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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Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: Ehehalt, Florian, Franke, Ellen, Pilarsky, Christian, Grützmann, Robert
Materialtyp: Artigo
Språk:Inglês
Publicerad: MDPI 2010
Ämnen:
Review
Länkar: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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