Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2009-3-2
pubmed:abstractText
CASE REPORTS: We present four cases: two males with Horner Syndrome, who were diagnosed by means of apraclonidine 0.5% and cocaine 4% tests respectively. Two children with anisocoria, one of whom had Horner Syndrome confirmed with apraclonidine 1% and the other, in whom an apraclonidine test ruled out this syndrome but in whom pilocarpine 0.125% confirmed Adie's pupil. DISCUSSION: Apraclonidine drops (1% and 0.5%) may aid in the diagnosis of Horner Syndrome and are easier to obtain than cocaine.
pubmed:language
spa
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1989-7286
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
84
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
105-8
pubmed:dateRevised
2010-6-16
pubmed:meshHeading
pubmed-meshheading:19253181-Adrenergic alpha-Agonists, pubmed-meshheading:19253181-Adult, pubmed-meshheading:19253181-Anisocoria, pubmed-meshheading:19253181-Birth Injuries, pubmed-meshheading:19253181-Brachial Plexus, pubmed-meshheading:19253181-Clonidine, pubmed-meshheading:19253181-Cocaine, pubmed-meshheading:19253181-Diagnosis, Differential, pubmed-meshheading:19253181-Female, pubmed-meshheading:19253181-Horner Syndrome, pubmed-meshheading:19253181-Humans, pubmed-meshheading:19253181-Infant, pubmed-meshheading:19253181-Male, pubmed-meshheading:19253181-Middle Aged, pubmed-meshheading:19253181-Neurilemmoma, pubmed-meshheading:19253181-Pilocarpine, pubmed-meshheading:19253181-Postoperative Complications, pubmed-meshheading:19253181-Thoracic Neoplasms, pubmed-meshheading:19253181-Tonic Pupil
pubmed:year
2009
pubmed:articleTitle
[Usefulness of apraclonidine in the diagnosis of Horner syndrome].
pubmed:affiliation
Servicio de Oftalmología, Hospital Universitario Miguel Servet, Zaragoza, España. aperezinigo@hotmail.com
pubmed:publicationType
Journal Article, English Abstract, Case Reports