Management of the hormonal syndrome of neuroendocrine tumors

Gastroenteropancreatic neuroendocrine tumors (GEP/NET) are unusual and rare neoplasms that present many clinical challenges. They characteristically synthesize store and secrete a variety of peptides and neuroamines which can lead to the development of distinct clinical syndrome, however many are cl...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Arch Med Sci
Prif Awduron: Gut, Paweł, Waligórska-Stachura, Joanna, Czarnywojtek, Agata, Sawicka-Gutaj, Nadia, Bączyk, Maciej, Ziemnicka, Katarzyna, Fischbach, Jakub, Woliński, Kosma, Kaznowski, Jarosław, Wrotkowska, Elżbieta, Ruchała, Marek
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Termedia Publishing House 2016
Pynciau:
State of the Art Paper
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5420621/
https://ncbi.nlm.nih.gov/pubmed/28507564
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5114/aoms.2016.60311
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