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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1952 1
1953 1
1954 1
1959 1
1960 1
1961 1
1975 1
1976 3
1977 1
1978 3
1979 4
1980 1
1981 4
1982 4
1983 7
1984 5
1985 3
1986 4
1987 7
1988 4
1989 8
1990 9
1991 4
1992 16
1993 9
1994 28
1995 56
1996 49
1997 40
1998 37
1999 24
2000 25
2001 31
2002 24
2003 27
2004 43
2005 35
2006 35
2007 34
2008 26
2009 21
2010 15
2011 20
2012 34
2013 29
2014 23
2015 32
2016 24
2017 24
2018 26
2019 21
2020 28
2021 25
2022 18
2023 15
2024 4

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915 results

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Page 1
Multiple endocrine neoplasia type 2: A review.
Mathiesen JS, Effraimidis G, Rossing M, Rasmussen ÅK, Hoejberg L, Bastholt L, Godballe C, Oturai P, Feldt-Rasmussen U. Mathiesen JS, et al. Semin Cancer Biol. 2022 Feb;79:163-179. doi: 10.1016/j.semcancer.2021.03.035. Epub 2021 Apr 1. Semin Cancer Biol. 2022. PMID: 33812987 Review.
Multiple endocrine neoplasias are rare hereditary syndromes some of them with malignant potential. Multiple endocrine neoplasia type 2 (MEN 2) is an autosomal dominant hereditary cancer syndrome due to germline variants in the REarranged
Multiple endocrine neoplasias are rare hereditary syndromes some of them with malignant potential. Multiple endocrin
Multiple endocrine neoplasia type 2B syndrome.
Malhotra R, Goyal A, Shamim SA. Malhotra R, et al. QJM. 2021 Jul 28;114(4):272-273. doi: 10.1093/qjmed/hcaa184. QJM. 2021. PMID: 32483633 No abstract available.
Multiple endocrine neoplasia type 2B and Hirschsprung's disease.
Kapur RP. Kapur RP. Clin Gastroenterol Hepatol. 2005 May;3(5):423-31. doi: 10.1016/s1542-3565(04)00676-7. Clin Gastroenterol Hepatol. 2005. PMID: 15880310 Review.
Multiple endocrine neoplasia type 2B and Hirschsprung's disease are genetic disorders characterized by gross and/or microscopic pathology of the enteric nervous system and associated dysmotility. A specific missense mutation in the RET proto-onc
Multiple endocrine neoplasia type 2B and Hirschsprung's disease are genetic disorders characterized by gr
Multiple endocrine neoplasia type 2: an overview.
Moline J, Eng C. Moline J, et al. Genet Med. 2011 Sep;13(9):755-64. doi: 10.1097/GIM.0b013e318216cc6d. Genet Med. 2011. PMID: 21552134 Free article. Review.
Multiple endocrine neoplasia type 2A, familial medullary thyroid carcinoma, and multiple endocrine neoplasia type 2B are collectively associated with a 70-100% risk of medullary thyroid carcinoma by age 70 years. Pheo
Multiple endocrine neoplasia type 2A, familial medullary thyroid carcinoma, and multiple endocrine
Multiple endocrine neoplasia type 2B: Frequency of physical stigmata-Results of the GPOH-MET registry.
Redlich A, Lessel L, Petrou A, Mier P, Vorwerk P. Redlich A, et al. Pediatr Blood Cancer. 2020 Feb;67(2):e28056. doi: 10.1002/pbc.28056. Epub 2019 Nov 13. Pediatr Blood Cancer. 2020. PMID: 31724322
BACKGROUND: Multiple endocrine neoplasia (MEN) 2B is characterized by early development of aggressive medullary thyroid carcinoma (MTC), visible physical stigmata, and associated symptoms. ...METHODS: Children with a diagnosis of MTC in MEN 2B r …
BACKGROUND: Multiple endocrine neoplasia (MEN) 2B is characterized by early development of aggressive medullary …
Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.
Wells SA Jr, Asa SL, Dralle H, Elisei R, Evans DB, Gagel RF, Lee N, Machens A, Moley JF, Pacini F, Raue F, Frank-Raue K, Robinson B, Rosenthal MS, Santoro M, Schlumberger M, Shah M, Waguespack SG; American Thyroid Association Guidelines Task Force on Medullary Thyroid Carcinoma. Wells SA Jr, et al. Thyroid. 2015 Jun;25(6):567-610. doi: 10.1089/thy.2014.0335. Thyroid. 2015. PMID: 25810047 Free PMC article. Review.
Prophylactic neck surgery for second-generation multiple endocrine neoplasia type 2B.
Machens A, Lorenz K, Weber F, Dralle H. Machens A, et al. Eur J Surg Oncol. 2021 Apr;47(4):924-927. doi: 10.1016/j.ejso.2020.11.006. Epub 2020 Nov 13. Eur J Surg Oncol. 2021. PMID: 33223415
There is no evidence-based guidance on the extent of prophylactic neck surgery for second-generation multiple endocrine neoplasia type 2B (MEN 2B), a newly emerging entity in the molecular era. In this investigation of MEN 2B child …
There is no evidence-based guidance on the extent of prophylactic neck surgery for second-generation multiple endocrine neo
Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.
Lee NC, Norton JA. Lee NC, et al. Surg Oncol. 2000 Nov;9(3):111-8. doi: 10.1016/s0960-7404(00)00038-4. Surg Oncol. 2000. PMID: 11356339 Review.
Multiple endocrine neoplasia (MEN) type 2B is a heritable endocrine disorder characterized by medullary thyroid carcinoma (MTC), pheochromocytoma, multiple mucosal neuromas, and a marfanoid habitus. ...The disease is inherited in a
Multiple endocrine neoplasia (MEN) type 2B is a heritable endocrine disorder characterized by medu
Molecular Diagnosis and Treatment of Multiple Endocrine Neoplasia Type 2B in Ethnic Han Chinese.
Zhang ZW, Guo X, Qi XP. Zhang ZW, et al. Endocr Metab Immune Disord Drug Targets. 2021;21(3):534-543. doi: 10.2174/1871530320666200910112230. Endocr Metab Immune Disord Drug Targets. 2021. PMID: 32914730
BACKGROUND: Multiple endocrine neoplasia type 2B (MEN 2B) is mainly caused by M918T RET germline mutation, and characterized by medullary thyroid carcinoma (MTC), pheochromocytoma (PHEO) and non-endocrine features. ...Recognition o …
BACKGROUND: Multiple endocrine neoplasia type 2B (MEN 2B) is mainly caused by M918T RET germline m …
Multiple endocrine neoplasias type 2B and RET proto-oncogene.
Martucciello G, Lerone M, Bricco L, Tonini GP, Lombardi L, Del Rossi CG, Bernasconi S. Martucciello G, et al. Ital J Pediatr. 2012 Mar 19;38:9. doi: 10.1186/1824-7288-38-9. Ital J Pediatr. 2012. PMID: 22429913 Free PMC article. Review.
Multiple Endocrine Neoplasia type 2B (MEN 2B) is an autosomal dominant complex oncologic neurocristopathy including medullary thyroid carcinoma, pheochromocytoma, gastrointestinal disorders, marphanoid face, and mucosal multiple ga
Multiple Endocrine Neoplasia type 2B (MEN 2B) is an autosomal dominant complex oncologic neurocris
915 results