eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | multiple endocrine neoplasia |
| Comorbidity | C0206754|neuroendocrine tumor |
| Sentences | 6 |
| 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- 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- 25460558 | multiple endocrine neoplasia type 1 with gastric neuroendocrine tumor presented with gastric polyposis. |
| 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- 25440487 | Metastasectomy of neuroendocrine tumors in patients with multiple endocrine neoplasia type 1. |
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