Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2012 2
2013 4
2014 4
2015 4
2016 6
2017 1
2018 6
2019 4
2020 6
2021 4
2022 2
2023 3
2024 3

Text availability

Article attribute

Article type

Publication date

Search Results

41 results

Results by year

Filters applied: . Clear all
Page 1
International consensus on initial screening and follow-up of asymptomatic SDHx mutation carriers.
Amar L, Pacak K, Steichen O, Akker SA, Aylwin SJB, Baudin E, Buffet A, Burnichon N, Clifton-Bligh RJ, Dahia PLM, Fassnacht M, Grossman AB, Herman P, Hicks RJ, Januszewicz A, Jimenez C, Kunst HPM, Lewis D, Mannelli M, Naruse M, Robledo M, Taïeb D, Taylor DR, Timmers HJLM, Treglia G, Tufton N, Young WF, Lenders JWM, Gimenez-Roqueplo AP, Lussey-Lepoutre C. Amar L, et al. Among authors: buffet a. Nat Rev Endocrinol. 2021 Jul;17(7):435-444. doi: 10.1038/s41574-021-00492-3. Epub 2021 May 21. Nat Rev Endocrinol. 2021. PMID: 34021277 Free PMC article. Review.
Pheochromocytoma: When to search a germline defect?
Buffet A, Burnichon N, Amar L, Gimenez-Roqueplo AP. Buffet A, et al. Presse Med. 2018 Jul-Aug;47(7-8 Pt 2):e109-e118. doi: 10.1016/j.lpm.2018.07.003. Epub 2018 Aug 9. Presse Med. 2018. PMID: 30100270 Review.
Mitochondrial Deficiencies in the Predisposition to Paraganglioma.
Lussey-Lepoutre C, Buffet A, Gimenez-Roqueplo AP, Favier J. Lussey-Lepoutre C, et al. Among authors: buffet a. Metabolites. 2017 May 4;7(2):17. doi: 10.3390/metabo7020017. Metabolites. 2017. PMID: 28471419 Free PMC article. Review.
EPAS1-mutated paragangliomas associated with haemoglobin disorders.
Mancini M, Buffet A, Porte B, Amar L, Lussey-Lepoutre C, Crinière L, Baudin E, Meatchi T, Gimenez-Roqueplo AP, Favier J, Burnichon N. Mancini M, et al. Among authors: buffet a. Br J Haematol. 2024 Mar;204(3):1054-1060. doi: 10.1111/bjh.19278. Epub 2024 Jan 9. Br J Haematol. 2024. PMID: 38195958
Comprehensive in silico and functional studies for classification of EPAS1/HIF2A genetic variants identified in patients with erythrocytosis.
Karaghiannis V, Maric D, Garrec C, Maaziz N, Buffet A, Schmitt L, Antunes V, Airaud F, Aral B, Le Roy A, Corbineau S, Mansour-Hendili L, Lesieur V, Rimbert A, Laporte F, Delamare M, Rab M, Bézieau S, Cassinat B, Galacteros F, Gimenez-Roqueplo AP, Burnichon N, Cario H, Van Wijk R, Bento C, Girodon F, Hoogewijs D, Gardie B. Karaghiannis V, et al. Among authors: buffet a. Haematologica. 2023 Jun 1;108(6):1652-1666. doi: 10.3324/haematol.2022.281698. Haematologica. 2023. PMID: 36700397 Free PMC article.
Transcriptome Analysis of lncRNAs in Pheochromocytomas and Paragangliomas.
Job S, Georges A, Burnichon N, Buffet A, Amar L, Bertherat J, Bouatia-Naji N, de Reyniès A, Drui D, Lussey-Lepoutre C, Favier J, Gimenez-Roqueplo AP, Castro-Vega LJ. Job S, et al. Among authors: buffet a. J Clin Endocrinol Metab. 2020 Mar 1;105(3):dgz168. doi: 10.1210/clinem/dgz168. J Clin Endocrinol Metab. 2020. PMID: 31678991
41 results