|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
4
|
|
pubmed:dateCreated |
2001-7-13
|
|
pubmed:abstractText |
Several inherited conditions have been associated with an increased or decreased incidence of retinal vein occlusion (RVO). The A allele in the 20210 G/A prothrombin gene has been found to be associated with systemic venous thrombosis. The aim of this study has been to verify the prevalence of this mutation in patients affected by central RVO (CRVO) or branch RVO (BRVO).
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Apr
|
|
pubmed:issn |
0721-832X
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
239
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
251-6
|
|
pubmed:dateRevised |
2004-11-17
|
|
pubmed:meshHeading |
pubmed-meshheading:11450488-Aged,
pubmed-meshheading:11450488-Aged, 80 and over,
pubmed-meshheading:11450488-Alleles,
pubmed-meshheading:11450488-DNA Mutational Analysis,
pubmed-meshheading:11450488-Female,
pubmed-meshheading:11450488-Genotype,
pubmed-meshheading:11450488-Humans,
pubmed-meshheading:11450488-Male,
pubmed-meshheading:11450488-Middle Aged,
pubmed-meshheading:11450488-Mutation,
pubmed-meshheading:11450488-Pilot Projects,
pubmed-meshheading:11450488-Polymerase Chain Reaction,
pubmed-meshheading:11450488-Prevalence,
pubmed-meshheading:11450488-Prothrombin,
pubmed-meshheading:11450488-Retinal Vein Occlusion,
pubmed-meshheading:11450488-Retrospective Studies
|
|
pubmed:year |
2001
|
|
pubmed:articleTitle |
The heterozygous 20210 G/A genotype prevalence in patients affected by central and branch retinal vein occlusion: a pilot study.
|
|
pubmed:affiliation |
Department of Ophthalmology, University of Ferrara, Corso Giovecca 203, 44100 Ferrara, Italy. sbd@dns.unife.it
|
|
pubmed:publicationType |
Journal Article,
Clinical Trial
|
