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Rheumatology (Oxford, England)|December 8, 2020
Amyloid storm: acute kidney injury and massive proteinuria, rapidly progressing to end-stage kidney disease in AA amyloidosis of familial Mediterranean feverOlga L Kukuy, Pazit Beckerman, Dganit Dinour, 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.
The Journal of Clinical Endocrinology and Metabolism|August 18, 2016
High Normal Uric Acid Levels Are Associated with an Increased Risk of Diabetes in Lean, Normoglycemic Healthy WomenMichal Shani, Shlomo Vinker, Dganit Dinour, et al.
Biomed Research International|November 6, 2015
Inflammatory Biomarkers in Refractory Congestive Heart Failure Patients Treated with Peritoneal DialysisMargarita Kunin, Vered Carmon, Michael Arad, et al.
Journal of Vascular and Interventional Radiology : JVIR|March 15, 2022
Treatment of Severe Renal Artery Stenosis with Acute Kidney Injury Requiring Hemodialysis by Percutaneous Transluminal Renal Angioplasty and Stent ImplantationNabil Abu-Amer, Olga L Kukuy, Margarita Kunin, et al.
The Journal of Urology|March 20, 2009
Late diagnosis of primary hyperoxaluria type 2 in the adult: effect of a novel mutation in GRHPR gene on enzymatic activity and molecular modelingNomy Levin-Iaina, Dganit Dinour, Lina Romero, et al.
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.
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