A Clinical Perspective on Ethical Issues in Genetic Testing von Sijmons, R. H., Van Langen, I. M., Sijmons, J. G.

Volltext

CT texture analysis in colorectal liver metastases and the surrounding liver parenchyma and its potential as an imaging biomarker of disease aggressiveness, response and survival von Beckers, R.C.J., Trebeschi, S., Maas, M., Schnerr, R.S., Sijmons, J.M.L., Beets, G.L., Houwers, J.B., Beets-Tan, R.G.H., Lambregts, D.M.J.

Volltext

A multicentre comparative prospective blinded analysis of EUS and MRI for screening of pancreatic cancer in high-risk individuals von Harinck, F, Konings, I C A W, Kluijt, I, Poley, J W, van Hooft, J E, van Dullemen, H M, Nio, C Y, Krak, N C, Hermans, J J, Aalfs, C M, Wagner, A, Sijmons, R H, Biermann, K, van Eijck, C H, Gouma, D J, Dijkgraaf, M G W, Fockens, P, Bruno, M J

Volltext

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts von Vasen, Hans F A, Blanco, Ignacio, Aktan-Collan, Katja, Gopie, Jessica P, Alonso, Angel, Aretz, Stefan, Bernstein, Inge, Bertario, Lucio, Burn, John, Capella, Gabriel, Colas, Chrystelle, Engel, Christoph, Frayling, Ian M, Genuardi, Maurizio, Heinimann, Karl, Hes, Frederik J, Hodgson, Shirley V, Karagiannis, John A, Lalloo, Fiona, Lindblom, Annika, Mecklin, Jukka-Pekka, Møller, Pal, Myrhoj, Torben, Nagengast, Fokko M, Parc, Yann, Ponz de Leon, Maurizio, Renkonen-Sinisalo, Laura, Sampson, Julian R, Stormorken, Astrid, Sijmons, Rolf H, Tejpar, Sabine, Thomas, Huw J W, Rahner, Nils, Wijnen, Juul T, Järvinen, Heikki Juhani, Möslein, Gabriela

Volltext

TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes von Ruijs, Marielle W G, Verhoef, Senno, Rookus, Matti A, Pruntel, Roelof, van der Hout, Annemarie H, Hogervorst, Frans B L, Kluijt, I, Sijmons, Rolf H, Aalfs, Cora M, Wagner, Anja, Ausems, Margreet G E M, Hoogerbrugge, Nicoline, van Asperen, Christi J, Gomez Garcia, Encarna B, Meijers-Heijboer, Hanne, ten Kate, Leo P, Menko, Fred H, van 't Veer, Laura J

Volltext

Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics von Sikkema-Raddatz, Birgit, Johansson, Lennart F., de Boer, Eddy N., Almomani, Rowida, Boven, Ludolf G., van den Berg, Maarten P., van Spaendonck-Zwarts, Karin Y., van Tintelen, J. Peter, Sijmons, Rolf H., Jongbloed, Jan D. H., Sinke, Richard J.

Volltext

Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk von ten Broeke, Sanne W, Brohet, Richard M, Tops, Carli M, van der Klift, Heleen M, Velthuizen, Mary E, Bernstein, Inge, Capellá Munar, Gabriel, Gomez Garcia, Encarna, Hoogerbrugge, Nicoline, Letteboer, Tom G W, Menko, Fred H, Lindblom, Annika, Mensenkamp, Arjen R, Moller, Pal, van Os, Theo A, Rahner, Nils, Redeker, Bert J W, Sijmons, Rolf H, Spruijt, Liesbeth, Suerink, Manon, Vos, Yvonne J, Wagner, Anja, Hes, Frederik J, Vasen, Hans F, Nielsen, Maartje, Wijnen, Juul T

Volltext

What is the impact of miniscrew-assisted rapid palatal expansion on the midfacial soft tissues? A prospective three-dimensional stereophotogrammetry study von Krijt, Laura L., Kapetanović, Aldin, Sijmons, Wouter J.L., Bruggink, Robin, Baan, Frank, Bergé, Stefaan J., Noverraz, René R.M., Xi, Tong, Schols, Jan G.J.H.

