@article{murphy_imaging_2016,
	title = {Imaging of {Cystic} {Fibrosis} and {Pediatric} {Bronchiectasis}},
	volume = {206},
	issn = {0361-803X},
	url = {http://proxy.library.upenn.edu:2908/doi/full/10.2214/AJR.15.14437},
	doi = {10.2214/AJR.15.14437},
	abstract = {Choose
                    Top of pageABSTRACT {\textless}{\textless}Disease Epidemiologic Pro...Pathophysiologic Basis of...Imaging StrategiesConclusionAcknowledgmentReferences  Key Points  CT is superior to pulmonary function tests and chest radiography for the assessment and monitoring of cystic fibrosis (CF)–related lung disease and, also, of pediatric bronchiectasis not caused by CF (hereafter referred to as non-CF bronchiectasis). Low-dose CT protocols that impart radiation doses similar to those used in chest radiography are feasible for the surveillance of patients with bronchiectasis. Chest radiography is still most commonly used as the first-line imaging examination of choice for the assessment of acute complications related to bronchiectasis. Pulmonary MRI, with or without the use of inhaled hyperpolarized gas, can be performed to obtain functional information, and, in dedicated centers, it may yield imaging results comparable to those obtained by CT. Gastrointestinal and pancreaticobiliary manifestations of CF are observed with greater frequency in adults, because of increased life expectancy.},
	number = {3},
	urldate = {2017-06-14TZ},
	journal = {American Journal of Roentgenology},
	author = {Murphy, Kevin P. and Maher, Michael M. and O'Connor, Owen J.},
	month = feb,
	year = {2016},
	keywords = {bronchiectasis, cystic fibrosis, high-resolution CT, low-dose CT, pulmonary MRI},
	pages = {448--454}
}

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