Works matching IS 17312302 AND DT 2023 AND VI 21 AND IP 1


Results: 28
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    "Go ahead and screen" - advice to healthcare systems for routine lynch syndrome screening from interviews with newly diagnosed colorectal cancer patients.

    Published in:
    Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00270-4
    By:
    • Schneider, Jennifer L.;
    • Firemark, Alison J.;
    • Gille, Sara;
    • Davis, James;
    • Pawloski, Pamala A.;
    • Liang, Su-Ying;
    • Epstein, Mara M.;
    • Lowery, Jan;
    • Lu, Christine Y.;
    • Sharaf, Ravi N.;
    • Burnett-Hartman, Andrea N.;
    • Schlieder, Victoria;
    • Salvati, Zachary M.;
    • Cragun, Deborah;
    • Rahm, Alanna Kulchak;
    • Hunter, Jessica Ezzell
    Publication type:
    Article
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    Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes - an EHTG, PLSD position statement.

    Published in:
    Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00263-3
    By:
    • Møller, Pal;
    • Seppälä, Toni T.;
    • Ahadova, Aysel;
    • Crosbie, Emma J.;
    • Holinski-Feder, Elke;
    • Scott, Rodney;
    • Haupt, Saskia;
    • Möslein, Gabriela;
    • Winship, Ingrid;
    • Broeke, Sanne W. Bajwa-ten;
    • Kohut, Kelly E.;
    • Ryan, Neil;
    • Bauerfeind, Peter;
    • Thomas, Laura E.;
    • Evans, D. Gareth;
    • Aretz, Stefan;
    • Sijmons, Rolf H.;
    • Half, Elizabeth;
    • Heinimann, Karl;
    • Horisberger, Karoline
    Publication type:
    Article
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    Using a multistep approach with multidisciplinary team to increase the diagnosis rate of Lynch syndrome-associated colorectal cancer after universal screening: a single-center study in Japan.

    Published in:
    Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00258-0
    By:
    • Tatsuta, Kyota;
    • Sakata, Mayu;
    • Iwaizumi, Moriya;
    • Kojima, Risa;
    • Yamanaka, Katsumasa;
    • Baba, Satoshi;
    • Suzuki, Katsunori;
    • Morita, Yoshifumi;
    • Kikuchi, Hirotoshi;
    • Hiramatsu, Yoshihiro;
    • Kurachi, Kiyotaka;
    • Takeuchi, Hiroya
    Publication type:
    Article
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    Germline heterozygous exons 8–11 pathogenic BARD1 gene deletion reported for the first time in a family with suspicion of a hereditary colorectal cancer syndrome: more than an incidental finding?

    Published in:
    Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00246-4
    By:
    • Carrera, Sergio;
    • Rodríguez-Martínez, Ana Belén;
    • Garin, Intza;
    • Sarasola, Esther;
    • Martínez, Cristina;
    • Maortua, Hiart;
    • Callejo, Almudena;
    • Ruiz de Lobera, Abigail;
    • Muñoz, Alberto;
    • Miñambres, Nagore;
    • Jiménez-Labaig, Pablo
    Publication type:
    Article
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