Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1999-2-8
pubmed:abstractText
To determine whether heritable thrombophilia and hypofibrinolysis were risk factors for retinal vein occlusion.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0003-9950
pubmed:author
pubmed:issnType
Print
pubmed:volume
117
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
43-9
pubmed:dateRevised
2005-11-17
pubmed:meshHeading
pubmed-meshheading:9930159-Adult, pubmed-meshheading:9930159-Aged, pubmed-meshheading:9930159-Antibodies, Antiphospholipid, pubmed-meshheading:9930159-Blood Coagulation Tests, pubmed-meshheading:9930159-DNA, Complementary, pubmed-meshheading:9930159-Factor V, pubmed-meshheading:9930159-Female, pubmed-meshheading:9930159-Fibrinolysis, pubmed-meshheading:9930159-Humans, pubmed-meshheading:9930159-Lipoprotein(a), pubmed-meshheading:9930159-Male, pubmed-meshheading:9930159-Methylenetetrahydrofolate Reductase (NADPH2), pubmed-meshheading:9930159-Middle Aged, pubmed-meshheading:9930159-Oxidoreductases Acting on CH-NH Group Donors, pubmed-meshheading:9930159-Plasminogen Activator Inhibitor 1, pubmed-meshheading:9930159-Point Mutation, pubmed-meshheading:9930159-Polymerase Chain Reaction, pubmed-meshheading:9930159-Polymorphism, Genetic, pubmed-meshheading:9930159-Prothrombin, pubmed-meshheading:9930159-Retinal Vein Occlusion, pubmed-meshheading:9930159-Thrombophilia
pubmed:year
1999
pubmed:articleTitle
Heritable thrombophilia and hypofibrinolysis. Possible causes of retinal vein occlusion.
pubmed:affiliation
Cholesterol Center, Jewish Hospital, Cincinnati, Ohio, USA. glueckch@healthall.com
pubmed:publicationType
Journal Article