Works matching IS 17312302 AND DT 2017

Results: 22

Meeting abstracts from the Annual Conference on Hereditary Cancers 2015.

Published in:: 2017
Publication type:: Abstract

The potential role of miRNAs in therapy of breast and ovarian cancers associated with BRCA1 mutation.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0076-7

By:

Strumidło, Agnieszka;
Skiba, Sylwia;
Scott, Rodney J.;
Lubiński, Jan

Publication type:

Article

Motivators and barriers of tamoxifen use as risk-reducing medication amongst women at increased breast cancer risk: a systematic literature review.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0075-8

By:

Meiser, B.;
Wong, W. K. T.;
Peate, M.;
Julian-Reynier, C.;
Kirk, J.;
Mitchell, G.

Publication type:

Article

Evaluation of psychosocial aspects in participants of cancer genetic counseling.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0073-x

By:

González-Ramírez, Leivy Patricia;
Martínez-Arriaga, Reyna;
Camacho-Cárdenas, Erendira;
Del Toro-Valero, Azucena;
Oceguera-Villanueva, Antonio;
Zagamé, Livia;
Silva-García, Aída Araceli;
Daneri-Navarro, Adrián

Publication type:

Article

Emotional impact on the results of BRCA1 and BRCA2 genetic test: an observational retrospective study.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0077-6

By:

Mella, Sara;
Muzzatti, Barbara;
Dolcetti, Riccardo;
Annunziata, Maria Antonietta

Publication type:

Article

Meeting abstracts from the Annual Conference on Hereditary Cancers 2016.

Published in:: Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0081-x
Publication type:: Article

Exome sequencing characterizes the somatic mutation spectrum of early serrated lesions in a patient with serrated polyposis syndrome (SPS).

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0082-9

By:

Horpaopan, Sukanya;
Kirfel, Jutta;
Peters, Sophia;
Kloth, Michael;
Hüneburg, Robert;
Altmüller, Janine;
Drichel, Dmitriy;
Odenthal, Margarete;
Kristiansen, Glen;
Strassburg, Christian;
Nattermann, Jacob;
Hoffmann, Per;
Nürnberg, Peter;
Büttner, Reinhard;
Thiele, Holger;
Kahl, Philip;
Spier, Isabel;
Aretz, Stefan

Publication type:

Article

The BRCA2 variant c.68-7 T>A is associated with breast cancer.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0080-y

By:

Møller, Pål;
Hovig, Eivind

Publication type:

Article

Clinical and genetic characterization of hereditary breast cancer in a Chinese population.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0079-4

By:

Wenjing Jian;
Kang Shao;
Qi Qin;
Xiaohong Wang;
Shufen Song;
Xianming Wang

Publication type:

Article

Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report.

Published in:

Hereditary Cancer in Clinical Practice, 2017, p. 1, doi. 10.1186/s13053-017-0078-5

By:

Seppälä, Toni;
Pylvänäinen, Kirsi;
Gareth Evans, Dafydd;
Järvinen, Heikki;
Renkonen-Sinisalo, Laura;
Bernstein, Inge;
Holinski-Feder, Elke;
Sala, Paola;
Lindblom, Annika;
Macrae, Finlay;
Blanco, Ignacio;
Sijmons, Rolf;
Jeffries, Jacqueline;
Vasen, Hans;
Burn, John;
Nakken, Sigve;
Hovig, Eivind;
Rødland, Einar Andreas;
Tharmaratnam, Kukatharmini;
de Vos tot Nederveen Cappel, Wouter H.

