Diagnosis of silent pheochromocytoma and paraganglioma
Author:
Publisher
Informa UK Limited
Subject
Endocrinology, Diabetes and Metabolism
Link
http://www.tandfonline.com/doi/pdf/10.1586/eem.12.76
Reference98 articles.
1. Pheochromocytoma: State-of-the-Art and Future Prospects
2. Pheochromocytoma in Italy: a multicentric retrospective study
3. Year of Diagnosis, Features at Presentation, and Risk of Recurrence in Patients with Pheochromocytoma or Secreting Paraganglioma
4. Frequent incidental discovery of phaeochromocytoma: data from a German cohort of 201 phaeochromocytoma
5. One Hundred Two Patients With Pheochromocytoma Treated at a Single Institution Since the Introduction of Laparoscopic Adrenalectomy
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1. Massive Biochemically Silent Pheochromocytoma Masquerading as Nonfunctioning Adrenocortical Cancer;JCEM Case Reports;2023-05
2. Silent pheochromocytoma and paraganglioma: Systematic review and proposed definitions for standardized terminology;Frontiers in Endocrinology;2022-10-17
3. Pre- and peri-operative characteristics, complications and outcomes of patients with biochemically silent pheochromocytomas; a case series;Endocrine;2022-09-08
4. Spontaneous Retroperitoneal Bleeding as a Complication of Unusual Renal Paraganglioma;Case Reports in Nephrology;2022-08-30
5. Biochemically normal adrenal pheochromocytoma following extensive central necrosis in a child with von Hippel-Lindau (VHL) gene mutation;BMJ Case Reports;2021-12
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