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Page 1
Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators.
Pranke IM, Hatton A, Simonin J, Jais JP, Le Pimpec-Barthes F, Carsin A, Bonnette P, Fayon M, Stremler-Le Bel N, Grenet D, Thumerel M, Mazenq J, Urbach V, Mesbahi M, Girodon-Boulandet E, Hinzpeter A, Edelman A, Sermet-Gaudelus I. Pranke IM, et al. Among authors: stremler le bel n. Sci Rep. 2017 Aug 7;7(1):7375. doi: 10.1038/s41598-017-07504-1. Sci Rep. 2017. PMID: 28785019 Free PMC article.
[Fat overload syndrome].
Picon J, Carsin A, Baravalle-Einaudi M, Coste ME, Wasier AP, Stremler-Le Bel N, Bosdure E, Dubus JC. Picon J, et al. Among authors: stremler le bel n. Arch Pediatr. 2016 Aug;23(8):836-9. doi: 10.1016/j.arcped.2016.05.011. Epub 2016 Jun 28. Arch Pediatr. 2016. PMID: 27369104 French.
Prevalence of Mycobacterium lentiflavum in cystic fibrosis patients, France.
Phelippeau M, Dubus JC, Reynaud-Gaubert M, Gomez C, Stremler le Bel N, Bedotto M, Prudent E, Drancourt M. Phelippeau M, et al. Among authors: stremler le bel n. BMC Pulm Med. 2015 Oct 26;15:131. doi: 10.1186/s12890-015-0123-y. BMC Pulm Med. 2015. PMID: 26503635 Free PMC article.
[Nanoparticles and health].
Dubus JC, Bosdure E, David M, Stremler-Lebel N. Dubus JC, et al. Arch Pediatr. 2010 Jun;17(6):600-1. doi: 10.1016/S0929-693X(10)70017-8. Arch Pediatr. 2010. PMID: 20654799 French. No abstract available.
23 results