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Handbook of cystic fibrosis[electron...

Filbrun, Amy G.

Handbook of cystic fibrosis[electronic resource] /

紀錄類型:	書目-電子資源 : Monograph/item
杜威分類號:	616.37
書名/作者:	Handbook of cystic fibrosis/ by Amy G. Filbrun, Thomas Lahiri, Clement L Ren.
作者:	Filbrun, Amy G.
其他作者:	Lahiri, Thomas.
出版者:	Cham : : Springer International Publishing :, 2016.
面頁冊數:	xii, 99 p. : : ill., digital ;; 24 cm.
Contained By:	Springer eBooks
標題:	Cystic fibrosis.
標題:	Medicine & Public Health.
標題:	Pneumology/Respiratory System.
ISBN:	9783319325040
ISBN:	9783319325026
內容註:	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.
摘要、提要註:	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.
電子資源:	http://dx.doi.org/10.1007/978-3-319-32504-0

Handbook of cystic fibrosis[electronic resource] /
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

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

438405
Cystic fibrosis.

LC Class. No.: RC858.C95

Dewey Class. No.: 616.37

Handbook of cystic fibrosis[electronic resource] /
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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.
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650 2 4 $a Pneumology/Respiratory System. $3 464971
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700 1 $a Ren, Clement L. $3 673130
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