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Pediatric Nephrology (Berlin, Germany)|October 7, 2009
Dent's disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg?Yaacov Frishberg, Dganit Dinour, Ruth Belostotsky, et al.
The Journal of Rheumatology|October 17, 2013
Familial Mediterranean fever (FMF) with proteinuria: clinical features, histology, predictors, and prognosis in a cohort of 25 patientsOlga Kukuy, Avi Livneh, Aharon Ben-David, 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.
The Journal of Biological Chemistry|October 9, 2004
A novel missense mutation in the sodium bicarbonate cotransporter (NBCe1/SLC4A4) causes proximal tubular acidosis and glaucoma through ion transport defectsDganit Dinour, Min-Hwang Chang, Jun-ichi Satoh, 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.
International Journal of Molecular Sciences|May 27, 2023
The Prognostic Value of Anti-PLA2R Antibodies Levels in Primary Membranous NephropathyOlga Lesya Kukuy, Ron Cohen, Boris Gilburd, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 4, 2011
Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2Dganit Dinour, Nicola K Gray, Liat Ganon, et al.
Nature Genetics|May 29, 2002
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene familyKarl P Schlingmann, Stefanie Weber, Melanie Peters, et al.
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