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Autor:
Matthias Kroiss, Yiling Xu, Sergei G. Tevosian, Graeme Eisenhofer, Raymond J. Bergeron, Arthur S. Tischler, Mercedes Robledo, Heather M. Hatch, Sudhir K. Rai, Dan Plant, Srilaxami Kalavalapalli, Robert Hromas, Karel Pacak, Henri J L M Timmers, Felix Beuschlein, David Taïeb, Bruna Calsina, Kenneth Cusi, Priyanaka Gupta, James A. Bibb, Susan Richter, Timothy J. Garrett, Fernando Bril, Prodip Bose, Hans K. Ghayee
Publikováno v:
Journal of the Endocrine Society
Background: Pheochromocytomas (PCCs) and paragangliomas (PGLs) are neuroendocrine tumors that are mostly benign. Metastatic disease occurs in about 10% of cases, and for these patients no effective therapies are available. Patients with mutations in