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1 e potential to cause per se narcoleptic-like sleep disruption.
2 acterized by recurrent nocturnal hypoxia and sleep disruption.
3 leep associated with oxygen desaturation and sleep disruption.
4 e, bowel/bladder and sexual dysfunction, and sleep disruption.
5 termine the effect of environmental noise on sleep disruption.
6 hey generally suggest modest and nonspecific sleep disruptions.
7 g neural mechanisms that explain age-related sleep disruption?
8 anisms linking non-rapid-eye-movement (NREM) sleep disruption, Abeta, and AD; (ii) a role for NREM sl
10 C1 cell activation likely contributes to the sleep disruption and adverse autonomic consequences of s
12 e and central types of sleep apnea result in sleep disruption and arterial oxyhemoglobin desaturation
14 echanisms underlying the interaction between sleep disruption and behavior remain poorly understood.
15 sis of a direct pathological role of PLMS in sleep disruption and can be important for the discussion
18 logy with both non-rapid eye movement (NREM) sleep disruption and memory impairment in older adults.
19 latonin supplementation for the treatment of sleep disruption and other neurological diseases such as
20 topic dermatitis (AD) experience significant sleep disruption, and clinically, the disease is noted t
21 arly-onset patients had more energy, minimal sleep disruption, and greater suicidality, while typical
23 han 40 million Americans suffer from chronic sleep disruption, and the development of effective treat
24 han 40 million Americans suffer from chronic sleep disruption, and the development of effective treat
26 with impaired NREM SWA, these data implicate sleep disruption as a mechanistic pathway through which
27 ii) the potential diagnostic utility of NREM sleep disruption as a new biomarker of AD; and (iv) the
28 ruption, Abeta, and AD; (ii) a role for NREM sleep disruption as a novel factor linking cortical Abet
29 ed in many atopic diseases that can underlie sleep disruptions as a consequence of the presence of no
30 Clinicians need to consider that the chronic sleep disruption associated with nightmares may affect t
31 adequate interventions to prevent and treat sleep disruption because of their high relevance to our
32 survivors suffering from moderate or greater sleep disruption between 2 and 24 months after surgery,
33 mproved with sleeping drugs, suggesting that sleep disruption contributes to their neurological decli
35 quality of life caused by intense pruritus, sleep disruption, dietary and nutritional concerns, and
36 tion and those with more negative affect and sleep disruption during marijuana withdrawal were more l
37 r the functional consequences of age-related sleep disruption, focusing on memory impairment as an ex
38 the MICU appeared to be more susceptible to sleep disruptions from environmental factors than patien
40 rat model is associated with large long-term sleep disruption, however, the vehicle, DMSO/PEG had as
41 with PTCHD1 deletion show symptoms of ADHD, sleep disruption, hypotonia, aggression, ASD, and ID.
42 urst; however, the effects of other forms of sleep disruption (i.e. spontaneous arousals and apnoea-i
44 ynchrony, a characteristic of shift work and sleep disruption in humans, also leads to metabolic path
45 sleep loss, we quantified a new procedure of sleep disruption in mice by a week of consecutive sleep
47 nderstanding the neural mechanism underlying sleep disruption in response to environmental perturbati
52 exposed to high sound levels and substantial sleep disruption irrespective of factors including previ
54 ENT In the light of increasing evidence that sleep disruption is crucially involved in the progressio
56 er emerging studies suggest that age-related sleep disruption may be one key factor that renders the
57 a support a neuropathological model in which sleep disruption may contribute to the maintenance and/o
58 ing that like many other stressors, extended sleep disruption may lead to a state of sustained microg
61 rimental studies of these different forms of sleep disruption show deranged physiology from subcellul
62 dation is more susceptible to the effects of sleep disruption than is the acquisition (learning) of s
63 may affect the degree of hypoxic stress and sleep disruption that occurs in response to upper airway
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