Pacak K - Search Results

1

Somatic HIF2A gain-of-function mutations in paraganglioma with polycythemia.

Zhuang Z, Yang C, Lorenzo F, Merino M, Fojo T, Kebebew E, Popovic V, Stratakis CA, Prchal JT, Pacak K. Zhuang Z, et al. Among authors: pacak k. N Engl J Med. 2012 Sep 6;367(10):922-30. doi: 10.1056/NEJMoa1205119. N Engl J Med. 2012. PMID: 22931260 Free PMC article.

2

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: pacak k. Cancer Res. 2000 Nov 15;60(22):6223-6. Cancer Res. 2000. PMID: 11103773

3

Genetic aspects of pheochromocytoma.

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

4

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: pacak k. Oncogene. 2002 Jan 17;21(3):479-82. doi: 10.1038/sj.onc.1205133. Oncogene. 2002. PMID: 11821960

5

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: pacak k. Endocr Pathol. 2002 Spring;13(1):17-27. doi: 10.1385/ep:13:1:17. Endocr Pathol. 2002. PMID: 12114747

6

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: pacak k. 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.

7

Localization of medullary thyroid carcinoma metastasis in a multiple endocrine neoplasia type 2A patient by 6-[18F]-fluorodopamine positron emission tomography.

Gourgiotis L, Sarlis NJ, Reynolds JC, VanWaes C, Merino MJ, Pacak K. Gourgiotis L, et al. Among authors: pacak k. J Clin Endocrinol Metab. 2003 Feb;88(2):637-41. doi: 10.1210/jc.2002-021354. J Clin Endocrinol Metab. 2003. PMID: 12574193

8

Unusual locations of involvement by malignancies: Case 2. Metastatic pheochromocytoma to the colon.

Padmanabhan H, Ehrlich LD, Quazedo M, Fojo T, Louie A, Walther M, Pacak K. Padmanabhan H, et al. Among authors: pacak k. J Clin Oncol. 2003 Sep 1;21(17):3369-71. doi: 10.1200/JCO.2003.09.100. J Clin Oncol. 2003. PMID: 12947075 No abstract available.

9

Distinct gene expression profiles in norepinephrine- and epinephrine-producing hereditary and sporadic pheochromocytomas: activation of hypoxia-driven angiogenic pathways in von Hippel-Lindau syndrome.

Eisenhofer G, Huynh TT, Pacak K, Brouwers FM, Walther MM, Linehan WM, Munson PJ, Mannelli M, Goldstein DS, Elkahloun AG. Eisenhofer G, et al. Among authors: pacak k. Endocr Relat Cancer. 2004 Dec;11(4):897-911. doi: 10.1677/erc.1.00838. Endocr Relat Cancer. 2004. PMID: 15613462

10

Differential expression of erythropoietin and its receptor in von hippel-lindau-associated and multiple endocrine neoplasia type 2-associated pheochromocytomas.

Vogel TW, Brouwers FM, Lubensky IA, Vortmeyer AO, Weil RJ, Walther MM, Oldfield EH, Linehan WM, Pacak K, Zhuang Z. Vogel TW, et al. Among authors: pacak k. J Clin Endocrinol Metab. 2005 Jun;90(6):3747-51. doi: 10.1210/jc.2004-1899. Epub 2005 Mar 15. J Clin Endocrinol Metab. 2005. PMID: 15769989

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