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Items: 10

1.

Rare manifestation of multiple endocrine neoplasia type 2A & cutaneous lichen amyloidosis in a family with RET gene mutation.

Birla S, Singla R, Sharma A, Tandon N.

Indian J Med Res. 2014 May;139(5):779-81. No abstract available.

2.

Diagnosis and surgical treatment of multiple endocrine neoplasia type 2A.

Tang KL, Lin Y, Li LM.

World J Surg Oncol. 2014 Jan 9;12:8. doi: 10.1186/1477-7819-12-8.

3.

An unusual presentation of MEN2A.

Casey R, Bell M, Keane M, Smyth A.

BMJ Case Rep. 2013 Jun 6;2013. pii: bcr2012007171. doi: 10.1136/bcr-2012-007171.

4.

Hedgehog signaling in human medullary thyroid carcinoma: a novel signaling pathway.

Bohinc B, Michelotti G, Diehl AM.

Thyroid. 2013 Sep;23(9):1119-26. doi: 10.1089/thy.2012.0474.

5.

Non-invasive prenatal diagnosis of multiple endocrine neoplasia type 2A using COLD-PCR combined with HRM genotyping analysis from maternal serum.

Macher HC, Martinez-Broca MA, Rubio-Calvo A, Leon-Garcia C, Conde-Sanchez M, Costa A, Navarro E, Guerrero JM.

PLoS One. 2012;7(12):e51024. doi: 10.1371/journal.pone.0051024. Epub 2012 Dec 7.

6.

Correlation between Calcitonin Levels and [(18)F]FDG-PET/CT in the Detection of Recurrence in Patients with Sporadic and Hereditary Medullary Thyroid Cancer.

Skoura E, Datseris IE, Rondogianni P, Tsagarakis S, Tzanela M, Skilakaki M, Exarhos D, Alevizaki M.

ISRN Endocrinol. 2012;2012:375231. doi: 10.5402/2012/375231. Epub 2012 May 10.

7.

Pheochromocytoma associated with neurofibromatosis type 1: concepts and current trends.

Zografos GN, Vasiliadis GK, Zagouri F, Aggeli C, Korkolis D, Vogiaki S, Pagoni MK, Kaltsas G, Piaditis G.

World J Surg Oncol. 2010 Mar 10;8:14. doi: 10.1186/1477-7819-8-14.

8.

Development and characterization of reference materials for MTHFR, SERPINA1, RET, BRCA1, and BRCA2 genetic testing.

Barker SD, Bale S, Booker J, Buller A, Das S, Friedman K, Godwin AK, Grody WW, Highsmith E, Kant JA, Lyon E, Mao R, Monaghan KG, Payne DA, Pratt VM, Schrijver I, Shrimpton AE, Spector E, Telatar M, Toji L, Weck K, Zehnbauer B, Kalman LV.

J Mol Diagn. 2009 Nov;11(6):553-61. doi: 10.2353/jmoldx.2009.090078. Epub 2009 Sep 18.

9.

Hereditary cancer syndromes.

Rahner N, Steinke V.

Dtsch Arztebl Int. 2008 Oct;105(41):706-14. doi: 10.3238/arztebl.2008.0706. Epub 2008 Oct 10.

10.

Correlation of RET somatic mutations with clinicopathological features in sporadic medullary thyroid carcinomas.

Moura MM, Cavaco BM, Pinto AE, Domingues R, Santos JR, Cid MO, Bugalho MJ, Leite V.

Br J Cancer. 2009 Jun 2;100(11):1777-83. doi: 10.1038/sj.bjc.6605056. Epub 2009 Apr 28.

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