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The Journal of Clinical Endocrinology and Metabolism|July 23, 2014
Exome sequencing identifies a novel homozygous mutation in the phosphate transporter SLC34A1 in hypophosphatemia and nephrocalcinosisAbbhirami Rajagopal, Débora Braslavsky, James T Lu, et al.Pediatric Nephrology (Berlin, Germany)|July 11, 2018
Clinical parameters, LysoGb3, podocyturia, and kidney biopsy in children with Fabry disease: is a correlation possible?Juan Politei, Valeria Alberton, Oscar Amoreo, et al.Pediatric Nephrology (Berlin, Germany)|February 19, 2021
Hemolytic uremic syndrome associated with Shiga toxin-producing Escherichia coli infection in Argentina: update of serotypes and genotypes and their relationship with severity of the diseaseLaura F Alconcher, Alejandro Balestracci, Paula A Coccia, et al.Pediatric Nephrology (Berlin, Germany)|July 2, 2018
Hyponatremia: a new predictor of mortality in patients with Shiga toxin-producing Escherichia coli hemolytic uremic syndromeLaura F Alconcher, Paula A Coccia, Angela Del C Suarez, et al.Pageof 2