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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
5
|
| pubmed:dateCreated |
1985-8-22
|
| pubmed:abstractText |
An abnormal variant of antithrombin III is reported in a young male with deep vein thrombosis. The heparin cofactor, progressive thrombin inhibition, and factor Xa inactivation are decreased. The abnormality seems to be a mutation which is transmitted in an autosomaldominant way. The half-life and fractional catabolic rate of 125I antithrombin III concentrate is the same in this patient as in patients with the classic type of antithrombin III deficiency and in a control.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
May
|
| pubmed:issn |
0036-553X
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
34
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
412-6
|
| pubmed:dateRevised |
2008-11-21
|
| pubmed:meshHeading |
pubmed-meshheading:4012220-Adult,
pubmed-meshheading:4012220-Antithrombin III,
pubmed-meshheading:4012220-Child,
pubmed-meshheading:4012220-Female,
pubmed-meshheading:4012220-Genetic Variation,
pubmed-meshheading:4012220-Humans,
pubmed-meshheading:4012220-Male,
pubmed-meshheading:4012220-Pedigree,
pubmed-meshheading:4012220-Sweden,
pubmed-meshheading:4012220-Thrombophlebitis
|
| pubmed:year |
1985
|
| pubmed:articleTitle |
A Swedish family with abnormal antithrombin III.
|
| pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|