Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement
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Published:2023-12-14
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Volume:
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ISSN:1759-5029
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Container-title:Nature Reviews Endocrinology
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language:en
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Short-container-title:Nat Rev Endocrinol
Author:
Taïeb David, Nölting Svenja, Perrier Nancy D., Fassnacht MartinORCID, Carrasquillo Jorge A.ORCID, Grossman Ashley B.ORCID, Clifton-Bligh RoderickORCID, Wanna George B., Schwam Zachary G., Amar LaurenceORCID, Bourdeau Isabelle, Casey Ruth T., Crona JoakimORCID, Deal Cheri L.ORCID, Del Rivero Jaydira, Duh Quan-Yang, Eisenhofer Graeme, Fojo Tito, Ghayee Hans K., Gimenez-Roqueplo Anne-PauleORCID, Gill Antony J., Hicks Rodney, Imperiale Alessio, Jha AbhishekORCID, Kerstens Michiel N., de Krijger Ronald R., Lacroix AndréORCID, Lazurova Ivica, Lin Frank I., Lussey-Lepoutre CharlotteORCID, Maher Eamonn R.ORCID, Mete Ozgur, Naruse Mitsuhide, Nilubol Naris, Robledo MercedesORCID, Sebag Frédéric, Shah Nalini S., Tanabe AkiyoORCID, Thompson Geoffrey B., Timmers Henri J. L. M., Widimsky Jiri, Young William J., Meuter Leah, Lenders Jacques W. M.ORCID, Pacak KarelORCID
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference191 articles.
1. Kastriti, M. E. et al. Schwann cell precursors generate the majority of chromaffin cells in zuckerkandl organ and some sympathetic neurons in paraganglia. Front. Mol. Neurosci. 12, 6 (2019). 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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