-
Paediatr Respir Rev · Dec 2012
ReviewThe evolution of exercise capacity and its limiting factors in cystic fibrosis.
- Athari Almajed and Larry C Lands.
- Division of Pediatric Respiratory Medicine, Department of Pdiatrics, Montreal Children's Hospital-McGill University Health Centre, 2300 Tupper Street, Room D380, Montreal, Québec, Canada, H3H 1P3.
- Paediatr Respir Rev. 2012 Dec 1;13(4):195-9.
AbstractThe ability to perform exercise is an important determinant of both longevity and quality of life for patients with Cystic Fibrosis. There are a variety of physical and behavioural factors that contribute to exercise limitation. These, such as lung function or habitual physical activity, change over time. However, these factors can also be modified by treatments and interventions. This review discusses the various factors that contribute to exercise limitation in Cystic Fibrosis, and how these change with age.Copyright © 2012 Elsevier Ltd. All rights reserved.
Notes
Knowledge, pearl, summary or comment to share?You can also include formatting, links, images and footnotes in your notes
- Simple formatting can be added to notes, such as
*italics*,_underline_or**bold**. - Superscript can be denoted by
<sup>text</sup>and subscript<sub>text</sub>. - Numbered or bulleted lists can be created using either numbered lines
1. 2. 3., hyphens-or asterisks*. - Links can be included with:
[my link to pubmed](http://pubmed.com) - Images can be included with:
 - For footnotes use
[^1](This is a footnote.)inline. - Or use an inline reference
[^1]to refer to a longer footnote elseweher in the document[^1]: This is a long footnote..