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 …

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 …

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

Objective: To report long-term follow-up of patients with multiple endocrine neoplasia type 1
(MEN1) and nonfunctioning pancreatic neuroendocrine tumors (NF-PET). Background …

Gastrinomas are neuroendocrine neoplasms (NENs), that occur primarily in the duodenum
and pancreas, which ectopically secrete gastrin, resulting in the Zollinger-Ellison syndrome …

Background The optimal surgical strategy for pancreatic neuroendocrine tumors (PNETs) is
unknown. However, current guidelines recommend a watch-and-wait strategy for small …

The relationship between surgical treatments and medical treatments in the various
management aspects of the Zollinger-Ellison syndrome (ZES) has taken many forms. In …

This guideline was created for the first time and is intended as a practical aid for the
diagnosis and therapy of neuroendocrine tumors. The aim is to represent the current state of …

Mutations of the multiple endocrine neoplasia type 1 (MEN1) gene lead to loss of function of
its protein product menin. In keeping with its tumor suppressor function in endocrine tissues …

Approximately 15–20% of breast cancers (BC) show either membrane overexpression of
ErbB-2 (MErbB-2), a member of the ErbBs family of receptor tyrosine kinases, or ERBB2 …