Cystic Fibrosis: Evolution from a Fatal Disease of Infancy with a Clear Phenotype to a Chronic Disease of Adulthood with Diverse Manifestations
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Immunology and Allergy
Link
http://link.springer.com/content/pdf/10.1007/s12016-008-8077-y.pdf
Reference13 articles.
1. Andersen D (1938) Cystic fibrosis of the pancreas and its relation to celiac disease: a clinical and pathological study. Am J Dis Child 56:344–399
2. Davis PB (2001) Cystic fibrosis. Pediatr Rev 22:257–264
3. Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, Grzelczak Z et al (1989) Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science 245:1066–1073
4. Davis PB (2006) Cystic fibrosis since 1938. Am J Respir Crit Care Med 173:475–482
5. Cantin A (1995) Cystic fibrosis lung inflammation: early, sustained, and severe. Am J Respir Crit Care Med 151:939–941
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2. Inhalation Treatment with Glutathione in Patients with Cystic Fibrosis. A Randomized Clinical Trial;American Journal of Respiratory and Critical Care Medicine;2013-07
3. Optimization of a Yellow Fluorescent Protein-Based Iodide Influx High-Throughput Screening Assay for Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Modulators;ASSAY and Drug Development Technologies;2010-12
4. Current World Literature;Current Opinion in Pulmonary Medicine;2009-11
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