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P H Kann, E Balakina, D Ivan, D K Bartsch, S Meyer, K-J Klose, Th Behr, and P Langer

Clinical Endocrinology and Metabolism 89 1694 –1697. Kann PH , Kann B, Fassbender WJ, Forst T, Bartsch DK, Langer P 2006 Small neuroendocrine pancreatic tumors in multiple endocrine neoplasia type 1 (MEN1): least

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C R C Pieterman, E B Conemans, K M A Dreijerink, J M de Laat, H Th M Timmers, M R Vriens, and G D Valk

Introduction Thoracic and duodenopancreatic neuroendocrine tumors (dpNETs) can occur either sporadically or as a manifestation of an inherited syndrome, most importantly the multiple endocrine neoplasia type 1 (MEN1) syndrome. This is an autosomal

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Elizabeth Grubbs, Daniel Halperin, Steven G Waguespack, and Robert F Gagel

Overview The multiple endocrine neoplasia syndromes are a varied group of disorders that include multiple endocrine neoplasia types 1 and 2 (MEN 1, MEN 2), von Hippel-Lindau (VHL) disease , Carney complex (CC), hereditary pheochromocytoma

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Jerena Manoharan, Max B Albers, and Detlef K Bartsch

Okumura T Shioyama Y Kiyoshima M Asato Y Saito H Iijima T Amemiya R Nagai H 2008 FDG PET/CT findings of thymic carcinoid and bronchial carcinoid in a patient with multiple neuroendocrine neoplasia type1 . Clinical Nuclear

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S M Sadowski, G Cadiot, E Dansin, P Goudet, and F Triponez

Apitzsch JC Walthers EM Fink L Fendrich V Slater EP Waldmann J Anlauf M 2016 Bronchopulmonary neuroendocrine neoplasms and their precursor lesions in multiple endocrine neoplasia type 1 . Neuroendocrinology 103 240 – 247

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Yulong Li and William F Simonds

hyperparathyroidism and including endocrine tumors with malignant potential Multiple endocrine neoplasia type 1 syndrome MEN1 Loss of function Malignant duodenopancreatic neuroendocrine tumor; thymic and bronchial neuroendocrine tumors Multiple

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Rachel S van Leeuwaarde, Joanne M de Laat, Carolina R C Pieterman, Koen Dreijerink, Menno R Vriens, and Gerlof D Valk

Introduction Multiple endocrine neoplasia type 1 (MEN1) (OMIM 131100) is a rare autosomal inherited disorder associated with a high risk for patients to simultaneously develop tumors of the parathyroid glands, duodenopancreatic neuroendocrine

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Rami Alrezk, Fady Hannah-Shmouni, and Constantine A Stratakis

Introduction Among the multiple endocrine neoplasia (MEN) syndromes, the most frequent is type 1 or MEN1 (OMIM #131100). MEN1 is characterized by primary hyperparathyroidism (PHPT) due to parathyroid gland hyperplasia, and functional or

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Zijie Feng, Jian Ma, and Xianxin Hua

Introduction In recent years, prevalence of neuroendocrine tumors is increasing ( Jiao et al. 2011 ), and the multiple endocrine neoplasia type 1 (MEN1) gene, which encodes protein menin, is genetically well characterized for its function in

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Simona Grozinsky-Glasberg, Kate E Lines, Shani Avniel-Polak, Chas Bountra, and Rajesh V Thakker

neuroendocrine neoplasms; PRL, prolactin; RET, rearranged during transfection gene; TSH, thyroid stimulating hormone; VIPomas, vasointestinal polypeptide secreting tumours. Multiple endocrine neoplasia type 1 (MEN1, Wermer's syndrome) MEN1 was