Results 91 to 100 of about 2,264 (160)

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

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

[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

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

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

Dornase alpha use in patients with cystic fibrosis. [PDF]

Rev Paul Pediatr, 2013
Marostica PJ.
europepmc   +1 more source

Fibrosis quística. Aspectos diagnósticos

, 2007
Cystic fibrosis (CF) is one of the most frequent inherited mortal diseases in Caucasian population. Dysfunction in exocrine glands is described in CF patients, with severe pancreatic insufficiency and chronic lung disease. CF is inherited as an autosomal
Ortigosa, Luis
core  

Abordaje dietético-nutricional en Fibrosis Quística

Revista Española de Nutrición Humana y Dietética, 2017
María Garriga García
doaj   +2 more sources