Primary Hyperoxaluria Type 3 Latest Advances

Find the Latest Research About Primary Hyperoxaluria Type 3

Last Updated: 09/26/2026

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Found 37 publications

Combined Liver-Kidney Transplantation in Pediatric Patients From Colombia: A Case Series.

Combined Liver-Kidney Transplantation in Pediatric Patients From Colombia: A Case Series.

Journal: Pediatric transplantation
Published: April 13, 2026

Identification of Primary Hyperoxaluria Type III by Gas Chromatography/Mass Spectrometry-Based Urine Metabolomics.

Identification of Primary Hyperoxaluria Type III by Gas Chromatography/Mass Spectrometry-Based Urine Metabolomics.

Journal: Metabolites
Published: February 09, 2026

Urine microscopy revealing a metabolic disorder: a case report.

Urine microscopy revealing a metabolic disorder: a case report.

Journal: BMC nephrology
Published: December 28, 2025

Coexistence of autosomal dominant polycystic kidney disease and primary hyperoxaluria type 3.

Coexistence of autosomal dominant polycystic kidney disease and primary hyperoxaluria type 3.

Journal: Kidney international
Published: July 19, 2025

Differential clinical characteristics of Chinese children with primary hyperoxaluria type 3.

Differential clinical characteristics of Chinese children with primary hyperoxaluria type 3.

Journal: Pediatric nephrology (Berlin, Germany)
Published: June 05, 2025

Normal urinary oxalate excretion in 4-hydroxy-2-oxo-glutarate aldolase 1 (HOGA1) deficient mice with AGT expression in peroxisomes and not in mitochondria.

Normal urinary oxalate excretion in 4-hydroxy-2-oxo-glutarate aldolase 1 (HOGA1) deficient mice with AGT expression in peroxisomes and not in mitochondria.

Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: April 23, 2025

Liver Transplantation in Childhood: A 2-Year Single Center Experience.

Liver Transplantation in Childhood: A 2-Year Single Center Experience.

Journal: Transplantation proceedings
Published: March 26, 2025

Human glyoxylate metabolism revisited: New insights pointing to multi-organ involvement with implications for siRNA-based therapies in primary hyperoxaluria.

Human glyoxylate metabolism revisited: New insights pointing to multi-organ involvement with implications for siRNA-based therapies in primary hyperoxaluria.

Journal: Journal of inherited metabolic disease
Published: May 24, 2024

Genetic Diagnosis of Hyperoxaluria Type 3 Patients Using Haplotype Analysis.

Genetic Diagnosis of Hyperoxaluria Type 3 Patients Using Haplotype Analysis.

Journal: Kidney & blood pressure research
Published: May 04, 2024

4-hydroxy-2-oxoglutarate metabolism in a mouse model of Primary Hyperoxaluria Type 3.

4-hydroxy-2-oxoglutarate metabolism in a mouse model of Primary Hyperoxaluria Type 3.

Journal: Biochemistry and biophysics reports
Published: April 27, 2024

Primary hyperoxaluria type 3: from infancy to adulthood in a genetically unique cohort.

Primary hyperoxaluria type 3: from infancy to adulthood in a genetically unique cohort.

Journal: Pediatric nephrology (Berlin, Germany)
Published: February 27, 2024

Characterization of Stone Events in Patients With Type 3 Primary Hyperoxaluria.

Characterization of Stone Events in Patients With Type 3 Primary Hyperoxaluria.

Journal: The Journal of urology
Published: March 08, 2023
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Last Updated: 09/26/2026