FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2162308691> ?p ?o ?g. }

• W2162308691 endingPage "60" @default.
• W2162308691 startingPage "53" @default.
• W2162308691 abstract "Background: Idiopathic steroid resistant nephrotic syndrome (ISRNS) represents about 10-20% of children with nephrotic syndrome with variable outcome. Objectives: To determine the histological patterns of ISRNS in Egyptian children and the histological details of the commonest types which might be the reason for the steroid resistance. Patients and Methods: The study included 53 cases with ISRNS. Their renal biopsies were retrieved from the archive of Electron microscopy unit and pathology department, Ain Shams University Specialized Hospital (ASUSH) in the duration from 2005-2011. The biopsies were examined histologically, with immunohistochemistry, and by electron microscopy. Results: They were 36 males (67.9%) and 17 females (32.1%), the age at diagnosis ranged from 1.5- 16 years with a mean of 6.71 years. Lower limb oedema was the commonest presentation (100%), haematuria was revealed in (17%) of cases. Histological examination showed three major patterns; Focal segmental glomerulosclerosis (FSGS) in 30.2%, minimal change glomerulopathy (MCG) in 24.5% and IgA nephropathy in 13.2 %. Mesangial hypercellularity was very common among MCG patients (85.3% ±6.7). Tubulointerstitial inflammation and fibrosis were common among cases with IgA nephropathy (40.4% ±11, 53.7% ±8 respectively). Conclusions: ISRNS in Egyptian children could be attributed mainly to three major diseases (FSGS, MCG and IgA nephropathy). Mesangial hypercellularity and severe tubulointerstitial disease might be the major causes for steroid resistance in MCG and IgA nephropathy respectively. Renal biopsy with electron microscopy examination should be done for all children with nephrotic syndrome at first time of presentation for proper assignment of treatment protocol." @default.
• W2162308691 created "2016-06-24" @default.
• W2162308691 creator A5043337256 @default.
• W2162308691 creator A5055784812 @default.
• W2162308691 creator A5060847222 @default.
• W2162308691 creator A5075895986 @default.
• W2162308691 date "2013-01-01" @default.
• W2162308691 modified "2023-09-26" @default.
• W2162308691 title "Histological patterns of idiopathic steroid resistant nephrotic syndrome in Egyptian children: A single centre study" @default.
• W2162308691 cites W1980782330 @default.
• W2162308691 cites W1988853097 @default.
• W2162308691 cites W2000752351 @default.
• W2162308691 cites W2006815696 @default.
• W2162308691 cites W2014116714 @default.
• W2162308691 cites W2030581712 @default.
• W2162308691 cites W2034118721 @default.
• W2162308691 cites W2045748071 @default.
• W2162308691 cites W2074850565 @default.
• W2162308691 cites W2083485009 @default.
• W2162308691 cites W2088248991 @default.
• W2162308691 cites W2106132002 @default.
• W2162308691 cites W2122252782 @default.
• W2162308691 cites W2137087916 @default.
• W2162308691 cites W2140062805 @default.
• W2162308691 cites W4210848327 @default.
• W2162308691 cites W4212860823 @default.
• W2162308691 doi "https://doi.org/10.5812/nephropathol.8997" @default.
• W2162308691 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3886174" @default.
• W2162308691 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24475425" @default.
• W2162308691 hasPublicationYear "2013" @default.
• W2162308691 type Work @default.
• W2162308691 sameAs 2162308691 @default.
• W2162308691 citedByCount "24" @default.
• W2162308691 countsByYear W21623086912012 @default.
• W2162308691 countsByYear W21623086912013 @default.
• W2162308691 countsByYear W21623086912014 @default.
• W2162308691 countsByYear W21623086912015 @default.
• W2162308691 countsByYear W21623086912016 @default.
• W2162308691 countsByYear W21623086912017 @default.
• W2162308691 countsByYear W21623086912018 @default.
• W2162308691 countsByYear W21623086912021 @default.
• W2162308691 countsByYear W21623086912022 @default.
• W2162308691 crossrefType "journal-article" @default.
• W2162308691 hasAuthorship W2162308691A5043337256 @default.
• W2162308691 hasAuthorship W2162308691A5055784812 @default.
• W2162308691 hasAuthorship W2162308691A5060847222 @default.
• W2162308691 hasAuthorship W2162308691A5075895986 @default.
• W2162308691 hasBestOaLocation W21623086912 @default.
• W2162308691 hasConcept C126322002 @default.
• W2162308691 hasConcept C134018914 @default.
• W2162308691 hasConcept C142724271 @default.
• W2162308691 hasConcept C2775934546 @default.
• W2162308691 hasConcept C2777747828 @default.
• W2162308691 hasConcept C2778415529 @default.
• W2162308691 hasConcept C2778930706 @default.
• W2162308691 hasConcept C2780091579 @default.
• W2162308691 hasConcept C2780199430 @default.
• W2162308691 hasConcept C2780368995 @default.
• W2162308691 hasConcept C2780688133 @default.
• W2162308691 hasConcept C2781087799 @default.
• W2162308691 hasConcept C2781184683 @default.
• W2162308691 hasConcept C555293320 @default.
• W2162308691 hasConcept C71924100 @default.
• W2162308691 hasConcept C90924648 @default.
• W2162308691 hasConceptScore W2162308691C126322002 @default.
• W2162308691 hasConceptScore W2162308691C134018914 @default.
• W2162308691 hasConceptScore W2162308691C142724271 @default.
• W2162308691 hasConceptScore W2162308691C2775934546 @default.
• W2162308691 hasConceptScore W2162308691C2777747828 @default.
• W2162308691 hasConceptScore W2162308691C2778415529 @default.
• W2162308691 hasConceptScore W2162308691C2778930706 @default.
• W2162308691 hasConceptScore W2162308691C2780091579 @default.
• W2162308691 hasConceptScore W2162308691C2780199430 @default.
• W2162308691 hasConceptScore W2162308691C2780368995 @default.
• W2162308691 hasConceptScore W2162308691C2780688133 @default.
• W2162308691 hasConceptScore W2162308691C2781087799 @default.
• W2162308691 hasConceptScore W2162308691C2781184683 @default.
• W2162308691 hasConceptScore W2162308691C555293320 @default.
• W2162308691 hasConceptScore W2162308691C71924100 @default.
• W2162308691 hasConceptScore W2162308691C90924648 @default.
• W2162308691 hasIssue "1" @default.
• W2162308691 hasLocation W21623086911 @default.
• W2162308691 hasLocation W21623086912 @default.
• W2162308691 hasLocation W21623086913 @default.
• W2162308691 hasLocation W21623086914 @default.
• W2162308691 hasOpenAccess W2162308691 @default.
• W2162308691 hasPrimaryLocation W21623086911 @default.
• W2162308691 hasRelatedWork W1994218053 @default.
• W2162308691 hasRelatedWork W2045527150 @default.
• W2162308691 hasRelatedWork W2116977443 @default.
• W2162308691 hasRelatedWork W2139847128 @default.
• W2162308691 hasRelatedWork W2349992554 @default.
• W2162308691 hasRelatedWork W2361901137 @default.
• W2162308691 hasRelatedWork W2381256826 @default.
• W2162308691 hasRelatedWork W2384732301 @default.
• W2162308691 hasRelatedWork W4229757522 @default.
• W2162308691 hasRelatedWork W4386254247 @default.
• W2162308691 hasVolume "2" @default.

• next