Pheochromocytomatosis Treated By Radio-Guided Surgery
Open Access
- 1 January 2017
- journal article
- Published by Elsevier BV in AACE Clinical Case Reports
- Vol. 3 (2), e170-e175
- https://doi.org/10.4158/ep151053.cr
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Familial pheochromocytomas and paragangliomasMolecular and Cellular Endocrinology, 2014
- Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneityNature Reviews Cancer, 2014
- Pheochromocytoma and paraganglioma syndromes: genetics and management updateCurrent Oncology, 2013
- Long-Term Outcomes of Surgical Treatment for Hereditary PheochromocytomaJournal of the American College of Surgeons, 2013
- Clinical Risk Factors for Malignancy and Overall Survival in Patients with Pheochromocytomas and Sympathetic Paragangliomas: Primary Tumor Size and Primary Tumor Location as Prognostic IndicatorsJournal of Clinical Endocrinology & Metabolism, 2011
- Initial work-up and long-term follow-up in patients with phaeochromocytomas and paragangliomasBest Practice & Research Clinical Endocrinology & Metabolism, 2006
- Year of Diagnosis, Features at Presentation, and Risk of Recurrence in Patients with Pheochromocytoma or Secreting ParagangliomaJournal of Clinical Endocrinology & Metabolism, 2005
- Clinical Experience Over 48 Years With PheochromocytomaAnnals of Surgery, 1999
- Long‐term evaluation following resection of apparently benign pheochromocytoma(s)/paraganglioma(s)World Journal of Surgery, 1990
- Persistent and recurrent pheochromocytoma: The role of surgeryWorld Journal of Surgery, 1982