Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement-Reference-Cited by-同舟云学术

Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement

Published:2023-12-14 Issue: Volume: Page:
ISSN:1759-5029
Container-title:Nature Reviews Endocrinology
language:en
Short-container-title:Nat Rev Endocrinol

Author:

Taïeb David,Nölting Svenja,Perrier Nancy D.,Fassnacht Martin^ORCID,Carrasquillo Jorge A.^ORCID,Grossman Ashley B.^ORCID,Clifton-Bligh Roderick^ORCID,Wanna George B.,Schwam Zachary G.,Amar Laurence^ORCID,Bourdeau Isabelle,Casey Ruth T.,Crona Joakim^ORCID,Deal Cheri L.^ORCID,Del Rivero Jaydira,Duh Quan-Yang,Eisenhofer Graeme,Fojo Tito,Ghayee Hans K.,Gimenez-Roqueplo Anne-Paule^ORCID,Gill Antony J.,Hicks Rodney,Imperiale Alessio,Jha Abhishek^ORCID,Kerstens Michiel N.,de Krijger Ronald R.,Lacroix André^ORCID,Lazurova Ivica,Lin Frank I.,Lussey-Lepoutre Charlotte^ORCID,Maher Eamonn R.^ORCID,Mete Ozgur,Naruse Mitsuhide,Nilubol Naris,Robledo Mercedes^ORCID,Sebag Frédéric,Shah Nalini S.,Tanabe Akiyo^ORCID,Thompson Geoffrey B.,Timmers Henri J. L. M.,Widimsky Jiri,Young William J.,Meuter Leah,Lenders Jacques W. M.^ORCID,Pacak Karel^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.nature.com/articles/s41574-023-00926-0.pdf

Reference191 articles.

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2. Furlan, A. et al. Multipotent peripheral glial cells generate neuroendocrine cells of the adrenal medulla. Science 357, eaal3753 (2017).

3. Baysal, B. E. et al. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science 287, 848–851 (2000).

4. Astuti, D. et al. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. Am. J. Hum. Genet. 69, 49–54 (2001).

5. Niemann, S. & Muller, U. Mutations in SDHC cause autosomal dominant paraganglioma, type 3. Nat. Genet. 26, 268–270 (2000).

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