Similar articles for PMID: 15827097

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1978	1
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1998	1
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2007	2
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1

Codon-specific development of pheochromocytoma in multiple endocrine neoplasia type 2.

Machens A, Brauckhoff M, Holzhausen HJ, Thanh PN, Lehnert H, Dralle H. Machens A, et al. J Clin Endocrinol Metab. 2005 Jul;90(7):3999-4003. doi: 10.1210/jc.2005-0064. Epub 2005 Apr 12. J Clin Endocrinol Metab. 2005. PMID: 15827097

2

Pheochromocytoma and medullary thyroid carcinoma: a new genotype-phenotype correlation of the RET protooncogene 891 germline mutation.

Jimenez C, Habra MA, Huang SC, El-Naggar A, Shapiro SE, Evans DB, Cote G, Gagel RF. Jimenez C, et al. J Clin Endocrinol Metab. 2004 Aug;89(8):4142-5. doi: 10.1210/jc.2004-0041. J Clin Endocrinol Metab. 2004. PMID: 15292360

3

Multiple endocrine neoplasia type 2: evaluation of the genotype-phenotype relationship.

Yip L, Cote GJ, Shapiro SE, Ayers GD, Herzog CE, Sellin RV, Sherman SI, Gagel RF, Lee JE, Evans DB. Yip L, et al. Arch Surg. 2003 Apr;138(4):409-16; discussion 416. doi: 10.1001/archsurg.138.4.409. Arch Surg. 2003. PMID: 12686527

4

Incidence and clinical relevance of RET proto-oncogene germline mutations in pheochromocytoma patients.

Januszewicz A, Neumann HP, Loń I, Szmigielski C, Symonides B, Kabat M, Apel TW, Wocial B, Lapiński M, Januszewicz W. Januszewicz A, et al. J Hypertens. 2000 Aug;18(8):1019-23. doi: 10.1097/00004872-200018080-00005. J Hypertens. 2000. PMID: 10953992

5

Peak incidence of pheochromocytoma and primary hyperparathyroidism in multiple endocrine neoplasia 2: need for age-adjusted biochemical screening.

Machens A, Lorenz K, Dralle H. Machens A, et al. J Clin Endocrinol Metab. 2013 Feb;98(2):E336-45. doi: 10.1210/jc.2012-3192. Epub 2013 Jan 2. J Clin Endocrinol Metab. 2013. PMID: 23284010

6

Pheochromocytoma penetrance varies by RET mutation in MEN 2A.

Quayle FJ, Fialkowski EA, Benveniste R, Moley JF. Quayle FJ, et al. Surgery. 2007 Dec;142(6):800-5; discussion 805.e1. doi: 10.1016/j.surg.2007.09.013. Epub 2007 Nov 5. Surgery. 2007. PMID: 18063059

7

High penetrance of pheochromocytoma associated with the novel C634Y/Y791F double germline mutation in the RET protooncogene.

Toledo RA, Wagner SM, Coutinho FL, Lourenço DM Jr, Azevedo JA, Longuini VC, Reis MT, Siqueira SA, Lucon AM, Tavares MR, Fragoso MC, Pereira AA, Dahia PL, Mulligan LM, Toledo SP. Toledo RA, et al. J Clin Endocrinol Metab. 2010 Mar;95(3):1318-27. doi: 10.1210/jc.2009-1355. Epub 2010 Jan 15. J Clin Endocrinol Metab. 2010. PMID: 20080836

8

Intronic single nucleotide polymorphisms in the RET protooncogene are associated with a subset of apparently sporadic pheochromocytoma and may modulate age of onset.

McWhinney SR, Boru G, Binkley PK, Peczkowska M, Januszewicz AA, Neumann HP, Eng C. McWhinney SR, et al. J Clin Endocrinol Metab. 2003 Oct;88(10):4911-6. doi: 10.1210/jc.2003-030245. J Clin Endocrinol Metab. 2003. PMID: 14557473

9

[The clinical patterns and RET proto-oncogene identification of pheochromocytoma in 13 multiple endocrine neoplasia type 2A pedigrees].

Qi XP, Chen ZG, Jin HY, Li F, Cheng J, Ying RB, Zhao JQ, Guo DG, Luo SY, Chen GP, Zhang XN. Qi XP, et al. Zhonghua Yi Xue Za Zhi. 2013 Jul 23;93(28):2200-4. Zhonghua Yi Xue Za Zhi. 2013. PMID: 24169328 Chinese.

10

The clinical spectrum of multiple endocrine neoplasia type 2a caused by the rare intracellular RET mutation S891A.

Schulte KM, Machens A, Fugazzola L, McGregor A, Diaz-Cano S, Izatt L, Aylwin S, Talat N, Beck-Peccoz P, Dralle H. Schulte KM, et al. J Clin Endocrinol Metab. 2010 Sep;95(9):E92-7. doi: 10.1210/jc.2010-0375. Epub 2010 Jun 16. J Clin Endocrinol Metab. 2010. PMID: 20554711

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