Pancreatic Neuroendocrine Neoplasms in Multiple Endocrine Neoplasia Type 1
Pancreatic Neuroendocrine Neoplasms in Multiple Endocrine Neoplasia Type 1
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Publisher
Switzerland: MDPI AG
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Language
English
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Publisher
Switzerland: MDPI AG
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Contents
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 multiple microadenomas. pNETs in patients with MEN...
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Full title
Pancreatic Neuroendocrine Neoplasms in Multiple Endocrine Neoplasia Type 1
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8070788
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8070788
Other Identifiers
ISSN
1422-0067,1661-6596
E-ISSN
1422-0067
DOI
10.3390/ijms22084041
