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Zeitschrift

Familial Cancer

Familial Cancer 1/2021

Ausgabe 1/2021

Inhaltsverzeichnis ( 12 Artikel )

28.09.2020 | Editorial | Ausgabe 1/2021

New surveillance guidelines for Li-Fraumeni and hereditary TP53 related cancer syndrome: implications for germline TP53 testing in breast cancer

D. Gareth Evans, Emma R. Woodward

09.01.2021 | Editorial Comment | Ausgabe 1/2021

The CAPP II trial of aspirin in Lynch syndrome/HNPCC: is it time for everyone to be treated?

Patrick M. Lynch

11.06.2020 | Original Article | Ausgabe 1/2021 Open Access

Improving primary care identification of familial breast cancer risk using proactive invitation and decision support

Nadeem Qureshi, Brittany Dutton, Stephen Weng, Christina Sheehan, Wendy Chorley, John F. R. Robertson, Denise Kendrick, Joe Kai

08.06.2020 | Review | Ausgabe 1/2021

Chemoprevention in familial adenomatous polyposis: past, present and future

Phillip M. Kemp Bohan, Gautam Mankaney, Timothy J. Vreeland, Robert C. Chick, Diane F. Hale, Jessica L. Cindass, Annelies T. Hickerson, Daniel C. Ensley, Vance Sohn, G. Travis Clifton, George E. Peoples, Carol A. Burke

08.06.2020 | Review | Ausgabe 1/2021 Open Access

Prospective observational data informs understanding and future management of Lynch syndrome: insights from the Prospective Lynch Syndrome Database (PLSD)

Toni T. Seppälä, Mev Dominguez-Valentin, Julian R. Sampson, Pål Møller

21.05.2020 | Original Article | Ausgabe 1/2021

Low accuracy of self-reported family history of melanoma in high-risk patients

Nicholas D. Flint, Michael D. Bishop, Tristan C. Smart, Jennifer L. Strunck, Kenneth M. Boucher, Douglas Grossman, Aaron M. Secrest

26.05.2020 | Original Article | Ausgabe 1/2021

Small fraction of testicular cancer cases may be causatively related to CHEK2 inactivating germ-line mutations: evidence for somatic loss of the remaining CHEK2 allele in the tumor tissue

Valeriya I. Ni, Alexandr O. Ivantsov, Mariya A. Kotkova, Sofia V. Baskina, Elena V. Ponomareva, Rashida V. Orlova, Eldar E. Topuzov, Kirill K. Kryukov, Kseniya V. Shelekhova, Svetlana N. Aleksakhina, Anna P. Sokolenko, Evgeny N. Imyanitov

06.06.2020 | Short Communication | Ausgabe 1/2021

Two cases of somatic STK11 mosaicism in Danish patients with Peutz–Jeghers syndrome

Anne Marie Jelsig, Birgitte Bertelsen, Isabel Forss, John Gásdal Karstensen

06.06.2020 | Original Article | Ausgabe 1/2021

Germline variants discovered in lymphoma patients undergoing tumor profiling: a case series

Anthony J. Scott, Molly C. Tokaz, Michelle F. Jacobs, Arul M. Chinnaiyan, Tycel J. Phillips, Ryan A. Wilcox

02.07.2020 | Review | Ausgabe 1/2021 Open Access

Report of the fifth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Leiden, The Netherlands, July 6th 2019

M. Suerink, K. Wimmer, L. Brugieres, C. Colas, R. Gallon, T. Ripperger, P. R. Benusiglio, E. M. A. Bleiker, Z. Ghorbanoghli, Y. Goldberg, J. C. H. Hardwick, M. Kloor, M. le Mentec, M. Muleris, M. Pineda, C. Ruiz-Ponte, H. F. A. Vasen

15.07.2020 | Short Communication | Ausgabe 1/2021

Complete response of hereditary leiomyomatosis and renal cell cancer (HLRCC)-associated renal cell carcinoma to nivolumab and ipilimumab combination immunotherapy by: a case report

Yasuhiro Iribe, Mitsuko Furuya, Yousuke Shibata, Masato Yasui, Makoto Funahashi, Junichi Ota, Hiromichi Iwashita, Yoji Nagashima, Hisashi Hasumi, Narihiko Hayashi, Kazuhide Makiyama, Keiichi Kondo, Reiko Tanaka, Masahiro Yao, Noboru Nakaigawa

20.07.2020 | Short Communication | Ausgabe 1/2021

Multiple primary cancers (renal papillary, lymphoma and teratoma) and hepatic cysts in association with a pathogenic germline mutation in the MET gene

Julian Adlard

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