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 …

Six multiple endocrine neoplasia (MEN) syndromes have received a level of attention that
might seem disproportionate to their low prevalence. The attention has been given because …

Context: Familial pituitary adenomas occur rarely in the absence of multiple endocrine
neoplasia type 1 (MEN1) and Carney complex (CNC). Objective: Our objective was to …

Stratakis CA, Tichomirowa MA, Boikos S, Azevedo MF, Lodish M, Martari M, Verma S, Daly
AF, Raygada M, Keil MF, Papademetriou J, Drori‐Herishanu L, Horvath A, Tsang KM …

Somatostatin-producing neuroendocrine tumors (SOM-NETs) of the duodenum and
pancreas appear to be heterogeneous. To determine their clinicopathological profiles …

Pituitary adenomas occur in a familial setting in multiple endocrine neoplasia type 1 (MEN1)
and Carney's complex (CNC), which occur due to mutations in the genes MEN1 and …

The identification of the multiple endocrine neoplasia type 1 (MEN1) gene in 1997 has
shown that germline heterozygous mutations in the MEN1 gene located on chromosome …

Pancreatic neuroendocrine tumors (PanNENs) are rare sporadic cancers or develop as part
of hereditary syndromes. PanNENs can be both functioning and non-functioning based on …

Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant inherited tumor
syndrome, associated with parathyroid, pituitary, and gastro-entero-pancreatic (GEP) …

Abstract Approximately 5–10% of neuroendocrine tumors (NETs) of the
gastroenteropancreatic system (GEP) have a hereditary background. The known inherited …