Functional Imaging Signature of Patients Presenting with Polycythemia/Paraganglioma Syndromes

Pheochromocytoma/paraganglioma (PPGL) syndromes associated with polycythemia have previously been described in association with mutations in the von Hippel–Lindau gene. Recently, mutations in the prolyl hydroxylase gene (PHD) 1 and 2 and in the hypoxia-inducible factor 2 α (HIF2A) were also found to...

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Detaylı Bibliyografya
Yayımlandı:J Nucl Med
Asıl Yazarlar: Janssen, Ingo, Chen, Clara C., Zhuang, Zhenping, Millo, Corina M., Wolf, Katherine I., Ling, Alexander, Lin, Frank I., Adams, Karen T., Herscovitch, Peter, Feelders, Richard A., Fojo, Antonio T., Taieb, David, Kebebew, Electron, Pacak, Karel
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Society of Nuclear Medicine 2017
Konular:
Oncology
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5537614/
https://ncbi.nlm.nih.gov/pubmed/28336782
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2967/jnumed.116.187690
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