Showing results (41-50 of 70) with videos related to
Sort By:
Pageof 7
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.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.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)|September 8, 2014
Maternal and infantile hypercalcemia caused by vitamin-D-hydroxylase mutations and vitamin D intakeDganit Dinour, Miriam Davidovits, Shraga Aviner, 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 Molecular Medicine (Berlin, Germany)|May 20, 2018
Translation inhibition corrects aberrant localization of mutant alanine-glyoxylate aminotransferase: possible therapeutic approach for hyperoxaluriaRuth Belostotsky, Roman Lyakhovetsky, Michael Y Sherman, 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.Frontiers in Pediatrics|October 2, 2024
Efficacy and safety of lumasiran for infants and young children with primary hyperoxaluria type 1: 30-month analysis of the phase 3 ILLUMINATE-B trialYaacov Frishberg, Wesley Hayes, Hadas Shasha-Lavsky, 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 7