Buys CH - Search Results

1

First-trimester use of paroxetine and congenital heart defects: a population-based case-control study.

Bakker MK, Kerstjens-Frederikse WS, Buys CH, de Walle HE, de Jong-van den Berg LT. Bakker MK, et al. Among authors: buys ch. Birth Defects Res A Clin Mol Teratol. 2010 Feb;88(2):94-100. doi: 10.1002/bdra.20641. Birth Defects Res A Clin Mol Teratol. 2010. PMID: 19937603

2

Severe myocardial fibrosis caused by a deletion of the 5' end of the lamin A/C gene.

van Tintelen JP, Tio RA, Kerstjens-Frederikse WS, van Berlo JH, Boven LG, Suurmeijer AJ, White SJ, den Dunnen JT, te Meerman GJ, Vos YJ, van der Hout AH, Osinga J, van den Berg MP, van Veldhuisen DJ, Buys CH, Hofstra RM, Pinto YM. van Tintelen JP, et al. Among authors: buys ch. J Am Coll Cardiol. 2007 Jun 26;49(25):2430-9. doi: 10.1016/j.jacc.2007.02.063. Epub 2007 Jun 11. J Am Coll Cardiol. 2007. PMID: 17599607 Free article.

3

A Hirschsprung disease locus at 22q11?

Kerstjens-Frederikse WS, Hofstra RM, van Essen AJ, Meijers JH, Buys CH. Kerstjens-Frederikse WS, et al. Among authors: buys ch. J Med Genet. 1999 Mar;36(3):221-4. J Med Genet. 1999. PMID: 10204849 Free PMC article.

4

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.

Niessen RC, Berends MJ, Wu Y, Sijmons RH, Hollema H, Ligtenberg MJ, de Walle HE, de Vries EG, Karrenbeld A, Buys CH, van der Zee AG, Hofstra RM, Kleibeuker JH. Niessen RC, et al. Among authors: buys ch. Gut. 2006 Dec;55(12):1781-8. doi: 10.1136/gut.2005.090159. Epub 2006 Apr 24. Gut. 2006. PMID: 16636019 Free PMC article.

5

Clinical definition of hereditary non-polyposis colorectal cancer: a search for the impossible?

Berends MJ, Wu Y, Sijmons RH, Hofstra RM, van der Zee AG, Buys CH, Kleibeuker JH. Berends MJ, et al. Among authors: buys ch. Scand J Gastroenterol Suppl. 2001;(234):61-7. doi: 10.1080/003655201753265127. Scand J Gastroenterol Suppl. 2001. PMID: 11768563 Review.

6

Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2.

Burzynski GM, Nolte IM, Osinga J, Ceccherini I, Twigt B, Maas S, Brooks A, Verheij J, Plaza Menacho I, Buys CH, Hofstra RM. Burzynski GM, et al. Among authors: buys ch. Eur J Hum Genet. 2004 Aug;12(8):604-12. doi: 10.1038/sj.ejhg.5201199. Eur J Hum Genet. 2004. PMID: 15138456

7

Oncological implications of RET gene mutations in Hirschsprung's disease.

Sijmons RH, Hofstra RM, Wijburg FA, Links TP, Zwierstra RP, Vermey A, Aronson DC, Tan-Sindhunata G, Brouwers-Smalbraak GJ, Maas SM, Buys CH. Sijmons RH, et al. Among authors: buys ch. Gut. 1998 Oct;43(4):542-7. doi: 10.1136/gut.43.4.542. Gut. 1998. PMID: 9824583 Free PMC article.

8

Determination of TP53 mutation is more relevant than microsatellite instability status for the prediction of disease-free survival in adjuvant-treated stage III colon cancer patients.

Westra JL, Schaapveld M, Hollema H, de Boer JP, Kraak MM, de Jong D, ter Elst A, Mulder NH, Buys CH, Hofstra RM, Plukker JT. Westra JL, et al. Among authors: buys ch. J Clin Oncol. 2005 Aug 20;23(24):5635-43. doi: 10.1200/JCO.2005.04.096. J Clin Oncol. 2005. PMID: 16110022 Clinical Trial.

9

FISH and array-CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions.

Dijkhuizen T, van Essen T, van der Vlies P, Verheij JB, Sikkema-Raddatz B, van der Veen AY, Gerssen-Schoorl KB, Buys CH, Kok K. Dijkhuizen T, et al. Among authors: buys ch. Am J Med Genet A. 2006 Nov 15;140(22):2482-7. doi: 10.1002/ajmg.a.31487. Am J Med Genet A. 2006. PMID: 17036314

10

Comprehensive TP53-denaturing gradient gel electrophoresis mutation detection assay also applicable to archival paraffin-embedded tissue.

Hayes VM, Bleeker W, Verlind E, Timmer T, Karrenbeld A, Plukker JT, Marx MP, Hofstra RM, Buys CH. Hayes VM, et al. Among authors: buys ch. Diagn Mol Pathol. 1999 Mar;8(1):2-10. doi: 10.1097/00019606-199903000-00002. Diagn Mol Pathol. 1999. PMID: 10408787

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