Works matching IS 13899600 AND DT 2018 AND VI 17 AND IP 4

Results: 20

Molecular analysis of an asbestos-exposed Belgian family with a high prevalence of mesothelioma.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 569, doi. 10.1007/s10689-018-0095-1

By:

Hylebos, Marieke;
Op de Beeck, Ken;
van den Ende, Jenneke;
Pauwels, Patrick;
Lammens, Martin;
van Meerbeeck, Jan P.;
Van Camp, Guy

Publication type:

Article

Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to decline.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 547, doi. 10.1007/s10689-018-0078-2

By:

Kanga-Parabia, Anaita;
Gaff, Clara;
Flander, Louisa;
Jenkins, Mark;
Keogh, Louise A.

Publication type:

Article

Response to letter to editor regarding published article—metachronous colorectal cancer following segmental or extended colectomy in Lynch syndrome: a systematic review and meta-analysis.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 545, doi. 10.1007/s10689-018-0077-3

By:

Lythgoe, Mark P.;
Malik, Salim S.;
McPhail, Mark;
Monahan, Kevin J.

Publication type:

Article

A retrospective review of 48 individuals, including 12 families, molecularly diagnosed with hereditary leiomyomatosis and renal cell cancer (HLRCC).

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 615, doi. 10.1007/s10689-018-0076-4

By:

Bhola, Priya T.;
Gilpin, Cathy;
Smith, Amanda;
Graham, Gail E.

Publication type:

Article

The first two confirmed sub-Saharan African families with germline TP53 mutations causing Li-Fraumeni syndrome.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 607, doi. 10.1007/s10689-018-0075-5

By:

Macaulay, Shelley;
Goodyear, Quintin Clive;
Kruger, Mia;
Chen, Wenlong;
Essop, Fahmida;
Krause, Amanda

Publication type:

Article

Commentary: PREMM5 threshold of 2.5% is recommended to improve identification of PMS2 carriers.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 567, doi. 10.1007/s10689-018-0074-6

By:

Kastrinos, Fay;
Uno, Hajime;
Syngal, Sapna

Publication type:

Article

Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 601, doi. 10.1007/s10689-018-0073-7

By:

Huq, A. J.;
Walsh, M.;
Rajagopalan, B.;
Finlay, M.;
Trainer, A. H.;
Bonnet, F.;
Sevenet, N.;
Winship, I. M.

Publication type:

Article

APC mosaicism in a young woman with desmoid type fibromatosis and familial adenomatous polyposis.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 539, doi. 10.1007/s10689-018-0072-8

By:

Stormorken, Astrid Tenden;
Berg, Thomas;
Norum, Ole-Jacob;
Hølmebakk, Toto;
Aaberg, Kristin;
Steigen, Sonja E.;
Grindedal, Eli Marie

Publication type:

Article

Risk management adherence following genetic testing for hereditary cancer syndromes: a Singaporean experience.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 621, doi. 10.1007/s10689-018-0071-9

By:

Courtney, Eliza;
Chin, Xin Wei;
Yuen, Jeanette;
Li, Shao-Tzu;
Chen, Yanni;
Allen, John Carson;
Tan, Veronique;
Lim, Geok Hoon;
Ngeow, Joanne

Publication type:

Article

Clinical interpretation of pathogenic ATM and CHEK2 variants on multigene panel tests: navigating moderate risk.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 495, doi. 10.1007/s10689-018-0070-x

By:

West, Allison H.;
Blazer, Kathleen R.;
Stoll, Jessica;
Jones, Matthew;
Weipert, Caroline M.;
Nielsen, Sarah M.;
Kupfer, Sonia S.;
Weitzel, Jeffrey N.;
Olopade, Olufunmilayo I.

Publication type:

Article

Letter to the editor.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 565, doi. 10.1007/s10689-018-0069-3

By:

Anele, C. C.;
Latchford, A.;
Faiz, O.;
Clark, S. K.

