Primary Hyperoxaluria Type 1 Latest Advances
Find the Latest Research About Primary Hyperoxaluria Type 1
Last Updated: 09/26/2026
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Found 665 publications
Skeletal oxalosis in a child on maintenance hemodialysis.
Journal: Kidney international
Published: August 04, 2026
68Ga-FAPI-04 PET/CT Findings in Primary Hyperoxaluria Type 1.
Journal: Clinical nuclear medicine
Published: June 20, 2026
A Case Report of Familial Primary Hyperoxaluria Type 1 Nephropathy with c.781C>G Gene Mutation and Literature Review.
Journal: Annals of clinical and laboratory science
Published: June 08, 2026
Kidney imaging for the diagnosis and follow-up of a primary hyperoxaluria type 1 patient with NC, NL, and severe chronic kidney disease: a case report with literature review.
Journal: Medical ultrasonography
Published: June 02, 2026
Case Report: A rare AGXT pathogenic variant associated with young-adult-onset end-stage kidney disease.
Journal: Frontiers in genetics
Published: May 13, 2026
Combined Liver-Kidney Transplantation in Pediatric Patients From Colombia: A Case Series.
Journal: Pediatric transplantation
Published: April 13, 2026
Multimodal retinal imaging of primary hyperoxaluria type 1.
Journal: Eye (London, England)
Published: April 09, 2026
Primary Hyperoxaluria Type 1 Diagnosed After Kidney Transplantation in the Absence of Classical Features.
Journal: Case reports in nephrology
Published: April 01, 2026
Targeting the Highly Deleterious G161C and Y260C SNP Variants of the AGXT Protein Involved in Glyoxylate Metabolism Using Tauroursodeoxycholic Acid: A Computational Study.
Journal: International journal of molecular sciences
Published: March 27, 2026
Last Updated: 09/26/2026