4 results match your criteria: "tulassay.zsolt@med.semmelweis-univ.hu.[Affiliation]"
Dig Dis
May 2020
Department of Gastroenterology, Medical Centre Hungarian Defence Forces, Semmelweis University Teaching Hospital Budapest, Budapest, Hungary.
Background: The clinical importance of microscopic colitis (MC) is increasing. This is explained by both the increasing incidence and the challenges posed by the disease. However, recent MC data also reveal a number of doubts and uncertainties.
View Article and Find Full Text PDFDig Dis
February 2019
Internal and Gastroenterological Clinic, Semmelweis University Budapest, Budapest, Hungary,
BMC Gastroenterol
October 2015
2nd Department of Medicine, Semmelweis University, Szentkirályi st. 46., 1088, Budapest, Hungary.
Background: Celiac disease, Crohn disease and ulcerative colitis are inflammatory disorders of the gastrointestinal tract with some common genetic, immunological and environmental factors involved in their pathogenesis. Several research shown that patients with celiac disease have increased risk of developing inflammatory bowel disease when compared with that of the general population. The aim of this study is to determine the prevalence of inflammatory bowel disease in our celiac patient cohort over a 15-year-long study period.
View Article and Find Full Text PDFDiagn Pathol
July 2015
Molecular Medicine Research Unit, Hungarian Academy of Sciences, Budapest, Hungary.
Background: A recently published transcript set is suitable for gene expression-based discrimination of normal colonic and colorectal cancer (CRC) biopsy samples. Our aim was to test the discriminatory power of the CRC-specific transcript set on independent biopsies and on formalin-fixed, paraffin-embedded (FFPE) tissue samples.
Methods: Total RNA isolations were performed with the automated MagNA Pure 96 Cellular RNA Large Volume Kit (Roche) from fresh frozen biopsies stored in RNALater (CRC (n = 15) and healthy colonic (n = 15)), furthermore from FFPE specimens including CRC (n = 15) and normal adjacent tissue (NAT) (n = 15) specimens next to the tumor.