Publication type:

Article

Hereditary gynaecologic cancers in Nepal: a proposed model of care to serve high risk populations in developing countries.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0072-y

By:

Pokharel, Hanoon P.;
Hacker, Neville F.;
Andrews, Lesley

Publication type:

Article

Preoperative genetic testing impacts surgical decision making in BRCA mutation carriers with breast cancer: a retrospective cohort analysis.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0071-z

By:

Yadav, Siddhartha;
Reeves, Ashley;
Campian, Sarah;
Sufka, Amy;
Zakalik, Dana

Publication type:

Article

Late onset asymptomatic pancreatic neuroendocrine tumor -- A case report on the phenotypic expansion for MEN1.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0070-0

By:

Kaiwar, Charu;
Macklin, Sarah K.;
Gass, Jennifer M.;
Jackson, Jessica;
Klee, Eric W.;
Hines, Stephanie L.;
Stauffer, John A.;
Atwal, Paldeep S.

Publication type:

Article

Hereditary pancreatic cancer: related syndromes and clinical perspective.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0069-6

By:

Carrera, Sergio;
Sancho, Aintzane;
Azkona, Eider;
Azkuna, Josune;
Lopez-Vivanco, Guillermo

Publication type:

Article

ARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0068-7

By:

Yan Jiang;
Chen-Yang Zhao;
Li-Chun Cheng;
Bing Xu;
Hui-Yi Lv

Publication type:

Article

Hereditary and non-hereditary branches of family eligible for BRCA test: cancers in other sites.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0067-8

By:

Digennaro, M.;
Sambiasi, D.;
Tommasi, S.;
Pilato, B.;
Diotaiuti, S.;
Kardhashi, A.;
Trojano, G.;
Tufaro, A.;
Paradiso, A. V.

Publication type:

Article

A case report of Muir-Torre syndrome in a woman with breast cancer and MSI-Low skin squamous cell carcinoma.

Published in:

2017

By:

Kientz, Caroline;
Joly, Marie-Odile;
Faivre, Laurence;
Clemenson, Alix;
Dalac, Sophie;
Lepage, Côme;
Chapusot, Caroline;
Jacquot, Caroline;
Schiappa, Renaud;
Lebrun, Marine

Publication type:

Case Study

The genetic basis of colonic adenomatous polyposis syndromes.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0065-x

By:

Talseth-Palmer, Bente A.

Publication type:

Article

Screening with magnetic resonance imaging, mammography and ultrasound in women at average and intermediate risk of breast cancer.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0064-y

By:

Huzarski, Tomasz;
Górecka-Szyld, Barbara;
Huzarska, Jowita;
Psut-Muszyńska, Grażyna;
Wilk, Grazyna;
Sibilski, Robert;
Cybulski, Cezary;
Kozak-Klonowska, Beata;
Siolek, Monika;
Kilar, Ewa;
Czudowska, Dorota;
Janiszewska, Hanna;
Godlewski, Dariusz;
Mackiewicz, Andrzej;
Jarkiewicz-Tretyn, Joanna;
Szabo-Moskal, Jadwiga;
Gronwald, Jacek;
Lubiński, Jan;
Narod, Steven A.

Publication type:

Article

Hereditary cancer syndromes in Latino populations: genetic characterization and surveillance guidelines.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0063-z

By:

Cruz-Correa, Marcia;
Pérez-Mayoral, Julyann;
Dutil, Julie;
Echenique, Miguel;
Mosquera, Rafael;
Rivera-Román, Keila;
Umpierre, Sharee;
Rodriguez-Quilichini, Segundo;
Gonzalez-Pons, Maria;
Olivera, Myrta I.;
Pardo, Sherly

Publication type:

Article

Anxiety and depression symptoms among women attending group-based patient education courses for hereditary breast and ovarian cancer.

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-016-0062-5

By:

Listøl, Wenche;
Høberg-Vetti, Hildegunn;
Eide, Geir Egil;
Bjorvatn, Cathrine

Publication type:

Article

How does genetic risk information for Lynch syndrome translate to risk management behaviours?

Published in:

Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-016-0061-6

By:

Steel, Emma;
Robbins, Andrew;
Jenkins, Mark;
Flander, Louisa;
Gaff, Clara;
Keogh, Louise

Publication type:

Article