Vortmeyer AO - Search Results

1

Somatic VHL gene alterations in MEN2-associated medullary thyroid carcinoma.

Koch CA, Brouwers FM, Vortmeyer AO, Tannapfel A, Libutti SK, Zhuang Z, Pacak K, Neumann HP, Paschke R. Koch CA, et al. Among authors: vortmeyer ao. BMC Cancer. 2006 May 17;6:131. doi: 10.1186/1471-2407-6-131. BMC Cancer. 2006. PMID: 16707008 Free PMC article.

2

Somatic VHL gene deletion and point mutation in MEN 2A-associated pheochromocytoma.

Koch CA, Huang SC, Zhuang Z, Stolle C, Azumi N, Chrousos GP, Vortmeyer AO, Pacak K. Koch CA, et al. Among authors: vortmeyer ao. Oncogene. 2002 Jan 17;21(3):479-82. doi: 10.1038/sj.onc.1205133. Oncogene. 2002. PMID: 11821960

3

Somatic point mutation of the wild-type allele detected in tumors of patients with VHL germline deletion.

Vortmeyer AO, Huang SC, Pack SD, Koch CA, Lubensky IA, Oldfield EH, Zhuang Z. Vortmeyer AO, et al. Oncogene. 2002 Feb 14;21(8):1167-70. doi: 10.1038/sj.onc.1205121. Oncogene. 2002. PMID: 11850836

4

New insights into the genetics of familial chromaffin cell tumors.

Koch CA, Vortmeyer AO, Zhuang Z, Brouwers FM, Pacak K. Koch CA, et al. Among authors: vortmeyer ao. Ann N Y Acad Sci. 2002 Sep;970:11-28. doi: 10.1111/j.1749-6632.2002.tb04409.x. Ann N Y Acad Sci. 2002. PMID: 12381538 Review.

5

Amplification and overexpression of mutant RET in multiple endocrine neoplasia type 2-associated medullary thyroid carcinoma.

Huang SC, Torres-Cruz J, Pack SD, Koch CA, Vortmeyer AO, Mannan P, Lubensky IA, Gagel RF, Zhuang Z. Huang SC, et al. Among authors: vortmeyer ao. J Clin Endocrinol Metab. 2003 Jan;88(1):459-63. doi: 10.1210/jc.2002-021254. J Clin Endocrinol Metab. 2003. PMID: 12519890

6

Does the expression of c-kit (CD117) in neuroendocrine tumors represent a target for therapy?

Koch CA, Gimm O, Vortmeyer AO, Al-Ali HK, Lamesch P, Ott R, Kluge R, Bierbach U, Tannapfel A. Koch CA, et al. Among authors: vortmeyer ao. Ann N Y Acad Sci. 2006 Aug;1073:517-26. doi: 10.1196/annals.1353.055. Ann N Y Acad Sci. 2006. PMID: 17102120

7

Proteomic profiling of von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 pheochromocytomas reveals different expression of chromogranin B.

Brouwers FM, Gläsker S, Nave AF, Vortmeyer AO, Lubensky I, Huang S, Abu-Asab MS, Eisenhofer G, Weil RJ, Park DM, Linehan WM, Pacak K, Zhuang Z. Brouwers FM, et al. Among authors: vortmeyer ao. Endocr Relat Cancer. 2007 Jun;14(2):463-71. doi: 10.1677/ERC-06-0038. Endocr Relat Cancer. 2007. PMID: 17639059

8

Somatic von Hippel-Lindau gene mutations detected in sporadic endolymphatic sac tumors.

Vortmeyer AO, Huang SC, Koch CA, Governale L, Dickerman RD, McKeever PE, Oldfield EH, Zhuang Z. Vortmeyer AO, et al. Cancer Res. 2000 Nov 1;60(21):5963-5. Cancer Res. 2000. PMID: 11085513

9

Duplication of the mutant RET allele in trisomy 10 or loss of the wild-type allele in multiple endocrine neoplasia type 2-associated pheochromocytomas.

Huang SC, Koch CA, Vortmeyer AO, Pack SD, Lichtenauer UD, Mannan P, Lubensky IA, Chrousos GP, Gagel RF, Pacak K, Zhuang Z. Huang SC, et al. Among authors: vortmeyer ao. Cancer Res. 2000 Nov 15;60(22):6223-6. Cancer Res. 2000. PMID: 11103773

10

Allelic imbalance of the mutant and wild-type RET allele in MEN 2A-associated medullary thyroid carcinoma.

Koch CA, Huang SC, Moley JF, Azumi N, Chrousos GP, Gagel RF, Zhuang Z, Pacak K, Vortmeyer AO. Koch CA, et al. Among authors: vortmeyer ao. Oncogene. 2001 Nov 22;20(53):7809-11. doi: 10.1038/sj.onc.1204991. Oncogene. 2001. PMID: 11753660

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