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Nephron. Clinical Practice|June 24, 2009
Truncating mutations in the chloride/proton ClC-5 antiporter gene in Seven Jewish Israeli families with Dent's 1 diseaseDganit Dinour, Miriam Davidovitz, Nomy Levin-Iaina, et al.
Pediatric Transplantation|January 30, 2009
Ocular complications in children and adolescents following renal transplantationIrit Krause, Moshe Snir, Roxana Cleper, et al.
Spinal Cord|August 27, 2021
Asymptomatic bacteriuria and antibiotic resistance profile in children with neurogenic bladder who require clean intermittent catheterizationReuben Ben-David, Fred Carroll, Emmanuel Kornitzer, et al.
Clinical Journal of the American Society of Nephrology : CJASN|July 3, 2010
Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutationsGil Chernin, Virginia Vega-Warner, Dominik S Schoeb, et al.
Clinical Transplantation|August 5, 2016
Focal segmental glomerulosclerosis in pediatric kidney transplantation: 30 years' experienceRoxana Cleper, Irit Krause, Nathan Bar Nathan, et al.
Pediatric Neurology|October 15, 2025
Blood Pressure Profile in Pediatric Moyamoya: Longitudinal Analysis and Revascularization ImpactNour Suliman, Roxana Cleper, Shelly I Shiran, et al.
Pediatric Transplantation|June 20, 2012
Post-transplantation lymphoproliferative disorder in pediatric kidney-transplant recipients - a national studyRoxana Cleper, Efrat Ben Shalom, Daniel Landau, et al.
Translational Pediatrics|January 24, 2022
Improving renal phenotype and evolving extra-renal features of 17q12 deletion encompassing the <i>HNF1B</i> geneRoxana Cleper, Adi Reches, Dana Shapira, et al.
Pediatric Nephrology (Berlin, Germany)|January 18, 2021
Long-term outcomes during 37 years of pediatric kidney transplantation: a cohort study comparing ethnic groupsMiriam Davidovits, Lewis Reisman, Roxana Cleper, et al.
Pediatric Nephrology (Berlin, Germany)|February 6, 2026
Single relapse at ≥ 0.5 mg/kg alternate-day prednisone predicts course of childhood nephrotic syndromeAbigail A Lazar, Elena Zion, Evgenia Gurevich, et al.
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