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Journal of Clinical Hypertension (Greenwich, Conn.)|February 12, 2016
Dipping in Ambulatory Blood Pressure Monitoring Correlates With Overnight Urinary Excretion of Catecholamines and SodiumRoland Därr, Michael Bursztyn, Christina Pamporaki, et al.
Therapeutic Advances in Endocrinology and Metabolism|November 14, 2012
Pheochromocytoma - update on disease managementRoland Därr, Jacques W M Lenders, Lorenz C Hofbauer, et al.
Endocrine|April 14, 2017
Accuracy of recommended sampling and assay methods for the determination of plasma-free and urinary fractionated metanephrines in the diagnosis of pheochromocytoma and paraganglioma: a systematic reviewRoland Därr, Matthias Kuhn, Christoph Bode, et al.
Endocrine Connections|September 2, 2020
Clinical decision making in small non-functioning VHL-related incidentalomasRoland Därr, Jonas Kater, Peggy Sekula, et al.
Clinical Endocrinology|March 7, 2013
Plasma-free vs deconjugated metanephrines for diagnosis of phaeochromocytomaChristina Pamporaki, Roland Därr, Michael Bursztyn, et al.
Endocrine|April 22, 2011
Is there still a place for adrenal venous sampling in the diagnostic localization of pheochromocytoma?Roland Därr, Graeme Eisenhofer, Jörg Kotzerke, et al.
Cellular and Molecular Neurobiology|April 7, 2018
Continued Tumor Reduction of Metastatic Pheochromocytoma/Paraganglioma Harboring Succinate Dehydrogenase Subunit B Mutations with Cyclical ChemotherapyIrfan Jawed, Margarita Velarde, Roland Därr, et al.
European Journal of Endocrinology|March 19, 2020
Overnight/first-morning urine free metanephrines and methoxytyramine for diagnosis of pheochromocytoma and paraganglioma: is this an option?Mirko Peitzsch, Denise Kaden, Christina Pamporaki, et al.
Clinical Endocrinology|October 10, 2013
Biochemical diagnosis of phaeochromocytoma using plasma-free normetanephrine, metanephrine and methoxytyramine: importance of supine sampling under fasting conditionsRoland Därr, Christina Pamporaki, Mirko Peitzsch, et al.
European Journal of Endocrinology|November 22, 2017
Next-generation panel sequencing identifies <i>NF1</i> germline mutations in three patients with pheochromocytoma but no clinical diagnosis of neurofibromatosis type 1Laura Gieldon, Jimmy Rusdian Masjkur, Susan Richter, et al.
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