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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Detalles Bibliográficos
Autores principales: Ehehalt, Florian, Franke, Ellen, Pilarsky, Christian, Grützmann, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840460/
https://www.ncbi.nlm.nih.gov/pubmed/24281208
http://dx.doi.org/10.3390/cancers2041901

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840460/
https://www.ncbi.nlm.nih.gov/pubmed/24281208
http://dx.doi.org/10.3390/cancers2041901

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