Does the effect of comprehensive respiratory physiotherapy home-program differ in children with cystic fibrosis and non-cystic fibrosis bronchiectasis?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00431-022-04509-5.pdf
Reference41 articles.
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2. Dodd JD, Lavelle LP, Fabre A, Brady D editors (2015) Imaging in cystic fibrosis and non–cystic fibrosis bronchiectasis. Seminars in respiratory and critical care medicine. Thieme Med Publ. https://doi.org/10.1055/s-0035-1546749
3. Denizoglu Kulli H, Gurses HN, Zeren M, Ucgun H, Cakir E (2020) Do pulmonary and extrapulmonary features differ among cystic fibrosis, primary ciliary dyskinesia, and healthy children? Pediatr Pulmonol 55(11):3067–3073. https://doi.org/10.1002/ppul.25052
4. Wells GD, Wilkes DL, Schneiderman JE, Rayner T, Elmi M, Selvadurai H et al (2011) Skeletal muscle metabolism in cystic fibrosis and primary ciliary dyskinesia. Pediatr Res 69(1):40–45. https://doi.org/10.1203/PDR.0b013e3181fff35f
5. Bar-Yoseph R, Ilivitzki A, Cooper DM, Gur M, Mainzer G, Hakim F et al (2019) Exercise capacity in patients with cystic fibrosis vs. non-cystic fibrosis bronchiectasis. PloS One 14(6):e0217491. https://doi.org/10.1371/journal.pone.0217491
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