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Titlebook: Brain Edema IX; Proceedings of the N Umeo Ito (Director and Neurosurgeon in Chief),Alex Conference proceedings 1994 Springer-Verlag/Wien 19

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https://doi.org/10.1007/0-387-31804-6at its isosbestic point. At this wavelength the probe is ion-insensitive and the fluorescent signals emitted is dependent on variations in the concentration of the dye. Variations in cell volume thus lead to changes in fluorescence intensity as the probe concentration is changed in the lightened del
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https://doi.org/10.1007/0-387-31804-6ransient reversible vacuolation in neurons in the posterior cingulate cortex of rats. Similar effects have also been observed with competitive glutamate antagonists such as CPP, CGS 19755 and CGP 37849. This transient morphological change has been noted to be coincident anatomically with brain regio
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https://doi.org/10.1007/0-387-31804-6uspended in an incubation chamber under continuous control of pH, pO., and temperature. Cell swelling was quantified by flow cytometry. After a control period, the suspension was added with AA at concentrations of 0.01 to 1.0 mM. Administration of AA induced an immediate, dose dependent swelling in
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Delivery of Contrast Media for MDCTg was reduced by 74% when temperature was lowered from 37°C to 24°C. Reduction in temperature to 24°C also resulted in inhibition of glutamate-stimulated K+ uptake. When both extracellular and intracellular Ca. were removed with BAP-TA/AM (50 μM) and 0.1 mMEGTA and in the absence of extracellular Ca
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Guide to Clinical Workstation Usen exposed to hypotonic solution, C6 cells swelled slowly to 5 times their normal volume and burst, whereas N18 cells swelled more rapidly, forming blebs, and then burst partially. The time to burst was 410.6 ± 45.7 s (mean ± SD, n = 5) for C6, and 69.3 ± 10.4 s (n = 5, p < 0.01) for N18, respectivel
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Image Reconstruction and Reviewwere dissected into oxygenated (95% O., 5% CO.) Ames medium, a physiologic solution resembling cerebrospinal fluid, and randomly assigned to either experimental hypoxic conditions (95% N., 5% CO.) or control conditions. All retinas were incubated and maintained at 37°C. Changes in extracellular K+ a
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