Primary Hyperoxaluria Type 2 Latest Advances
Find the Latest Research About Primary Hyperoxaluria Type 2
Last Updated: 04/28/2026
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Found 87 publications
Publisher Correction: Clinical burden, genetic heterogeneity, and diagnostic implications in primary hyperoxaluria type 2.
Journal: Pediatric nephrology (Berlin, Germany)
Published: March 16, 2026
N-Propargylglycine Restores Survival by Preventing Calcium Oxalate Stone Formation, Tubular Injury, and Kidney Dysfunction in a Lethal Mouse Model of Primary Hyperoxaluria Type 2.
Journal: Kidney international
Published: December 22, 2025
Clinical burden, genetic heterogeneity, and diagnostic implications in primary hyperoxaluria type 2.
Clinical burden, genetic heterogeneity, and diagnostic implications in primary hyperoxaluria type 2.
Journal: Pediatric nephrology (Berlin, Germany)
Published: November 06, 2025
Primary hyperoxaluria: insights into its clinical presentation, genetic mutations, and transplantation outcomes in a pediatric population in a tertiary care center.
Journal: Orphanet journal of rare diseases
Published: June 25, 2025
Phenotypes and the Importance of Genetic Analysis in Adult Patients with Nephrolithiasis and/or Nephrocalcinosis: A Single-Center Experience.
Journal: Genes
Published: March 20, 2025
Clinical features and mutational spectrum of Chinese patients with primary hyperoxaluria type 2.
Journal: Urolithiasis
Published: February 26, 2024
Modified by the Innovative Drugs and Strategies-Pattern of Selected Indications for Pediatric Liver Transplantation.
Journal: Pediatric transplantation
Published: January 23, 2024
Late-onset retinal oxalosis in primary hyperoxaluria type 2.
Journal: American journal of ophthalmology case reports
Published: December 14, 2023
Last Updated: 04/28/2026