Volltext

Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome von ENGEL, Christoph, LOEFFLER, Markus, SCHMIEGEL, Wolff, BUETTNER, Reinhard, MOESLEIN, Gabriela, LETTEBOER, Tom G. W, GOMEZ GARCIA, Encarna, HES, Frederik J, HOOGERBRUGGE, Nicoline, MENKO, Fred H, VAN OS, Theo A. M, SIJMONS, Rolf H, STEINKE, Verena, WAGNER, Anja, KLUIJT, Irma, PROPPING, Peter, VASEN, Hans F. A, RAHNER, Nils, HOLINSKI-FEDER, Elke, DIETMAIER, Wolfgang, SCHACKERT, Hans K, GOERGENS, Heike, VON KNEBEL DOEBERITZ, Magnus, GOECKE, Timm O

Volltext

Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling von Bokkers, K., Bleiker, E. M. A., Aalfs, C. M., van Dalen, T., Velthuizen, M. E., Duijveman, P., Sijmons, R. H., Koole, W., Schoenmaeckers, E. J. P., Ausems, M. G. E. M.

Volltext

Guidelines for the Li-Fraumeni and heritable TP53-related cancer syndromes von Frebourg, Thierry, Bajalica Lagercrantz, Svetlana, Oliveira, Carla, Magenheim, Rita, Evans, D Gareth

Volltext

CDH1-related hereditary diffuse gastric cancer syndrome: Clinical variations and implications for counseling von Kluijt, Irma, Siemerink, Ester J.M., Ausems, Margreet G.E.M., van Os, Theo A.M., de Jong, Daphne, Simões-Correia, Joana, van Krieken, J. Han, Ligtenberg, Marjolijn J., Figueiredo, Joana, van Riel, Els, Sijmons, Rolf H., Plukker, John T.M., van Hillegersberg, Richard, Dekker, Evelien, Oliveira, Carla, Cats, Annemieke, Hoogerbrugge, Nicoline

Volltext

Evolution of surgical approach to rectal cancer resection: A multinational registry assessment von Sijmons, Julie M L, Dekker, Jan Willem T, Tuynman, Jurriaan B, Mohan, Helen M, Smart, Philip, Heriot, Alexander G, Walker, Kate, Kuryba, Angela, Matthiessen, Peter, Tanis, Pieter J

Volltext

Characteristics of Lynch syndrome associated ovarian cancer von Woolderink, J.M., De Bock, G.H., de Hullu, J.A., Hollema, H., Zweemer, R.P., Slangen, B.F.M., Gaarenstroom, K.N., van Beurden, M., van Doorn, H.C., Sijmons, R.H., Vasen, H.F.A., Mourits, M.J.E.

Volltext

The additional value of endometrial sampling in the early detection of endometrial cancer in women with Lynch syndrome von Helder-Woolderink, J.M, De Bock, G.H, Sijmons, R.H, Hollema, H, Mourits, M.J.E

Volltext

Probing the expression and adhesion of glycans involved in Helicobacter pylori infection von Sijmons, Daniel, Collett, Simon, Soliman, Caroline, Guy, Andrew J., Scott, Andrew M., Durrant, Lindy G., Elbourne, Aaron, Walduck, Anna K., Ramsland, Paul A.

Volltext

Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome von Tischkowitz, Marc, Colas, Chrystelle, Pouwels, Sjaak, Hoogerbrugge, Nicoline

Volltext

Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP) von Nielsen, M, Franken, P F, Reinards, T H C M, Weiss, M M, Wagner, A, van der Klift, H, Kloosterman, S, Houwing-Duistermaat, J J, Aalfs, C M, Ausems, M G E M, Bröcker-Vriends, A H J T, Gomez Garcia, E B, Hoogerbrugge, N, Menko, F H, Sijmons, R H, Verhoef, S, Kuipers, E J, Morreau, H, Breuning, M H, Tops, C M J, Wijnen, J T, Vasen, H F A, Fodde, R, Hes, F J

Volltext

ASO Visual Abstract: Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling von Bokkers, Kyra, Bleiker, Eveline M. A., Aalfs, Cora M., van Dalen, Thijs, Velthuizen, Mary E., Duijveman, Petra, Sijmons, Rolf H., Koole, Wouter, Schoenmaeckers, Ernst J. P., Ausems, Margreet G. E. M.

Volltext

A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound von Corsten‐Janssen, Nicole, Bouman, Katelijne, Diphoorn, Janouk C. D., Scheper, Arjen J., Kinds, Rianne, Mecky, Julia, Breet, Hanna, Verheij, Joke B. G. M., Suijkerbuijk, Ron, Duin, Leonie K., Manten, Gwendolyn T. R., Langen, Irene M., Sijmons, Rolf H., Sikkema‐Raddatz, Birgit, Westers, Helga, Diemen, Cleo C.

Volltext