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Gerkes, E. H., Fock, J. M., den Dunnen, W. F. A., van Belzen, M. J., van der Lans, C. A., Hoving, E. W., Fakkert, I. E., Smith, M. J., Evans, D. G., Olderode-Berends, M. J. W.
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Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal cancer
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Is colorectal surveillance indicated in patients with PTEN mutations?
Nieuwenhuis, M. H., Kets, C. M., Murphy-Ryan, M., Colas, C., Möller, P., Hes, F. J., Hodgson, S. V., Olderode-Berends, M. J. W., Aretz, S., Heinimann, K., Gomez Garcia, E. B., Douglas, F., Spigelman, A., Timshel, S., Lindor, N. M., Vasen, H. F. A.
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Homozygous TMEM127 mutations in 2 patients with bilateral pheochromocytomas
Eijkelenkamp, K., Olderode‐Berends, M.J.W., van der Luijt, R.B., Robledo, M., van Dooren, M., Feelders, R.A., de Vries, J., Kerstens, M.N., Links, T.P., van der Horst‐Schrivers, A.N.A.
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Association of Hereditary Nonpolyposis Colorectal Cancer–Related Tumors Displaying Low Microsatellite Instability with MSH6 Germline Mutations
Wu, Ying, Berends, Maran J.W., Mensink, Rob G.J., Kempinga, Claudia, Sijmons, Rolf H., van der Zee, Ate G.J., Hollema, Harry, Kleibeuker, Jan H., Buys, Charles H.C.M., Hofstra, Robert M.W.
Published in American journal of human genetics (01.11.1999)
Published in American journal of human genetics (01.11.1999)
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A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrum
Van Reeuwijk, J, Olderode-Berends, MJW, Van Den Elzen, C, Brouwer, OF, Roscioli, T, Van Pampus, MG, Scheffer, H, Brunner, HG, Van Bokhoven, H, Hol, FA
Published in Clinical genetics (01.09.2010)
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Chronic overproduction of islet amyloid polypeptide/amylin in transgenic mice: lysosomal localization of human islet amyloid polypeptide and lack of marked hyperglycaemia or hyperinsulinaemia
Höppener, J W, Verbeek, J S, de Koning, E J, Oosterwijk, C, van Hulst, K L, Visser-Vernooy, H J, Hofhuis, F M, van Gaalen, S, Berends, M J, Hackeng, W H
Published in Diabetologia (01.12.1993)
Published in Diabetologia (01.12.1993)
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Clinical Screening as Compared with DNA Analysis in Families with Multiple Endocrine Neoplasia Type 2A
Lips, Cornelis, Landsvater, Rudy M, Hoppener, Jo, Geerdink, Rolf A, Blijham, Geert, van Veen, Joke M. Jansen-Schillhorn, van Gils, Adriaan, de Wit, Mireille J, Zewald, Richard A, Berends, Marianne, Beemer, Frits A, Brouwers-Smalbraak, Joanneke, Jansen, Rumo, van Amstel, Hans Kristian Ploos, van Vroonhoven, Theo, Vroom, Thea M
Published in The New England journal of medicine (29.09.1994)
Published in The New England journal of medicine (29.09.1994)
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Hereditary non-polyposis colorectal cancer: identification of mutation carriers and assessing pathogenicity of mutations
Niessen, R C, Sijmons, R H, Berends, M J W, Ou, J, Hofstra, R M W, Kleibeuker, J H
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Detection of calcitonin-encoding mRNA by radioactive and non- radioactive in situ hybridization: improved colorimetric detection and cellular localization of mRNA in thyroid sections
Denijn, M, De Weger, RA, Berends, MJ, Compier-Spies, PI, Jansz, H, Van Unnik, JA, Lips, CJ
Published in The journal of histochemistry and cytochemistry (01.03.1990)
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The importance of family history in young patients with endometrial cancer
