Results 51 to 60 of about 588 (121)

Chronic lung infection by <i>Achromobacter xylosoxidans</i> in a patient with cystic fibrosis successfully treated with cefiderocol as a pre and post-lung transplant regimen. [PDF]

Rev Esp Quimioter
Ramos-Oliveira S, Alonso-Moralejo R, Pérez V, Quezada CA, de Pablo A, Muñoz-Gallego I, Silva JT, Aguado JM, López-Medrano F.   +8 more
europepmc   +1 more source

Estimation of care costs for individuals with cystic fibrosis at a referral center: cohort study, Salvador, 2005-2022. [PDF]

Epidemiol Serv Saude
Costa JCB, Sorte NCAB, D'Souza EL.
europepmc   +1 more source

Infections, autoimmunity and immunodeficiencies are the leading etiologies of non-cystic fibrosis bronchiectasis in adults from the southwest of Colombia. [PDF]

Biomedica
Zea-Vera AF, Rodríguez CA, Giraldo S, Chacón MA, Guerrero LF, Mosquera R, Vallejo RA, Vargas FS, García MA, Rengifo MA, Bonelo A, Parra M.   +11 more
europepmc   +1 more source

Short-term Tolerance to Inhaled Antibiotics in Patients With Bronchial Infection not Associated With Cystic Fibrosis. [PDF]

Open Respir Arch
Máiz L, Nieto R, Durán D, Máiz J, Ruiz-Calvo G, Muriel A, Barbero E, Vélez-Díaz-Pallarés M, Morillo R.   +8 more
europepmc   +1 more source

[Genetic testing in Primary Care]. [PDF]

Aten Primaria, 2023
Fernández Torres S, Ejarque Doménech I.   +1 more
europepmc   +1 more source

[Self-care capacity of adult cystic fibrosis patients during transition/transfer between services]. [PDF]

An Sist Sanit Navar
Coca Barbado A, Zamarrón de Lucas E, Álvarez-Sala Walther R, Prados Sánchez MC.   +3 more
europepmc   +1 more source

Long term follow-up of a tobacco prevention and cessation program in cystic fibrosis patients. [PDF]

Adicciones, 2016
Ortega-García JA, Perales JE, Cárceles-Álvarez A, Sánchez-Sauco MF, Villalona S, Mondejar-López P, Pastor-Vivero MD, Mira Escolano P, James-Vega DC, Sánchez-Solís M.   +9 more
europepmc   +1 more source

Look at the wood and not at the tree: The Microbiome in Chronic Obstructive Lung Disease and Cystic Fibrosis. [PDF]

Arch Bronconeumol, 2020
Monsó E.
europepmc   +1 more source

Hipoplasia tímica en un niño con fibrosis quística

Revista Cubana de Hematología, Inmunología y Hemoterapia
La fibrosis quística es la enfermedad autosómica recesiva más frecuente en poblaciones caucásicas; en Cuba, uno de cada 5 000 recién nacidos están afectados. En 1989 fue clonado el gen regulador de la conductancia transmembranal de la fibrosis quística e
Odalis de la Guardia-Peña, Catalino Ustariz-García, María de los Á García-García, Luz M Morera-Barrios, Arturo Chang-Monteagudo, Kalia Lavaut-Sánchez   +5 more
doaj  

IRT/IRT as a newborn cystic fibrosis screening method: optimal cutoff points for a mixed population. [PDF]

Cad Saude Publica
Godoy C, Brito PP, Amorim T, Souza EL, Boa-Sorte N.   +4 more
europepmc   +1 more source