I. Introduction F AMILIAL multiple endocrine endocrine neoplasia type I (FMENI) is a
complex hereditary disorder encompassing pancreatic and pituitary tumors and hyperplasia …

Endocrine pancreatic tumors are rare neoplasms that occur sporadically or as part of a
multiple endocrine neoplasia type 1 (MEN1) syndrome. Germ-line mutations of the MEN1 …

Thompson NW (University of Michigan, Ann Arbor, MI, USA). Current concepts in the
surgical management of multiple endocrine neoplasia type 1 pancreatic-duodenal disease …

Objective: We sought to develop a comprehensive program for clinical genetic testing in a
large group of extended families with multiple endocrine neoplasia type 1 (MEN 1), with the …

OBJECTIVE Multiple endocrine neoplasia type 1 (MEN1) is a familial tumour syndrome of
endocrine tumours involving parathyroids, anterior pituitary and enteropancreatic …

Abstract Multiple endocrine neoplasia‐1 (MEN‐1) is an autosomal dominant inherited
syndrome that occurs due to inactivating mutations of the MEN1 gene locus, coding for a …

Prospective Endoscopic Ultrasonographic Evaluation of the Fr... : Official journal of the
American College of Gastroenterology | ACG Prospective Endoscopic Ultrasonographic …

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder
characterized by tumors of the parathyroids, pancreatic islets, and anterior pituitary. The …

More than 50% of patients with typical MEN-2B have a de novo M918T germline mutation of
the RET protooncogene. However, even in typical MEN-2B, extrathyroidal manifestations of …

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 …