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

Year Number of Results
1952 1
1953 3
1954 1
1955 1
1956 1
1957 1
1958 2
1959 1
1960 3
1961 1
1962 2
1964 4
1965 3
1974 1
1978 1
1980 3
1981 1
1982 2
1983 3
1984 5
1985 1
1986 9
1987 6
1988 7
1989 15
1990 17
1991 20
1992 34
1993 25
1994 55
1995 62
1996 66
1997 97
1998 114
1999 115
2000 130
2001 100
2002 91
2003 69
2004 93
2005 84
2006 95
2007 107
2008 97
2009 103
2010 97
2011 101
2012 148
2013 96
2014 84
2015 95
2016 97
2017 118
2018 98
2019 97
2020 111
2021 101
2022 127
2023 108
2024 60

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2,980 results

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Page 1
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 geneticis …
OBJECTIVE: The aim was to provide guidelines for evaluation, treatment, and genetic testing for multiple endocrine neoplasi
Multiple Endocrine Neoplasia Type 1: Latest Insights.
Brandi ML, Agarwal SK, Perrier ND, Lines KE, Valk GD, Thakker RV. Brandi ML, et al. Endocr Rev. 2021 Mar 15;42(2):133-170. doi: 10.1210/endrev/bnaa031. Endocr Rev. 2021. PMID: 33249439 Free PMC article. Review.
Multiple endocrine neoplasia type 1 (MEN1), a rare tumor syndrome that is inherited in an autosomal dominant pattern, is continuing to raise great interest for endocrinology, gastroenterology, surgery, radiology, genetics, and molecular b
Multiple endocrine neoplasia type 1 (MEN1), a rare tumor syndrome that is inherited in an autosoma
Clinical aspects of multiple endocrine neoplasia type 1.
Al-Salameh A, Cadiot G, Calender A, Goudet P, Chanson P. Al-Salameh A, et al. Nat Rev Endocrinol. 2021 Apr;17(4):207-224. doi: 10.1038/s41574-021-00468-3. Epub 2021 Feb 9. Nat Rev Endocrinol. 2021. PMID: 33564173 Review.
Multiple endocrine neoplasia type 1 (MEN1) is a rare syndrome characterized by the co-occurrence of primary hyperparathyroidism, duodenopancreatic neuroendocrine tumours (NETs) and/or pituitary adenomas. ...
Multiple endocrine neoplasia type 1 (MEN1) is a rare syndrome characterized by the co-occurrence o
Multiple Endocrine Neoplasia Type 1 and the Pancreas: Diagnosis and Treatment of Functioning and Non-Functioning Pancreatic and Duodenal Neuroendocrine Neoplasia within the MEN1 Syndrome - An International Consensus Statement.
Niederle B, Selberherr A, Bartsch DK, Brandi ML, Doherty GM, Falconi M, Goudet P, Halfdanarson TR, Ito T, Jensen RT, Larghi A, Lee L, Öberg K, Pavel M, Perren A, Sadowski SM, Tonelli F, Triponez F, Valk GD, O'Toole D, Scott-Coombes D, Thakker RV, Thompson GB, Treglia G, Wiedenmann B. Niederle B, et al. Neuroendocrinology. 2021;111(7):609-630. doi: 10.1159/000511791. Epub 2020 Sep 24. Neuroendocrinology. 2021. PMID: 32971521 Free article. Review.
The better understanding of the biological behavior of multiple endocrine neoplasia type 1 (MEN1) organ manifestations and the increase in clinical experience warrant a revision of previously published guidelines. ...
The better understanding of the biological behavior of multiple endocrine neoplasia type 1 (MEN1) …
Causes of death and prognostic factors in multiple endocrine neoplasia type 1: a prospective study: comparison of 106 MEN1/Zollinger-Ellison syndrome patients with 1613 literature MEN1 patients with or without pancreatic endocrine tumors.
Ito T, Igarashi H, Uehara H, Berna MJ, Jensen RT. Ito T, et al. Medicine (Baltimore). 2013 May;92(3):135-181. doi: 10.1097/MD.0b013e3182954af1. Medicine (Baltimore). 2013. PMID: 23645327 Free PMC article.
Multiple endocrine neoplasia type 1 (MEN1) is classically characterized by the development of functional or nonfunctional hyperplasia or tumors in endocrine tissues (parathyroid, pancreas, pituitary, adrenal). ...
Multiple endocrine neoplasia type 1 (MEN1) is classically characterized by the development of func
Multiple endocrine neoplasia type 1 (MEN1).
Carroll RW. Carroll RW. Asia Pac J Clin Oncol. 2013 Dec;9(4):297-309. doi: 10.1111/ajco.12046. Epub 2012 Dec 26. Asia Pac J Clin Oncol. 2013. PMID: 23279763 Review.
Multiple endocrine neoplasia type 1 (MEN1) is inherited in an autosomal dominant fashion and predisposes to the development of hyperplastic or neoplastic changes in the parathyroid and pituitary glands and the endocrine pancreas, along wi
Multiple endocrine neoplasia type 1 (MEN1) is inherited in an autosomal dominant fashion and predi
Multiple endocrine neoplasia type 1 (MEN1).
Thakker RV. Thakker RV. Best Pract Res Clin Endocrinol Metab. 2010 Jun;24(3):355-70. doi: 10.1016/j.beem.2010.07.003. Best Pract Res Clin Endocrinol Metab. 2010. PMID: 20833329 Review.
Multiple Endocrine Neoplasia type 1 (MEN1) is an autosomal-dominant disorder characterised by the occurrence of tumours of the parathyroids, pancreas and anterior pituitary. ...
Multiple Endocrine Neoplasia type 1 (MEN1) is an autosomal-dominant disorder characterised by the
Diagnosis and treatment of multiple endocrine neoplasia type 1 (MEN1).
Gaztambide S, Vazquez F, Castaño L. Gaztambide S, et al. Minerva Endocrinol. 2013 Mar;38(1):17-28. Minerva Endocrinol. 2013. PMID: 23435440 Review.
Multiple endocrine neoplasia type 1 (MEN1; formerly known as Wermer syndrome) is a rare disorder characterized by the combined occurrence of two or more tumors involving parathyroid, pancreatic islets and anterior pituitary glands; some o
Multiple endocrine neoplasia type 1 (MEN1; formerly known as Wermer syndrome) is a rare disorder c
2,980 results