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1 white-light endoscopy and preferably optical chromoendoscopy.
2 'smarter' mucosal biopsy when combined with chromoendoscopy.
3 methods include magnification endoscopy and chromoendoscopy.
4 of preneoplastic lesions with methylene blue chromoendoscopy.
5 ite light endoscopy, narrow band imaging and chromoendoscopy.
6 ocedure and withdrawal times with pancolonic chromoendoscopy (30.7 +/- 12.8 minutes and 18.3 +/- 7.6
7 nce in adenoma detection rates by pancolonic chromoendoscopy (34.4%; 95% CI 26.4%-43.3%) vs white-lig
9 nition endoscopy in combination with digital chromoendoscopy allowed real-time in vivo prediction of
11 ia are constantly being evaluated, including chromoendoscopy and biomarkers of carcinoma, in an attem
12 using high-definition endoscopy with digital chromoendoscopy and the accuracy of predicting histology
14 BE) using dye-based chromoendoscopy, optical chromoendoscopy, autofluorescence imaging, or confocal l
15 ithin this study we assessed whether digital chromoendoscopy can accurately predict the histology of
18 of high-definition white light endoscopy and chromoendoscopy compared with white light endoscopy alon
21 endoscopy [i-scan], and Fujinon intelligent chromoendoscopy [FICE]), confocal laser endomicroscopy (
22 nsitivity and specificity of pCLE to virtual chromoendoscopy for classification of colorectal polyps
23 light endoscopy is noninferior to pancolonic chromoendoscopy for detection of adenomas in patients wi
26 e for ACF detection using high-magnification chromoendoscopy has demonstrated considerable variabilit
27 y, cap-fitted colonoscopy, and dye-based pan-chromoendoscopy have each shown to increase polyp detect
30 ds (narrow band imaging, Fujinon Intelligent ChromoEndoscopy, i-scan, and autofluorescence) have been
31 ight endoscopy is not inferior to pancolonic chromoendoscopy if performed by experienced and dedicate
36 de enhancements in diagnostic optics such as chromoendoscopy, magnification endoscopy, and confocal l
37 Newer technology and techniques, including chromoendoscopy, magnification endoscopy, optical cohere
39 hite-light endoscopy (n = 128) or pancolonic chromoendoscopy (n = 128) evaluations by 24 colonoscopis
41 ith Barrett's esophagus (BE) using dye-based chromoendoscopy, optical chromoendoscopy, autofluorescen
44 More convenient methods, such as "digital" chromoendoscopy, show promise but have had mixed results
46 rrounding mucosa, and preliminary support of chromoendoscopy to target dysplasia better during colono
47 nsitivity and specificity of pCLE to virtual chromoendoscopy using a modified gold standard that assu
51 E had higher sensitivity compared to virtual chromoendoscopy when considering histopathology as gold
52 ence in specificity between pCLE and virtual chromoendoscopy when considering histopathology or modif
53 ng (NBI) with magnifying endoscopy (ME), and chromoendoscopy with 1.5% Lugol's solution, before defin
54 er, these methods and several other methods (chromoendoscopy with magnification, confocal laser micro
56 o DNA is increased in Barrett's mucosa after chromoendoscopy with methylene blue, an effect apparentl