… endocrine neoplasia type 1 (MEN1) is one of the most well-known hereditary endocrine
syndromes, first … However, in patients with gastrinomas the incidence of MEN1 is 16−38%, which …

… Multiple endocrine neoplasia type 1 (MEN1) is a rare syndrome … neuroendocrine tumours
(NETs) and/or pituitary adenomas. MEN1 can predispose patients to other endocrine and non-…

… Each MEN syndrome exhibits different combinations of … and molecular genetics of each
endocrine tumour syndrome. … occult metastatic disease is more prevalent in MEN1 patients …

… molecular details of the MEN1 and MEN4 syndromes. The gene causing … MEN1 associated
endocrine tumor is generally similar to that for the respective tumors occurring in non-MEN1 …

… Lipomas, facial angiofibromas, and collagenomas are also common and can be useful in
visually identifying the MEN1 syndrome in patients with otherwise equivocal features. …

… type 1 (MEN-1), which is also referred to as Wermer's syndrome. In … with MEN-1.96, 165 In
MEN type 2 (MEN-2), which is also called Sipple's syndrome, 136 medullary thyroid carcinoma …

… Gastric neuroendocrine neoplasms occurring in MEN1 patients are related to … -Ellison
syndrome and complicated genetic changes, which are called gastric neuroendocrine neoplasms …

… Immunostaining for basic FGF in the gastric endocrine cells of a patient with MEN1 syndrome
and ZES. The peptide is expressed by both intraglandular cells showing hyperplastic pre- …

… MEN1 syndrome. How these results translate into clinical practice needs to be determined
in future research. In conclusion, multiple endocrine neoplasia type 1 (MEN1) is a syndrome …