rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
1
|
pubmed:dateCreated |
2005-3-8
|
pubmed:abstractText |
Exhaled nitric oxide has previously been found to be low in cystic fibrosis. The aim of this study was to determine whether exhaled nitric oxide levels would increase in response to oral L-arginine supplementation administered daily for 4 weeks. Exhaled and nasal nitric oxide was measured weekly. Plasma L-arginine levels increased in response to supplementation but this was not reflected in an increase in eNO levels.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
1569-1993
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pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
4
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
67-9
|
pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15752684-Administration, Oral,
pubmed-meshheading:15752684-Adolescent,
pubmed-meshheading:15752684-Arginine,
pubmed-meshheading:15752684-Breath Tests,
pubmed-meshheading:15752684-Child,
pubmed-meshheading:15752684-Cystic Fibrosis,
pubmed-meshheading:15752684-Female,
pubmed-meshheading:15752684-Follow-Up Studies,
pubmed-meshheading:15752684-Forced Expiratory Volume,
pubmed-meshheading:15752684-Humans,
pubmed-meshheading:15752684-Male,
pubmed-meshheading:15752684-Nerve Tissue Proteins,
pubmed-meshheading:15752684-Nitric Oxide,
pubmed-meshheading:15752684-Nitric Oxide Synthase,
pubmed-meshheading:15752684-Nitric Oxide Synthase Type I,
pubmed-meshheading:15752684-Nitric Oxide Synthase Type III,
pubmed-meshheading:15752684-Pilot Projects,
pubmed-meshheading:15752684-Treatment Outcome,
pubmed-meshheading:15752684-Vital Capacity
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pubmed:year |
2005
|
pubmed:articleTitle |
A pilot study of oral L-arginine in cystic fibrosis.
|
pubmed:affiliation |
m.l.everard@sheffield.ac.uk
|
pubmed:publicationType |
Journal Article,
Comparative Study
|