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1978
2025

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Year Number of Results
1978 1
1979 1
1986 1
1988 1
1989 1
1990 2
1991 2
1992 2
1994 8
1995 16
1996 11
1997 16
1998 9
1999 6
2000 10
2001 6
2002 4
2003 6
2004 11
2005 16
2006 10
2007 9
2008 7
2009 5
2010 4
2011 1
2012 5
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2015 9
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2017 7
2018 3
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2020 5
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2023 2
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2025 1

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216 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
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.
Multiple Endocrine Neoplasia Type 1, Type 2A, and Type 2B.
Greenberg LA. Greenberg LA. Prim Care. 2024 Sep;51(3):483-494. doi: 10.1016/j.pop.2024.03.006. Epub 2024 May 23. Prim Care. 2024. PMID: 39067973 Review.
Multiple endocrine neoplasia type 1 is a rare genetic neuroendocrine syndrome caused by over 1500 different germline mutations. ...Multiple endocrine neoplasia type 2A (MEN2A) and Multiple endocrine neoplasi
Multiple endocrine neoplasia type 1 is a rare genetic neuroendocrine syndrome caused by over 1500 different germ
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 …
Rare syndromes.
Jabbour SA, Davidovici BB, Wolf R. Jabbour SA, et al. Clin Dermatol. 2006 Jul-Aug;24(4):299-316. doi: 10.1016/j.clindermatol.2006.04.005. Clin Dermatol. 2006. PMID: 16828412 Review.
In some patients with multiple endocrine neoplasia type 2A, cutaneous lichen amyloidosis may also be present. Multiple endocrine neoplasia type 2B is characterized by medullary thyroid cancer and pheochromocytoma but …
In some patients with multiple endocrine neoplasia type 2A, cutaneous lichen amyloidosis may also be present. …
Patient quality of life and prognosis in multiple endocrine neoplasia type 2.
Grey J, Winter K. Grey J, et al. Endocr Relat Cancer. 2018 Feb;25(2):T69-T77. doi: 10.1530/ERC-17-0335. Epub 2017 Oct 24. Endocr Relat Cancer. 2018. PMID: 29066504 Review.
Multiple endocrine neoplasia type 2 (MEN2) refers to the autosomal-dominant neuroendocrine tumour syndromes, MEN type 2A (MEN2A) and MEN type 2B (MEN2B). ...In the absence, at the time of writing, of any large-scale research into q
Multiple endocrine neoplasia type 2 (MEN2) refers to the autosomal-dominant neuroendocrine tumour syndromes, MEN
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
A comprehensive review on MEN2B.
Castinetti F, Moley J, Mulligan L, Waguespack SG. Castinetti F, et al. Endocr Relat Cancer. 2018 Feb;25(2):T29-T39. doi: 10.1530/ERC-17-0209. Epub 2017 Jul 11. Endocr Relat Cancer. 2018. PMID: 28698189 Review.
MEN2B is a very rare autosomal dominant hereditary tumor syndrome associated with medullary thyroid carcinoma (MTC) in 100% cases, pheochromocytoma in 50% cases and multiple extra-endocrine features, many of which can be quite disabling. Only few data are available …
MEN2B is a very rare autosomal dominant hereditary tumor syndrome associated with medullary thyroid carcinoma (MTC) in 100% cases, pheochrom …
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 2b.
Carney JA, Sizemore GW, Hayles AB. Carney JA, et al. Pathobiol Annu. 1978;8:105-53. Pathobiol Annu. 1978. PMID: 364372 Review.
Multiple endocrine neoplasia, type 2b, is a disorder of unknown etiology with major involvement of the thyroid and adrenal glands, the autonomic nervous system, and connective tissue. ...We are aware of only 2 patients who, 5 years after thyroid
Multiple endocrine neoplasia, type 2b, is a disorder of unknown etiology with major involvement of the th
216 results