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Handbook of cystic fibrosis

Filbrun, Amy G.

Handbook of cystic fibrosis

Record Type:	Electronic resources : Monograph/item
Title/Author:	Handbook of cystic fibrosisby Amy G. Filbrun, Thomas Lahiri, Clement L Ren.
Author:	Filbrun, Amy G.
other author:	Lahiri, Thomas.
Published:	Cham :Springer International Publishing :2016.
Description:	xii, 99 p. :ill., digital ;24 cm.
Contained By:	Springer eBooks
Subject:	Cystic fibrosis.
Online resource:	http://dx.doi.org/10.1007/978-3-319-32504-0
ISBN:	9783319325040$q(electronic bk.)

Handbook of cystic fibrosis
Filbrun, Amy G.

Handbook of cystic fibrosis[electronic resource] /by Amy G. Filbrun, Thomas Lahiri, Clement L Ren. - Cham :Springer International Publishing :2016. - xii, 99 p. :ill., digital ;24 cm.

Introduction and epidemiology of cystic fibrosis -- Pathophysiology of cystic fibrosis -- Clinical features and complications of cystic fibrosis -- Diagnosis of cystic fibrosis -- Monitoring and evaluation of patients with cystic fibrosis -- Treatment of cystic fibrosis.

This concise manual provides clinicians and other related health care professionals with an essential reference tool to the background of cystic fibrosis, and the management and treatment of this disease. The latest guidelines are reviewed and current and emerging treatments are discussed in the latter chapters. Cystic fibrosis is an inherited condition where a mutation in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) causes loss of function. The dysfunction of CFTR results in the production of thick mucus in the lungs and digestive tract, causing pulmonary and gastrointestinal manifestations. The incidence of cystic fibrosis in Europe and the US ranges between 1 in 2,000 and 1 in 25,000.

ISBN: 9783319325040$q(electronic bk.)

Standard No.: 10.1007/978-3-319-32504-0doiSubjects--Topical Terms:

520584
Cystic fibrosis.

LC Class. No.: RC858.C95

Dewey Class. No.: 616.37

Handbook of cystic fibrosis
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245 1 0 $a Handbook of cystic fibrosis $h [electronic resource] / $c by Amy G. Filbrun, Thomas Lahiri, Clement L Ren.
260 $a Cham : $b Springer International Publishing : $b Imprint: Adis, $c 2016.
300 $a xii, 99 p. : $b ill., digital ; $c 24 cm.
505 0 $a Introduction and epidemiology of cystic fibrosis -- Pathophysiology of cystic fibrosis -- Clinical features and complications of cystic fibrosis -- Diagnosis of cystic fibrosis -- Monitoring and evaluation of patients with cystic fibrosis -- Treatment of cystic fibrosis.
520 $a This concise manual provides clinicians and other related health care professionals with an essential reference tool to the background of cystic fibrosis, and the management and treatment of this disease. The latest guidelines are reviewed and current and emerging treatments are discussed in the latter chapters. Cystic fibrosis is an inherited condition where a mutation in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) causes loss of function. The dysfunction of CFTR results in the production of thick mucus in the lungs and digestive tract, causing pulmonary and gastrointestinal manifestations. The incidence of cystic fibrosis in Europe and the US ranges between 1 in 2,000 and 1 in 25,000.
650 0 $a Cystic fibrosis. $3 520584
650 1 4 $a Medicine & Public Health. $3 273799
650 2 4 $a Pneumology/Respiratory System. $3 274253
700 1 $a Lahiri, Thomas. $3 761643
700 1 $a Ren, Clement L. $3 761644
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