Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1964 1
1969 1
1972 1
1973 1
1974 1
1975 2
1976 6
1977 5
1978 6
1979 5
1980 1
1981 7
1982 4
1983 14
1984 17
1985 19
1986 16
1987 26
1988 14
1989 36
1990 22
1991 27
1992 37
1993 31
1994 33
1995 37
1996 50
1997 35
1998 43
1999 47
2000 56
2001 39
2002 47
2003 41
2004 45
2005 58
2006 67
2007 51
2008 59
2009 48
2010 55
2011 48
2012 80
2013 62
2014 54
2015 65
2016 62
2017 66
2018 60
2019 57
2020 79
2021 71
2022 61
2023 52
2024 10

Text availability

Article attribute

Article type

Publication date

Search Results

1,783 results

Results by year

Filters applied: . Clear all
Page 1
Multiple endocrine neoplasia: an update.
McDonnell JE, Gild ML, Clifton-Bligh RJ, Robinson BG. McDonnell JE, et al. Intern Med J. 2019 Aug;49(8):954-961. doi: 10.1111/imj.14394. Intern Med J. 2019. PMID: 31387156 Review.
The multiple endocrine neoplasia (MEN) syndromes include MEN1, MEN2 (formerly MEN2A), MEN3 (formerly MEN2B) and the recently identified MEN4. ...
The multiple endocrine neoplasia (MEN) syndromes include MEN1, MEN2 (formerly MEN2A), MEN3 (formerly MEN2B) and the rec …
Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1).
Thakker RV, Newey PJ, Walls GV, Bilezikian J, Dralle H, Ebeling PR, Melmed S, Sakurai A, Tonelli F, Brandi ML; Endocrine Society. Thakker RV, et al. J Clin Endocrinol Metab. 2012 Sep;97(9):2990-3011. doi: 10.1210/jc.2012-1230. Epub 2012 Jun 20. J Clin Endocrinol Metab. 2012. PMID: 22723327 Review.
OBJECTIVE: The aim was to provide guidelines for evaluation, treatment, and genetic testing for multiple endocrine neoplasia type 1 (MEN1). PARTICIPANTS: The group, which comprised 10 experts, including physicians, surgeons, and geneticists from international …
OBJECTIVE: The aim was to provide guidelines for evaluation, treatment, and genetic testing for multiple endocrine neoplasi …
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 during Transfection ( …
Multiple endocrine neoplasias are rare hereditary syndromes some of them with malignant potential. Multiple endocrine neopl …
Update on the clinical management of multiple endocrine neoplasia type 1.
Pieterman CRC, Valk GD. Pieterman CRC, et al. Clin Endocrinol (Oxf). 2022 Oct;97(4):409-423. doi: 10.1111/cen.14727. Epub 2022 Apr 1. Clin Endocrinol (Oxf). 2022. PMID: 35319130 Free PMC article. Review.
This review provides an overview of novel insights in the clinical management of patients with Multiple Endocrine Neoplasia Type 1, focusing on the last decade since the last update of the MEN1 guidelines. ...
This review provides an overview of novel insights in the clinical management of patients with Multiple Endocrine Neoplasia …
Dermal hyperneury.
Marušić Z, Korša L, Calonje E. Marušić Z, et al. Clin Dermatol. 2021 Mar-Apr;39(2):291-294. doi: 10.1016/j.clindermatol.2020.10.008. Epub 2020 Oct 16. Clin Dermatol. 2021. PMID: 34272024
Clinically, it can present with or without visible lesions, within a syndrome or sporadically, and in solitary or multiple fashion. The syndromes most commonly associated with DN include multiple endocrine neoplasia 2B and 2A, neurofibromatosis type II, and C …
Clinically, it can present with or without visible lesions, within a syndrome or sporadically, and in solitary or multiple fashion. The synd …
MENX.
Pellegata NS. Pellegata NS. Ann Endocrinol (Paris). 2012 Apr;73(2):65-70. doi: 10.1016/j.ando.2012.04.001. Epub 2012 Apr 25. Ann Endocrinol (Paris). 2012. PMID: 22542001 Review.
Multiple Endocrine Neoplasia: Genetics and Clinical Management.
Norton JA, Krampitz G, Jensen RT. Norton JA, et al. Surg Oncol Clin N Am. 2015 Oct;24(4):795-832. doi: 10.1016/j.soc.2015.06.008. Epub 2015 Jul 27. Surg Oncol Clin N Am. 2015. PMID: 26363542 Free PMC article. Review.
Early diagnosis of multiple endocrine neoplasia (MEN) syndromes is critical for optimal clinical outcomes; before the MEN syndromes can be diagnosed, they must be suspected. ...
Early diagnosis of multiple endocrine neoplasia (MEN) syndromes is critical for optimal clinical outcomes; before the M …
Multiple endocrine neoplasia.
Caruso DR, O'Dorisio TM, Mazzaferri EL. Caruso DR, et al. Curr Opin Oncol. 1991 Feb;3(1):103-8. doi: 10.1097/00001622-199102000-00015. Curr Opin Oncol. 1991. PMID: 1675123 Review.
The multiple endocrine neoplasia (MEN) syndromes are well-defined disorders characterized by familial inheritance of specific endocrine tumors. ...
The multiple endocrine neoplasia (MEN) syndromes are well-defined disorders characterized by familial inheritance of sp …
Update on multiple endocrine neoplasia Type 1 and 2.
Al-Salameh A, Baudry C, Cohen R. Al-Salameh A, et al. Presse Med. 2018 Sep;47(9):722-731. doi: 10.1016/j.lpm.2018.03.005. Epub 2018 Jun 13. Presse Med. 2018. PMID: 29909163 Review.
Multiple endocrine neoplasia type 1 is a rare genetic syndrome, characterized by the co-occurrence, in the same individual or in related individuals of the same family, of hyperparathyroidism, duodenopancraetic neuroendocrine tumors, pituitary adenomas, adren …
Multiple endocrine neoplasia type 1 is a rare genetic syndrome, characterized by the co-occurrence, in the same individ …
Multiple endocrine neoplasia type 1 (MEN-1) and neuroendocrine neoplasms (NENs).
Effraimidis G, Knigge U, Rossing M, Oturai P, Rasmussen ÅK, Feldt-Rasmussen U. Effraimidis G, et al. Semin Cancer Biol. 2022 Feb;79:141-162. doi: 10.1016/j.semcancer.2021.04.011. Epub 2021 Apr 24. Semin Cancer Biol. 2022. PMID: 33905872 Review.
The increased incidence is mainly due to increased awareness and improved detection methods both in the majority of sporadic NENs (non-inherited), but also the inherited groups of neoplasms appearing in at least ten genetic syndromes. The most important one is multiple …
The increased incidence is mainly due to increased awareness and improved detection methods both in the majority of sporadic NENs (non-inher …
1,783 results