Liat Ganon

Tel Litwinsky, TA, Israel

Last Updated: 09/26/2026

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Found 9 publications

Childhood Hypercalciuric Hypercalcemia With Elevated Vitamin D and Suppressed Parathyroid Hormone: Long-Term Follow Up.

Childhood Hypercalciuric Hypercalcemia With Elevated Vitamin D and Suppressed Parathyroid Hormone: Long-Term Follow Up.

Journal: Frontiers in pediatrics

Published: August 02, 2021

Familial Hyperkalemia and Hypertension (FHHt) and KLHL3: Description of a Family with a New Recessive Mutation (S553L) Compared to a Family with a Dominant Mutation, Q309R, with Analysis of Urinary Sodium Chloride Cotransporter.

Familial Hyperkalemia and Hypertension (FHHt) and KLHL3: Description of a Family with a New Recessive Mutation (S553L) Compared to a Family with a Dominant Mutation, Q309R, with Analysis of Urinary Sodium Chloride Cotransporter.

Journal: Nephron

Published: March 15, 2017

Hyponatremia in refractory congestive heart failure patients treated with icodextrin-based peritoneal dialysis: A case series.

Hyponatremia in refractory congestive heart failure patients treated with icodextrin-based peritoneal dialysis: A case series.

Journal: Nefrologia

Published: November 21, 2016

Loss of function of NaPiIIa causes nephrocalcinosis and possibly kidney insufficiency.

Loss of function of NaPiIIa causes nephrocalcinosis and possibly kidney insufficiency.

Journal: Pediatric nephrology (Berlin, Germany)

Published: March 31, 2016

Evaluation of an infant with hypercalcemia.

Evaluation of an infant with hypercalcemia.

Journal: Pediatric nephrology (Berlin, Germany)

Published: October 06, 2014

Maternal and infantile hypercalcemia caused by vitamin-D-hydroxylase mutations and vitamin D intake.

Maternal and infantile hypercalcemia caused by vitamin-D-hydroxylase mutations and vitamin D intake.

Journal: Pediatric nephrology (Berlin, Germany)

Published: January 01, 2014

Chronic hypercalcaemia from inactivating mutations of vitamin D 24-hydroxylase (CYP24A1): implications for mineral metabolism changes in chronic renal failure.

Chronic hypercalcaemia from inactivating mutations of vitamin D 24-hydroxylase (CYP24A1): implications for mineral metabolism changes in chronic renal failure.

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

Published: November 16, 2013

Wild-type uromodulin prevents NFkB activation in kidney cells, while mutant uromodulin, causing FJHU nephropathy, does not.

Wild-type uromodulin prevents NFkB activation in kidney cells, while mutant uromodulin, causing FJHU nephropathy, does not.

Journal: Journal of nephrology

Published: November 03, 2013

Loss-of-function mutations of CYP24A1, the vitamin D 24-hydroxylase gene, cause long-standing hypercalciuric nephrolithiasis and nephrocalcinosis.

Loss-of-function mutations of CYP24A1, the vitamin D 24-hydroxylase gene, cause long-standing hypercalciuric nephrolithiasis and nephrocalcinosis.

Journal: The Journal of urology

Published: February 26, 2013

Showing 1-9 of 9

Last Updated: 09/26/2026