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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease multiple endocrine neoplasia type 1
Comorbidity C0206754|neuroendocrine tumor
Sentences 11
PubMedID- 25713781 Management of pancreatic neuroendocrine tumors in patients with men 1.
PubMedID- 24819502 The aim of this study was to characterize the molecular basis of a case of men1-like syndrome with a neuroendocrine tumor and persistent primary hyperparathyroidism (phpt).
PubMedID- 23569534 Gastrinoma and insulinoma are the 2 most common functional pancreatic neuroendocrine tumors in patients with men1 [7].
PubMedID- 23091757 Simultaneous eus-fna diagnosis and tnm staging of a pancreatic neuroendocrine tumor in a patient with an unrecognized men type 1.
PubMedID- 25440487 Metastasectomy of neuroendocrine tumors in patients with multiple endocrine neoplasia type 1.
PubMedID- 25565142 Biallelic inactivation of men1 encoding menin in pancreatic neuroendocrine tumors (pnets) associated with the multiple endocrine neoplasia type 1 (men1) syndrome is well established, but how menin loss/inactivation initiates tumorigenesis is not well understood.
PubMedID- 25460558 multiple endocrine neoplasia type 1 with gastric neuroendocrine tumor presented with gastric polyposis.
PubMedID- 26113081 Objective: the prevalence and clinical behavior of bronchopulmonary neuroendocrine tumors (bnet) associated with multiple endocrine neoplasia type 1 (men1) are not well defined.
PubMedID- 23093487 Objective: the aim of the study was to determine whether there is an association of abo blood type with the development of neuroendocrine tumors in patients with multiple endocrine neoplasia, type 1 (men-1).
PubMedID- 21455335 Aim: to search for the optimal surgery for gastrinoma and duodenopancreatic neuroendocrine tumors in patients with multiple endocrine neoplasia type 1.
PubMedID- 19960369 Further evaluation of the captem regimen in patients with pituitary neuroendocrine tumors which fail to respond to classic treatments is warranted.

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