New Insights into the Nuclear Imaging Phenotypes of Cluster 1 Pheochromocytoma and Paraganglioma

2017/09/01 by David Taïeb, Karel Pacak, Karel Pacák
Biochemistry, Genetics and Molecular Biology · Medicine · #Adrenal and Paraganglionic Tumors #Cancer, Hypoxia, and Metabolism #Hormonal Regulation and Hypertension

paper · doi:10.1016/j.tem.2017.08.001

openalex publication_date 2017/09/01 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/29

Citations

• Non-pheochromocytoma (PCC)/paraganglioma (PGL) tumors in patients with succinate dehydrogenase-related PCC–PGL syndromes: a clinicopathological and molecular analysis
• Hallmarks of Cancer: The Next Generation
• SDHA is a tumor suppressor gene causing paraganglioma
• Accumulation of Krebs cycle intermediates and over-expression of HIF1α in tumours which result from germline FH and SDH mutations