Pancreatic neuroendocrine tumors (PNETs) are frequent and can be non-functional (NF) in
patients with multiple endocrine neoplasia type 1 (MEN1). Their identification is of clinical …

Multiple endocrine neoplasia type 1 (MEN1) is inherited as an autosomal dominant disorder.
1, 2 It has a prevalence of 2 to 3 per 100,000 3 and is reported to be present in 0.22% to …

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 …

Objective: Little data are available on the natural history of untreated multiple endocrine
neoplasia type 1 (MEN-1). These data are essential in deciding treatment that may carry …

Zollinger-Ellison syndrome (ZES) is characterized classically by peptic ulcer, diarrhea, and
gastric acid hypersecretion related to gastrin producing tumor (s)[1] usually originating in the …

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

In 1982, a prospective study was initiated of 52 consecutive patients with proven Zollinger-
Ellison syndrome (ZES), involving surgical exploration with the goal of removing the …

Background Pancreatic tumours are common in patients with multiple endocrine neoplasia
type 1 (MEN1), and close surveillance is needed to detect pancreatic lesions at an early …

Objective Effect of genetic screening on outcome in multiple endocrine neoplasia type 1
(MEN1) remains unclear. Expression of MEN1 is described using currently available …

The lethality of the endocrine tumors associated with multiple endocrine neoplasia type I
(MEN-I), particularly the pancreatic islet cell tumors, has been controversial. We evaluated …