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Choni Rinat

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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 26, 2009
A comprehensive study of cardiovascular risk factors, cardiac function and vascular disease in children with chronic renal failureChoni Rinat, Rachel Becker-Cohen, Amiram Nir, et al.
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.
Molecular Genetics and Metabolism|December 14, 2005
Molecular, biochemical, and genetic characterization of a female patient with Lesch-Nyhan diseaseChoni Rinat, Esther Zoref-Shani, Ziva Ben-Neriah, et al.
Pediatric Nephrology (Berlin, Germany)|March 2, 2021
Long-term complications of systemic oxalosis in children-a retrospective single-center cohort studyEfrat Ben-Shalom, Ruth Cytter-Kuint, Choni Rinat, et al.
American Journal of Human Genetics|January 25, 2011
Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndromeRuth Belostotsky, Efrat Ben-Shalom, Choni Rinat, et al.
Pediatric Nephrology (Berlin, Germany)|January 18, 2022
Metabolic alkalosis in infants treated with peritoneal dialysisShimrit Tzvi-Behr, Alon Bnaya, Rachel Becker-Cohen, et al.
Pediatric Nephrology (Berlin, Germany)|November 9, 2023
Acute glomerulonephritis with concurrent suspected bacterial pneumonia - is it the tip of the iceberg?Shimrit Tzvi-Behr, Yaacov Frishberg, Orli Megged, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2007
Misleading findings of homozygosity mapping resulting from three novel mutations in NPHS1 encoding nephrin in a highly inbred communityYaacov Frishberg, Ziva Ben-Neriah, Maija Suvanto, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 30, 2019
Early puberty in end stage renal failure and renal transplant recipientsCarmit Avnon Ziv, Shimrit Tzvi-Behr, Efrat Ben-Shalom, et al.
American Journal of Nephrology|June 18, 2005
Intra-familial clinical heterogeneity: absence of genotype-phenotype correlation in primary hyperoxaluria type 1 in IsraelYaacov Frishberg, Choni Rinat, Adel Shalata, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

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Pageof 4
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 26, 2009
A comprehensive study of cardiovascular risk factors, cardiac function and vascular disease in children with chronic renal failureChoni Rinat, Rachel Becker-Cohen, Amiram Nir, et al.
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.
Molecular Genetics and Metabolism|December 14, 2005
Molecular, biochemical, and genetic characterization of a female patient with Lesch-Nyhan diseaseChoni Rinat, Esther Zoref-Shani, Ziva Ben-Neriah, et al.
Pediatric Nephrology (Berlin, Germany)|March 2, 2021
Long-term complications of systemic oxalosis in children-a retrospective single-center cohort studyEfrat Ben-Shalom, Ruth Cytter-Kuint, Choni Rinat, et al.
American Journal of Human Genetics|January 25, 2011
Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndromeRuth Belostotsky, Efrat Ben-Shalom, Choni Rinat, et al.
Pediatric Nephrology (Berlin, Germany)|January 18, 2022
Metabolic alkalosis in infants treated with peritoneal dialysisShimrit Tzvi-Behr, Alon Bnaya, Rachel Becker-Cohen, et al.
Pediatric Nephrology (Berlin, Germany)|November 9, 2023
Acute glomerulonephritis with concurrent suspected bacterial pneumonia - is it the tip of the iceberg?Shimrit Tzvi-Behr, Yaacov Frishberg, Orli Megged, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2007
Misleading findings of homozygosity mapping resulting from three novel mutations in NPHS1 encoding nephrin in a highly inbred communityYaacov Frishberg, Ziva Ben-Neriah, Maija Suvanto, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 30, 2019
Early puberty in end stage renal failure and renal transplant recipientsCarmit Avnon Ziv, Shimrit Tzvi-Behr, Efrat Ben-Shalom, et al.
American Journal of Nephrology|June 18, 2005
Intra-familial clinical heterogeneity: absence of genotype-phenotype correlation in primary hyperoxaluria type 1 in IsraelYaacov Frishberg, Choni Rinat, Adel Shalata, et al.
Pageof 4