We briefly review the characteristics of pituitary tumors associated with multiple endocrine
neoplasia type 1. Multiple endocrine neoplasia type 1 is an autosomal-dominant disorder …

Patients affected by the multiple endocrine neoplasia type I syndrome (MEN1) display a high
incidence of pituitary adenomas, though it is still unknown whether these pituitary tumors …

Multiple endocrine neoplasia type I (MEN-1) is an autosomal dominant syndrome
associated with anterior pituitary, parathyroid, and enteropancreatic endocrine tumors as …

Abstract Multiple endocrine neoplasia Type 1 (MENl) is a rare hereditary tumor syndrome
predisposingto tum or development in severalendocrine organs. Its major manifestations …

Multiple endocrine neoplasia type 1 (MEN 1) is associated with parathyroid,
enteropancreatic, pituitary, and other tumors. The MEN1 gene, a tumor suppressor, is …

Disease characteristics. Multiple endocrine neoplasia type 1 (MEN1) syndrome includes a
varying combination of more than 20 endocrine and non-endocrine tumors. Endocrine …

Multiple Endocrine Neoplasia type 1 (MEN1) is a rare hereditary endocrine cancer
syndrome characterized primarily by tumors of the parathyroid glands (95% of cases) …

Background. In contrast with multiple endocrine neoplasia type 2, malignancies are of minor
importance in multiple endocrine neoplasia type 1 (MEN 1) syndrome. Methods. The data for …

M ultiple endocrine neoplasia type 1 (MEN1) is inherited in an autosomal dominant fashion
and predisposes to the development of hyperplastic or neoplastic changes in the …

OBJECTIVE Multiple endocrine neoplasia type 1 (MEN1) is a rare, autosomal-dominant
tumor disorder characterized by the development of pituitary tumors and other endocrine …