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 …

Multiple endocrine neoplasia type I (MEN‐I) is an autosomal dominant disorder
characterized by endocrinopathies involving the anterior pituitary gland, parathyroid glands …

Pancreaticoduodenal tumors develop in a majority of patients with multiple endocrine
neoplasia type 1 (MEN 1) and have a pronounced effect on life expectancy as the principal …

Objective To determine the role of surgery in patients with Zollinger-Ellison syndrome (ZES)
and multiple endocrine neoplasia type 1 (MEN1) with either limited or advanced pancreatic …

The syndrome of multiple endocrine neoplasia type 1 is an autosomal dominantly inherited
disease affecting several endocrine organs. The affected organs include the pituitary, the …

Multiple endocrine neoplasia type 1 (MEN-1) is an interesting genetic syndrome of
polyendocrinopathies. Clinical knowledge about MEN-1 is essential as it appears to be …

Objective: The aim was to provide guidelines for evaluation, treatment, and genetic testing
for multiple endocrine neoplasia type 1 (MEN1). Participants: The group, which comprised …

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder
characterized by the combined occurrence of parathyroid, pancreatic islet and anterior …

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 …