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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 131
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 97
2019 98
2020 111
2021 101
2022 125
2023 107
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2026 71

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3,171 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 Free article. 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.
Manoharan J, Albers MB, Rinke A, Adelmeyer J, Görlach J, Bartsch DK. Manoharan J, et al. Dtsch Arztebl Int. 2024 Aug 9;121(16):527-533. doi: 10.3238/arztebl.m2024.0094. Dtsch Arztebl Int. 2024. PMID: 38863299 Free PMC article. Review.
BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a rare genetic disease of autosomal dominant inheritance, with an estimated prevalence of 3-20/100 000. ...
BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a rare genetic disease of autosomal domi …
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
Pancreatic Neuroendocrine Neoplasms in Multiple Endocrine Neoplasia Type 1.
Marini F, Giusti F, Tonelli F, Brandi ML. Marini F, et al. Int J Mol Sci. 2021 Apr 14;22(8):4041. doi: 10.3390/ijms22084041. Int J Mol Sci. 2021. PMID: 33919851 Free PMC article. Review.
About 10% of pNETs arise within endocrine tumor syndromes, such as Multiple Endocrine Neoplasia type 1 (MEN1). pNETs affect 30-80% of MEN1 patients, manifesting prevalently as multiple microadenomas. pNETs in patients with MEN1 are partic …
About 10% of pNETs arise within endocrine tumor syndromes, such as Multiple Endocrine Neoplasia type 1 ( …
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
Expressions of Cushing's syndrome in multiple endocrine neoplasia type 1.
Simonds WF. Simonds WF. Front Endocrinol (Lausanne). 2023 Jun 20;14:1183297. doi: 10.3389/fendo.2023.1183297. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37409236 Free PMC article. Review.
Cushing's syndrome (CS) resulting from endogenous hypercortisolism can be sporadic or can occur in the context of familial disease because of pituitary or extra-pituitary neuroendocrine tumors. Multiple endocrine neoplasia type 1 (MEN1) i …
Cushing's syndrome (CS) resulting from endogenous hypercortisolism can be sporadic or can occur in the context of familial disease because o …
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 and Zollinger-Ellison syndrome: a prospective study of 107 cases and comparison with 1009 cases from the literature.
Gibril F, Schumann M, Pace A, Jensen RT. Gibril F, et al. Medicine (Baltimore). 2004 Jan;83(1):43-83. doi: 10.1097/01.md.0000112297.72510.32. Medicine (Baltimore). 2004. PMID: 14747767 Free article. Review.
In patients with multiple endocrine neoplasia type 1 (MEN1), the most common functional pancreatic endocrine tumor (PET) syndrome is Zollinger-Ellison syndrome (ZES). ...
In patients with multiple endocrine neoplasia type 1 (MEN1), the most common functional pancreatic …
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
Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene.
Lemos MC, Thakker RV. Lemos MC, et al. Hum Mutat. 2008 Jan;29(1):22-32. doi: 10.1002/humu.20605. Hum Mutat. 2008. PMID: 17879353 Review.
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the occurrence of tumors of the parathyroids, pancreas, and anterior pituitary. ...
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the
3,171 results