van Nederveen FH - Search Results

1

Parasympathetic paragangliomas are part of the Von Hippel-Lindau syndrome.

Gaal J, van Nederveen FH, Erlic Z, Korpershoek E, Oldenburg R, Boedeker CC, Kontny U, Neumann HP, Dinjens WN, de Krijger RR. Gaal J, et al. Among authors: van nederveen fh. J Clin Endocrinol Metab. 2009 Nov;94(11):4367-71. doi: 10.1210/jc.2009-1479. Epub 2009 Oct 6. J Clin Endocrinol Metab. 2009. PMID: 19808854

2

p53 alterations and their relationship to SDHD mutations in parasympathetic paragangliomas.

van Nederveen FH, Dannenberg H, Sleddens HF, de Krijger RR, Dinjens WN. van Nederveen FH, et al. Mod Pathol. 2003 Sep;16(9):849-56. doi: 10.1097/01.MP.0000084111.03922.4D. Mod Pathol. 2003. PMID: 13679447

3

Clinical characteristics of pheochromocytoma patients with germline mutations in SDHD.

Dannenberg H, van Nederveen FH, Abbou M, Verhofstad AA, Komminoth P, de Krijger RR, Dinjens WN. Dannenberg H, et al. Among authors: van nederveen fh. J Clin Oncol. 2005 Mar 20;23(9):1894-901. doi: 10.1200/JCO.2005.07.198. J Clin Oncol. 2005. PMID: 15774781

4

Microarray-based CGH of sporadic and syndrome-related pheochromocytomas using a 0.1-0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p.

Aarts M, Dannenberg H, deLeeuw RJ, van Nederveen FH, Verhofstad AA, Lenders JW, Dinjens WN, Speel EJ, Lam WL, de Krijger RR. Aarts M, et al. Among authors: van nederveen fh. Genes Chromosomes Cancer. 2006 Jan;45(1):83-93. doi: 10.1002/gcc.20268. Genes Chromosomes Cancer. 2006. PMID: 16215979

5

PTEN gene loss, but not mutation, in benign and malignant phaeochromocytomas.

van Nederveen FH, Perren A, Dannenberg H, Petri BJ, Dinjens WN, Komminoth P, de Krijger RR. van Nederveen FH, et al. J Pathol. 2006 Jun;209(2):274-80. doi: 10.1002/path.1968. J Pathol. 2006. PMID: 16538614

6

Genetic analyses of apparently sporadic pheochromocytomas: the Rotterdam experience.

Korpershoek E, Van Nederveen FH, Dannenberg H, Petri BJ, Komminoth P, Perren A, Lenders JW, Verhofstad AA, De Herder WW, De Krijger RR, Dinjens WN. Korpershoek E, et al. Among authors: van nederveen fh. Ann N Y Acad Sci. 2006 Aug;1073:138-48. doi: 10.1196/annals.1353.014. Ann N Y Acad Sci. 2006. PMID: 17102080

7

Frequent genetic changes in childhood pheochromocytomas.

De Krijger RR, Petri BJ, Van Nederveen FH, Korpershoek E, De Herder WW, De Muinck Keizer-Schrama SM, Dinjens WN. De Krijger RR, et al. Among authors: van nederveen fh. Ann N Y Acad Sci. 2006 Aug;1073:166-76. doi: 10.1196/annals.1353.017. Ann N Y Acad Sci. 2006. PMID: 17102083

8

The occurrence of SDHB gene mutations in pheochromocytoma.

Van Nederveen FH, Dinjens WN, Korpershoek E, De Krijger RR. Van Nederveen FH, et al. Ann N Y Acad Sci. 2006 Aug;1073:177-82. doi: 10.1196/annals.1353.018. Ann N Y Acad Sci. 2006. PMID: 17102084

9

New developments in the detection of the clinical behavior of pheochromocytomas and paragangliomas.

de Krijger RR, van Nederveen FH, Korpershoek E, Dinjens WN. de Krijger RR, et al. Among authors: van nederveen fh. Endocr Pathol. 2006 Summer;17(2):137-41. doi: 10.1385/ep:17:2:137. Endocr Pathol. 2006. PMID: 17159246 Review.

10

Expression of activin and inhibin subunits, receptors and binding proteins in human pheochromocytomas: a study based on mRNA analysis and immunohistochemistry.

Hofland J, van Nederveen FH, Timmerman MA, Korpershoek E, de Herder WW, Lenders JW, Verhofstad AA, de Krijger RR, de Jong FH. Hofland J, et al. Among authors: van nederveen fh. Clin Endocrinol (Oxf). 2007 Mar;66(3):335-40. doi: 10.1111/j.1365-2265.2007.02732.x. Clin Endocrinol (Oxf). 2007. PMID: 17302865

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