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Cystic fibrosis : etiology, diagnosis and treatments.

Author: Paul N Leatte
Publisher: Nova Science Publishers Inc, 2010.
Edition/Format:   Print book : EnglishView all editions and formats
Summary:

Cystic Fibrosis is a hereditary disease affecting the exocrine (mucus) glands of the lungs, liver, pancreas, and intestines, causing progressive disability due to multisystem failure. Individuals  Read more...

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Details

Document Type: Book
All Authors / Contributors: Paul N Leatte
ISBN: 9781607418337 1607418339
OCLC Number: 1036214415
Description: 275 pages
Contents: Preface; Newborn screening for cystic fibrosis; Cystic fibrosis and respiratory viral infections; Cystic fibrosis, pseudomonas aeruginosa infection, and relevance of innate immune response: challenge for hematopoietic stem cell transplantation; Neutrophil elastase-mediated modulation of pathophysiology in cystic fibrosis lung disease; Genotypic hetereogeneity of the molecular basis of cystic fibrosis: the paradigm of lithuanian population genetic testing; Serum transferrin microheterogeneity in cystic fibrosis; Effects of the lack of transport of thiocyanate in cystic fibrosis lung disease; Treatments for cystic fibrosis: the role of adherence, importance and burden; Cystic Fibrosis -- update on diagnosis and treatment; How effective are nutritional interventions in children and adults with cystic fibrosis?; Sweat test: recommendations for good practice and analytical criteria of the methods used; New trends in the inhibition of Pseudomonas aeruginosa quorum sensing activity; Ocular surface changes in patients with cystic fibrosis; Pseudo-Bartter Syndrome in cystic fibrosis; Management of cystic fibrosis-related arthritis; Cumbria Medicines for Children Research; Index.

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