… endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary tumor syndrome
… tumor suppressor gene MEN1, and is characterized by a predisposition to a multitude of …

… neoplasms appearing in at least ten genetic syndromes. The most important one is multiple
endocrine neoplasia type 1 (MEN-1), caused by mutations in the tumour suppressor … MEN1. …

… 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-…

… 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- …

… also include skin lesions, especially tumor-type lesions. This is a … MEN1 and dermatological
issues (apart from dermatologic features of each endocrine tumor/neuroendocrine neoplasia)…

… Multiple endocrine neoplasia type 1 Multiple endocrine neoplasia type 1 (MEN1) is an
autosomal dominant syndrome resulting from mutation of the tumor suppressor gene on …

… the same MEN1 mutation as our proband and, around the same time, their father was
diagnosed with a neuroendocrine carcinoma, this tumor was investigated for the MEN1 mutation …

… diagnosis of MEN1, genetics of sporadic endocrine tumors, MEN1-related conditions, the
biological functions of menin, potential pharmacological therapies, disease pathogenesis, …