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    • A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study 

      Bancroft, E. K.; Page, E. C.; Brook, M. N.; Thomas, S.; Taylor, N.; Pope, J.; McHugh, J.; Jones, A. B.; Karlsson, Q.; Merson, S.; Ong, K. R.; Hoffman, J.; Huber, C.; Maehle, L.; Grindedal, E. M.; Stormorken, A.; Evans, D. G.; Rothwell, J.; Lalloo, F.; Brady, A. F.; Bartlett, M.; Snape, K.; Hanson, H.; James, P.; McKinley, J.; Mascarenhas, L.; Syngal, S.; Ukaegbu, C.; Side, L.; Thomas, T.; Barwell, J.; Teixeira, M. R.; Izatt, L.; Suri, M.; Macrae, F. A.; Poplawski, N.; Chen-Shtoyerman, R.; Ahmed, M.; Musgrave, H.; Nicolai, N.; Greenhalgh, L.; Brewer, C.; Pachter, N.; Spigelman, A. D.; Azzabi, A.; Helfand, B. T.; Halliday, D.; Buys, S.; Ramon, Y. Cajal T.; Donaldson, A.; Cooney, K. A.; Harris, M.; McGrath, J.; Davidson, R.; Taylor, A.; Cooke, P.; Myhill, K.; Hogben, M.; Aaronson, N. K.; Ardern-Jones, A.; Bangma, C. H.; Castro, E.; Dearnaley, D.; Dias, A.; Dudderidge, T.; Eccles, D. M.; Green, K.; Eyfjord, J.; Falconer, A.; Foster, C. S.; Gronberg, H.; Hamdy, F. C.; Johannsson, O.; Khoo, V.; Lilja, H.; Lindeman, G. J.; Lubinski, J.; Axcrona, K.; Mikropoulos, C.; Mitra, A. V.; Moynihan, C.; Ni Raghallaigh, H.; Rennert, G.; Collier, R.; Offman, J.; Kote-Jarai, Z.; Eeles, R. A. (Elsevier, 2021-11-01)
      BACKGROUND: Lynch syndrome is a rare familial cancer syndrome caused by pathogenic variants in the mismatch repair genes MLH1, MSH2, MSH6, or PMS2, that cause predisposition to various cancers, predominantly colorectal and ...