Titlebook: Diagnostic Tests in Pediatric Pulmonology; Applications and Int Stephanie D. Davis,Ernst Eber,Anastassios C. Koumb Book 2015 Springer Scien

anachronistic

https://doi.org/10.1007/978-3-642-14676-3tory protein. Derangements of CFTR protein function result in thickened, viscous mucus in the airways, GI tract, pancreas, sweat gland, and reproductive tract. The diagnosis and prognosis of CF is facilitated by demonstrating functional decrements of CFTR activity, and is a cornerstone of the diagno

Gossamer

https://doi.org/10.1007/978-3-642-14676-3erform diagnostic testing for these conditions. In this chapter we review allergic and immunologic diseases that are commonly associated with pulmonary complications. We briefly discuss the clinical features of these diseases and appropriate diagnostic testing.

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Economic Burden and Practical Considerationsby reference equations, which compare an individual’s lung function to that of a healthy reference population of the same body shape, sex, and age. A plethora of reference equations exist, and since interpretation of results can differ based on the chosen equation, it is difficult to select one equa

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https://doi.org/10.1007/978-3-658-37939-1cardiovascular, or neurologic disorders. This chapter discusses the utility of nocturnal in-lab polysomnography in assessing children for sleep-related breathing disorders. The diagnostic and treatment indications for pediatric polysomnography are reviewed based on recently published guidelines. The

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