Yakın Doğu Üniversitesi
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Clinical course of primary focal segmental glomerulosclerosis (FSGS) in Turkish children: a report from the Turkish Pediatric Nephrology FSGS Study Group. (Kayıt no. 243866)

MARC ayrıntıları
000 -LEADER
fixed length control field naa a22 7ar4500
016 ## - NATIONAL BIBLIOGRAPHIC AGENCY CONTROL NUMBER
Record control number 000281020000004
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 00414301
040 ## - CATALOGING SOURCE
Original cataloging agency NEU
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title eng
050 04 - LIBRARY OF CONGRESS CALL NUMBER
Classification number WJ 301
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20160411133210.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 150313t xxu||||| |||| 00| 0 tu d
001 - CONTROL NUMBER
control field 267199
100 1# - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 576308
Personal name Besbas, N.
245 10 - TITLE STATEMENT
Title Clinical course of primary focal segmental glomerulosclerosis (FSGS) in Turkish children: a report from the Turkish Pediatric Nephrology FSGS Study Group.
Statement of responsibility, etc. Nesrin Besbas, Fatih Ozaltin, Sevinc Emre et al.
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Date of publication, distribution, etc. 2010.
Name of publisher, distributor, etc. Turkish J Pediatrics,
520 ## - SUMMARY, ETC.
Summary, etc. The clinical course of focal segmental glomerulosclerosis (FSGS) is heterogeneous in children. To evaluate the clinical course and the predictors of outcome in Turkish children with primary FSGS, a retrospective study was conducted by the Turkish Pediatric Nephrology Study Group in 14 pediatric nephrology centers. Two hundred twenty-two patients (92 boys, 130 girls, aged 1-16 years) with biopsy-proven primary FSGS were included. One hundred forty-eight patients were followed-up for a median of 51 months (range: 0.26-270). The clinical course was characterized by complete remission in 50 (33.8%), persistent proteinuria in 50 (33.8%) and progression to renal failure in 48 (32.4%) patients. Progression to end-stage renal disease (ESRD) was significantly higher in patients who did not attain remission. Complete remission, partial remission and progress to renal failure were recorded in 37%, 32% and 28%, respectively, of the patients (n=73) treated with prednisone combined cyclophosphamide/cyclosporine A. However, in patients (n=33) treated with pulse methyl prednisolone plus oral prednisone (up to 20 months) combined with cyclophosphamide, complete remission in 51.5% and partial remission in 27.3% of the patients were noted. Progression to renal failure was observed in 9.1% of this group of patients. Multivariate analysis showed that only plasma creatinine at presentation was an independent predictive value for outcome. Patients with serum creatinine level higher than 1.5 mg/dl had 6.6 times increased rate of progression to renal failure. Failure to achieve remission is a predictor of renal failure in children with primary FSGS. The use of immunosuppressive treatment in conjunction with prolonged steroid seems beneficial in primary FSGS in children.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 576309
Topical term or geographic name entry element Kidney
General subdivision Disease
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 572720
Topical term or geographic name entry element Near East University Article
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 572723
Topical term or geographic name entry element Yakın Doğu Üniversitesi Makale
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 118290
Topical term or geographic name entry element Children
773 ## - HOST ITEM ENTRY
Main entry heading Turkish Journal Of Pediatrics
Related parts MAY-JUN, 2010, 52 3, p255-p261, 7p.
International Standard Serial Number 00414301
942 ## - ADDED ENTRY ELEMENTS (KOHA)
-- 1000007
Call number prefix WJ0000301C552010
Koha item type Online Electronic Document
Mevcut
Total checkouts Full call number Barcode Koha item type Lost status Damaged status Not for loan Withdrawn status Home library Current library Shelving location
  WJ 301 .C55 2010 EOL-1479 Online Electronic Document         NEU Grand Library NEU Grand Library Online electronic