Amiloride Inhalation Therapy in Cystic Fibrosis: Influence on Ion Content, Hydration, and Rheology of Sputum-Reference-Cited by-同舟云学术

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Amiloride Inhalation Therapy in Cystic Fibrosis: Influence on Ion Content, Hydration, and Rheology of Sputum

Published:1993-10 Issue:4_pt_1 Volume:148 Page:1002-1007
ISSN:0003-0805
Container-title:American Review of Respiratory Disease
language:en
Short-container-title:Am Rev Respir Dis

Author:

Tomkiewicz R. P.,App E. M.,Zayas J. G.,Ramirez O.,Church N.,Boucher R. C.,Knowles M. R.,King M.

Publisher

American Thoracic Society

Subject

Pulmonary and Respiratory Medicine

Reference26 articles.

1. Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation.

2. Cystic fibrosis: a disease in electrolyte transport

3. Abnormal regulation of ion channels in cystic fibrosis epithelia

4. Molecular and cellular biology of cystic fibrosis

5. Acute and Long-term Amiloride Inhalation in Cystic Fibrosis Lung Disease: A Rational Approach to Cystic Fibrosis Therapy

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