Works matching IS 13899600 AND DT 2023 AND VI 22 AND IP 2

Results: 12

2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.

Published in:: Familial Cancer, 2023, v. 22, n. 2, p. 237, doi. 10.1007/s10689-022-00324-x
Publication type:: Article

Laboratory variation in the grading of dysplasia of duodenal adenomas in familial adenomatous polyposis patients.

Published in:

Familial Cancer, 2023, v. 22, n. 2, p. 177, doi. 10.1007/s10689-022-00320-1

By:

Soons, E.;
Siersema, P. D.;
van Lierop, L. M. A.;
Bisseling, T. M.;
van Kouwen, M. C. A.;
Nagtegaal, I. D.;
van der Post, R. S.;
Atsma, F.

Publication type:

Article

Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review.

Published in:

Familial Cancer, 2023, v. 22, n. 2, p. 167, doi. 10.1007/s10689-022-00319-8

By:

Aziz, Shahram;
O'Sullivan, Hazel;
Heelan, Kara;
Alam, Afrina;
McVeigh, Terri P.

Publication type:

Article

A need to tailor surveillance based on family history: describing a highly penetrant familial paraganglioma kindred with an SDHD pathogenic variant.

Published in:

Familial Cancer, 2023, v. 22, n. 2, p. 217, doi. 10.1007/s10689-022-00318-9

By:

Foley, Madeline;
Sharma, Anu;
Garfield, Kinley;
Maese, Luke;
Buchmann, Luke;
Boyle, Julie;
Kohlmann, Wendy;
Jeter, Joanne;
Greenberg, Samantha

Publication type:

Article

Next-generation universal hereditary cancer screening: implementation of an automated hereditary cancer screening program for patients with advanced cancer undergoing tumor sequencing in a large HMO.

Published in:

Familial Cancer, 2023, v. 22, n. 2, p. 225, doi. 10.1007/s10689-022-00317-w

By:

Hoffman, Trevor L.;
Kershberg, Hilary;
Goff, John;
Holmquist, Kimberly J.;
Haque, Reina;
Alvarado, Monica

Publication type:

Article

Barriers to completion of cascade genetic testing: how can we improve the uptake of testing for hereditary breast and ovarian cancer syndrome?

Published in:

Familial Cancer, 2023, v. 22, n. 2, p. 127, doi. 10.1007/s10689-022-00316-x

By:

Kahn, Ryan Matthew;
Ahsan, Muhammad Danyal;
Chapman-Davis, Eloise;
Holcomb, Kevin;
Nitecki, Roni;
Rauh-Hain, Jose Alejandro;
Fowlkes, Rana Khan;
Tubito, Francesca;
Pires, Maira;
Christos, Paul J;
Tkachuk, Kaitlyn;
Krinsky, Hannah;
Sharaf, Ravi N.;
Offit, Kenneth;
Lipkin, Steven;
Frey, Melissa K.

Publication type:

Article

Determinants of adherence to recommendations on physical activity, red and processed meat intake, and body weight among lynch syndrome patients.

Published in:

Familial Cancer, 2023, v. 22, n. 2, p. 155, doi. 10.1007/s10689-022-00315-y

By:

Hoedjes, M;
Vrieling, A;
de Brauwer, L;
Visser, A;
Gómez García, E;
Hoogerbrugge, N;
Kampman, E

Publication type:

Article

Identifying the BRCA1 c.-107A > T variant in Dutch patients with a tumor BRCA1 promoter hypermethylation.

Published in:

Familial Cancer, 2023, v. 22, n. 2, p. 151, doi. 10.1007/s10689-022-00314-z

By:

de Jong, Vincent M. T.;
Pruntel, Roelof;
Steenbruggen, Tessa G.;
Bleeker, Fonnet E.;
Nederlof, Petra;
Hogervorst, Frans B. L.;
linn, Sabine C.

Publication type:

Article

A pilot study investigating feasibility of mainstreaming germline BRCA1 and BRCA2 testing in high-risk patients with breast and/or ovarian cancer in three tertiary Cancer Centres in Ireland.

Published in:

Familial Cancer, 2023, v. 22, n. 2, p. 135, doi. 10.1007/s10689-022-00313-0

By:

McVeigh, Terri Patricia;
Sweeney, Karl J.;
Brennan, Donal J.;
McVeigh, Una M.;
Ward, Simon;
Strydom, Ann;
Seal, Sheila;
Astbury, Katherine;
Donnellan, Paul;
Higgins, Joanne;
Keane, Maccon;
Kerin, Michael J.;
Malone, Carmel;
McGough, Pauline;
McLaughlin, Ray;
O'Leary, Michael;
Rushe, Margaret;
Barry, Michael Kevin;
MacGregor, Geraldine;
Sugrue, Michael

Publication type:

Article

Disclosure of genetic risk to dating partners among young adults with von Hippel-Lindau disease.

Published in:

Familial Cancer, 2023, v. 22, n. 2, p. 203, doi. 10.1007/s10689-022-00311-2

By:

Bond, Elysa;
Yashar, Beverly;
Else, Tobias;
Osborne, Jenae;
Marvin, Monica

Publication type:

Article

Analysis of uveal melanomas and paired constitutional DNA for exclusion of a BAP1-tumor predisposition syndrome.

Published in:

Familial Cancer, 2023, v. 22, n. 2, p. 193, doi. 10.1007/s10689-022-00310-3

By:

Abbassi, Yasaman Arjmand;
Le Guin, Claudia;
Bornfeld, Norbert;
Bechrakis, Nikolaos E.;
Zeschnigk, Michael;
Lohmann, Dietmar R.

Publication type:

Article

CDH1 mutations recurrence and global clustering in genetically tested families with hereditary diffuse gastric cancer syndrome: results from a systematic study.

Published in:

Familial Cancer, 2023, v. 22, n. 2, p. 187, doi. 10.1007/s10689-022-00309-w

By:

Corso, Giovanni;
Tagliaferri, Valentina;
Massari, Giulia;
Cioffi, Antonio;
Rossi, Elisabetta Maria Cristina;
Veronesi, Paolo;
Magnoni, Francesca

Publication type:

Article