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Multiple endocrine neoplasia syndrome

open access: yesУкраїнський радіологічний та онкологічний журнал, 2021
Background. Multiple endocrine neoplasia type 1 is a rare inherited disease that combines heterogeneous autosomal inherited disorders, the pathogenesis of which is based on hyperplasia or tumor transformation of several neuro- endocrine glands.
М. В. Красносельський   +3 more
doaj   +4 more sources

Surgical treatment of pancreatic endocrine tumors in multiple endocrine neoplasia type 1

open access: yesClinics, 2012
Surgical approaches to pancreatic endocrine tumors associated with multiple endocrine neoplasia type 1 may differ greatly from those applied to sporadic pancreatic endocrine tumors.
Marcel Cerqueira Cesar Machado
doaj   +4 more sources

Multiple endocrine neoplasia: the Chilean experience

open access: yesClinics, 2012
Multiple endocrine neoplasia (MEN) types 1 and 2 are genetic diseases that are inherited as autosomal traits. The major clinical manifestations of multiple endocrine neoplasia type 1 include the so-called "3 P's": parathyroid, pituitary, and pancreatic ...
René E. Diaz, Nelson Wohllk
doaj   +2 more sources

Genotype-phenotype correlation in multiple endocrine neoplasia type 2

open access: yesClinics, 2012
Multiple endocrine neoplasia type 2 is an autosomal-dominant hereditary cancer syndrome caused by missense gain-of-function mutations of the rearranged during transfection proto-oncogene, which encodes the receptor tyrosine kinase, on chromosome 10.
Friedhelm Raue, Karin Frank-Raue
doaj   +2 more sources

Clinical case: multiple endocrine neoplasia type 1 (MEN 1)

open access: yesОжирение и метаболизм, 2012
Multiple endocrine neoplasia syndrome type 1 (MEN1, Wermer syndrome) – group o а heterogeneous inherited deseases, caused by hyperlasia or neoplasia of several endocrine glands.

doaj   +3 more sources

Multiple endocrine neoplasia

open access: yesMedicine, 2001
Multiple endocrine neoplasia (MEN) is characterized by the occurrence of tumours involving two or more endocrine glands; two major forms, referred to as MEN1 and MEN2, are recognized. MEN1 is characterized by parathyroid, pancreatic islet and anterior pituitary tumours, whilst MEN2 is characterized by medullary thyroid carcinoma (MTC) in association ...
Thakker, Rajesh, Thakker, RV
core   +6 more sources

Multiple endocrine neoplasia type 2 – solving the puzzle

open access: yesJournal of Family Medicine and Primary Care, 2023
Multiple endocrine neoplasia (MEN) are tumors that involve two or more endocrine glands. It can also involve other organs and tissues as well. Out of the four types of MEN type 2 is the most common.
Ajay K. Jha   +2 more
doaj   +2 more sources

Multimodality appearance of multiple endocrine neoplasia type 1: A case report

open access: yesRadiology Case Reports, 2019
Multiple endocrine neoplasia type 1 is a rare autosomal dominant disorder classically characterized by a predisposition to tumors of the parathyroid glands, anterior pituitary, and enteropancreatic endocrine cells.
John Monge, MD   +2 more
doaj   +2 more sources

Multiple Endocrine Neoplasia Syndromes from Genetic and Epigenetic Perspectives

open access: yesBiomarker Insights, 2018
Multiple endocrine neoplasia (MEN) syndromes are infrequent inherited disorders in which more than one endocrine glands develop noncancerous (benign) or cancerous (malignant) tumors or grow excessively without forming tumors.
Fatemeh Khatami, Seyed Mohammad Tavangar
doaj   +2 more sources

Multiple endocrine neoplasia type 2: achievements and current challenges

open access: yesClinics, 2012
Incremental advances in medical technology, such as the development of sensitive hormonal assays for routine clinical care, are the drivers of medical progress.
Andreas Machens, Henning Dralle
doaj   +2 more sources

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