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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...
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| Publicado no: | Arch Med Sci |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Termedia Publishing House
2016
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| Assuntos: | |
| Acesso em linha: | 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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