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1 excessive brain tissue oxygenation, elevated brain temperature).
2 eration of normal EEG and the maintenance of brain temperature.
3 thy data we built HEATWAVE-a 4D map of human brain temperature.
4 ennes bioheat equation was used to propagate brain temperature.
5 ons and a force behind associated changes in brain temperature.
6 creased excitability consequent to increased brain temperature.
7 rain temperature since it reflects body, not brain temperature.
9 immediately by 1 hr of either normothermia (brain temperature 37 +/- 0.5 degrees C) or hypothermia (
10 ure ranged from 36.1 to 40.9 degrees C; mean brain temperature (38.5 +/- 0.4 degrees C) exceeded oral
11 ranged from 32.6 to 42.3 degrees C and mean brain temperature (38.5 +/- 0.8 degrees C) exceeded body
12 mployed in the present study with respect to brain temperatures, a dynamic parameter that reflects me
13 undergo interventions to achieve a 'normal' brain temperature; a parameter that remains undefined fo
14 that imaging through a cranial window lowers brain temperature, an effect capable of affecting cerebr
15 hermocouples were placed to measure core and brain temperature and a composite probe placed in the pa
16 brile seizures are associated with increased brain temperature and are often resistant to treatments
22 l stimulation can cause local changes in the brain temperature and subsequent local changes in the ox
23 use does not lead to profound elevations in brain temperature and sustained vasoconstriction, two cr
24 pport the potential importance of monitoring brain temperature and the importance of controlling feve
25 s are remarkable for surviving near-freezing brain temperatures and near cessation of neural activity
27 tions of the impact of the light-dark cycle, brain temperature, and blood flow on the function of the
28 he profound influence of sleep-wake state on brain temperature, and can be harnessed to differentiate
33 e additional support for the hypothesis that brain temperatures are elevated during winter depression
35 they are in the ICU for a week or more, and brain temperatures are likely to be as much as 2 degrees
39 n tissue PO(2) in the thalamus (PtO(2)), and brain temperature (Bt) simultaneously during acute hyper
40 th cocaine and PRO their ability to increase brain temperature but failed to induce temperature decre
41 ethylone and MDPV dose-dependently increased brain temperature, but even at high doses that induced r
42 S-201 (1.5-2.5 mg/kg, i.p.) reduces body and brain temperature by 2-5 degrees C in 15-30 min in a dos
44 ogical parameters, such as body temperature, brain temperature, cerebral blood flow, blood gases, blo
47 hermometry to provide an estimate of in vivo brain temperature changes during MR-ARFI, and pressure a
49 , real-time data acquisition, and continuous brain temperature control, in this new rat model, provid
52 -4.2 mmHg to 14.8+/-5.2 mmHg (P=0.004) while brain temperature decreased from 36.5+0.3 degrees C to 3
53 ter immersion objective at room temperature, brain temperature decreases by ~2-3 degrees C, causing d
56 th increasing time after stroke, ipsilateral brain temperature did not change, but contralateral hemi
58 Adenosine treatment significantly lowered brain temperature during recovery, and a part of the neu
60 To explore this possibility, we measured brain temperature dynamics during a 10-min forced swim i
63 studies are required to determine why early brain temperature elevation is highest in potential penu
66 ic brain activation as the primary source of brain temperature fluctuations and a force behind associ
67 med with the same dose/pattern as SA induced brain temperature fluctuations similar in many ways to t
68 mimicked cocaine in its ability to increase brain temperature following the initial injection and to
70 g/kg, s.c.) or MDPV (0.1-1.0 mg/kg, s.c.) on brain temperature homeostasis in rats maintained in a st
71 aimed to determine the clinical relevance of brain temperature in patients by establishing how much i
75 G desynchronization, EMG activation, a large brain temperature increase, but weaker hyperlocomotion.
76 ortical blood flow among groups with varying brain temperature, indicating that delayed deterioration
79 perficial cortex regions, where the baseline brain temperature is lower than the temperature of incom
80 mic brain temperature variation-not absolute brain temperature-is one way in which human brain physio
82 mary endpoint was the time required to reach brain temperature less than 35 degrees C beginning from
83 on would decrease the time required to reach brain temperature less than 35 degrees C compared to act
87 y after acute ischaemic stroke, elevation of brain temperature might augment tissue metabolic rate an
88 neural cells is accompanied by heat release, brain temperature monitoring provides insight into behav
89 e was no effect of drug treatment on body or brain temperature, nor on the duration or rate of Type I
92 Compared with anesthetized controls, core brain temperatures of the saline and slurry groups dropp
93 companied by heat production, measurement of brain temperature offers a method for assessing global a
94 rebral blood flow, changes in blood gases or brain temperature, or rat strain; (3) the neuroprotectiv
96 alysis, 25 displayed a daily rhythm, and the brain temperature range decreased in older patients (P =
99 eous vasodilation; (2) drastic drops in deep brain temperature (reaching a nadir of 22.44 +/- 0.74 de
101 ody temperatures, because cooler and varying brain temperatures reduce brain performance and thus fit
102 ole of regional cerebral blood flow in local brain temperature regulation has received scant attentio
103 pplying oxygen for neuromodulator synthesis, brain temperature regulation, signaling to neurons, stab
105 led the gradients and regional variations in brain temperatures reported in the literature for awake
109 E in patients, we found that lack of a daily brain temperature rhythm increased the odds of death in
110 rature monitoring and management, with daily brain temperature rhythmicity emerging as one of the str
113 els during the hibernation season keep their brain temperature significantly elevated above ambient t
114 ure measurement is not a good measurement of brain temperature since it reflects body, not brain temp
115 e primary triggering force behind changes in brain temperature that are sufficient to affect body tem
116 schemia (HI) is neuroprotective; the precise brain temperature that provides optimal protection is un
118 observed during warm water forced swim, when brain temperature transiently increased (0.5 degrees C)
119 imals, passive animals had the same pattern; brain temperatures transiently decreased after cocaine i
121 oach, we previously demonstrated that hourly brain temperature values co-varied strongly with time sp
130 e treatment groups: (1) normothermic (Normo)-brain temperature was maintained at 37 degrees C; (2) in
135 brupt hypodynamia after drug infusion), mean brain temperature was very stable at an elevated plateau
136 perature than dorsal striatum, each of these brain temperatures was higher than that in deep temporal
138 , end tidal Pco2, arterial Po2 and Pco2, and brain temperature were observed before inducing cardiac
142 ve drug administration of a session elevated brain temperature, while subsequent repeated injections
144 ed that fentanyl induces biphasic changes in brain temperature, with an initial decrease that results
145 negatively correlated with average body and brain temperature, with the largest amount of REM sleep