Reply: Evaluation of management of desmoid tumours associated with familial adenomatous polyposis in Dutch patients

Por Nieuwenhuis, M H, Vasen, H F A
Publicado em 2011

Is Breast Cancer Part of the Tumor Spectrum of Hereditary Nonpolyposis Colorectal Cancer?

Por Vasen, H. F. A., Morreau, H., Nortier, J. W. R.
Publicado em 2001

An alternative to prophylactic colectomy for colon cancer prevention in HNPCC syndrome

Por Vasen, H F A, de Vos tot Nederveen Cappel, W H
Publicado em 2005

Duodenal adenomatosis in familial adenomatous polyposis

Por Bülow, S, Björk, J, Christensen, I J, Fausa, O, Järvinen, H, Moesgaard, F, Vasen, H F A
Publicado em 2004

Family history is neglected in the work-up of patients with colorectal cancer: a quality assessment using cancer registry data

Por van Dijk, D. A., Oostindiër, M. J., Kloosterman-Boele, W. M., Krijnen, P., Vasen, H. F. A.
Publicado em 2007

Increased risk of colorectal neoplasia in asymptomatic liver‐transplant recipients

Por Koornstra, J J, Wesseling, J, de Jong, A E, Vasen, H F A, Kleibeuker, J H, Haagsma, E B
Publicado em 2007

Is surveillance of the small bowel indicated for Lynch syndrome families?

Por Kate, G L ten, Kleibeuker, J H, Nagengast, F M, Craanen, M, Cats, A, Menko, F H, Vasen, H F A
Publicado em 2007

Identification of HNPCC by Molecular Analysis of Colorectal and Endometrial Tumors

Por Vasen, H. F. A., Hendriks, Y., de Jong, A. E., van Puijenbroek, M., Tops, C., Bröcker-Vriends, A. H. J. T., Wijnen, J. Th., Morreau, H.
Publicado em 2004

Duodenal carcinoma in MUTYH‐associated polyposis

Por Nielsen, M, Poley, J W, Verhoef, S, van Puijenbroek, M, Weiss, M M, Burger, G T, Dommering, C J, Vasen, H F A, Kuipers, E J, Wagner, A, Morreau, H, Hes, F J
Publicado em 2006

Screening for BRCA2 mutations in 81 Dutch breast–ovarian cancer families

Por Peelen, T, Vliet, M van, Bosch, A, Bignell, G, Vasen, H F A, Klijn, J G M, Meijers-Heijboer, H, Stratton, M, Ommen, G-J B van, Cornelisse, C J, Devilee, P
Publicado em 2000

Genetic Testing for Breast Cancer Predisposition in 1999: Which Molecular Strategy and which Family Criteria?

Por Stoppa-Lyonnet, D., Caligo, M., Eccles, D., Evans, D. G. R., Haites, N. E., Hodgson, N. S., Møller, P., Morrison, P. J., Steel, C. M., Vasen, H. F. A., Chang-Claude, J.
Publicado em 1999

Linkage to markers for the chromosome region 17q12-q21 in 13 Dutch breast cancer kindreds

Por Devilee, P., Cornelis, R. S., Bootsma, A., Bardoel, A., van Vliet, M., van Leeuwen, I., Cletor, F. J., de Klein, A., Lindhout, D., Vasen, H. F. A., Cornelisse, C. J., Khan, P. Meera
Publicado em 1993

Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defect

Por de Vos tot Nederveen Cappel, W H, Buskens, E, van Duijvendijk, P, Cats, A, Menko, F H, Griffioen, G, Slors, J F, Nagengast, F M, Kleibeuker, J H, Vasen, H F A
Publicado em 2003

Insurance Implications for Individuals with a High Risk of Breast and Ovarian Cancer in Europe

Por Morrison, P. J., Steel, C. M., Vasen, H. F. A., Eccles, D., Evans, D. G. R., Møller, P., Hodgson, S., Stoppa-Lyonnet, D., Chang-Claude, J., Caligo, M., Olah, E., Haites, N. E., Nevin, N. C.
Publicado em 1999

Current Policies for Surveillance and Management in Women at Risk for Breast and Ovarian Cancer: A Survey among 16 European Family Cancer Clinics

Por Vasen, H. F. A., Haites, N. E., Evans, D. G. R., Steel, C. M., Møller, P., Hodgson, S., Eccles, D., Morrison, P., Stoppa-Lyonnet, D., Chang-Claude, J., Caligo, M., European Familial Breast Cancer Collaborative Group
Publicado em 1999

Cost effectiveness of a new strategy to identify HNPCC patients

Por Kievit, W, de Bruin, J H F M, Adang, E M M, Severens, J L, Kleibeuker, J H, Sijmons, R H, Ruers, T J, Nagengast, F M, Vasen, H F A, van Krieken, J H J M, Ligtenberg, M J L, Hoogerbrugge, N
Publicado em 2005

Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers

Por Ghorbanoghli, Z., Nieuwenhuis, M. H., Houwing-Duistermaat, J. J., Jagmohan-Changur, S., Hes, F. J., Tops, C. M., Wagner, A., Aalfs, C. M., Verhoef, S., Gómez García, E. B., Sijmons, R. H., Menko, F. H., Letteboer, T. G., Hoogerbrugge, N., van Wezel, T., Vasen, H. F. A., Wijnen, J. T.
Publicado no Fam Cancer (2016)

Guidelines for the clinical management of Lynch syndrome (hereditary non‐polyposis cancer)

Por Vasen, H F A, Möslein, G, Alonso, A, Bernstein, I, Bertario, L, Blanco, I, Burn, J, Capella, G, Engel, C, Frayling, I, Friedl, W, Hes, F J, Hodgson, S, Mecklin, J‐P, Møller, P, Nagengast, F, Parc, Y, Renkonen‐Sinisalo, L, Sampson, J R, Stormorken, A, Wijnen, J
Publicado em 2007

Evaluation of management of desmoid tumours associated with familial adenomatous polyposis in Dutch patients

Por Nieuwenhuis, M H, Mathus-Vliegen, E M, Baeten, C G, Nagengast, F M, van der Bijl, J, van Dalsen, A D, Kleibeuker, J H, Dekker, E, Langers, A M, Vecht, J, Peters, F T, van Dam, R, van Gemert, W G, Stuifbergen, W N, Schouten, W R, Gelderblom, H, Vasen, H F A
Publicado em 2011

A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families

Por Peelen, T., van Vliet, M., Petrij-Bosch, A., Mieremet, R., Szabo, C., van den Ouweland, A. M. W., Hogervorst, F., Brohet, R., Ligtenberg, M. J. L., Teugels, E., van der Luijt, R., van der Hout, A. H., Gille, J. J. P., Pals, G., Jedema, I., Olmer, R., van Leeuwen, I., Newman, B., Plandsoen, M., van der Est, M., Brink, G., Hageman, S., Arts, P. J. W., Bakker, M. M., Willems, H. W., van der Looij, E., Neyns, B., Bonduelle, M., Jansen, R., Oosterwijk, J. C., Sijmons, R., Smeets, H. J. M., van Asperen, C. J., Meijers-Heijboer, H., Klijn, J. G. M., de Greve, J., King, M.-C., Menko, F. H., Brunner, H. G., Halley, D., van Ommen, G.-J. B., Vasen, H. F. A., Cornelisse, C. J., van 'tVeer, L. J., de Knijff, P., Bakker, E., Devilee, P.
Publicado em 1997