Source:http://linkedlifedata.com/resource/pubmed/id/21464714
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2011-7-12
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pubmed:abstractText |
Lipoprotein glomerulopathy is a rare disorder characterized by proteinuria, renal insufficiency and disturbances in lipoprotein metabolism closely related to those observed in type III hyperlipidemia. Rare mutations in apolipoprotein E (apoE) gene may contribute to the pathogenesis of the disease. This article reviews the clinical and laboratory features of lipoprotein glomerulopathy, discusses the mechanisms that may be implicated in its pathogenesis and summarizes the currently available therapeutic options.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1473-6535
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
262-9
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pubmed:meshHeading |
pubmed-meshheading:21464714-Animals,
pubmed-meshheading:21464714-Apolipoproteins E,
pubmed-meshheading:21464714-Humans,
pubmed-meshheading:21464714-Hyperlipidemias,
pubmed-meshheading:21464714-Kidney,
pubmed-meshheading:21464714-Mutation, Missense,
pubmed-meshheading:21464714-Nephrosis,
pubmed-meshheading:21464714-Proteinuria
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pubmed:year |
2011
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pubmed:articleTitle |
Lipoprotein glomerulopathy.
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pubmed:affiliation |
Department of Internal Medicine, Medical School, University of Ioannina, Ioannina, Greece.
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pubmed:publicationType |
Journal Article,
Review
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