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Page 1
Lumacaftor/Ivacaftor Population Pharmacokinetics in Pediatric Patients with Cystic Fibrosis: A First Step Toward Personalized Therapy.
Bouazza N, Urien S, Foissac F, Choupeaux L, Lui G, Froelicher Bournaud L, Rouillon S, Zheng Y, Bardin E, Stremler N, Bessaci K, Bihouee T, Coirier-Duet E, Marguet C, Deneuville E, Laurans M, Reix P, Gerardin M, Mittaine M, Epaud R, Thumerelle C, Weiss L, Berthaud R, Semeraro M, Treluyer JM, Benaboud S, Sermet-Gaudelus I. Bouazza N, et al. Among authors: laurans m. Clin Pharmacokinet. 2024 Mar;63(3):333-342. doi: 10.1007/s40262-023-01342-3. Epub 2024 Feb 4. Clin Pharmacokinet. 2024. PMID: 38310629
Neonatal screening of cystic fibrosis: diagnostic problems with CFTR mild mutations.
Roussey M, Le Bihannic A, Scotet V, Audrezet MP, Blayau M, Dagorne M, David V, Deneuville E, Giniès JL, Laurans M, Moisan-Petit V, Rault G, Vigneron P, Férec C. Roussey M, et al. Among authors: laurans m. J Inherit Metab Dis. 2007 Aug;30(4):613. doi: 10.1007/s10545-007-0633-8. Epub 2007 Jul 12. J Inherit Metab Dis. 2007. PMID: 17632692
[Recommendations for the management of bone demineralization in cystic fibrosis].
Sermet-Gaudelus I, Nove-Josserand R, Loeille GA, Dacremont G, Souberbielle JC, Fritsch J, Laurans M, Moulin P, Cortet B, Salles JP, Ginies JL, Guillot M, Perez-Martin S, Ruiz JC, Montagne V, Cohen-Solal M, Cormier C, Garabédian M, Mallet E; Fédération française des centres de ressource et de compétence en mucoviscidose. Sermet-Gaudelus I, et al. Among authors: laurans m. Arch Pediatr. 2008 Mar;15(3):301-12. doi: 10.1016/j.arcped.2007.12.003. Epub 2008 Mar 5. Arch Pediatr. 2008. PMID: 18325750 French.
[Bone health in cystic fibrosis].
Sermet-Gaudelus I, Castanet M, Souberbielle JC, Mallet E; Le Groupe de Travail sur Minéralisation Osseuse et Mucoviscidose de la Fédération Française des Centres de Ressource et de Compétence en Mucoviscidose. Sermet-Gaudelus I, et al. Arch Pediatr. 2009 Jun;16(6):616-8. doi: 10.1016/S0929-693X(09)74088-6. Arch Pediatr. 2009. PMID: 19541106 French. No abstract available.
Reference percentiles for FEV(1) and BMI in European children and adults with cystic fibrosis.
Boëlle PY, Viviani L, Busson PF, Olesen HV, Ravilly S, Stern M, Assael BM, Barreto C, Drevinek P, Thomas M, Krivec U, Mei-Zahav M, Vibert JF, Clement A, Mehta A, Corvol H; French CF Modifier Gene Study Investigators; European CF Registry Working Group. Boëlle PY, et al. Orphanet J Rare Dis. 2012 Sep 7;7:64. doi: 10.1186/1750-1172-7-64. Orphanet J Rare Dis. 2012. PMID: 22958330 Free PMC article.
Measurement properties of the one-minute sit-to-stand test in children and adolescents with cystic fibrosis: A multicenter randomized cross-over trial.
Combret Y, Boujibar F, Gennari C, Medrinal C, Sicinski S, Bonnevie T, Gravier FE, Laurans M, Marguet C, Le Roux P, Lamia B, Prieur G, Reychler G. Combret Y, et al. Among authors: laurans m. PLoS One. 2021 Feb 12;16(2):e0246781. doi: 10.1371/journal.pone.0246781. eCollection 2021. PLoS One. 2021. PMID: 33577586 Free PMC article. Clinical Trial.
Rapid Improvement after Starting Elexacaftor-Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis and Advanced Pulmonary Disease.
Burgel PR, Durieu I, Chiron R, Ramel S, Danner-Boucher I, Prevotat A, Grenet D, Marguet C, Reynaud-Gaubert M, Macey J, Mely L, Fanton A, Quetant S, Lemonnier L, Paillasseur JL, Da Silva J, Martin C; French Cystic Fibrosis Reference Network Study Group. Burgel PR, et al. Am J Respir Crit Care Med. 2021 Jul 1;204(1):64-73. doi: 10.1164/rccm.202011-4153OC. Am J Respir Crit Care Med. 2021. PMID: 33600738
Chest physiotherapy enhances detection of Pseudomonas aeruginosa in nonexpectorating children with cystic fibrosis.
Marguet C, Houdouin V, Pin I, Reix P, Huet F, Mittaine M, Ramel S, Wizla-Derambure N, Abely M, Dalphin ML, Fayon M, Bihouée T, Le Bourgeois M, Deneuville E, Corvol H, Laurans M, Couderc L, Leroux E, Lémée L. Marguet C, et al. Among authors: laurans m. ERJ Open Res. 2021 Mar 8;7(1):00513-2020. doi: 10.1183/23120541.00513-2020. eCollection 2021 Jan. ERJ Open Res. 2021. PMID: 33718497 Free PMC article.
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