic stimulation (TMS) is commonly used to non-invasively probe and alter human motor cortex excitability via a time-varying magnetic field [1]. In principle, a magnetic stimulator consists ... See full document

22

Evolution of premotor cortical excitability after cathodal inhibition of the primary motor cortex: a sham-controlled serial navigated TMS study.

Evolution of premotor cortical excitability after cathodal inhibition of the primary motor cortex: a sham-controlled serial navigated TMS study.

... of motor network compen- sation ...contralateral motor areas depending on the amount of deficit ...secondary motor regions change their interaction patterns, ... See full document

10

Robust control in water management

Robust control in water management

... bu¤er role of groundwater in a static setting and shows that it is positive under standard concavity assumptions of the bene…t function, and Tsur and Graham-Tomasi (1991) provide a similar analysis for a dynamic ... See full document

20

ALS pathogenesis: role of motor neuron-derived exosomes in microglia activation and dysfunction

ALS pathogenesis: role of motor neuron-derived exosomes in microglia activation and dysfunction

... Figure I. 3 – Involvement of exosomes in interneuronal communication. Many studies have reported the release of exosomes by neurons, oligodendrocytes, astrocytes and microglia. It is proposed that these exosomes are ... See full document

112

Multiplexed simultaneous representations of cognitive and motor features, in the mouse medial prefrontal cortex, during a memory guided behavior

Multiplexed simultaneous representations of cognitive and motor features, in the mouse medial prefrontal cortex, during a memory guided behavior

... We fitted the coefficients associated with the bins of the sliding kernel used to predict speed at each cm of each trial (Figure 4.1 ), consequently, all speed values were decoded the same way. This assumed that speed ... See full document

213

The role of the medial Prefrontal Cortex in nociception : functional characterization of Prelimbic and Infralimbic nuclei

The role of the medial Prefrontal Cortex in nociception : functional characterization of Prelimbic and Infralimbic nuclei

... the role of the prefrontal cortex (PFC) in this ...the role of these two PFC areas in pain modulation by using behavioural and electrophysiological techniques to (i) characterize the ... See full document

87

Robust Control in Water Management

Robust Control in Water Management

... In this paper, results for water use were derived with and without stock e¤ects on cost, and presented for varying levels of model uncer- tainty, as expressed by levels of the penalty parameter θ, to explore and ... See full document

23

Robust statistical modeling of portfolios

Robust statistical modeling of portfolios

... three robust and classical baseline ...the robust (classical) portfolios of the three ...the robust portfolios are more stable, with a distribution located at higher values and possessing smaller ... See full document

28

Involvement of the hippocampus, amygdala, entorhinal cortex and posterior parietal cortex in memory consolidation

Involvement of the hippocampus, amygdala, entorhinal cortex and posterior parietal cortex in memory consolidation

... entorhinal cortex 90 or 180 min after training confirm those of Ferreira et ...entorhinal cortex and that of the parietal cortex in memory pro- ...parietal cortex, respectively (16). For ... See full document

6

Low frequency (0.5Hz) rTMS over THe rigHT (non-doMinanT) MoTor corTex doeS noT affecT ipSiLaTeraL Hand perforMance in HeaLTHy HuManS

Low frequency (0.5Hz) rTMS over THe rigHT (non-doMinanT) MoTor corTex doeS noT affecT ipSiLaTeraL Hand perforMance in HeaLTHy HuManS

... We have also shown an overall better performance with the right hand than with the left or both hands. This might be expected given the right-handedness of the subjects. It is reasonable to assume that the task involved ... See full document

6

Excitability of the motor cortex ipsilateral to the moving body side depends on spatio-temporal task complexity and hemispheric specialization.

Excitability of the motor cortex ipsilateral to the moving body side depends on spatio-temporal task complexity and hemispheric specialization.

... of motor areas ipsilateral to the moving hand is asymmetric such that the left hemisphere is more activated when a complex movement task is executed with the ipsilateral, left body side than the right hemisphere ... See full document

10

The prefrontal cortex and chronic pain : the role of metabotropic glutamatergic receptors in the descending modulation of pain

The prefrontal cortex and chronic pain : the role of metabotropic glutamatergic receptors in the descending modulation of pain

... the role of the prefrontal cortex upon descending modulation of ...prefrontal cortex, some studies propose a similarity between human and primates and between primates and ...orbitofrontal ... See full document

94

Robust partial least squares path modeling

Robust partial least squares path modeling

... Although robust PLS and PLSc produce almost undistorted estimates when the outliers arise randomly and initial evidence is obtained that they are robust against systematic outliers, future research should ... See full document

28

Differential expression of secreted phosphoprotein 1 in the motor cortex among primate species and during postnatal development and functional recovery.

Differential expression of secreted phosphoprotein 1 in the motor cortex among primate species and during postnatal development and functional recovery.

... visual cortex neurons of the rhesus macaque and marmoset but not in that of the mouse ...association cortex neurons of the rhesus macaque and marmoset but not in that of the mouse ... See full document

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