 | Articles: Pediatric Nephrology |
Duplication of paternal IGF2 or loss of maternal IGF2 imprinting occurs in half of Wilms tumors with various structural WT1 abnormalities
Genes, Chromosomes and Cancer, 06/11/08
Urological issues in pediatric renal transplantation
Current Opinion in Urology, 06/10/08
Prenatal hydronephrosis: early evaluation
Current Opinion in Urology, 06/10/08
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Determination of reference values for plasma cystatin C and comparison with creatinine in premature infants
Pediatric Nephrology, 06/10/08
Obstacles to the prescribing of growth hormone in children with chronic kidney disease
Pediatric Nephrology, 06/09/08
Molecular evidence of the independent origin of multiple Wilms tumors in a case of WAGR syndrome
Pediatric Blood & Cancer, 06/06/08
Hypertension and microalbuminuria in children with congenital solitary kidneys
Journal of Paediatrics and Child Health, 06/06/08
Selection of modalities, prescription, and technical issues in children on peritoneal dialysis
Pediatric Nephrology, 06/05/08
A novel Wilms tumor 1 gene mutation in a child with severe renal dysfunction and persistent renal blastema
Pediatric Nephrology, 06/03/08
Clinical outcomes in pediatric hemodialysis patients in the USA: lessons from CMS ESRD CPM Project
Pediatric Nephrology, 06/02/08
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Indexed Journals: Kidney International, Hemodialysis International, Nephrology Dialysis Transplantation
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