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 …

The better understanding of the biological behavior of multiple endocrine neoplasia type 1
(MEN1) organ manifestations and the increase in clinical experience warrant a revision of …

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

Pancreatic endocrine tumors (PETs) have long fascinated clini-cians, because some can
release biologically active hormones that cause distinct syndromes and provide important …

This review provides an overview of novel insights in the clinical management of patients
with Multiple Endocrine Neoplasia Type 1, focusing on the last decade since the last update …

Multiple endocrine neoplasia type 1 (MEN1) is classically characterized by the development
of functional or nonfunctional hyperplasia or tumors in endocrine tissues (parathyroid …

In patients with multiple endocrine neoplasia type 1 (MEN1), the most common functional
pancreatic endocrine tumor (PET) syndrome is Zollinger-Ellison syndrome (ZES). ZES has …

Objective: To analyze the penetrance and clinical course of isolated nonfunctioning tumors
of the pancreas (NFTP) in MEN 1 patients, and to propose a strategy for managing them …

Little is known of the natural history of thymic carcinoids in multiple endocrine neoplasia type
1 (MEN1). This is important because in 1993 they were identified as a frequent cause of …

Context: Guidelines advise lifelong radiological followup for asymptomatic pituitary
adenomas (PITs) because of the risk for growth and subsequent visual field defects. In the …