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1 METHODS: Single-dose pharmacokinetics of low-osmolar 1% maraviroc (MVC), 1% tenofovir (TFV), or 1% MV
3 mmercial lubricants were compounded into iso-osmolar and hyperosmolar mixtures (283 and 3429 mOsm/kg,
6 tions, ranging from thermal, tactile, taste, osmolar, and fluid flow sensing to transepithelial Ca2+
9 the escaped animals were also markedly hypo-osmolar compared to controls as a result of water loadin
10 similarly after treatment with NaCl, an equi-osmolar concentration of sorbitol, or ABA, whereas AtNHX
11 activity was robust in these cells in normal osmolar conditions and increased by approximately twofol
12 L. interrogans serovar Copenhageni adapts to osmolar conditions that correspond with invasion of a ma
13 the primary choline transporters under hypo-osmolar conditions whereas BetT3 was the major choline t
14 rons is markedly exacerbated by chronic hypo-osmolar conditions, but neuronal survival is not enhance
16 a single biphasic injection of 130 mL of iso-osmolar contrast material (100 mL at 5 mL/sec and 30 mL
17 erwent intravenous administration of the iso-osmolar contrast material (IOCM) iodixanol 320 and patie
18 approximately 3.6 times higher with all low-osmolar contrast media (2.3%) than with high-osmolar med
19 s to all available high-osmolar and four low-osmolar contrast media (ioxaglate, iohexol, iopamidol, a
20 ar contrast medium (IOCM) iodixanol with low-osmolar contrast media (LOCM) and to identify predictors
21 e versus IV saline in patients receiving low-osmolar contrast media (RR, 0.65 [CI, 0.33 to 1.25]; low
22 a slight reduction in CIN risk with the iso-osmolar contrast media agent iodixanol compared with a d
23 investigate the cardiovascular effect of iso-osmolar contrast media and the image quality achieved.
25 g coronary angioplasty, the use of ionic low osmolar contrast media reduces the risk of ischemic comp
27 cification can be achieved with iso- and low-osmolar contrast media when it is injected at the same i
29 at comparable iodine delivery rates, the iso-osmolar contrast medium iodixanol 270 is not inferior to
30 medium iodixanol 270 is not inferior to low-osmolar contrast medium iopromide 300 for assessment of
31 consent were obtained for the Effect of Iso-osmolar Contrast Medium on Coronary Opacification and He
33 myelinolysis who are subjected to aggressive osmolar correction may be rescued with appropriate fluid
36 interrogans involves a transition from a low osmolar environment outside the host to a higher physiol
40 with the hyperosmolar gel than with the iso-osmolar formulation (median toxicity grade, 2.50 vs. 1.1
41 re determined by comparing serum lactate and osmolar gap at baseline, after 48 hrs, and at end of the
42 assium and bicarbonate levels, and anion and osmolar gap determination, as well as hepatic and renal
44 nce of a methanol concentration, the osmolal/osmolar gap may be informative; or, in the context of im
47 oncentration at 10 cm, compared with the iso-osmolar gel (median, 8.9% vs. 54.6% of administered conc
51 cific toxic effect of monomeric nonionic low-osmolar iodinated contrast medium in ICU patients with m
52 dose in utero exposure to water-soluble, low-osmolar, iodinated intravenous products, such as iohexol
53 were prospectively randomized to receive iso-osmolar iodixanol 270 or low-osmolar iopromide 300 contr
57 osure to 25 mmol/L d-glucose, but not to iso-osmolar mannitol, 1) reduced the ability of L-ASA to inh
58 for 60 min with 5-25 mmol/L d-glucose or iso-osmolar mannitol, we evaluated the influence of a 30-min
59 osmolar contrast media (2.3%) than with high-osmolar media (0.6%), usually in patients with pathologi
61 media compared with the three noncharged low-osmolar media, the incidence (per million examinations)
63 corneal epithelial cells cultured in normal osmolar medium (312 mOsM) were exposed to media with hig
65 ells were cultured in vitro with cycled hypo-osmolar or hyper-osmolar stresses, the AQY1 null yeast s
67 by aggressive correction of a hyper- or hypo-osmolar state and until recently has been associated wit
68 thy, symptomatic cerebral edema due to a low osmolar state, is a medical emergency and often encounte
71 d in vitro with cycled hypo-osmolar or hyper-osmolar stresses, the AQY1 null yeast showed significant
72 atient-level and hospital-level variation in osmolar therapy use and the substantial amount of sustai
73 use and the substantial amount of sustained osmolar therapy without intracranial pressure monitoring
74 Cl(-) reversal potential, particularly when osmolar transmembrane gradients are minimized, for examp
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