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

Year Number of Results
1982 1
1983 1
2001 1
2004 1
2005 1
2006 1
2007 1
2008 5
2009 1
2010 4
2011 4
2012 6
2013 5
2014 11
2015 10
2016 8
2017 9
2018 3
2019 2
2020 13
2021 12
2022 8
2023 3
2024 4

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98 results

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Page 1
The French Compassionate Program of elexacaftor-tezacaftor-ivacaftor in people with cystic fibrosis with advanced lung disease and no F508del CFTR variant.
Burgel PR, Sermet-Gaudelus I, Durieu I, Kanaan R, Macey J, Grenet D, Porzio M, Coolen-Allou N, Chiron R, Marguet C, Douvry B, Dufeu N, Danner-Boucher I, Foucaud P, Lemonnier L, Girodon E, Da Silva J, Martin C; French CF Reference Network study group. Burgel PR, et al. Among authors: chiron r. Eur Respir J. 2023 Feb 16:2202437. doi: 10.1183/13993003.02437-2022. Online ahead of print. Eur Respir J. 2023. PMID: 36796836
Gathering real-world compassionate data to expand eligibility for elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with N1303K or other rare CFTR variants: a viewpoint.
Burgel PR, Sermet-Gaudelus I, Girodon E, Kanaan R, Le Bihan J, Remus N, Ravoninjatovo B, Grenet D, Porzio M, Houdouin V, Le Clainche-Viala L, Durieu I, Nove-Josserand R, Languepin J, Coltey B, Guillaumot A, Audousset C, Chiron R, Weiss L, Fajac I, Da Silva J, Martin C; French CF Reference Network study group. Burgel PR, et al. Among authors: chiron r. Eur Respir J. 2024 Jan 25;63(1):2301959. doi: 10.1183/13993003.01959-2023. Print 2024 Jan. Eur Respir J. 2024. PMID: 38242629 No abstract available.
Nonsense mutations accelerate lung disease and decrease survival of cystic fibrosis children.
Orenti A, Pranke I, Faucon C, Varilh J, Hatton A, Golec A, Dehillotte C, Durieu I, Reix P, Burgel PR, Grenet D, Tasset C, Gachelin E, Perisson C, Lepissier A, Dreano E, Tondelier D, Chevalier B, Weiss L, Kiefer S, Laurans M, Chiron R, Lemonnier L, Marguet C, Jung A, Edelman A, Kerem BS, Girodon E, Taulan-Cadars M, Hinzpeter A, Kerem E, Naehrlich L, Sermet-Gaudelus I; ECFSPR Steering group. Orenti A, et al. Among authors: chiron r. J Cyst Fibros. 2023 Nov;22(6):1070-1079. doi: 10.1016/j.jcf.2023.06.005. Epub 2023 Jul 6. J Cyst Fibros. 2023. PMID: 37422433
Amikacin Liposomal Inhalation Suspension in the Treatment of Mycobacterium abscessus Lung Infection: A French Observational Experience.
Chiron R, Hoefsloot W, Van Ingen J, Marchandin H, Kremer L, Morisse-Pradier H, Charriot J, Mallet JP, Herrmann JL, Caimmi D, Moreau J, Dumont Y, Godreuil S, Bergeron A, Drevait M, Bouzat-Rossigneux E, Terrail N, Andrejak C, Veziris N, Grenet D, Coudrat A, Catherinot E. Chiron R, et al. Open Forum Infect Dis. 2022 Sep 11;9(10):ofac465. doi: 10.1093/ofid/ofac465. eCollection 2022 Oct. Open Forum Infect Dis. 2022. PMID: 36267258 Free PMC article.
A model for active and healthy ageing with a rare genetic disease: cystic fibrosis.
Chiron R, Caimmi D, Valiulis A, Durieu I, Tejedor P, Le Cam Y, Boudes M, Jonquet O, Strandberg T, Michel JP, de Manuel Keenoy E, Demoly P, Mercier J, Bourret R, Bousquet J; MACVIA-LR European Innovation Partnership on Active and Healthy Ageing Reference Site. Chiron R, et al. Eur Respir J. 2016 Mar;47(3):714-9. doi: 10.1183/13993003.01237-2015. Eur Respir J. 2016. PMID: 26929314 Free article. Review. No abstract available.
[National consensus regarding azithromycin use in cystic fibrosis].
Abely M, Jubin V, Bessaci-Kabouya K, Chiron R, Bui S, Fayon M. Abely M, et al. Among authors: chiron r. Rev Mal Respir. 2015 Jun;32(6):557-65. doi: 10.1016/j.rmr.2014.10.733. Epub 2015 May 21. Rev Mal Respir. 2015. PMID: 26003196 Review. French.
98 results