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Ocular sequelae of epidermal necrolysis: French national audit of practices, literature review and proposed management.
Thorel D, Ingen-Housz-Oro S, Benaïm D, Daien V, Gabison E, Saunier V, Béral L, Touboul D, Brémond-Gignac D, Robert M, Vasseur R, Royer G, Dereure O, Milpied B, Bernier C, Welfringer-Morin A, Bodemer C, Cordel N, Tauber M, Burillon C, Servant M, Couret C, Vabres B, Tétart F, Cassagne M, Kuoch MA, Muraine M, Delcampe A, Gueudry J. Thorel D, et al. Orphanet J Rare Dis. 2023 Mar 11;18(1):51. doi: 10.1186/s13023-023-02616-6. Orphanet J Rare Dis. 2023. PMID: 36906580 Free PMC article. Review.
[Acute orbital inflammation in VEXAS syndrome: Case report].
Rimbert N, Retout A, Muraine M, Thorel D. Rimbert N, et al. Among authors: thorel d. J Fr Ophtalmol. 2024 Mar 5:104128. doi: 10.1016/j.jfo.2024.104128. Online ahead of print. J Fr Ophtalmol. 2024. PMID: 38448312 French. No abstract available.
Management of ocular involvement in the acute phase of Stevens-Johnson syndrome and toxic epidermal necrolysis: french national audit of practices, literature review, and consensus agreement.
Thorel D, Ingen-Housz-Oro S, Royer G, Delcampe A, Bellon N, Bodemer C, Welfringer-Morin A, Bremond-Gignac D, Robert MP, Tauber M, Malecaze F, Dereure O, Daien V, Colin A, Bernier C, Couret C, Vabres B, Tetart F, Milpied B, Cornut T, Ben Said B, Burillon C, Cordel N, Beral L, de Prost N, Wolkenstein P, Muraine M, Gueudry J. Thorel D, et al. Orphanet J Rare Dis. 2020 Sep 22;15(1):259. doi: 10.1186/s13023-020-01538-x. Orphanet J Rare Dis. 2020. PMID: 32962748 Free PMC article. Review.
FUBP1: a new protagonist in splicing regulation of the DMD gene.
Miro J, Laaref AM, Rofidal V, Lagrafeuille R, Hem S, Thorel D, Méchin D, Mamchaoui K, Mouly V, Claustres M, Tuffery-Giraud S. Miro J, et al. Among authors: thorel d. Nucleic Acids Res. 2015 Feb 27;43(4):2378-89. doi: 10.1093/nar/gkv086. Epub 2015 Feb 6. Nucleic Acids Res. 2015. PMID: 25662218 Free PMC article.
Comprehensive oligonucleotide array-comparative genomic hybridization analysis: new insights into the molecular pathology of the DMD gene.
Ishmukhametova A, Khau Van Kien P, Méchin D, Thorel D, Vincent MC, Rivier F, Coubes C, Humbertclaude V, Claustres M, Tuffery-Giraud S. Ishmukhametova A, et al. Among authors: thorel d. Eur J Hum Genet. 2012 Oct;20(10):1096-100. doi: 10.1038/ejhg.2012.51. Epub 2012 Apr 18. Eur J Hum Genet. 2012. PMID: 22510846 Free PMC article.
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