Andrea Kerti
Budapest, BU 1083, Hungary
Last Updated: 09/26/2026
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Found 10 publications
Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 20, 2020
QMPSF is sensitive and specific in the detection of NPHP1 heterozygous deletions.
Journal: Clinical chemistry and laboratory medicine
Published: September 12, 2016
Prevalence of obesity and metabolic changes after kidney transplantation: Hungarian pediatric cohort study.
Journal: Transplantation proceedings
Published: August 19, 2014
Bone metabolism and arterial stiffness after renal transplantation.
Journal: Kidney & blood pressure research
Published: July 18, 2014
Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndrome.
Journal: Nature genetics
Published: November 23, 2013
Ambulatory arterial stiffness index in children after kidney transplantation.
Journal: Pediatric transplantation
Published: June 12, 2013
NPHS2 homozygous p.R229Q variant: potential modifier instead of causal effect in focal segmental glomerulosclerosis.
Journal: Pediatric nephrology (Berlin, Germany)
Published: March 20, 2013
NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndrome.
Journal: Pediatric nephrology (Berlin, Germany)
Published: July 24, 2012
Cardiovascular risk assessment in children with chronic kidney disease.
Journal: Pediatric nephrology (Berlin, Germany)
Published: July 03, 2012
Cardiovascular risk assessment in children following kidney transplantation.
Journal: Pediatric transplantation
Published: June 15, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026