Treatment of cystic fibrosis and 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 in...

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Bibliographic Details
Other Authors: Azuma, Arata, (Editor), Schechter, Michael S., (Editor)
Format: eBook
Language: English
Published: Switzerland : Springer, 2017.
Series: Milestones in drug therapy.
Subjects:
nemoci plic
cystická fibróza
pulmonary diseases
cystic fibrosis
elektronické knihy
sborníky
electronic books
papers of several authors
ISBN: 9783034809771
9783034809757
Physical Description: 1 online resource

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Table of contents

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080 |a (0.034.2:08)   |2 MRF 
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245 0 0 |a Treatment of cystic fibrosis and other rare lung diseases /  |c Arata Azuma, Michael S. Schechter, editors. 
264 1 |a Switzerland :  |b Springer,  |c 2017. 
300 |a 1 online resource 
336 |a text  |b txt  |2 rdacontent 
337 |a počítač  |b c  |2 rdamedia 
338 |a online zdroj  |b cr  |2 rdacarrier 
490 1 |a Milestones in drug therapy,  |x 2296-6056 
504 |a Includes bibliographical references. 
506 |a Plný text je dostupný pouze z IP adres počítačů Univerzity Tomáše Bati ve Zlíně nebo vzdáleným přístupem pro zaměstnance a studenty 
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.- Resumé vydavatel 
590 |a SpringerLink  |b Springer Complete eBooks 
650 0 7 |a nemoci plic  |2 czenas  |7 ph134927 
650 0 7 |a cystická fibróza  |2 czenas  |7 ph119277 
650 0 9 |a pulmonary diseases  |2 eczenas 
650 0 9 |a cystic fibrosis  |2 eczenas 
655 7 |a elektronické knihy  |7 fd186907  |2 czenas 
655 7 |a sborníky  |7 fd163935  |2 czenas 
655 9 |a electronic books  |2 eczenas 
655 9 |a papers of several authors  |2 eczenas 
700 1 |a Azuma, Arata,  |e editor. 
700 1 |a Schechter, Michael S.,  |e editor. 
776 0 8 |i Printed edition:  |z 9783034809757 
830 0 |a Milestones in drug therapy. 
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992 |c NTK-SpringerBLS 
993 |x NEPOSILAT  |y EIZ 

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