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Molecular Pathogenesis of Pancreatic Neuroendocrine Tumors
Pancreatic neuroendocrine tumors (PNETs) are rare primary neoplasms of the pancreas and arise sporadically or in the context of genetically determined syndromes. Depending on hormone production and sensing, PNETs clinically manifest due to a hormone-related syndrome (functional PNET) or by symptoms...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3840460/ https://ncbi.nlm.nih.gov/pubmed/24281208 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cancers2041901 |
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