東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

Handbook of cystic fibrosis

Filbrun, Amy G.

FindBook

Google Book

Amazon

博客來

Handbook of cystic fibrosis

紀錄類型:	書目-電子資源 : Monograph/item
正題名/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.
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.
Contained By:	Springer eBooks
標題:	Cystic fibrosis. -
電子資源:	http://dx.doi.org/10.1007/978-3-319-32504-0
ISBN:	9783319325040

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

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

820635
Cystic fibrosis.

LC Class. No.: RC858.C95

Dewey Class. No.: 616.37

Handbook of cystic fibrosis
LDR:01927nmm a2200313 a 4500 001 2053813
003 DE-He213
005 20161006125322.0
006 m d
007 cr nn 008maaau
008 170510s2016 gw s 0 eng d
020 $a 9783319325040 $q (electronic bk.)
020 $a 9783319325026 $q (paper)
024 7 $a 10.1007/978-3-319-32504-0 $2 doi
035 $a 978-3-319-32504-0
040 $a GP $c GP
041 0 $a eng
050 4 $a RC858.C95
072 7 $a MJL $2 bicssc
072 7 $a MED079000 $2 bisacsh
082 0 4 $a 616.37 $2 23
090 $a RC858.C95 $b F479 2016
100 1 $a Filbrun, Amy G. $3 3166954
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 820635
650 1 4 $a Medicine & Public Health. $3 890906
650 2 4 $a Pneumology/Respiratory System. $3 894348
700 1 $a Lahiri, Thomas. $3 3166955
700 1 $a Ren, Clement L. $3 3166956
710 2 $a SpringerLink (Online service) $3 836513
773 0 $t Springer eBooks
856 4 0 $u http://dx.doi.org/10.1007/978-3-319-32504-0
950 $a Medicine (Springer-11650)