Linked Life Data

20865641

Source:http://linkedlifedata.com/resource/pubmed/id/20865641

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2010-9-24
pubmed:abstractText
In the last 10 years the knowledge of the pathophysiology of atypical hemolytic uremic syndrome (aHUS) has substantially increased. Nevertheless, aHUS remains a severe disorder, in which early recognition of symptoms remains a key issue. The landmark discovery of genetic abnormalities in complement regulatory genes in most patients gave us new insights into the influence of each abnormality on the disease outcome and opened new perspectives for patient management. This allows a potentially more tailored approach in treating aHUS patients.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1098-9064
pubmed:author
pubmed:copyrightInfo
© Thieme Medical Publishers.
pubmed:issnType
Electronic
pubmed:volume
36
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
641-52
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
Atypical hemolytic uremic syndrome associated with mutations in complement regulator genes.
pubmed:affiliation
Service de Néphrologie, Hôpital Foch, 40 rue Worth, Suresnes, Paris, France.
pubmed:publicationType
Journal Article, Review, Research Support, Non-U.S. Gov't