Dannenberg H - Search Results

1

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: dannenberg h. Ann N Y Acad Sci. 2006 Aug;1073:138-48. doi: 10.1196/annals.1353.014. Ann N Y Acad Sci. 2006. PMID: 17102080

2

Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas.

Dannenberg H, De Krijger RR, van der Harst E, Abbou M, IJzendoorn Y, Komminoth P, Dinjens WN. Dannenberg H, et al. Int J Cancer. 2003 Jun 10;105(2):190-5. doi: 10.1002/ijc.11060. Int J Cancer. 2003. PMID: 12673678 Free article.

3

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. Among authors: dannenberg h. Mod Pathol. 2003 Sep;16(9):849-56. doi: 10.1097/01.MP.0000084111.03922.4D. Mod Pathol. 2003. PMID: 13679447

4

Molecular genetic alterations in adrenal and extra-adrenal pheochromocytomas and paragangliomas.

Dannenberg H, Komminoth P, Dinjens WN, Speel EJ, de Krijger RR. Dannenberg H, et al. Endocr Pathol. 2003 Winter;14(4):329-50. doi: 10.1385/ep:14:4:329. Endocr Pathol. 2003. PMID: 14739490 Review.

5

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. J Clin Oncol. 2005 Mar 20;23(9):1894-901. doi: 10.1200/JCO.2005.07.198. J Clin Oncol. 2005. PMID: 15774781

6

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: dannenberg h. Genes Chromosomes Cancer. 2006 Jan;45(1):83-93. doi: 10.1002/gcc.20268. Genes Chromosomes Cancer. 2006. PMID: 16215979

7

Frequent loss of 17p, but no p53 mutations or protein overexpression in benign and malignant pheochromocytomas.

Petri BJ, Speel EJ, Korpershoek E, Claessen SM, van Nederveen FH, Giesen V, Dannenberg H, van der Harst E, Dinjens WN, de Krijger RR. Petri BJ, et al. Among authors: dannenberg h. Mod Pathol. 2008 Apr;21(4):407-13. doi: 10.1038/modpathol.3801013. Epub 2008 Jan 25. Mod Pathol. 2008. PMID: 18223555 Free article.

8

An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis.

van Nederveen FH, Gaal J, Favier J, Korpershoek E, Oldenburg RA, de Bruyn EM, Sleddens HF, Derkx P, Rivière J, Dannenberg H, Petri BJ, Komminoth P, Pacak K, Hop WC, Pollard PJ, Mannelli M, Bayley JP, Perren A, Niemann S, Verhofstad AA, de Bruïne AP, Maher ER, Tissier F, Méatchi T, Badoual C, Bertherat J, Amar L, Alataki D, Van Marck E, Ferrau F, François J, de Herder WW, Peeters MP, van Linge A, Lenders JW, Gimenez-Roqueplo AP, de Krijger RR, Dinjens WN. van Nederveen FH, et al. Among authors: dannenberg h. Lancet Oncol. 2009 Aug;10(8):764-71. doi: 10.1016/S1470-2045(09)70164-0. Epub 2009 Jul 1. Lancet Oncol. 2009. PMID: 19576851 Free PMC article. Clinical Trial.

9

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. Among authors: dannenberg h. J Pathol. 2006 Jun;209(2):274-80. doi: 10.1002/path.1968. J Pathol. 2006. PMID: 16538614

10

Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma.

Dannenberg H, Dinjens WN, Abbou M, Van Urk H, Pauw BK, Mouwen D, Mooi WJ, de Krijger RR. Dannenberg H, et al. Clin Cancer Res. 2002 Jul;8(7):2061-6. Clin Cancer Res. 2002. PMID: 12114404

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