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Last Updated: 01/07/2026
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Found 84 publications
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
Young Male With End-Stage Renal Disease Due to Primary Hyperoxaluria Type 2: A Rare Presentation.
Journal: Cureus
Published: August 19, 2023
Clinical characteristics, genetic profile and short-term outcomes of children with primary hyperoxaluria type 2: a nationwide experience.
Journal: Pediatric nephrology (Berlin, Germany)
Published: July 15, 2023
Simultaneous Liver Kidney Transplantation in a Primary Type 2 Hyperoxaluria With Corrected TOF and Severe Cardiomyopathy: A Case Report.
Journal: Journal of clinical and experimental hepatology
Published: June 30, 2023
Pediatric combined living donor liver and kidney transplantation for primary hyperoxaluria type 2.
Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
Published: April 01, 2023
Last Updated: 01/07/2026