Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas-Reference-Cited by-同舟云学术

Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas

Published:2016-11-18 Issue:4 Volume:13 Page:233-247
ISSN:1759-5029
Container-title:Nature Reviews Endocrinology
language:en
Short-container-title:Nat Rev Endocrinol

Author:

Toledo Rodrigo A., ,Burnichon Nelly,Cascon Alberto,Benn Diana E.,Bayley Jean-Pierre,Welander Jenny,Tops Carli M.,Firth Helen,Dwight Trish,Ercolino Tonino,Mannelli Massimo,Opocher Giuseppe,Clifton-Bligh Roderick,Gimm Oliver,Maher Eamonn R.,Robledo Mercedes,Gimenez-Roqueplo Anne-Paule,Dahia Patricia L. M.

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.nature.com/articles/nrendo.2016.185.pdf

Reference124 articles.

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2. Favier, J., Amar, L. & Gimenez-Roqueplo, A. P. Paraganglioma and phaeochromocytoma: from genetics to personalized medicine. Nat. Rev. Endocrinol. 11, 101–111 (2015).

3. Piccini, V. et al. Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients. Endocr. Relat. Cancer 19, 149–155 (2012).

4. Lenders, J. W. et al. Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. J. Clin. Endocrinol. Metab. 99, 1915–1942 (2014).

5. van Nederveen, F. H. et al. An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis. Lancet Oncol. 10, 764–771 (2009).

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