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    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 revision

    Zaffaroni, Gloria; Mannucci, Alessandro; Koskenvuo, Laura; de Lacy, Borja; Maffioli, Anna; Bisseling, Tanya; Half, Elizabeth; Cavestro, Giulia Martina; Valle, Laura; Ryan, Neil; Aretz, Stefan; Brown, Karen; Buttitta, Francesco; Carneiro, Fatima; Claber, Oonagh; Blanco-Colino, Ruth; Collard, Maxime; Crosbie, Emma; Cunha, Miguel; Doulias, Triantafyllos; Fleming, Christina; Heinrich, Henriette; Hüneburg, Robert; Metras, Julie; Nagtegaal, Iris; Negoi, Ionut; Nielsen, Maartje; Pellino, Gianluca; Ricciardiello, Luigi; Sagir, Abdurrahman; Sánchez-Guillén, Luis; Seppälä, Toni T; Siersema, Peter; Striebeck, Benedikt; Sampson, Julian R; Latchford, Andrew; Parc, Yann; Burn, John; Möslein, Gabriela.
    Br. j. surg; 111 (5), 2024
    Hereditary adenomatous polyposis syndromes, including familial adenomatous polyposis and other rare adenomatous polyposis syndromes, increase the lifetime risk of colorectal and other cancers. A team of 38 experts convened to update the 2008 European recommendations for the clinical management of patient...
    Polypose adénomateuse colique/imagerie diagnostique, Polypose adénomateuse colique/génétique, Endoscopie, Dépistage génétique, Antinéoplasiques/usage thérapeutique
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