Multiple endocrine neoplasia (MEN) is characterized by the occurrence of tumors involving
two or more endocrine glands within a single patient. Four major forms of MEN, which are …

This is a consensus statement from an international group, mostly of clinical
endocrinologists. MEN1 and MEN2 are hereditary cancer syndromes. The commonest …

This volume covers tumors of the pituary, the thyroid and parathyroid, the adrenal gland, the
endocrine pancreas, and inherited tumor syndromes. Each entity is extensively discussed …

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder
characterized by the occurrence of tumors of the parathyroids, pancreas, and anterior …

Multiple endocrine neoplasia (MEN) refers to a group of autosomal dominant disorders with
generally high penetrance that lead to the development of a wide spectrum of endocrine and …

To date, data on pituitary adenomas in MEN type 1 (MEN1) still have to be evaluated. We
analyzed the data of a large series of 324 MEN1 patients from a French and Belgian …

The protein menin is encoded by the MEN1 gene, which is mutated in patients with multiple
endocrine neoplasia type 1 (MEN1) syndrome. Although menin acts as a tumor suppressor …

Background The natural history of multiple endocrine neoplasia type 1 (MEN1) is known
through single-institution or single-family studies. We aimed to analyze the risk factors and …

MEN1 is a tumor suppressor gene that encodes a 610 amino acid nuclear protein (menin) of
previously unknown function. Using a yeast two-hybrid screen with menin as the bait, we …

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant cancer syndrome,
characterized primarily by multiple tumors in the parathyroid glands, endocrine pancreas …