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United European Gastroenterology Journal|July 21, 2022
Benign inheritable disorders of bilirubin metabolism manifested by conjugated hyperbilirubinemia-A narrative reviewMariana B Morais, Mariana Verdelho Machado
United European Gastroenterology Journal|August 2, 2014
Tetramer-visualized gluten-specific CD4+ T cells in blood as a potential diagnostic marker for coeliac disease without oral gluten challengeAsbjørn Christophersen, Melinda Ráki, Elin Bergseng, et al.
United European Gastroenterology Journal|August 2, 2014
Reappraisal of the so-called 'villous tumours' of the rectosigmoid, based on histological, immunohistochemical and genotypic featuresLaure Droy-Dupré, Sébastien Küry, Emmanuel Coron, et al.
United European Gastroenterology Journal|April 19, 2016
Crohn's disease and skinA G Gravina, A Federico, E Ruocco, et al.
United European Gastroenterology Journal|April 19, 2016
Sleep disturbance due to heartburn and regurgitation is common in patients with functional dyspepsiaN Vakil, B Wernersson, J Wissmar, et al.
United European Gastroenterology Journal|April 19, 2016
In vitro fertilization-induced pregnancies predispose to gastroesophageal reflux diseaseIlker Turan, Gul Kitapcioglu, Ege Tavmergen Goker, et al.
United European Gastroenterology Journal|April 19, 2016
CT texture analysis in colorectal liver metastases: A better way than size and volume measurements to assess response to chemotherapy?Sheng-Xiang Rao, Doenja Mj Lambregts, Roald S Schnerr, et al.
United European Gastroenterology Journal|April 19, 2016
Short-term prognosis of potential celiac disease in Indian patientsRaghuram Kondala, Amarender S Puri, Ameet K Banka, et al.
United European Gastroenterology Journal|April 19, 2016
Risk factors for complications in patients with ulcerative colitisChristine N Manser, Jan Borovicka, Frank Seibold, et al.
United European Gastroenterology Journal|April 19, 2016
Type 1 serrated polyposis represents a predominantly female disease with a high prevalence of dysplastic serrated adenomas, without germline mutation in MUTYH, APC, and PTEN genesMarco Petronio, Stephane Pinson, Thomas Walter, et al.
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