Phaeochromocytomas and Paragangliomas: A difference in disease behaviour and clinical outcomes-Reference-Cited by-同舟云学术

Phaeochromocytomas and Paragangliomas: A difference in disease behaviour and clinical outcomes

Published:2015-09-04 Issue:5 Volume:112 Page:486-491
ISSN:0022-4790
Container-title:Journal of Surgical Oncology
language:en
Short-container-title:J. Surg. Oncol.

Author:

Ezzat Abdel-Aziz Tarek¹²,Prete Francesco¹,Conway Gerard³,Gaze Mark³,Bomanji Jamshed³,Bouloux Pierre⁴,Khoo Bernard⁴,Caplin Martyn⁴,Mushtaq Imran¹,Smart James¹,Kurzawinski Tom R.¹

Affiliation:

1. Centre for Endocrine Surgery; University College London Hospital and Great Ormond Street Hospital; London UK

2. Department of General Surgery; University of Alexandria; Egypt

3. Departments of Oncology; Endocrinology and Nuclear Medicine; University College London Hospital; London UK

4. Department of Endocrinology; Oncology and Neuroendocrine Unit; Royal Free Hospital; London UK

Publisher

Wiley

Subject

Oncology,General Medicine,Surgery

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jso.24030/fullpdf

Reference21 articles.

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2. Pheochromocytoma in Sweden 1958-1981. An analysis of the National Cancer Registry Data;Stenström;Acta Med Scand,1986

3. An overview of pheochromocytoma: history, current concepts, vagaries, and diagnostic challenges;Manger;Ann N Y Acad Sci,2006

4. Pheochromocytoma in children;Ciftci;J Pediatr Surg,2001

5. Prevalence of clinically unsuspected pheochromocytoma. Review of a 50-year;Sutton;Mayo Clin Proc,1981

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