Publication type:

Article

Gene expression analysis in peripheral blood cells of patients with hereditary leiomyomatosis and renal cell cancer syndrome (HLRCC): identification of NRF2 pathway activation.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 587, doi. 10.1007/s10689-017-0068-9

By:

Arenas Valencia, Carolina;
Lopez Kleine, Liliana;
Pinzon Velasco, Andres M.;
Cardona Barreto, Andrea Y.;
Arteaga Diaz, Clara E.

Publication type:

Article

Haplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutation.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 531, doi. 10.1007/s10689-017-0067-x

By:

von Salomé, Jenny;
Liu, Tao;
Keihäs, Markku;
Morak, Moni;
Holinski-Feder, Elke;
Berry, Ian R.;
Moilanen, Jukka S.;
Baert-Desurmont, Stéphanie;
Lindblom, Annika;
Lagerstedt-Robinson, Kristina

Publication type:

Article

Adaptation of couples living with a high risk of breast/ovarian cancer and the association with risk-reducing surgery.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 485, doi. 10.1007/s10689-017-0065-z

By:

Shapira, Rachel;
Turbitt, Erin;
Erby, Lori H.;
Biesecker, Barbara B.;
Klein, William M. P.;
Hooker, Gillian W.

Publication type:

Article

Urological sequelae of desmoids associated with familial adenomatous polyposis.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 525, doi. 10.1007/s10689-017-0064-0

By:

Walton, S. J.;
Malietzis, G.;
Clark, S. K.;
Havranek, E.

Publication type:

Article

Feasibility of endoscopic resection using bipolar snare for nonampullary duodenal tumours in familial adenomatous polyposis patients.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 517, doi. 10.1007/s10689-017-0063-1

By:

Inoki, Kazuya;
Nakajima, Takeshi;
Nonaka, Satoru;
Abe, Seiichiro;
Suzuki, Haruhisa;
Yoshinaga, Shigetaka;
Oda, Ichiro;
Yamada, Masayoshi;
Takatsu, Mizuki;
Yoshida, Hiroshi;
Taniguchi, Hirokazu;
Sekine, Shigeki;
Ohe, Yuichiro;
Saito, Yutaka

Publication type:

Article

Metachronous colorectal cancer following segmental or extended colectomy in Lynch syndrome: a systematic review and meta-analysis.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 557, doi. 10.1007/s10689-017-0062-2

By:

Malik, Salim S.;
Lythgoe, Mark P.;
McPhail, Mark;
Monahan, Kevin J.

Publication type:

Article

SNP association study in PMS2-associated Lynch syndrome.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 507, doi. 10.1007/s10689-017-0061-3

By:

ten Broeke, Sanne W.;
Elsayed, Fadwa A.;
Pagan, Lisa;
Olderode-Berends, Maran J. W.;
Garcia, Encarna Gomez;
Gille, Hans J. P.;
van Hest, Liselot P.;
Letteboer, Tom G. W.;
van der Kolk, Lizet E.;
Mensenkamp, Arjen R.;
van Os, Theo A.;
Spruijt, Liesbeth;
Redeker, Bert J. W.;
Suerink, Manon;
Vos, Yvonne J.;
Wagner, Anja;
Wijnen, Juul T.;
Steyerberg, E. W.;
Tops, Carli M. J.;
van Wezel, Tom

Publication type:

Article

Correlation of IL-31 gene polymorphisms with susceptibility and clinical recurrence of bladder cancer.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 577, doi. 10.1007/s10689-017-0060-4

By:

Li, Qin;
Tang, Tielong;
Zhang, Peng;
Liu, Chenlu;
Pu, Yan;
Zhang, Yan;
Song, Huizi;
Wang, Yanyun;
Song, Yaping;
Su, Min;
Zhou, Bin;
Zhang, Lin

Publication type:

Article

Mutations in context: implications of BRCA testing in diverse populations.

Published in:

Familial Cancer, 2018, v. 17, n. 4, p. 471, doi. 10.1007/s10689-017-0038-2

By:

Felix, Gabriela E. S.;
Zheng, Yonglan;
Olopade, Olufunmilayo I.

Publication type:

Article