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Moreover, the hemispheric encoding/retrieval asymmetry model (HERA) (Habib et al., 2003) also suggests more involvement of the left hemisphere in episodic encoding which, in this case, may be reflected by sleep spindle activity.
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When maximum N3 sleep is achieved, any further need for repose could be reflected by the less restful N1 sleep.
Applied to the current sleep study, a difference in the level of attentional control of predictable and unpredictable response processing at encoding before sleep would be reflected by different amplitude of negative SPs.
Based on our previous findings, a general sleep defensive mechanism is postulated to be triggered by rare tones which should be reflected by an crossmodal NBR also in brain areas not directly targeted by the acoustic paradigm.
This may be reflected by their tumorigenicity.
The importance of sleep times is reflected by the observation that when sleep deprived, experimental human and animal subjects exhibit a 'sleep rebound' proportional to the amount of sleep lost [10], indicating that the amount of sleep, or of some specific component of sleep, is physiologically relevant.
Sleep propensity, increasingly depending on extended time spent awake, is reflected by process S. In this model, the sleep intensity (process S) is at its maximum at sleep onset, declining during consecutive sleep.
The sympathetic tone is reduced in sleep, which is reflected by a reduction of heart rate (HR).
The differences in impulsiveness are reflected in sleep architecture as well.
Sleep disturbance was reflected, for example, in the measure of sleep efficiency, with a mean value of 77.58% (± 19.28).
The changes of sleep patterns were mainly reflected by altered sleep stage distribution and increased sleep fragmentation.
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CEO of Professional Science Editing for Scientists @ prosciediting.com