Jansen JC - Search Results

1

The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family.

Hensen EF, Jansen JC, Siemers MD, Oosterwijk JC, Vriends AH, Corssmit EP, Bayley JP, van der Mey AG, Cornelisse CJ, Devilee P. Hensen EF, et al. Among authors: jansen jc. Eur J Hum Genet. 2010 Jan;18(1):62-6. doi: 10.1038/ejhg.2009.112. Eur J Hum Genet. 2010. PMID: 19584903 Free PMC article.

2

First experiences with genetic counselling based on predictive DNA diagnosis in hereditary glomus tumours (paragangliomas).

Oosterwijk JC, Jansen JC, van Schothorst EM, Oosterhof AW, Devilee P, Bakker E, Zoeteweij MW, van der Mey AG. Oosterwijk JC, et al. Among authors: jansen jc. J Med Genet. 1996 May;33(5):379-83. doi: 10.1136/jmg.33.5.379. J Med Genet. 1996. PMID: 8733047 Free PMC article.

3

Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2-cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes.

van Schothorst EM, Jansen JC, Bardoel AF, van der Mey AG, James MJ, Sobol H, Weissenbach J, van Ommen GJ, Cornelisse CJ, Devilee P. van Schothorst EM, et al. Among authors: jansen jc. Eur J Hum Genet. 1996;4(5):267-73. doi: 10.1159/000472213. Eur J Hum Genet. 1996. PMID: 8946172

4

Color Doppler imaging of paragangliomas in the neck.

Jansen JC, Baatenburg de Jong RJ, Schipper J, van der Mey AG, van Gils AP. Jansen JC, et al. J Clin Ultrasound. 1997 Nov-Dec;25(9):481-5. doi: 10.1002/(sici)1097-0096(199711/12)25:9<481::aid-jcu3>3.0.co;2-j. J Clin Ultrasound. 1997. PMID: 9350566

5

Founder effect at PGL1 in hereditary head and neck paraganglioma families from the Netherlands.

van Schothorst EM, Jansen JC, Grooters E, Prins DE, Wiersinga JJ, van der Mey AG, van Ommen GJ, Devilee P, Cornelisse CJ. van Schothorst EM, et al. Among authors: jansen jc. Am J Hum Genet. 1998 Aug;63(2):468-73. doi: 10.1086/301951. Am J Hum Genet. 1998. PMID: 9683583 Free PMC article.

6

Estimation of growth rate in patients with head and neck paragangliomas influences the treatment proposal.

Jansen JC, van den Berg R, Kuiper A, van der Mey AG, Zwinderman AH, Cornelisse CJ. Jansen JC, et al. Cancer. 2000 Jun 15;88(12):2811-6. Cancer. 2000. PMID: 10870065

7

Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene.

Taschner PE, Jansen JC, Baysal BE, Bosch A, Rosenberg EH, Bröcker-Vriends AH, van Der Mey AG, van Ommen GJ, Cornelisse CJ, Devilee P. Taschner PE, et al. Among authors: jansen jc. Genes Chromosomes Cancer. 2001 Jul;31(3):274-81. doi: 10.1002/gcc.1144. Genes Chromosomes Cancer. 2001. PMID: 11391798

8

Management of carotid body tumors.

van der Mey AG, Jansen JC, van Baalen JM. van der Mey AG, et al. Among authors: jansen jc. Otolaryngol Clin North Am. 2001 Oct;34(5):907-24, vi. doi: 10.1016/s0030-6665(05)70354-6. Otolaryngol Clin North Am. 2001. PMID: 11557446 Review.

9

Carotid body tumors in humans caused by a mutation in the gene for succinate dehydrogenase D (SDHD).

Dahan A, Taschner PE, Jansen JC, van der Mey A, Teppema LJ, Cornelisse CJ. Dahan A, et al. Among authors: jansen jc. Adv Exp Med Biol. 2004;551:71-6. doi: 10.1007/0-387-27023-x_12. Adv Exp Med Biol. 2004. PMID: 15602946 No abstract available.

10

Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas.

van Houtum WH, Corssmit EP, Douwes Dekker PB, Jansen JC, van der Mey AG, Bröcker-Vriends AH, Taschner PE, Losekoot M, Frölich M, Stokkel MP, Cornelisse CJ, Romijn JA. van Houtum WH, et al. Among authors: jansen jc. Eur J Endocrinol. 2005 Jan;152(1):87-94. doi: 10.1530/eje.1.01833. Eur J Endocrinol. 2005. PMID: 15762191

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