Works matching IS 13899600 AND DT 2021 AND VI 20 AND IP 1
Results: 12
The CAPP II trial of aspirin in Lynch syndrome/HNPCC: is it time for everyone to be treated?
- Published in:
- 2021
- By:
- Publication type:
- Editorial
New surveillance guidelines for Li-Fraumeni and hereditary TP53 related cancer syndrome: implications for germline TP53 testing in breast cancer.
- Published in:
- 2021
- By:
- Publication type:
- Editorial
Multiple primary cancers (renal papillary, lymphoma and teratoma) and hepatic cysts in association with a pathogenic germline mutation in the MET gene.
- Published in:
- Familial Cancer, 2021, v. 20, n. 1, p. 81, doi. 10.1007/s10689-020-00196-z
- By:
- Publication type:
- Article
Complete response of hereditary leiomyomatosis and renal cell cancer (HLRCC)-associated renal cell carcinoma to nivolumab and ipilimumab combination immunotherapy by: a case report.
- Published in:
- Familial Cancer, 2021, v. 20, n. 1, p. 75, doi. 10.1007/s10689-020-00195-0
- By:
- Publication type:
- Article
Report of the fifth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Leiden, The Netherlands, July 6th 2019.
- Published in:
- Familial Cancer, 2021, v. 20, n. 1, p. 67, doi. 10.1007/s10689-020-00194-1
- By:
- Publication type:
- Article
Prospective observational data informs understanding and future management of Lynch syndrome: insights from the Prospective Lynch Syndrome Database (PLSD).
- Published in:
- Familial Cancer, 2021, v. 20, n. 1, p. 35, doi. 10.1007/s10689-020-00193-2
- By:
- Publication type:
- Article
Germline variants discovered in lymphoma patients undergoing tumor profiling: a case series.
- Published in:
- Familial Cancer, 2021, v. 20, n. 1, p. 61, doi. 10.1007/s10689-020-00192-3
- By:
- Publication type:
- Article
Two cases of somatic STK11 mosaicism in Danish patients with Peutz–Jeghers syndrome.
- Published in:
- Familial Cancer, 2021, v. 20, n. 1, p. 55, doi. 10.1007/s10689-020-00191-4
- By:
- Publication type:
- Article
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.
- Published in:
- Familial Cancer, 2021, v. 20, n. 1, p. 49, doi. 10.1007/s10689-020-00190-5
- By:
- Publication type:
- Article
Chemoprevention in familial adenomatous polyposis: past, present and future.
- Published in:
- Familial Cancer, 2021, v. 20, n. 1, p. 23, doi. 10.1007/s10689-020-00189-y
- By:
- Publication type:
- Article
Improving primary care identification of familial breast cancer risk using proactive invitation and decision support.
- Published in:
- Familial Cancer, 2021, v. 20, n. 1, p. 13, doi. 10.1007/s10689-020-00188-z
- By:
- Publication type:
- Article
Low accuracy of self-reported family history of melanoma in high-risk patients.
- Published in:
- Familial Cancer, 2021, v. 20, n. 1, p. 41, doi. 10.1007/s10689-020-00187-0
- By:
- Publication type:
- Article