Vortmeyer AO - Search Results

1

Adrenal ganglioneuroma in a patient presenting with severe hypertension and diarrhea.

Koch CA, Brouwers FM, Rosenblatt K, Burman KD, Davis MM, Vortmeyer AO, Pacak K. Koch CA, et al. Among authors: vortmeyer ao. Endocr Relat Cancer. 2003 Mar;10(1):99-107. doi: 10.1677/erc.0.0100099. Endocr Relat Cancer. 2003. PMID: 12653673

2

Survivin: a novel neuroendocrine marker for pheochromocytoma.

Koch CA, Vortmeyer AO, Diallo R, Poremba C, Giordano TJ, Sanders D, Bornstein SR, Chrousos GP, Pacak K. Koch CA, et al. Among authors: vortmeyer ao. Eur J Endocrinol. 2002 Mar;146(3):381-8. doi: 10.1530/eje.0.1460381. Eur J Endocrinol. 2002. PMID: 11888845

3

Pheochromocytoma in von hippel-lindau disease: distinct histopathologic phenotype compared to pheochromocytoma in multiple endocrine neoplasia type 2.

Koch CA, Mauro D, Walther MM, Linehan WM, Vortmeyer AO, Jaffe R, Pacak K, Chrousos GP, Zhuang Z, Lubensky IA. Koch CA, et al. Among authors: vortmeyer ao. Endocr Pathol. 2002 Spring;13(1):17-27. doi: 10.1385/ep:13:1:17. Endocr Pathol. 2002. PMID: 12114747

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

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

6

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

7

Genetic aspects of pheochromocytoma.

Koch CA, Vortmeyer AO, Huang SC, Alesci S, Zhuang Z, Pacak K. Koch CA, et al. Among authors: vortmeyer ao. Endocr Regul. 2001 Mar;35(1):43-52. Endocr Regul. 2001. PMID: 11308996 Review.

8

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

9

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

10

Loss of heterozygosity for the NF2 gene in retinal and optic nerve lesions of patients with neurofibromatosis 2.

Chan CC, Koch CA, Kaiser-Kupfer MI, Parry DM, Gutmann DH, Zhuang Z, Vortmeyer AO. Chan CC, et al. Among authors: vortmeyer ao. J Pathol. 2002 Sep;198(1):14-20. doi: 10.1002/path.1174. J Pathol. 2002. PMID: 12210058 Free PMC article.

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