Cargando…
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...
Autores principales: | Gut, Paweł, Waligórska-Stachura, Joanna, Czarnywojtek, Agata, Sawicka-Gutaj, Nadia, Bączyk, Maciej, Ziemnicka, Katarzyna, Fischbach, Jakub, Woliński, Kosma, Kaznowski, Jarosław, Wrotkowska, Elżbieta, Ruchała, Marek |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420621/ https://www.ncbi.nlm.nih.gov/pubmed/28507564 http://dx.doi.org/10.5114/aoms.2016.60311 |
Ejemplares similares
-
Chromogranin A – unspecific neuroendocrine marker. Clinical utility and potential diagnostic pitfalls
por: Gut, Paweł, et al.
Publicado: (2016) -
Incidence of pituitary autoantibodies in idiopathic diabetes insipidus
por: Gut, Paweł, et al.
Publicado: (2018) -
Hindgut neuroendocrine neoplasms – characteristics and prognosis
por: Gut, Paweł, et al.
Publicado: (2017) -
Familial syndromes associated with neuroendocrine tumours
por: Gut, Paweł, et al.
Publicado: (2015) -
Clinical features of gastroenteropancreatic tumours
por: Gut, Paweł, et al.
Publicado: (2015)