Safety and immunogenicity of a subunit respiratory syncytial virus vaccine in children 24 to 48 months old
Clicks: 344
ID: 117149
1994
Article Quality & Performance Metrics
Overall Quality
Improving Quality
0.0
/100
Combines engagement data with AI-assessed academic quality
Reader Engagement
Emerging Content
7.8
/100
26 views
26 readers
Trending
AI Quality Assessment
Not analyzed
Abstract
A subunit vaccine for respiratory syncytial virus (RSV) consisting of purified fusion glycoprotein (designated PFP-1) was tested in children 24 to 48 months old. Two doses of 20 micrograms (n = 13) and 50 micrograms (n = 10) were compared with a saline (n = 24) placebo control group. Local and syste …
| Reference Key |
pr1994thesafety
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | Paradiso PR;Hildreth SW;Hogerman DA;Speelman DJ;Lewin EB;Oren J;Smith DH;; |
| Journal | the pediatric infectious disease journal |
| Year | 1994 |
| DOI |
DOI not found
|
| URL | |
| Keywords |
National Center for Biotechnology Information
NCBI
NLM
MEDLINE
humans
pubmed abstract
nih
national institutes of health
national library of medicine
female
male
Child
preschool
Clinical Trial
Randomized Controlled Trial
follow-up studies
Cohort Studies
neutralization tests
respiratory syncytial virus infections / prevention & control*
enzyme-linked immunosorbent assay
viral fusion proteins / immunology*
p r paradiso
human / immunology*
human / isolation & purification
respiratory syncytial virus
vaccination*
pmid:7808848
doi:10.1097/00006454-199409000-00008
s w hildreth
d h smith
|
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.