Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

117 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
[Cystic fibrosis: how to use pulmonary function tests].
Counil FP, Karila C, Le Bourgeois M, Matecki S, Lebras MN, Couderc L, Fajac I, Reynaud-Gaubert M, Bellet M, Gauthier R, Denjean A; Groupe de travail Explorations Fonctionnelles Respiratoires de la Société Française de la Mucoviscidose. Counil FP, et al. Among authors: fajac i. Rev Mal Respir. 2007 Jun;24(6):691-701. doi: 10.1016/s0761-8425(07)91145-6. Rev Mal Respir. 2007. PMID: 17632430 Review. French.
[Diagnosis of cystic fibrosis in adults].
Chinet T, Fajac I, Ferec C, Garcia Carmona T, Nguyen-Khoa T. Chinet T, et al. Among authors: fajac i. Rev Mal Respir. 2000 Aug;17(3 Pt 2):739-48. Rev Mal Respir. 2000. PMID: 11076384 Review. French.
Diagnosis of cystic fibrosis in adults with diffuse bronchiectasis.
Hubert D, Fajac I, Bienvenu T, Desmazes-Dufeu N, Ellaffi M, Dall'ava-Santucci J, Dusser D. Hubert D, et al. Among authors: fajac i. J Cyst Fibros. 2004 Mar;3(1):15-22. doi: 10.1016/j.jcf.2003.12.004. J Cyst Fibros. 2004. PMID: 15463882 Free article.
Non-classic cystic fibrosis associated with D1152H CFTR mutation.
Burgel PR, Fajac I, Hubert D, Grenet D, Stremler N, Roussey M, Siret D, Languepin J, Mely L, Fanton A, Labbé A, Domblides P, Vic P, Dagorne M, Reynaud-Gaubert M, Counil F, Varaigne F, Bienvenu T, Bellis G, Dusser D. Burgel PR, et al. Among authors: fajac i. Clin Genet. 2010 Apr;77(4):355-64. doi: 10.1111/j.1399-0004.2009.01294.x. Epub 2009 Oct 15. Clin Genet. 2010. PMID: 19843100
Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport.
Sermet-Gaudelus I, Girodon E, Sands D, Stremmler N, Vavrova V, Deneuville E, Reix P, Bui S, Huet F, Lebourgeois M, Munck A, Iron A, Skalicka V, Bienvenu T, Roussel D, Lenoir G, Bellon G, Sarles J, Macek M, Roussey M, Fajac I, Edelman A. Sermet-Gaudelus I, et al. Among authors: fajac i. Am J Respir Crit Care Med. 2010 Oct 1;182(7):929-36. doi: 10.1164/rccm.201003-0382OC. Epub 2010 Jun 10. Am J Respir Crit Care Med. 2010. PMID: 20538955
Amikacin liposome inhalation suspension for chronic Pseudomonas aeruginosa infection in cystic fibrosis.
Bilton D, Pressler T, Fajac I, Clancy JP, Sands D, Minic P, Cipolli M, Galeva I, Solé A, Quittner AL, Liu K, McGinnis JP 2nd, Eagle G, Gupta R, Konstan MW; CLEAR-108 Study Group. Bilton D, et al. Among authors: fajac i. J Cyst Fibros. 2020 Mar;19(2):284-291. doi: 10.1016/j.jcf.2019.08.001. Epub 2019 Aug 23. J Cyst Fibros. 2020. PMID: 31451351 Free PMC article. Clinical Trial.
117 results