Issue Highlights Clinical Gastroenterology and Hepatology

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Issue Highlights Clinical Gastroenterology and Hepatology Stephen B. Hanauer  Clinical Gastroenterology and Hepatology  Volume 13, Issue 10, Pages 1709-1710 (October 2015) DOI: 10.1016/j.cgh.2015.08.001 Copyright © 2015 AGA Institute Terms and Conditions

Figure 1 The total numbers of lesions with IN found using WL colonoscopy in stepwise, segmental, and targeted biopsy specimens or using NBI colonoscopy in segmental or targeted biopsy specimens, differentiated by non–adenoma-like and adenoma-like lesions or the sum of both (total). Furthermore, the sum of dysplastic lesions in stepwise and targeted biopsy specimens in WL colonoscopy and of targeted and segmental biopsy specimens in NBI colonoscopy is shown. Clinical Gastroenterology and Hepatology 2015 13, 1709-1710DOI: (10.1016/j.cgh.2015.08.001) Copyright © 2015 AGA Institute Terms and Conditions

Figure 2 Comparison of OffTime+OnTime between groups. CHE on paper-pencil tests. Mean±95% confidence interval depicted in the bars. Significantly higher OffTime+OnTime in patients with CHE than those without CHE in entire cirrhosis (Cirr) group compared with controls. Clinical Gastroenterology and Hepatology 2015 13, 1709-1710DOI: (10.1016/j.cgh.2015.08.001) Copyright © 2015 AGA Institute Terms and Conditions