Language:
English
繁體中文
Help
圖資館首頁
Login
Back
Switch To:
Labeled
|
MARC Mode
|
ISBD
Treatment of cystic fibrosis and oth...
~
Azuma, Arata.
Treatment of cystic fibrosis and other rare lung diseases
Record Type:
Electronic resources : Monograph/item
Title/Author:
Treatment of cystic fibrosis and other rare lung diseasesedited by Arata Azuma, Michael S. Schechter.
other author:
Azuma, Arata.
Published:
Basel :Springer Basel :2017.
Description:
viii, 263 p. :ill., digital ;24 cm.
Contained By:
Springer eBooks
Subject:
Cystic fibrosisTreatment.
Online resource:
http://dx.doi.org/10.1007/978-3-0348-0977-1
ISBN:
9783034809771$q(electronic bk.)
Treatment of cystic fibrosis and other rare lung diseases
Treatment of cystic fibrosis and other rare lung diseases
[electronic resource] /edited by Arata Azuma, Michael S. Schechter. - Basel :Springer Basel :2017. - viii, 263 p. :ill., digital ;24 cm. - Milestones in drug therapy,2296-6056. - Milestones in drug therapy..
Part I Etiopathology and Genetics of Rare Lung Diseases -- Part II Treatment of Cystic Fibrosis -- Part III Treatment of Other Rare Lung Diseases.
This volume describes the pathogenesis and pathophysiology of several pulmonary diseases as well as their treatment. It also discusses the underlying genetic and molecular biological basis, which opens the way for new treatments for these conditions. It focuses on the treatment of cystic fibrosis including CFTR (cystic fibrosis transmembrane-conductance regulator) modulator therapies, drug therapies that augment airway surface liquid as well as anti-inflammatory and anti-infective therapies. Further topics include long-term, low-dose macrolide therapy for diffuse panbronchiolitis; novel agents for previously untreatable idiopathic pulmonary fibrosis; possible new treatments for pulmonary alveolar proteinosis (PAP); and multiple novel therapeutic targets for treating lymphangiomyomatosis. Research into these conditions has led to major advances in our understanding of the underlying genetic and molecular basis of this disease, and to dramatic improvements in survival and quality of life for affected individuals.
ISBN: 9783034809771$q(electronic bk.)
Standard No.: 10.1007/978-3-0348-0977-1doiSubjects--Topical Terms:
731857
Cystic fibrosis
--Treatment.
LC Class. No.: RC858.C95
Dewey Class. No.: 616.372
Treatment of cystic fibrosis and other rare lung diseases
LDR
:02199nmm a2200325 a 4500
001
507088
003
DE-He213
005
20170201181627.0
006
m d
007
cr nn 008maaau
008
171030s2017 sz s 0 eng d
020
$a
9783034809771$q(electronic bk.)
020
$a
9783034809757$q(paper)
024
7
$a
10.1007/978-3-0348-0977-1
$2
doi
035
$a
978-3-0348-0977-1
040
$a
GP
$c
GP
041
0
$a
eng
050
4
$a
RC858.C95
072
7
$a
MMG
$2
bicssc
072
7
$a
MED071000
$2
bisacsh
082
0 4
$a
616.372
$2
23
090
$a
RC858.C95
$b
T784 2017
245
0 0
$a
Treatment of cystic fibrosis and other rare lung diseases
$h
[electronic resource] /
$c
edited by Arata Azuma, Michael S. Schechter.
260
$a
Basel :
$b
Springer Basel :
$b
Imprint: Springer,
$c
2017.
300
$a
viii, 263 p. :
$b
ill., digital ;
$c
24 cm.
490
1
$a
Milestones in drug therapy,
$x
2296-6056
505
0
$a
Part I Etiopathology and Genetics of Rare Lung Diseases -- Part II Treatment of Cystic Fibrosis -- Part III Treatment of Other Rare Lung Diseases.
520
$a
This volume describes the pathogenesis and pathophysiology of several pulmonary diseases as well as their treatment. It also discusses the underlying genetic and molecular biological basis, which opens the way for new treatments for these conditions. It focuses on the treatment of cystic fibrosis including CFTR (cystic fibrosis transmembrane-conductance regulator) modulator therapies, drug therapies that augment airway surface liquid as well as anti-inflammatory and anti-infective therapies. Further topics include long-term, low-dose macrolide therapy for diffuse panbronchiolitis; novel agents for previously untreatable idiopathic pulmonary fibrosis; possible new treatments for pulmonary alveolar proteinosis (PAP); and multiple novel therapeutic targets for treating lymphangiomyomatosis. Research into these conditions has led to major advances in our understanding of the underlying genetic and molecular basis of this disease, and to dramatic improvements in survival and quality of life for affected individuals.
650
0
$a
Cystic fibrosis
$x
Treatment.
$3
731857
650
0
$a
Lungs
$x
Diseases
$x
Treatment.
$3
489272
650
1 4
$a
Biomedicine.
$3
273648
650
2 4
$a
Pharmacology/Toxicology.
$3
273652
650
2 4
$a
Pneumology/Respiratory System.
$3
274253
650
2 4
$a
Internal Medicine.
$3
273839
650
2 4
$a
Immunology.
$3
189152
700
1
$a
Azuma, Arata.
$3
773549
700
1
$a
Schechter, Michael S.
$3
773550
710
2
$a
SpringerLink (Online service)
$3
273601
773
0
$t
Springer eBooks
830
0
$a
Milestones in drug therapy.
$3
557479
856
4 0
$u
http://dx.doi.org/10.1007/978-3-0348-0977-1
950
$a
Biomedical and Life Sciences (Springer-11642)
based on 0 review(s)
ALL
電子館藏
Items
1 records • Pages 1 •
1
Inventory Number
Location Name
Item Class
Material type
Call number
Usage Class
Loan Status
No. of reservations
Opac note
Attachments
000000138023
電子館藏
1圖書
電子書
EB RC858.C95 T784 2017
一般使用(Normal)
On shelf
0
1 records • Pages 1 •
1
Multimedia
Multimedia file
http://dx.doi.org/10.1007/978-3-0348-0977-1
Reviews
Add a review
and share your thoughts with other readers
Export
pickup library
Processing
...
Change password
Login