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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2-3
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pubmed:dateCreated |
2004-3-22
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pubmed:abstractText |
Idiopathic cerebral vein thrombosis (iCVT) represents approximately 30% of the cases of cerebral vein thrombosis (CVT). New, inherited - factor V Leiden (FVL) and prothrombin gene mutation (PTHRA20210) - and inherited/acquired - hyperhomocysteinemia (HHcy) - prothrombotic conditions have been detected recently.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1015-9770
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pubmed:author |
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pubmed:copyrightInfo |
Copyright 2004 S. Karger AG, Basel
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pubmed:issnType |
Print
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pubmed:volume |
17
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
153-9
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:14707415-Adult,
pubmed-meshheading:14707415-Antithrombin III,
pubmed-meshheading:14707415-Cerebral Veins,
pubmed-meshheading:14707415-Factor V,
pubmed-meshheading:14707415-Female,
pubmed-meshheading:14707415-Homocysteine,
pubmed-meshheading:14707415-Humans,
pubmed-meshheading:14707415-Hyperhomocysteinemia,
pubmed-meshheading:14707415-Intracranial Thrombosis,
pubmed-meshheading:14707415-Male,
pubmed-meshheading:14707415-Point Mutation,
pubmed-meshheading:14707415-Prevalence,
pubmed-meshheading:14707415-Protein C,
pubmed-meshheading:14707415-Protein S,
pubmed-meshheading:14707415-Prothrombin,
pubmed-meshheading:14707415-Risk Factors,
pubmed-meshheading:14707415-Thrombophilia,
pubmed-meshheading:14707415-Venous Thrombosis
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pubmed:year |
2004
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pubmed:articleTitle |
Hyperhomocysteinemia and other newly recognized inherited coagulation disorders (factor V Leiden and prothrombin gene mutation) in patients with idiopathic cerebral vein thrombosis.
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pubmed:affiliation |
Department of Internal Medicine, University of Modena and Reggio Emilia, Italy. paoloven@unimore.it
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pubmed:publicationType |
Journal Article
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