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3,060 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 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) …
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 …
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 …
Editorial: New insights into multiple endocrine neoplasia type 1.
Barlier A, Romanet P, Pellegata NS. Barlier A, et al. Front Endocrinol (Lausanne). 2023 Aug 11;14:1266148. doi: 10.3389/fendo.2023.1266148. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37635979 Free PMC article. No abstract available.
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: The Potential Role of microRNAs in the Management of the Syndrome.
Donati S, Ciuffi S, Marini F, Palmini G, Miglietta F, Aurilia C, Brandi ML. Donati S, et al. Int J Mol Sci. 2020 Oct 14;21(20):7592. doi: 10.3390/ijms21207592. Int J Mol Sci. 2020. PMID: 33066578 Free PMC article. Review.
Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited tumor syndrome, characterized by the development of multiple neuroendocrine tumors (NETs) in a single patient. ...
Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited tumor syndrome, characterized by th …
3,060 results