Ozde N. Turkkan - Publications

Clinical course of proteinuria due to cubilin variants: a large multicenter pediatric cohort.

Journal: Pediatric nephrology (Berlin, Germany)

Published: November 14, 2025

Predictors of kidney survival in children with autosomal recessive polycystic kidney disease.

Journal: Clinical and experimental nephrology

Published: April 21, 2025

Pediatric kidney care experience after the 2023 Türkiye earthquake.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: October 23, 2023

The relationship between urine heat shock protein 70 and congenital anomalies of the kidney and urinary tract: UTILISE study.

Journal: Frontiers in urology

Published: August 21, 2023

Catastrophic antiphospholipid syndrome accompanied by complement regulatory gene mutation.

Journal: The Turkish journal of pediatrics

Published: April 28, 2023

Urine soluble TLR4 levels may contribute to predict urinary tract infection in children: the UTILISE Study.

Journal: Pediatric nephrology (Berlin, Germany)

Published: January 04, 2023

Association between serum biomarkers and oral health status in children with chronic kidney disease: A cross-sectional study.

Journal: Clinical oral investigations

Published: December 20, 2022

Phenotypic and genotypic characteristics of children with Bartter syndrome.

Journal: The Turkish journal of pediatrics

Published: October 28, 2022

Clinical and genetic characterization of children with cubilin variants.

Journal: Pediatric nephrology (Berlin, Germany)

Published: April 22, 2022

Urinary HSP70 improves diagnostic accuracy for urinary tract infection in children: UTILISE study.

Journal: Pediatric nephrology (Berlin, Germany)

Published: February 23, 2022

Rituximab treatment for difficult-to-treat nephrotic syndrome in children: a multicenter, retrospective study

Journal: Turkish journal of medical sciences

Published: December 26, 2020

Primary coenzyme Q10 Deficiency-6 (COQ10D6): Two siblings with variable expressivity of the renal phenotype.

Journal: European journal of medical genetics

Published: June 01, 2018