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Familial Cancer|November 15, 2024
The genetic landscape of Lynch syndrome in the Israeli populationAasem Abu Shtaya, Sofia Naftaly Nathan, Inbal Kedar, et al.The British Journal of Surgery|May 9, 2024
Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revisionGloria Zaffaroni, Alessandro Mannucci, Laura Koskenvuo, et al.Gastroenterology|October 22, 2021
Timeline of Development of Pancreatic Cancer and Implications for Successful Early Detection in High-Risk IndividualsKasper A Overbeek, Michael G Goggins, Mohamad Dbouk, et al.Hereditary Cancer in Clinical Practice|October 11, 2023
Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statementPal Møller, Toni T Seppälä, Aysel Ahadova, et al.Eclinicalmedicine|May 14, 2023
Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome databaseMev Dominguez-Valentin, Saskia Haupt, Toni T Seppälä, et al.Hereditary Cancer in Clinical Practice|October 1, 2022
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortiumPål Møller, Toni Seppälä, James G Dowty, et al.Pageof 4