Berends, Maran J.W, Kleibeuker, Jan H, de Vries, Elisabeth G.E, Mourits, Marian J.E, Hollema, Harry, Pras, Elisabeth, van der Zee, Ate G.J
Published in European journal of obstetrics & gynecology and reproductive biology (01.02.1999)
Published in European journal of obstetrics & gynecology and reproductive biology (01.02.1999)
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Conference Proceeding
The clinical implications of a positive calcitonin test for C-cell hyperplasia in genetically unaffected members of an MEN2A kindred
LANDSVATER, R. M, ROMBOUTS, A. G. M, TE MEERMAN, G. J, SCHILLHORN-VAN VEEN, J. M. J, BERENDS, M. J. H, GEERDINK, R. A, STRUYVENBERG, A, BUYS, C. H. C. M, LIPS, C. J. M
Published in American journal of human genetics (01.02.1993)
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Published in American journal of human genetics (01.02.1993)
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The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers
Suerink, Manon, van der Klift, Heleen M., ten Broeke, Sanne W., Dekkers, Olaf M., Bernstein, Inge, Capellá Munar, Gabriel, Gomez Garcia, Encarna, Hoogerbrugge, Nicoline, Letteboer, Tom G.W., Menko, Fred H., Lindblom, Annika, Mensenkamp, Arjen, Moller, Pal, van Os, Theo A., Rahner, Nils, Redeker, Bert J.W., Olderode, Maran, Spruijt, Liesbeth, Vos, Yvonne J., Wagner, Anja, Morreau, Hans, Hes, Frederik J., Vasen, Hans F.A., Tops, Carli M., Wijnen, Juul T., Nielsen, Maartje
Published in Genetics in medicine (01.04.2016)
Published in Genetics in medicine (01.04.2016)
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From medical history and biochemical tests to presymptomatic treatment in a large MEN 2A family
Lips, C J, Landsvater, R M, Höppener, J W, Geerdink, R A, Blijham, G H, Jansen-Schillhorn van Veen, J M, Feldberg, M A, van Gils, A P, Hoogenboom, H, Berends, M J
Published in Journal of internal medicine (01.10.1995)
Published in Journal of internal medicine (01.10.1995)
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A role for MLH3 in hereditary nonpolyposis colorectal cancer
Hofstra, Robert M.W, Wu, Ying, Berends, Maran J.W, Sijmons, Rolf H, Mensink, Rob G.J, Verlind, Edwin, Kooi, Krista A, van der Sluis, Tineke, Kempinga, Claudia, van der Zee, Ate G.J, Hollema, Harry, Buys, Charles H.C.M, Kleibeuker, Jan H
Published in Nature genetics (01.10.2001)
Published in Nature genetics (01.10.2001)
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Germline mutations of EXO1 gene in patients with hereditary nonpolyposis colorectal cancer (HNPCC) and atypical HNPCC forms
Wu, Y, Berends, M J, Post, J G, Mensink, R G, Verlind, E, Van Der Sluis, T, Kempinga, C, Sijmons, R H, van der Zee, A G, Hollema, H, Kleibeuker, J H, Buys, C H, Hofstra, R M
Published in Gastroenterology (New York, N.Y. 1943) (01.06.2001)
Published in Gastroenterology (New York, N.Y. 1943) (01.06.2001)
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Small bites versus large bites for closure of abdominal midline incisions (STITCH): a double-blind, multicentre, randomised controlled trial
Deerenberg, Eva B, MD, Harlaar, Joris J, Dr, Steyerberg, Ewout W, Prof, Lont, Harold E, MD, van Doorn, Helena C, MD, Heisterkamp, Joos, MD, Wijnhoven, Bas PL, MD, Schouten, Willem R, MD, Cense, Huib A, MD, Stockmann, Hein BAC, MD, Berends, Frits J, MD, Dijkhuizen, F Paul HLJ, MD, Dwarkasing, Roy S, MD, Jairam, An P, MD, van Ramshorst, Gabrielle H, MD, Kleinrensink, Gert-Jan, Prof, Jeekel, Johannes, Prof, Lange, Johan F, Prof
Published in The Lancet (British edition) (26.09.2015)
Published in The Lancet (British edition) (26.09.2015)
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