Pheochromocytoma, guidelines

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by JWM Lenders · 2014 · Cited by 2163 — The aim was to formulate clinical practice guidelines for pheochromocytoma and paraganglioma (PPGL).Participants:. The Task Force included a chair s. by PF Plouin · 2016 · Cited by 343 — Pheochromocytoma and paraganglioma: an Endocrine Society Clinical Practice Guideline. Journal of Clinical Endocrinology and Metabolism 2014 99 1915–1942. Jun 19, 2014 — The aim was to formulate clinical practice guidelines for pheochromocytoma and paraganglioma (PPGL). Conclusions: The Task Force recommends that by JWM Lenders · 2014 · Cited by 2168 — Abstract. Objective: The aim was to formulate clinical practice guidelines for pheochromocytoma and paraganglioma (PPGL). Participants: The Task Force included by R Garcia‑Carbonero · 2021 · Cited by 27 — The North American neuroendocrine tumor society consensus guideline for the diagnosis and management of neu- roendocrine tumors: pheochromocytoma, paraganglioma Aug 20, 2021 — The ES/AACC/ESE guidelines recommend minimally invasive (eg, laparoscopic) adrenalectomy for most adrenal pheochromocytomas, with open resection by JWM Lenders · 2014 · Cited by 2160 — Guidelines on Pheochromocytoma and Paraganglioma. J Clin Endocrinol Metab, June 2014, 99(6):1915–1942. The Endocrine Society. The recommendations in the following guidelines may vary from those that appear in UpToDate topic reviews. Readers who are looking for UpToDate topic reviewsby R Garcia-Carbonero · 2021 · Cited by 26 — Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors that arise from chromaffin cells of the adrenal medulla and the

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