Pituitary adenomas in the setting of multiple endocrine neoplasia type 1: a single-institution experience

S Cohen-Cohen, DA Brown, BT Himes… - Journal of …, 2020 - thejns.org
OBJECTIVE Multiple endocrine neoplasia type 1 (MEN1) is a rare, autosomal-dominant
tumor disorder characterized by the development of pituitary tumors and other endocrine …

[引用][C] Insulinoma and prolactinoma in a young female: a variant of multiple endocrine neoplasia 1 (MEN-1)

MJT Cardino, FL Lantion-Ang - Phil J Intern Med, 2017

[HTML][HTML] Multiple Endocrine Neoplasia Type 1

G Singh, NJ Mulji, I Jialal - StatPearls [Internet], 2023 - ncbi.nlm.nih.gov
Multiple Endocrine Neoplasia Type 1 - StatPearls - NCBI Bookshelf US flag An official website
of the United States government Here's how you know NIH NLM Logo Access keys NCBI …

[HTML][HTML] Multiple endocrine neoplasia type 1 with a frameshift mutation in its gene accompanied by a giant cervical lipoma and multiple fatty deposits in the pancreas …

Y Fushimi, S Kamei, F Tatsumi, J Sanada… - BMC Endocrine …, 2021 - Springer
Background Multiple endocrine neoplasia type 1 (MEN1) is a syndrome characterized by
pituitary neoplasia, primary hyperparathyroidism and pancreatic endocrine tumor. Here we …

[HTML][HTML] Metastatic pancreatic gastrinoma, severe primary hyperparathyroidism, and adrenal cushing syndrome in a patient with multiple endocrine neoplasia type 1 …

FM de Oliveira, SS Maeda, MMS Marone… - AACE Clinical Case …, 2017 - Elsevier
Objective: Multiple endocrine neoplasia type 1 (MEN1) has an estimated incidence in the
general population of 0.01 to 2.5 cases per 1,000 individuals. Here we report on the case of …

Diagnosis by serendipity: Cushing syndrome attributable to cortisol-producing adrenal adenoma as the initial manifestation of multiple endocrine neoplasia type 1 due …

AS Alzahrani, N Al-Khaldi, Y Shi, RA Al-Rijjal, M Zou… - Endocrine Practice, 2008 - Elsevier
Objective To report a case that highlights the potential for Cushing syndrome to be the first
manifestation of multiple endocrine neoplasia type 1 (MEN 1) syndrome and to describe the …

[HTML][HTML] A case of familial multiple endocrine neoplasia type 1 with a novel mutation in the MEN1 gene

MJ Kim, EH Kim, MS Shin, JH Kim… - Endocrinology and …, 2011 - synapse.koreamed.org
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder
characterized by the occurrence of multiple tumors in the parathyroid gland, pancreatic islet …

Multiple endocrine neoplasia type 1 with suspicion of Zollinger Ellison syndrome in a family with history of renal stones and hypercalcemia in a limited resource setting …

K Hussain, J Nahar, F Abbas, J Nawar… - Oxford Medical Case …, 2022 - academic.oup.com
Multiple endocrine neoplasia type 1 (MEN 1) syndrome is a rare autosomal dominant
endocrine tumour syndrome, which can be diagnosed clinically based on family history and …

[PDF][PDF] An Indian family of multiple endocrine neoplasia type 1 (MEN1): molecular diagnosis, treatment and follow up

SR Shah, R Raghavan, DC Desai… - Indian Journal of …, 2008 - academia.edu
Background/Objective: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal,
dominant syndrome, characterized mainly by the combination of tumors involving the …

Diagnosis and surgical treatment of multiple endocrine neoplasia

G Zhou, WEI Yao, C Xi, X Jiang, X Li… - Chinese medical …, 2009 - journals.lww.com
Background Multiple endocrine neoplasia (MEN) is relatively rare. But more patients could
be found by detailed examination. We discuss the diagnosis and surgical treatment of MEN …