http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd
viii, 222 pages : illustrations ; 26 cm.
Cystic fibrosis : the first indentified glutathione transport disease -- Bile acid dysfunction in the cystic fibrosis intestine -- Electrolite depletion with metabolic alkalosis in infants with cystic fibrosis -- Markers of oxidative damage and antioxidant status in blood of children with cystic fibrosis -- Auxological and endocrine abnormalities in cystic fibrosis -- Agents that enhance mucociliary clearance in the treatment of cystic fibrosis related lung disease -- Molecular genetics of hispanic cystic fibrosis -- Pregnancy in cystic fibrosis - Scandinavian experience -- Interleukin-8 in sputum from cystic fibrosis patients during ibuprofen treatment -- Improving survival as a result of modern preventative care : an ageing Swedish cystic fibrous population
Includes bibliographical references and index.