Linked Life Data

16221337

Source:http://linkedlifedata.com/resource/pubmed/id/16221337

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2005-10-13
pubmed:abstractText
Idiopathic collapsing glomerulopathy (ICG) is a clinically and pathologically distinct variant of focal segmental glomerulosclerosis, which is characterized by proteinuria (often nephrotic range) and rapid progression to end-stage renal failure. The typical pathological changes are global/segmental glomerular collapse, hypertrophy and hyperplasia of podocytes and severe tubulointerstitial lesions. Most ICG patients who have been reported in previous published papers are adults. ICG in children is rare. The study aimed to analyze and investigate clinical manifestations, renal histopathological findings, treatment and outcomes of ICG in children.
pubmed:language
chi
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0578-1310
pubmed:author
pubmed:issnType
Print
pubmed:volume
42
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
731-3
pubmed:meshHeading
pubmed:year
2004
pubmed:articleTitle
[Idiopathic collapsing glomerulopathy in children: report of two cases].
pubmed:affiliation
Department of Pediatrics, The First Affiliated Hospital, SUN Yat-sen University, Guangzhou 510080, China.
pubmed:publicationType
Journal Article, English Abstract, Case Reports