Homozygous SLC2A9 Mutations Cause Severe Renal Hypouricemia

Dganit Dinour, Nicola K. Gray, Susan Campbell, +13

Journal of the American Society of Nephrology

GeneticsRenal PathologyGenetic EpidemiologyUric Acid AbsorptionMolecular Genetics +14

Loss-of-Function Mutations of <i>CYP24A1</i> , the Vitamin D 24-Hydroxylase Gene, Cause Long-standing Hypercalciuric Nephrolithiasis and Nephrocalcinosis

Dganit Dinour, Pazit Beckerman, Liat Ganon, +3

The Journal of Urology

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

Dganit Dinour, Miriam Davidovits, Shraga Aviner, +7

Pediatric Nephrology

NutritionMetabolic DisorderInherited Metabolic DiseaseClinical NutritionPediatrics +6

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

Giacomo Colussi, Liat Ganon, Silvana Penco, +6

Nephrology Dialysis Transplantation

Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2

Dganit Dinour, Nicola K. Gray, Liat Ganon, +9

Nephrology Dialysis Transplantation

URAT1 mutations cause renal hypouricemia type 1 in Iraqi Jews

Dganit Dinour, Andrew Bahn, Liat Ganon, +8

Nephrology Dialysis Transplantation

Loss of function of NaPiIIa causes nephrocalcinosis and possibly kidney insufficiency

Dganit Dinour, Miriam Davidovits, Liat Ganon, +6

Pediatric Nephrology

UrologyRenal FunctionMedicineKidney FailureRenal Pathology +7

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

Margarita Kunin, Liat Ganon, Eli J. Holtzman, +1

Nefrología

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

Margarita Kunin, Liat Ganon, Eli J. Holtzman, +1

Nefrología (English Edition)

HemodialysisHeart FailureRenal FunctionCardiovascular DiseaseSodium Homeostasis +13