Skip to main content

Hereditary Cancer in Clinical Practice

Ausgabe 1/2017

Inhalt (20 Artikel)

Open Access Research

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

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

Open Access Research

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

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

Open Access Review

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

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

Open Access Research

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

Tomasz Huzarski, Barbara Górecka-Szyld, Jowita Huzarska, Grażyna Psut-Muszyńska, Grażyna Wilk, Robert Sibilski, Cezary Cybulski, Beata Kozak-Klonowska, Monika Siołek, Ewa Kilar, Dorota Czudowska, Hanna Janiszewska, Dariusz Godlewski, Andrzej Mackiewicz, Joanna Jarkiewicz-Tretyn, Jadwiga Szabo-Moskal, Jacek Gronwald, Jan Lubiński, Steven A. Narod, T Byrski, T Dębniak, A Tołoczko-Grabarek, O Oszurek, M Michalak, H Rogowska-Droś, E Szatkowska, R Kulus, W Kwiecień, L Szyiński, I Winiarska, P Kasprzak, L Tomiak-Rówińska, M Kosterska-Spalska, T Dróżdż, P Sosnowski

Open Access Review

The genetic basis of colonic adenomatous polyposis syndromes

Bente A. Talseth-Palmer

Open Access Case report

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

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

Open Access Research

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

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

Open Access Review

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

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

Open Access Review

Hereditary pancreatic cancer: related syndromes and clinical perspective

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

Open Access Case report

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

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

Open Access Research

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

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

Open Access Research

Evaluation of psychosocial aspects in participants of cancer genetic counseling

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

Open Access Review

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

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

Open Access Research

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

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

Open Access Research

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

Toni Seppälä, Kirsi Pylvänäinen, Dafydd Gareth Evans, Heikki Järvinen, Laura Renkonen-Sinisalo, Inge Bernstein, Elke Holinski-Feder, Paola Sala, Annika Lindblom, Finlay Macrae, Ignacio Blanco, Rolf Sijmons, Jacqueline Jeffries, Hans Vasen, John Burn, Sigve Nakken, Eivind Hovig, Einar Andreas Rødland, Kukatharmini Tharmaratnam, Wouter H. de Vos tot Nederveen Cappel, James Hill, Juul Wijnen, Mark Jenkins, Maurizio Genuardi, Kate Green, Fiona Lalloo, Lone Sunde, Miriam Mints, Lucio Bertario, Marta Pineda, Matilde Navarro, Monika Morak, Ian M. Frayling, John-Paul Plazzer, Julian R. Sampson, Gabriel Capella, Gabriela Möslein, Jukka-Pekka Mecklin, Pål Møller

Open Access Research

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

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

Open Access Research

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

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

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.