Results 161 to 170 of about 925,943 (256)

Clinical Disorders in Cystic Fibrosis That Affect Emergency Procedures-A Case Report and Review. [PDF]

J Clin Med
Jarzynka S, Dobrosz M, Jaworski S, Jóźwicki K, Wierzba S, Barbarska O, Minkiewicz-Zochniak A.   +6 more
europepmc   +1 more source

Medical Management of Patients With Cystic Fibrosis

, 1965
Harry Shwachman
openalex   +1 more source

Serial lung function studies in cystic fibrosis in the first 5 years of life. [PDF]

, 1978
S. Godfrey, M B Mearns, G. Howlett
openalex   +1 more source

Achromobacter spp.: Emerging pathogens in the cystic fibrosis lung. [PDF]

PLoS Pathog
Bhowmik N, Stubbendieck RM.
europepmc   +1 more source

Serum alpha - fetoprotein levels in patients with cystic fibrosis and their parents and siblings. [PDF]

, 1975
R. K. Chandra, K Madhavankutty, R. C. Way   +2 more
openalex   +1 more source

Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation

Jornal de Pediatria, 2017
P. Farrell, Terry B. White, C. Ren, S. Hempstead, F. Accurso, N. Derichs, M. Howenstine, S. McColley, M. Rock, M. Rosenfeld, I. Sermet-Gaudelus, K. Southern, B. Marshall, P. Sosnay   +13 more
semanticscholar   +1 more source

Managing an ageing cystic fibrosis population: challenges and priorities. [PDF]

Eur Respir Rev
Frost FJ, Peckham DG, Felton IC, Snowball JE, Gray RD, Jones AM, Simmonds NJ, Lord RW, Lip GYH, Chandler H, Murphy K, Downey DG, Sheppard DN, Davies JC, Bull J, Sommer P, Cupid B, Allen L, Duckers J.   +18 more
europepmc   +1 more source

Altered Polyamine Metabolism in Cystic Fibrosis [PDF]

, 1979
Diane Haddock Russell, Michael G. Rosenblum, Robert C. Beckerman, Brian G.M. Durie, Lynn M. Taussig, Don R. Barnett   +5 more
openalex   +1 more source

Decoding the role of extracellular vesicles in pathogenesis of cystic fibrosis. [PDF]

Mol Cell Pediatr
Kalsi P, Gupta N, Goyal G, Sharma H.
europepmc   +1 more source

Microbiology of cystic fibrosis persons not chronically infected with P. aeruginosa: A quasi-experimental study on two different upper airways’ sampling methods

Heliyon
Background: The upper airways of cystic fibrosis (CF) persons are an evolutionary niche where genetically adapted bacterial strains are selected for lung infection.
Daniela Dolce, Novella Ravenni, Cristina Fevola, Michela Francalanci, Paolo Bonomi, Maria Chiara Cavicchi, Valeria Galici, Anna Silvia Neri, Giovanni Taccetti, Vito Terlizzi, Diletta Innocenti, Beatrice Ferrari, Chiara Bianchimani, Erica Camera, Tommaso Orioli, Silvia Campana   +15 more
doaj