Document Detail


Respiratory syncytial virus infection and chronic respiratory morbidity - is there a functional or genetic predisposition?
MedLine Citation:
PMID:  22963586     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
CONCLUSION:   Single-nucleotide polymorphisms in genes coding for IL-8, IL-19, IL-20, IL-13 mannose-binding lectin, IFNG and a RANTES polymorphism have been associated with subsequent wheeze following RSV LRTI in term-born infants.
Authors:
Simon B Drysdale; Anthony D Milner; Anne Greenough
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review     Date:  2012-09-11
Journal Detail:
Title:  Acta paediatrica (Oslo, Norway : 1992)     Volume:  101     ISSN:  1651-2227     ISO Abbreviation:  Acta Paediatr.     Publication Date:  2012 Nov 
Date Detail:
Created Date:  2012-10-02     Completed Date:  2013-03-07     Revised Date:  2014-07-31    
Medline Journal Info:
Nlm Unique ID:  9205968     Medline TA:  Acta Paediatr     Country:  Norway    
Other Details:
Languages:  eng     Pagination:  1114-20     Citation Subset:  IM    
Copyright Information:
© 2012 The Author(s)/Acta Paediatrica © 2012 Foundation Acta Paediatrica.
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MeSH Terms
Descriptor/Qualifier:
Asthma / etiology*,  genetics,  physiopathology
Bronchiolitis, Viral / complications*
Chronic Disease
Cough / etiology,  genetics,  physiopathology
Disease Susceptibility* / physiopathology
Genetic Markers
Genetic Predisposition to Disease
Humans
Infant
Infant, Newborn
Infant, Premature
Infant, Premature, Diseases / etiology,  genetics,  physiopathology
Lung / physiopathology
Polymorphism, Single Nucleotide
Respiratory Function Tests
Respiratory Sounds / etiology*,  genetics,  physiopathology
Respiratory Syncytial Virus Infections / complications*
Chemical
Reg. No./Substance:
0/Genetic Markers

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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