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Nefrologia|August 2, 2017
Hyponatremia in refractory congestive heart failure patients treated with icodextrin-based peritoneal dialysis: A case seriesMargarita Kunin, Liat Ganon, Eli J Holtzman, et al.Nephron. Clinical Practice|December 15, 2010
Molecular study of proteinuria in patients treated with B₁₂ supplements: do not forget megaloblastic anemia type 1Nomy Levin-Iaina, Dganit Dinour, Gabriel Morduchowicz, et al.Journal of Nephrology|March 21, 2014
Wild-type uromodulin prevents NFkB activation in kidney cells, while mutant uromodulin, causing FJHU nephropathy, does notDganit Dinour, Liat Ganon, Levin-Iaina Nomy, et al.The Journal of Urology|March 9, 2013
Loss-of-function mutations of CYP24A1, the vitamin D 24-hydroxylase gene, cause long-standing hypercalciuric nephrolithiasis and nephrocalcinosisDganit Dinour, Pazit Beckerman, Liat Ganon, et al.Pediatric Nephrology (Berlin, Germany)|February 4, 2009
Non-urate transporter 1-related renal hypouricemia and acute renal failure in an Israeli-Arab familyHilla Bahat, Dganit Dinour, Liat Ganon, et al.Frontiers in Pediatrics|December 3, 2021
Childhood Hypercalciuric Hypercalcemia With Elevated Vitamin D and Suppressed Parathyroid Hormone: Long-Term Follow UpEvgenia Gurevich, Shelly Levi, Yael Borovitz, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 16, 2013
Chronic hypercalcaemia from inactivating mutations of vitamin D 24-hydroxylase (CYP24A1): implications for mineral metabolism changes in chronic renal failureGiacomo Colussi, Liat Ganon, Silvana Penco, et al.Pediatric Nephrology (Berlin, Germany)|July 6, 2016
Loss of function of NaPiIIa causes nephrocalcinosis and possibly kidney insufficiencyDganit Dinour, Miriam Davidovits, Liat Ganon, et al.Pediatric Nephrology (Berlin, Germany)|September 8, 2014
Maternal and infantile hypercalcemia caused by vitamin-D-hydroxylase mutations and vitamin D intakeDganit Dinour, Miriam Davidovits, Shraga Aviner, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 15, 2010
URAT1 mutations cause renal hypouricemia type 1 in Iraqi JewsDganit Dinour, Andrew Bahn, Liat Ganon, et al.Pageof 4