Citations (9)
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Ioannis Ilias & Costas Thomopoulos. (2019) Addressing delays in the diagnosis of pheochromocytoma/paraganglioma. Expert Review of Endocrinology & Metabolism 14:5, pages 359-363.
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Georgiana A Dobri, Emmanuel Bravo & Amir H Hamrahian. (2014) Pheochromocytoma: pitfalls in the biochemical evaluation. Expert Review of Endocrinology & Metabolism 9:2, pages 123-135.
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Articles from other publishers (7)
Shejil Kumar, Katherine Wu, Natassia Rodrigo & Anthony Glover. (2023) Massive Biochemically Silent Pheochromocytoma Masquerading as Nonfunctioning Adrenocortical Cancer. JCEM Case Reports 1:3.
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Georgiana Constantinescu, Cristina Preda, Victor Constantinescu, Timo Siepmann, Stefan R. Bornstein, Jacques W. M. Lenders, Graeme Eisenhofer & Christina Pamporaki. (2022) Silent pheochromocytoma and paraganglioma: Systematic review and proposed definitions for standardized terminology. Frontiers in Endocrinology 13.
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Athanasios Fountas, Georgia Kanti, Spyridoula Glycofridi, Maria A. Christou, Athanasia Kalantzi, Irene Giagourta, Athina Markou, Georgia Ntali, Chrysanthi Aggeli, Eleftheria Saoulidou, Antonia Dimakopoulou, George N. Zografos, Theodora Kounadi, Stelios Tigas & Labrini Papanastasiou. (2022) Pre- and peri-operative characteristics, complications and outcomes of patients with biochemically silent pheochromocytomas; a case series. Endocrine 78:3, pages 570-579.
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Tawfeeq I. Sangey, Hamim Abdul Rusheke, Ansaar I. Sangey, Nimishkumar Chaya & Advera Ngaiza. (2022) Spontaneous Retroperitoneal Bleeding as a Complication of Unusual Renal Paraganglioma. Case Reports in Nephrology 2022, pages 1-8.
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Benjamin Wei-Liang Ng, Jeanne Sze-Lyn Wong & Teck-Hock Toh. (2021) Biochemically normal adrenal pheochromocytoma following extensive central necrosis in a child with von Hippel-Lindau (VHL) gene mutation. BMJ Case Reports 14:12, pages e245154.
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Samuel Joseph Withey, Stephen PerrioDimitra ChristodoulouLouise IzattPaul CarrollAnand VelusamyRupert ObholzerValerie LewingtonAudrey Eleanor Therese Jacques. (2019) Imaging Features of Succinate Dehydrogenase–deficient Pheochromocytoma-Paraganglioma Syndromes. RadioGraphics 39:5, pages 1393-1410.
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Carsten C. Boedeker, Erik F. Hensen, Hartmut P.H. Neumann, Wolfgang Maier, Francien H. van Nederveen, Carlos Suárez, Henricus P. Kunst, Juan P. Rodrigo, Robert P. Takes, Phillip K. Pellitteri, Alessandra Rinaldo & Alfio Ferlito. (2014) Genetics of hereditary head and neck paragangliomas. Head & Neck 36:6, pages 907-916.
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