Zobrazeno 1 - 10
of 44
pro vyhledávání: '"L. E. van der Kolk"'
Autor:
Carolien M. Kets, M. A. Legdeur, Jan C. Oosterwijk, Ellen M. A. Smets, Christianne A.R. Lok, Marian J.E. Mourits, L. E. van der Kolk, M. R. Buist, Cora M. Aalfs, I. van de Beek, J.A. de Hullu
Publikováno v:
van de Beek, I, Smets, E M A, Legdeur, M A, de Hullu, J A, Lok, C A R, Buist, M R, Mourits, M J E, Kets, C M, van der Kolk, L E, Oosterwijk, J C & Aalfs, C M 2020, ' Genetic counseling of patients with ovarian carcinoma: acceptance, timing, and psychological wellbeing ', Journal of Community Genetics, vol. 11, no. 2, pp. 183-191 . https://doi.org/10.1007/s12687-019-00427-6
Journal of Community Genetics
Journal of Community Genetics, 11, 2, pp. 183-191
Journal of community genetics, 11(2), 183-191. SPRINGER HEIDELBERG
Journal of Community Genetics, 11(2), 183-191. Springer Verlag
Journal of Community Genetics, 11, 183-191
Journal of community genetics, 11(2), 183-191. Springer Verlag
Journal of Community Genetics
Journal of Community Genetics, 11, 2, pp. 183-191
Journal of community genetics, 11(2), 183-191. SPRINGER HEIDELBERG
Journal of Community Genetics, 11(2), 183-191. Springer Verlag
Journal of Community Genetics, 11, 183-191
Journal of community genetics, 11(2), 183-191. Springer Verlag
Contains fulltext : 218565.pdf (Publisher’s version ) (Open Access) The new Dutch guidelines on hereditary and familial ovarian carcinoma recommend genetic testing of all patients with epithelial ovarian cancer (EOC). With this study, we aimed to o
Autor:
P. C. Johannesma, R. J. A. van Moorselaar, S. Horenblas, L. E. van der Kolk, E. Thunnissen, J. H. T. M. van Waesberghe, F. H. Menko, P. E. Postmus
Publikováno v:
Case Reports in Medicine, Vol 2014 (2014)
Birt-Hogg-Dubé (BHD) syndrome is a cancer disorder caused by a pathogenic FLCN mutation characterized by fibrofolliculomas, lung cysts, pneumothorax, benign renal cyst, and renal cell carcinoma (RCC). In this case we describe a patient with bilatera
Externí odkaz:
https://doaj.org/article/7ee9fba051cf4b6785e94fdd83c47525
Autor:
Petur Snaebjornsson, R T van der Kaaij, Karolina Sikorska, J P van Kessel, L. E. van der Kolk, J.W. van Sandick, O Balagué, J.M. Van Dieren, Annemieke Cats, F. van Coevorden
Publikováno v:
British Journal of Surgery. 105:e176-e182
Background Patients with hereditary diffuse gastric cancer and a CDH1 mutation have a 60–80 per cent lifetime risk of developing diffuse gastric cancer. Total prophylactic gastrectomy eliminates this risk, but is associated with considerable morbid
Autor:
H. van Boven, J. W. Wilmink, Sheima Farag, A.C.J. van Akkooi, Neeltje Steeghs, Geerard L. Beets, L. E. van der Kolk
Publikováno v:
Familial cancer, 17(2). Springer Netherlands
Familial Cancer, 17(2), 247-253. Springer Netherlands
Familial Cancer, 17(2), 247-253. Springer Netherlands
Gastrointestinal stromal tumors (GISTs) occur mostly sporadically. GISTs associated with a familial syndrome are very rare and are mostly wild type for KIT and platelet-derived growth factor alpha (PDGFRA). To date 35 kindreds and 8 individuals have
Autor:
Rashmie D. Debipersad, Gabe S. Sonke, Lennart Mulder, Esther H. Lips, Esther Scheerman, L. E. van der Kolk, J Wessling, Fbl Hogervorst, Petra M. Nederlof
Publikováno v:
Cancer Research. 77:P4-12
Background As estrogen receptor (ER)-positive breast cancer in BRCA1 mutation carriers arises at an older age with less aggressive tumor characteristics than ER negative BRCA1 mutated breast cancer, it has been suggested that these tumors are 'sporad
Autor:
Gerrit A. Meijer, Paul Roepman, Linda J.W. Bosch, Tineke E. Buffart, Kim Monkhorst, E. A. De Bruijn, K. van der Hoeven, L. E. van der Kolk, Kris G. Samsom, Luuk J. Schipper, Edwin Cuppen, Lieke Schoenmaker, Emile E. Voest, Immy Riethorst, L.R. Hoes
Publikováno v:
Annals of Oncology. 31:S784
Autor:
L. E. van der Kolk, Grace N. Sidharta, Neil K. Aaronson, Daniela E E Hahn, Willem Eijzenga, E. M. A. Bleiker
Publikováno v:
Familial Cancer
Familial Cancer, 14(4), 629-636. Springer Netherlands
Familial Cancer, 14(4), 629-636. Springer Netherlands
Only a minority of individuals who undergo cancer genetic counseling experience heightened levels of psychological distress, but many more experience a range of cancer genetic-specific psychosocial problems. The aim of this study was to estimate the
Autor:
Eveline M. A. Bleiker, L. E. van der Kolk, Grace N. Sidharta, Margreet G. E. M. Ausems, Neil K. Aaronson, Daniela E E Hahn, Mary E. Velthuizen, Willem Eijzenga
Publikováno v:
Clinical Genetics. 87:419-427
Approximately 70% of counselees undergoing cancer genetic counseling and testing (CGCT) experience some degree of CGCT-related psychosocial problems. We evaluated the efficacy of an intervention designed to increase detection and management of proble
Autor:
Luuk J. Schipper, H. van Snellenberg, Gerrit A. Meijer, Lieke Schoenmaker, E. A. De Bruijn, Edwin Cuppen, L. E. van der Kolk, Kris G. Samsom, Linda J.W. Bosch, Kim Monkhorst, Paul Roepman, Emile E. Voest, Immy Riethorst, L.R. Hoes
Publikováno v:
Annals of Oncology. 30:v575
Background Advances in DNA sequencing technology have strongly reduced costs of Whole Genome Sequencing (WGS) and have made it possible to perform WGS on tumor biopsies within 2 to 3 weeks. Despite its great potential, the value of WGS has so far onl
Publikováno v:
Leukemia, 17(8), 1658-1664. Nature Publishing Group
Antibody-dependent cellular cytotoxicity ( ADCC) is one of the possible mechanisms of action of the chimeric CD20 monoclonal antibody IDEC-C2B8 ( rituximab). As granulocyte-colony stimulating factor (G-CSF) greatly enhances the cytotoxicity of neutro