1. McIIwaine MP, Lee Son NM, Richmond ML. Physiotherapy and cystic fibrosis: what is the evidence base? Curr Opin Pulm Med. 2014;20:613--7. 2. Bento J, Goncalves M, Silva N, Pinto… Click to show full abstract
1. McIIwaine MP, Lee Son NM, Richmond ML. Physiotherapy and cystic fibrosis: what is the evidence base? Curr Opin Pulm Med. 2014;20:613--7. 2. Bento J, Goncalves M, Silva N, Pinto T, Marinho A, Winck JC. Indicaciones y cumplimiento con la insuflación-exuflación mecánica domiciliaria en pacientes con enfermedades neuromusculares. Arch Bronconeumol. 2010;46:420--5. 3. González Bellido V, González Conde W, Bermejo Moreno I, Ruiz Tajadura R, García Pérez L. Ensayo clínico aleatorizado de técnicas de aclaramiento mucociliar en niños con bronquiectasias sin fibrosis quística. Fisioterapia. 2013;35:92--8. 4. Alexander S, Alshafi K, Anderson AK, Balfour-Lynn I, Bentley S, Buchdahl R, et al. Clinical guidelines for the care of children with cystic fibrosis. 6th ed. Royal Brompton Hospital Paediatric Cystic Fibrosis Team; 2014. Available from: http://www.rbht. nhs.uk/childrencf [accessed 25.03.16]. 5. Konstan MW, Morgan WJ, Butler SM, Pasta DJ, Craib ML, Silva SJ, et al. Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis. J Pediatr. 2007;151:134--9.
               
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