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Discusses clinical manifestations and available therapies for cystic fibrosis. Amongst other relevant topics, the text examines complications of the disease and treatment strategies, and presents the genetics and genetic epidemiology of cystic fibrosis.
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First Sentence:
The cloning of the gene that is defective in cystic fibrosis (CF) has provided a means for accurate genetic diagnosis, defining the basic cellular defect, and developing new treatment strategies. Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
conventional chest physiotherapy, mist tent therapy, overt right heart failure, mucin peptide core, bronchiectatic cysts, chronic pseudomonas infection, reabsorptive duct, amiloride aerosol, secretory clearance, chronic endobronchial infection, distal intestinal obstruction syndrome, multilobular biliary cirrhosis, focal biliary cirrhosis, opsonized pseudomonas, cepacia colonization, pulmonary exacerbations, ductal segments, pancreatic duct cells, aeruginosa mucoid exopolysaccharide, basolateral cell membrane, pulmonary deterioration, mucin granules, mucus stasis, porcine submaxillary mucin, respiratory exacerbations Key Phrases - Capitalized Phrases (CAPs): (learn more)
New Engl, New York, Acta Paediatr, San Francisco, United States, Allergy Clin, Chest Med, Acta Pathol, Cell Biol, Raven Press, Agents Chemother, American Physiological Society, Liver Physiol, Marcel Dekker, The Gastrointestinal System, Academic Press, Johns Hopkins Med, Membrane Biol, Drug Intell, Elastic van Gieson, Hedman Cefsulodin, Hedman Ceftazidime, Pergamon Press, Van Asperen New!
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Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
The cloning of the gene that is defective in cystic fibrosis (CF) has provided a means for accurate genetic diagnosis, defining the basic cellular defect, and developing new treatment strategies. Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
conventional chest physiotherapy, mist tent therapy, overt right heart failure, mucin peptide core, bronchiectatic cysts, chronic pseudomonas infection, reabsorptive duct, amiloride aerosol, secretory clearance, chronic endobronchial infection, distal intestinal obstruction syndrome, multilobular biliary cirrhosis, focal biliary cirrhosis, opsonized pseudomonas, cepacia colonization, pulmonary exacerbations, ductal segments, pancreatic duct cells, aeruginosa mucoid exopolysaccharide, basolateral cell membrane, pulmonary deterioration, mucin granules, mucus stasis, porcine submaxillary mucin, respiratory exacerbations Key Phrases - Capitalized Phrases (CAPs): (learn more)
New Engl, New York, Acta Paediatr, San Francisco, United States, Allergy Clin, Chest Med, Acta Pathol, Cell Biol, Raven Press, Agents Chemother, American Physiological Society, Liver Physiol, Marcel Dekker, The Gastrointestinal System, Academic Press, Johns Hopkins Med, Membrane Biol, Drug Intell, Elastic van Gieson, Hedman Cefsulodin, Hedman Ceftazidime, Pergamon Press, Van Asperen New!
Books on Related Topics | Concordance | Text Stats Browse Sample Pages:
Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
Citations (learn more)
This book cites 88
books:
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100
books
cite this book:
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- Cystic Fibrosis by Margaret E. Hodson on 10 pages
- Cystic Fibrosis by Lynn M. Taussig on 9 pages
- Cellular and Molecular Basis of Cystic Fibrosis by G. Mastella on 5 pages
- Cystic Fibrosis (Experience of Illness) by Evan Willis on 4 pages
- The Metabolic and Molecular Bases of Inherited Disease, 4 volume set by Charles R. Scriver on 4 pages
See all 88 books this book cites
- Psychosocial Aspects of Cystic Fibrosis by Myra Bluebond-Langner on 7 pages
- The Cystic Fibrosis Transmembrane Conductance Regulator (Molecular Biology Intelligence Unit) by Kevin L. Kirk on 5 pages
- Cystic Fibrosis: Methods and Protocols (Methods in Molecular Medicine) by William R. Skach on 4 pages
- Cilia and Mucus: From Development to Respiratory Defense by Salathe in Front Matter (1), Front Matter (2), and page 359
- Defects of Secretion in Cystic Fibrosis (Advances in Experimental Medicine and Biology) by Carsten Schultz on page 34, page 111, and Back Matter
See all 100 books citing this book
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