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Pheochromocytoma and Paraganglioma: A Review of Diagnosis, Management and Treatment of Rare Causes of Hypertension

Pheochromocytomas (PHEO) and paragangliomas (PGL) are rare tumors originated in cells derived from the neural crest. The first ones are located in the adrenal medulla, and the second ones in the sympathetic and parasympathetic nervous system. These kind of tumors may secrete excess catecholamines, i...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Cureus
मुख्य लेखकों: Cerqueira, Ana, Seco, Tiago, Costa, Ana, Tavares, Maria, Cotter, Jorge
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Cureus 2020
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC7273359/
https://ncbi.nlm.nih.gov/pubmed/32523826
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.7969
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