Testing for germline mutations in sporadic pheochromocytoma/paraganglioma: a systematic review-Reference-Cited by-同舟云学术

Testing for germline mutations in sporadic pheochromocytoma/paraganglioma: a systematic review

Published:2014-07-07 Issue:3 Volume:82 Page:338-345
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clin Endocrinol

Author:

Brito Juan P.¹²,Asi Noor²,Bancos Irina¹,Gionfriddo Michael R.²³,Zeballos-Palacios Claudia L.²,Leppin Aaron L.²,Undavalli Chaitanya²,Wang Zhen²,Domecq Juan P.²,Prustsky Gabriela²,Elraiyah Tarig A.²,Prokop Larry J.²,Montori Victor M.¹²,Murad Mohammad H.²⁴

Affiliation:

1. Division of Endocrinology; Diabetes; Metabolism and Nutrition; Mayo Clinic; Rochester MN USA

2. Knowledge and Evaluation Research Unit; Mayo Clinic; Rochester MN USA

3. Mayo Graduate School; Mayo Clinic; Rochester MN USA

4. Division of Preventive Medicine; Mayo Clinic; Rochester MN USA

Funder

The Enodcrine Society

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Reference26 articles.

1. Occurence of pheochromocytoma in Rochester, Minnesota, 1950 through 1979;Beard;Mayo Clinic Proceedings,1983

2. Adrenal causes of hypertension: pheochromocytoma and primary aldosteronism;Young;Reviews In Endocrine & Metabolic Disorders,2007

3. An update on the genetics of paraganglioma, pheochromocytoma, and associated hereditary syndromes;Gimemez-Roqueplo;Hormone and Metabolic Research,2012

4. Review: should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes?;Jimenez;The Journal of Clinical Endocrinology and Metabolism,2006

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