Role of SDHAF2 and SDHD in von Hippel–Lindau Associated Pheochromocytomas-Reference-Cited by-同舟云学术

Role of SDHAF2 and SDHD in von Hippel–Lindau Associated Pheochromocytomas

Published:2013-12-10 Issue:3 Volume:38 Page:724-732
ISSN:0364-2313
Container-title:World Journal of Surgery
language:en
Short-container-title:World J Surg

Author:

Kugelberg Johan,Welander Jenny,Schiavi Francesca,Fassina Ambrogio,Bäckdahl Martin,Larsson Catharina,Opocher Giuseppe,Söderkvist Peter,Dahia Patricia L.,Neumann Hartmut P. H.,Gimm Oliver

Publisher

Springer Science and Business Media LLC

Subject

Surgery

Link

http://link.springer.com/content/pdf/10.1007/s00268-013-2373-2.pdf

Reference43 articles.

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2. Gimenez-Roqueplo AP, Burnichon N, Amar L et al (2008) Recent advances in the genetics of phaeochromocytoma and functional paraganglioma. Clin Exp Pharmacol Physiol 35:376–379

3. Neumann HP, Bausch B, McWhinney SR et al (2002) Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J Med 346:1459–1466

4. Welander J, Soderkvist P, Gimm O (2011) Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas. Endocr Relat Cancer 18:R253–R276

5. Woodward ER, Maher ER (2006) Von Hippel–Lindau disease and endocrine tumour susceptibility. Endocr Relat Cancer 13:415–425

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