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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease multiple endocrine neoplasia type 1
Symptom C0014132|endocrine tumor
Sentences 9
PubMedID- 25460558 multiple endocrine neoplasia type 1 with gastric neuroendocrine tumor presented with gastric polyposis.
PubMedID- 22584720 Surgical approaches to pancreatic endocrine tumors associated with multiple endocrine neoplasia type 1 may differ greatly from those applied to sporadic pancreatic endocrine tumors.
PubMedID- 22797396 Context: the surgical management of pancreatic endocrine tumors in patients with multiple endocrine neoplasia type 1 (men-1) is controversial and complicated by the fact that these tumors are frequently multifocal.
PubMedID- 20514321 Gastrinoma is the most frequent functional pancreaticoduodenal endocrine tumor in patients with multiple endocrine neoplasia type 1 (men 1).
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- 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- 21455335 Aim: to search for the optimal surgery for gastrinoma and duodenopancreatic neuroendocrine tumors in patients with multiple endocrine neoplasia type 1.
PubMedID- 22581216 Predicting the risk of multiple endocrine neoplasia type 1 for patients with commonly occurring endocrine tumors.
PubMedID- 25440487 Metastasectomy of neuroendocrine tumors in patients with multiple endocrine neoplasia type 1.

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