Pheochromocytoma/Paraganglioma: Update on Diagnosis and Management-Reference-Cited by-同舟云学术

Pheochromocytoma/Paraganglioma: Update on Diagnosis and Management

Published:2017-07-13 Issue: Volume: Page:261-310
ISSN:2523-3785
Container-title:Contemporary Endocrinology
language:
Short-container-title:

Author:

Jochmanova Ivana,Pacak Karel

Publisher

Springer International Publishing

Link

http://link.springer.com/content/pdf/10.1007/978-3-319-62470-9_12

Reference241 articles.

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2. Ayala-Ramirez M, Feng L, Johnson MM, Ejaz S, Habra MA, Rich T, Busaidy N, et al. Clinical risk factors for malignancy and overall survival in patients with pheochromocytomas and sympathetic paragangliomas: primary tumor size and primary tumor location as prognostic indicators. J Clin Endocrinol Metab. 2011;96(3):717–25. doi: 10.1210/jc.2010-1946 .

3. Brouwers FM, Eisenhofer G, Tao JJ, Kant JA, Adams KT, Linehan WM, Pacak K. High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing. J Clin Endocrinol Metab. 2006;91(11):4505–9. doi: 10.1210/jc.2006-0423 .

4. Eisenhofer G, Lenders JW, Siegert G, Bornstein SR, Friberg P, Milosevic D, Mannelli M, et al. Plasma methoxytyramine: a novel biomarker of metastatic pheochromocytoma and paraganglioma in relation to established risk factors of tumour size, location and SDHB mutation status. Eur J Cancer. 2012;48(11):1739–49. doi: 10.1016/j.ejca.2011.07.016 .

5. McNeil AR, Blok BH, Koelmeyer TD, Burke MP, Hilton JM. Phaeochromocytomas discovered during coronial autopsies in Sydney, Melbourne and Auckland. Aust NZ J Med. 2000;30(6):648–52.

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1. Diagnosis and management of metastatic pheochromocytoma and paraganglioma;Vnitřní lékařství;2017-09-01