Results 31 to 40 of about 65,584 (272)
Multiple endocrine neoplasia type 1
Indian Journal of Endocrinology and Metabolism, 2012 Multiple endocrine neoplasia type 1 (MEN1) is characterized by the occurrence of parathyroid, pancreatic islet and anterior pituitary tumors. Some patients may also develop carcinoid tumors, adrenocortical tumors, facial angiofibromas, collagenomas, and ...
R V Thakker
doaj +1 more source
Multiple endocrine neoplasia type 2
Orphanet Journal of Rare Diseases, 2006 Multiple Endocrine Neoplasia Type 2 (MEN2) is a rare hereditary complex disorder characterized by the presence of medullary thyroid carcinoma (MTC), unilateral or bilateral pheochromocytoma (PHEO) and other hyperplasia and/or neoplasia of different ...
Luzi Ettore +6 more
doaj +1 more source
Multiple endocrine neoplasia type 2A
Kaohsiung Journal of Medical Sciences, 2012 Multiple endocrine neoplasia type 2A (MEN 2A) is an autosomal dominant inherited cancer syndrome that expresses nonendocrine and endocrine tumors.
Chiung-Tang Huang +2 more
doaj +1 more source
Multiple endocrine neoplasia type 1
Orphanet Journal of Rare Diseases, 2006 Multiple Endocrine Neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary cancer syndrome presented mostly by tumours of the parathyroids, endocrine pancreas and anterior pituitary, and characterised by a very high penetrance and an equal sex ...
Luzi Ettore +6 more
doaj +1 more source
Multiple endocrine neoplasia 1: a broad overview
Therapeutic Advances in Chronic Disease, 2021 This review article discusses the diagnoses and treatment of patients with multiple endocrine neoplasia type 1 (MEN 1). The most common tumors associated with MEN 1 are located in the pancreas, pituitary, and parathyroid glands.
Rachel Thompson, Christine S. Landry
doaj +1 more source
Genotype-phenotype correlation in multiple endocrine neoplasia type 2
Clinics, 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 +1 more source
Frontiers in Endocrinology, 2019 Multiple endocrine neoplasia type 1 (MEN1) is a rare hereditary tumor syndrome inherited in an autosomal dominant manner and characterized by a predisposition to a multitude of endocrine neoplasms primarily of parathyroid, enteropancreatic, and anterior ...
C. Kamilaris, C. Stratakis
semanticscholar +1 more source
Multiple endocrine neoplasia: the Chilean experience
Clinics, 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 +1 more source
Clinical case: multiple endocrine neoplasia type 1 (MEN 1)
Ожирение 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 +1 more source
Journal of Clinical Endocrinology and Metabolism, 2019 Context The clinical phenotype of multiple endocrine neoplasia type 4 (MEN4) is undefined due to a limited number of published cases. Knowledge on disease manifestation in MEN4 is essential for developing prevention programs and treatment.
A. Frederiksen +5 more
semanticscholar +1 more source