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MON-376 A Novel Mutation in VHL Gene as Posible Cause of Metastasic Pheocromocytoma

A 62-year-old woman with no family history of hereditary diseases presented to the ER department in 2008 with the diagnosis of a subarachnoid hemorrhage that required urgent decompressive craniotomy. On February 2011, due to resistant hypertension, an abdominal CT scan was performed, revealing a lef...

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Detalhes bibliográficos
Publicado no:J Endocr Soc
Main Authors: Montes Barrón, Diego, Quintanilla Flores, Dania, De los Santos Aguilar, Ramon, De la Riva Espinoza, Claudia, Rodríguez Romo, Anabel, Garcia Tuomola, Aili, Reza-Albarran, Alfredo
Formato: Artigo
Idioma:Inglês
Publicado em: Endocrine Society 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6551159/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-MON-376
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