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Page 1
Functional assessment and phenotypic heterogeneity of SFTPA1 and SFTPA2 mutations in interstitial lung diseases and lung cancer.
Legendre M, Butt A, Borie R, Debray MP, Bouvry D, Filhol-Blin E, Desroziers T, Nau V, Copin B, Dastot-Le Moal F, Héry M, Duquesnoy P, Allou N, Bergeron A, Bermudez J, Cazes A, Chene AL, Cottin V, Crestani B, Dalphin JC, Dombret C, Doray B, Dupin C, Giraud V, Gondouin A, Gouya L, Israël-Biet D, Kannengiesser C, Le Borgne A, Leroy S, Longchampt E, Lorillon G, Nunes H, Picard C, Reynaud-Gaubert M, Traclet J, de Vuyst P, Coulomb L'Hermine A, Clement A, Amselem S, Nathan N. Legendre M, et al. Among authors: clement a. Eur Respir J. 2020 Dec 24;56(6):2002806. doi: 10.1183/13993003.02806-2020. Print 2020 Dec. Eur Respir J. 2020. PMID: 32855221 Free article.
Chronic eosinophilic pneumonia in a 13-year-old child.
Nathan N, Guillemot N, Aubertin G, Blanchon S, Chadelat K, Epaud R, Clément A, Fauroux B. Nathan N, et al. Among authors: clement a. Eur J Pediatr. 2008 Oct;167(10):1203-7. doi: 10.1007/s00431-007-0648-z. Epub 2008 Jan 17. Eur J Pediatr. 2008. PMID: 18202853
Lung alveolar epithelium and interstitial lung disease.
Corvol H, Flamein F, Epaud R, Clement A, Guillot L. Corvol H, et al. Among authors: clement a. Int J Biochem Cell Biol. 2009 Aug-Sep;41(8-9):1643-51. doi: 10.1016/j.biocel.2009.02.009. Epub 2009 Feb 23. Int J Biochem Cell Biol. 2009. PMID: 19433305 Review.
Loss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesia.
Duquesnoy P, Escudier E, Vincensini L, Freshour J, Bridoux AM, Coste A, Deschildre A, de Blic J, Legendre M, Montantin G, Tenreiro H, Vojtek AM, Loussert C, Clément A, Escalier D, Bastin P, Mitchell DR, Amselem S. Duquesnoy P, et al. Among authors: clement a. Am J Hum Genet. 2009 Dec;85(6):890-6. doi: 10.1016/j.ajhg.2009.11.008. Am J Hum Genet. 2009. PMID: 19944405 Free PMC article.
Interstitial lung diseases in children.
Clement A, Nathan N, Epaud R, Fauroux B, Corvol H. Clement A, et al. Orphanet J Rare Dis. 2010 Aug 20;5:22. doi: 10.1186/1750-1172-5-22. Orphanet J Rare Dis. 2010. PMID: 20727133 Free PMC article. Review.
713 results