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Page 1
Spanish consensus on the prevention and treatment of Pseudomonas aeruginosa bronchial infections in cystic fibrosis patients.
Cantón R, Máiz L, Escribano A, Olveira C, Oliver A, Asensio O, Gartner S, Roma E, Quintana-Gallego E, Salcedo A, Girón R, Barrio MI, Pastor MD, Prados C, Martínez-Martínez MT, Barberán J, Castón JJ, Martínez-Martínez L, Poveda JL, Vázquez C, de Gracia J, Solé A; en representación del Grupo Español de Consenso del Tratamiento Antimicrobiano en el Paciente con Fibrosis Quística. Cantón R, et al. Among authors: vazquez c. Arch Bronconeumol. 2015 Mar;51(3):140-50. doi: 10.1016/j.arbres.2014.09.021. Epub 2015 Jan 20. Arch Bronconeumol. 2015. PMID: 25614377 English, Spanish.
Antibiotic resistance and population structure of cystic fibrosis Pseudomonas aeruginosa isolates from a Spanish multi-centre study.
López-Causapé C, de Dios-Caballero J, Cobo M, Escribano A, Asensio Ó, Oliver A, Del Campo R, Cantón R, Solé A, Cortell I, Asensio O, García G, Martínez MT, Cols M, Salcedo A, Vázquez C, Baranda F, Girón R, Quintana E, Delgado I, de Miguel MÁ, García M, Oliva C, Prados MC, Barrio MI, Pastor MD, Olveira C, de Gracia J, Álvarez A, Escribano A, Castillo S, Figuerola J, Togores B, Oliver A, López C, de Dios Caballero J, Tato M, Máiz L, Suárez L, Cantón R. López-Causapé C, et al. Among authors: vazquez c. Int J Antimicrob Agents. 2017 Sep;50(3):334-341. doi: 10.1016/j.ijantimicag.2017.03.034. Epub 2017 Jul 20. Int J Antimicrob Agents. 2017. PMID: 28735882
[SEPAR (Spanish Society of Pneumology and Thoracic Surgery) Guidelines. Guideline for diagnosis and treatment of respiratory involvements in cystic fibrosis].
Máiz L, Baranda F, Coll R, Prados C, Vendrell M, Escribano A, Gartner S, de Gracia S, Martínez M, Salcedo A, Vázquez C; SEPAR (Spanish Society of Pneumology and Thoracic Surgery). Máiz L, et al. Among authors: vazquez c. Arch Bronconeumol. 2001 Sep;37(8):316-24. doi: 10.1016/s0300-2896(01)75101-0. Arch Bronconeumol. 2001. PMID: 11562317 Review. Spanish. No abstract available.
[Consensus on certain aspects of lung disease in cystic fibrosis patients].
Maiz L, Antelo C, Baquero F, Cobos N, Morales P, Pérez-Frías J, Vázquez C. Maiz L, et al. Among authors: vazquez c. Arch Bronconeumol. 1999 Jul-Aug;35(7):339-44. doi: 10.1016/s0300-2896(15)30072-7. Arch Bronconeumol. 1999. PMID: 10439132 Review. Spanish. No abstract available.
Population pharmacokinetics of high dose ibuprofen in cystic fibrosis.
Arranz I, Martín-Suárez A, Lanao JM, Mora F, Vázquez C, Escribano A, Juste M, Mercader J, Ripoll E. Arranz I, et al. Among authors: vazquez c. Arch Dis Child. 2003 Dec;88(12):1128-30. doi: 10.1136/adc.88.12.1128. Arch Dis Child. 2003. PMID: 14670788 Free PMC article.
Missense mutation R1066C in the second transmembrane domain of CFTR causes a severe cystic fibrosis phenotype: study of 19 heterozygous and 2 homozygous patients.
Casals T, Pacheco P, Barreto C, Giménez J, Ramos MD, Pereira S, Pinheiro JA, Cobos N, Curvelo A, Vázquez C, Rocha H, Séculi JL, Pérez E, Dapena J, Carrilho E, Duarte A, Palacio AM, Nunes V, Lavinha J, Estivill X. Casals T, et al. Among authors: vazquez c. Hum Mutat. 1997;10(5):387-92. doi: 10.1002/(SICI)1098-1004(1997)10:5<387::AID-HUMU9>3.0.CO;2-C. Hum Mutat. 1997. PMID: 9375855
916 results