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Scientific Reports|January 28, 2016
Activating mutations in CTNNB1 in aldosterone producing adenomasTobias Åkerström, Rajani Maharjan, Holger Sven Willenberg, et al.
European Journal of Nuclear Medicine and Molecular Imaging|August 29, 2012
EANM 2012 guidelines for radionuclide imaging of phaeochromocytoma and paragangliomaDavid Taïeb, Henri J Timmers, Elif Hindié, et al.
Endocrine-Related Cancer|August 20, 2015
Novel somatic mutations and distinct molecular signature in aldosterone-producing adenomasTobias Åkerström, Holger Sven Willenberg, Kenko Cupisti, et al.
Annals of Surgery|October 15, 2020
Surgical Outcomes After Neoadjuvant Chemoradiation Followed by Curative Surgery in Patients With Esophageal Cancer: An Intergroup Phase III Trial of the Swiss Group for Clinical Cancer Research (SAKK 75/08)Urs von Holzen, Sven Schmidt, Stefanie Hayoz, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 15, 2009
Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patientsZoran Erlic, Lisa Rybicki, Mariola Peczkowska, et al.
Langenbeck'S Archives of Surgery|April 3, 2019
Surgical therapy of adrenal tumors: guidelines from the German Association of Endocrine Surgeons (CAEK)K Lorenz, P Langer, B Niederle, et al.
Endocrine-Related Cancer|October 31, 2013
Long-term prognosis of patients with pediatric pheochromocytomaBirke Bausch, Ulrich Wellner, Dirk Bausch, et al.
The British Journal of Surgery|January 7, 2020
International multicentre review of perioperative management and outcome for catecholamine-producing tumoursH Groeben, M K Walz, B J Nottebaum, et al.
JAMA|October 27, 2005
Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC geneFrancesca Schiavi, Carsten C Boedeker, Birke Bausch, et al.
The New England Journal of Medicine|May 10, 2002
Germ-line mutations in nonsyndromic pheochromocytomaHartmut P H Neumann, Birke Bausch, Sarah R McWhinney, et al.
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