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

Year Number of Results
2002 1
2003 3
2005 4
2006 3
2007 2
2008 2
2009 2
2010 6
2011 6
2012 4
2013 8
2014 5
2015 7
2016 10
2017 7
2018 5
2019 9
2020 13
2021 12
2022 8
2023 6
2024 4

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114 results

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Page 1
The Diagnosis and Management of Lipodystrophy Syndromes: A Multi-Society Practice Guideline.
Brown RJ, Araujo-Vilar D, Cheung PT, Dunger D, Garg A, Jack M, Mungai L, Oral EA, Patni N, Rother KI, von Schnurbein J, Sorkina E, Stanley T, Vigouroux C, Wabitsch M, Williams R, Yorifuji T. Brown RJ, et al. Among authors: vigouroux c. J Clin Endocrinol Metab. 2016 Dec;101(12):4500-4511. doi: 10.1210/jc.2016-2466. Epub 2016 Oct 6. J Clin Endocrinol Metab. 2016. PMID: 27710244 Free PMC article. Review.
Seipin localizes at endoplasmic-reticulum-mitochondria contact sites to control mitochondrial calcium import and metabolism in adipocytes.
Combot Y, Salo VT, Chadeuf G, Hölttä M, Ven K, Pulli I, Ducheix S, Pecqueur C, Renoult O, Lak B, Li S, Karhinen L, Belevich I, Le May C, Rieusset J, Le Lay S, Croyal M, Tayeb KS, Vihinen H, Jokitalo E, Törnquist K, Vigouroux C, Cariou B, Magré J, Larhlimi A, Ikonen E, Prieur X. Combot Y, et al. Among authors: vigouroux c. Cell Rep. 2022 Jan 11;38(2):110213. doi: 10.1016/j.celrep.2021.110213. Cell Rep. 2022. PMID: 35021082 Free article.
RIPK3 dampens mitochondrial bioenergetics and lipid droplet dynamics in metabolic liver disease.
Afonso MB, Islam T, Magusto J, Amorim R, Lenoir V, Simões RF, Teixeira J, Silva LC, Wendum D, Jéru I, Vigouroux C, Castro RE, Oliveira PJ, Prip-Buus C, Ratziu V, Gautheron J, Rodrigues CMP. Afonso MB, et al. Among authors: vigouroux c. Hepatology. 2023 Apr 1;77(4):1319-1334. doi: 10.1002/hep.32756. Epub 2022 Oct 11. Hepatology. 2023. PMID: 36029129 Free PMC article.
Lipodystrophic syndromes: From diagnosis to treatment.
Sollier C, Vatier C, Capel E, Lascols O, Auclair M, Janmaat S, Fève B, Jéru I, Vigouroux C. Sollier C, et al. Among authors: vigouroux c. Ann Endocrinol (Paris). 2020 Feb;81(1):51-60. doi: 10.1016/j.ando.2019.10.003. Epub 2019 Dec 16. Ann Endocrinol (Paris). 2020. PMID: 31982105 Review.
Molecular and Cellular Bases of Lipodystrophy Syndromes.
Zammouri J, Vatier C, Capel E, Auclair M, Storey-London C, Bismuth E, Mosbah H, Donadille B, Janmaat S, Fève B, Jéru I, Vigouroux C. Zammouri J, et al. Among authors: vigouroux c. Front Endocrinol (Lausanne). 2022 Jan 3;12:803189. doi: 10.3389/fendo.2021.803189. eCollection 2021. Front Endocrinol (Lausanne). 2022. PMID: 35046902 Free PMC article. Review.
[Mutltifaceted biological roles of leptin].
Charchour R, Dufour-Rainfray D, Morineau G, Vatier C, Fellahi S, Vigouroux C, Genoux A, Capeau J, Lacorte JM, Collet C, Cuerq C, Bastard JP; groupe de travail RIHN Adipokines. Charchour R, et al. Among authors: vigouroux c. Ann Biol Clin (Paris). 2020 Jun 1;78(3):231-242. doi: 10.1684/abc.2020.1560. Ann Biol Clin (Paris). 2020. PMID: 32540812 Free article. Review. French.
[Mutltifaceted biological roles of adiponectin].
Cuerq C, Morineau G, Dufour-Rainfray D, Vatier C, Fellahi S, Vigouroux C, Genoux A, Lacorte JM, Charchour R, Fève B, Capeau J, Collet C, Bastard JP; groupe de travail RIHN Adipokines. Cuerq C, et al. Among authors: vigouroux c. Ann Biol Clin (Paris). 2020 Jun 1;78(3):243-252. doi: 10.1684/abc.2020.1562. Ann Biol Clin (Paris). 2020. PMID: 32540813 Free article. Review. French.
A-type lamin-linked lipodystrophies.
Vigouroux C, Capeau J. Vigouroux C, et al. Novartis Found Symp. 2005;264:166-77; discussion 177-82, 227-30. Novartis Found Symp. 2005. PMID: 15773753 Review.
Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling.
Schuermans N, El Chehadeh S, Hemelsoet D, Gautheron J, Vantyghem MC, Nouioua S, Tazir M, Vigouroux C, Auclair M, Bogaert E, Dufour S, Okawa F, Hilbert P, Van Doninck N, Taquet MC, Rosseel T, De Clercq G, Debackere E, Van Haverbeke C, Cherif FR, Urtizberea JA, Chanson JB, Funalot B, Authier FJ, Kaya S, Terryn W, Callens S, Depypere B, Van Dorpe J; Program for Undiagnosed Diseases (UD-PrOZA); Poppe B, Impens F, Mizushima N, Depienne C, Jéru I, Dermaut B. Schuermans N, et al. Among authors: vigouroux c. Nat Genet. 2023 Nov;55(11):1929-1940. doi: 10.1038/s41588-023-01535-3. Epub 2023 Nov 2. Nat Genet. 2023. PMID: 37919452
114 results