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Postoperative Management in Patients with Pheochromocytoma and Paraganglioma

Pheochromocytomas and paragangliomas (PPGLs) are rare catecholamine-secreting neuroendocrine tumors of the adrenal medulla and sympathetic/parasympathetic ganglion cells, respectively. Excessive release of catecholamines leads to episodic symptoms and signs of PPGL, which include hypertension, heada...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Cancers (Basel)
Päätekijät: Mamilla, Divya, Araque, Katherine A., Brofferio, Alessandra, Gonzales, Melissa K., Sullivan, James N., Nilubol, Naris, Pacak, Karel
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: MDPI 2019
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6678461/
https://ncbi.nlm.nih.gov/pubmed/31277296
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cancers11070936
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