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 …

MEN1 is a syndrome of parathyroid adenomas, gastrinomas, prolactinomas, and other
endocrine tumors. Collagenomas and facial angiofibromas are newly recognized but …

Multiple endocrine neoplasia type 1 (MEN1) provides a prime example of how a rare
disease can advance our understanding of basic cell biology, neoplasia and common …

Combined clinical and laboratory investigations of multiple endocrine neoplasia type 1
(MEN1) have resulted in an increased understanding of this disorder which may be inherited …

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 type 1 (MEN1) is characterized by the combined occurrence of
tumors of the parathyroids, pancreatic islets, and anterior pituitary. In addition, some patients …

Multiple endocrine neoplasia type 1 (MEN1), a rare tumor syndrome that is inherited in an
autosomal dominant pattern, is continuing to raise great interest for endocrinology …

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 …

Multiple Endocrine Neoplasia type 1 (MEN1) is an autosomal-dominant disorder
characterised by the occurrence of tumours of the parathyroids, pancreas and anterior …

Multiple endocrine neoplasia type 1 (MEN1), among all syndromes, causes tumors in the
highest number of tissue types. Most of the tumors are hormone producing (eg, parathyroid …