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Pancreatic Neuroendocrine Neoplasms in Multiple Endocrine Neoplasia Type 1
Pancreatic neuroendocrine tumors (pNETs) are a rare group of cancers accounting for about 1–2% of all pancreatic neoplasms. About 10% of pNETs arise within endocrine tumor syndromes, such as Multiple Endocrine Neoplasia type 1 (MEN1). pNETs affect 30–80% of MEN1 patients, manifesting prevalently as...
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| Izdano u: | Int J Mol Sci |
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| Glavni autori: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
MDPI
2021
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8070788/ https://ncbi.nlm.nih.gov/pubmed/33919851 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22084041 |
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