eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | multiple endocrine neoplasia type 1 |
| Comorbidity | C0021670|insulinoma |
| Sentences | 8 |
| PubMedID- 25047095 | Novel mutation 928g>c of men1 gene in a familial multiple endocrine neoplasia type 1 case (men1) with co-existence of insulinoma and glucagonoma. |
| PubMedID- 26527982 | The median age at diagnosis is about 47 years, except in insulinoma patients with men 1, in whom the median age is the mid-20’s [4]. |
| PubMedID- 24459236 | insulinoma may be associated with the multiple endocrine neoplasia type 1 in 4-6% of patients. |
| PubMedID- 22785103 | Clinical features of insulinoma in patients with multiple endocrine neoplasia type 1: analysis of the database of the men consortium of japan. |
| PubMedID- 23569534 | men1 patients with insulinoma are usually admitted to the hospital for a relapse of hypoglycemia. |
| PubMedID- 23102680 | Methods: eight 12-month-old conditional men1 knockout mice with insulinoma were assessed. |
| PubMedID- 20464709 | insulinoma in a patient with men 1 syndrome--9-year follow-up: case report. |
| PubMedID- 22584725 | There is general consensus to submit men1 patients with insulinoma and a hypoglycaemia syndrome to surgery after biochemical diagnosis and fasting test verification, more or less irrespective of tumor size, since no efficient medical treatment option is available (2),(11),(18),(19),(39)–(43). |
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