Identification of Primary Hyperoxaluria Type III by Gas Chromatography/Mass Spectrometry-Based Urine Metabolomics. [PDF]
Kuhara T +4 more
europepmc +1 more source
Molecular and Genetic Determinants of Nephrocalcinosis: Mechanisms, Genotype-Phenotype Correlations, and Precision Medicine. [PDF]
Popa S +6 more
europepmc +1 more source
Urine microscopy revealing a metabolic disorder: a case report. [PDF]
Santos D +6 more
europepmc +1 more source
Crystalline retinopathy in a child with hyperoxaluria type 1: Ultrawide field imaging before and after treatment. [PDF]
Borella Y +3 more
europepmc +1 more source
From recurrent flank pain to systemic oxalosis: a case of primary hyperoxaluria type 1 requiring dual organ transplantation. [PDF]
Hassan SMS +8 more
europepmc +1 more source
Teduglutide use in haemodialysis-dependent renal failure from secondary hyperoxaluria in short bowel syndrome and type 3 intestinal failure - A case report. [PDF]
Low ES, Chapman B, Wong D.
europepmc +1 more source
Kaleidoscopic Views in the Bone Marrow: Oxalate Crystals in a Patient Presenting with Bicytopenia
Yelda Dere +6 more
doaj +1 more source
Renal survival in hereditary urolithiasis: a monocentric cohort study from a Tunisian nephrology department. [PDF]
Bettaieb A +9 more
europepmc +1 more source
Hyperoxaluria and renal calculi [PDF]
R G, Woolfson, M A, Mansell
openaire +2 more sources

