Epidemiology of chronic kidney disease in children

J Harambat, KJ van Stralen, JJ Kim, EJ Tizard - Pediatric nephrology, 2012 - Springer
In the past 30 years there have been major improvements in the care of children with chronic
kidney disease (CKD). However, most of the available epidemiological data stem from end …

Chronic kidney disease in children: the global perspective

BA Warady, V Chadha - Pediatric nephrology, 2007 - Springer
In contrast to the increasing availability of information pertaining to the care of children with
chronic kidney disease (CKD) from large-scale observational and interventional studies …

Recent advances in the identification and management of inherited hyperoxalurias

DJ Sas, PC Harris, DS Milliner - Urolithiasis, 2019 - Springer
Primary hyperoxaluria (PH) is caused by genetic mutations resulting in oxalate
overproduction leading to nephrolithiasis, nephrocalcinosis, extrarenal manifestations …

Chronic kidney disease in children in Turkey

K Bek, S Akman, I Bilge, R Topaloğlu, S Çalışkan… - Pediatric …, 2009 - Springer
To determine the incidence, etiology and treatment patterns of chronic kidney disease (CKD)
in children a questionnaire was sent to pediatric nephrology centers in Turkey, asking them …

[HTML][HTML] Chronic renal failure in children

P Hari, IK Singla, M Mantan, M Kanitkar… - Indian …, 2003 - indianpediatrics.net
Objective: To determine the etiology of chronic renal failure amongst children attending the
Pediatric Nephrology services at a tertiary care center. Subjects: We reviewed the records of …

The spectrum of chronic renal failure among Jordanian children.

RM Hamed - Journal of nephrology, 2002 - europepmc.org
Background The causes of chronic renal failure (CRF) vary from one country to another. In
this study we reviewed our experience with the different types of renal disorders leading to …

[HTML][HTML] Primary hyperoxaluria type 1

DS Milliner, PC Harris, DJ Sas, AG Cogal, JC Lieske - 2022 - europepmc.org
Primary hyperoxaluria type 1 (PH1) is caused by a deficiency of the liver peroxisomal
enzyme alanine: glyoxylate-aminotransferase (AGT), which catalyzes the conversion of …

Pattern of renal diseases in children: A developing country experience

SP Yadav, GS Shah, OP Mishra… - Saudi Journal of Kidney …, 2016 - journals.lww.com
Spectrum of renal disease varies in different ethnic population, geographical location, and
by environmental factors. The purpose of this study was to find out the clinical spectrum and …

Consanguineous marriage, reproductive behaviour and postnatal mortality in contemporary Iran

M Hosseini-Chavoshi, MJ Abbasi-Shavazi, AH Bittles - Human heredity, 2014 - karger.com
Objectives: The aims of the study were to determine the prevalence, types and socio-
economic correlates of consanguineous marriages in Iran, and to gauge the extent to which …

Burden of chronic kidney disease in iran a screening program is of essential need

M Nafar, SM Mousavi, M Mahdavi, GF POURREZA… - 2008 - sid.ir
Introduction. The latent nature of CHRONIC KIDNEY DISEASE (CKD) in primary stages
precludes early diagnosis. This necessitates plans such as screening, but we should first …