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Page 1
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 biology …
Multiple endocrine neoplasia type 1 (MEN1), a rare tumor syndrome that is inherited in an autosomal domin …
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 …
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 dominant in …
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 of prima …
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 …
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) organ m …
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 …
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 particularly …
About 10% of pNETs arise within endocrine tumor syndromes, such as Multiple Endocrine Neoplasia type 1 (M …
Multiple endocrine neoplasia type 1 revealed by a hip pathologic fracture.
Slouma M, Abbes M, Dhahri R, Litaiem N, Gueddiche N, Mansouri N, Msekni I, Gharsallah I, Metoui L, Louzir B. Slouma M, et al. Clin Rheumatol. 2021 Feb;40(2):775-782. doi: 10.1007/s10067-020-05281-3. Epub 2020 Jul 14. Clin Rheumatol. 2021. PMID: 32666178 Review.
Multiple endocrine neoplasia type 1 is a rare autosomal inherited syndrome that affects a variety of endocrine tissues such as the parathyroid, endocrine pancreas, and anterior pituitary. ...A literature review was conducted by searching PubMed …
Multiple endocrine neoplasia type 1 is a rare autosomal inherited syndrome that affects a variety of endo …
Multiple Endocrine Neoplasia Type 1 Syndrome Pancreatic Neuroendocrine Tumor Genotype/Phenotype: Is There Any Advance on Predicting or Preventing?
Ramamoorthy B, Nilubol N. Ramamoorthy B, et al. Surg Oncol Clin N Am. 2023 Apr;32(2):315-325. doi: 10.1016/j.soc.2022.10.008. Surg Oncol Clin N Am. 2023. PMID: 36925188 Free PMC article. Review.
Multiple endocrine neoplasia type 1 syndrome (MEN1) is a disease caused by mutations in the MEN1 tumor suppressor gene leading to hyperparathyroidism, pituitary adenomas, and entero-pancreatic neuroendocrine tumors. ...
Multiple endocrine neoplasia type 1 syndrome (MEN1) is a disease caused by mutations in the MEN1 tumor su …
3,078 results