Dganit Dinour

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

Karl P. Schlingmann, Stefanie Weber, Melanie Peters et al. · Nature Genetics · 2002 · 784 citations

Life Sciences, Genetics, Molecular Genetics +11

Role of nitric oxide in renal medullary oxygenation. Studies in isolated and intact rat kidneys.

Mayer Brezis, Samuel N. Heyman, Dganit Dinour et al. · Journal of Clinical Investigation · 1991 · 284 citations · Full text

Medicine, Pharmacology, Physiology +16

Homozygous SLC2A9 Mutations Cause Severe Renal Hypouricemia

Dganit Dinour, Nicola K. Gray, Susan Campbell et al. · Journal of the American Society of Nephrology · 2009 · 241 citations

Medicine, Genetics, Molecular Genetics +17

A Novel Missense Mutation in the Sodium Bicarbonate Cotransporter (NBCe1/SLC4A4) Causes Proximal Tubular Acidosis and Glaucoma through Ion Transport Defects

Dganit Dinour, Min‐Hwang Chang, Jun-ichi Satoh et al. · Journal of Biological Chemistry · 2004 · 172 citations · Full text

Medicine, Genetics, Nephrology +15

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 et al. · The Journal of Urology · 2013 · 138 citations

Medicine, Genetics, Nephrology +17