• A Case of Infiltrative Cardiomyopathy Secondary to Primary Hyperoxaluria Type 2 - Utilization of Multimodality Imaging
• A case report of invasive infantile primary hyperoxaluria type 1 and literature review
• A mutation creating an out-of-frame alternative translation initiation site in the GRHPR 5'UTR causing primary hyperoxaluria type II
• A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2
• Brain abscess caused by Cladophialophora bantiana after renal allograft loss: A case report
• Calcified nodules on fingers in primary hyperoxaluria type 2
• Characterization of Stone Events in Patients With Type 3 Primary Hyperoxaluria
• Chiral liquid chromatography tandem mass spectrometry in the determination of the configuration of glyceric acid in urine of patients with D-glyceric and L-glyceric acidurias
• Clinical characteristics, genetic profile and short-term outcomes of children with primary hyperoxaluria type 2: a nationwide experience
• Clinical features and mutational spectrum of Chinese patients with primary hyperoxaluria type 2
• Clinical practice recommendations for primary hyperoxaluria: an expert consensus statement from ERKNet and OxalEurope
• Combined liver-kidney transplantation for hyperoxaluria type II?
• Combined Liver-Kidney Transplantation for Primary Hyperoxaluria Type 2: A Case Report
• Correction to: Three Tesla magnetic resonance imaging detects oxalate osteopathy in patients with primary hyperoxaluria type I
• Cristalline retinopathy from type 2 primary hyperoxaluria
• Cutaneous Oxalosis Due to Primary Hyperoxaluria
• D-glyceric aciduria
• d-Glyceric aciduria does not cause nonketotic hyperglycinemia: A historic co-occurrence
• D-glyceric aciduria is caused by genetic deficiency of D-glycerate kinase (GLYCTK)
• Detection of primary hyperoxaluria type 2 (L-glyceric aciduria) in patients with maintained renal function or end-stage renal failure
• Diagnostic Code-Based Screening for Identifying Children with Primary Hyperoxaluria
• Diagnostic policies on nephrolithiasis/nephrocalcinosis of possible genetic origin by Italian nephrologists: a survey by the Italian Society of Nephrology with an emphasis on primary hyperoxaluria
• Effect of liver transplantation with primary hyperoxaluria type 1: Five case reports and review of literature
• End-stage renal failure in primary hyperoxaluria type 2
• Ethnic differences in GRHPR mutations in patients with primary hyperoxaluria type 2
• Etiology, urine metabolic risk factors, and urine oxalate patterns in patients with significant hyperoxaluria and recurrent nephrolithiasis
• Evaluation of mutation screening as a first line test for the diagnosis of the primary hyperoxalurias
• Extracorporal shock wave lithotripsy in the management of stones in children with oxalosis--still the first choice?
• Failure of isolated kidney transplantation in a pediatric patient with primary hyperoxaluria type 2
• Glyoxylate reductase activity in blood mononuclear cells and the diagnosis of primary hyperoxaluria type 2
• Glyoxylate reductase/hydroxypyruvate reductase: a novel prognostic marker for hepatocellular carcinoma patients after curative resection
• Hemolytic Uremic Syndrome in an Infant with Primary Hyperoxaluria Type II: An Unreported Clinical Association
• High-performance liquid chromatographic assay for L-glyceric acid in body fluids. Application in primary hyperoxaluria type 2
• HOGA1 gene pathogenic variants in primary hyperoxaluria type III: Spectrum of pathogenic sequence variants, and phenotypic association
• HOGA1 variants in Chinese patients with primary hyperoxaluria type 3: genetic features and genotype-phenotype relationships
• Hypercalcemia in an Infant with Primary Hyperoxaluria Type 2: A Novel Association
• Hyperoxaluria, hyperglycoluria and renal oxalosis in Gilbert's potoroos (Potorous gilbertii)
• Improved Outcome of Infantile Oxalosis Over Time in Europe: Data From the OxalEurope Registry
• Incidence of Kidney Stones After Metabolic and Bariatric Surgery-Data from the Scandinavian Obesity Surgery Registry
• Invited response to recurrence of oxalate nephropathy after isolated kidney transplantation for primary hyperoxaluria type 2
• Is liver analysis still required for the diagnosis of primary hyperoxaluria type 2?
• Isolated kidney transplantation under lumasiran therapy in primary hyperoxaluria type 1: a report of five cases
• Kidney cysts in patients with <em>HOGA1</em> variants
• Kinetic analysis and tissue distribution of human D-glycerate dehydrogenase/glyoxylate reductase and its relevance to the diagnosis of primary hyperoxaluria type 2
• Lactate dehydrogenase A inhibitors with a 2,8-dioxabicyclo[3.3.1]nonane scaffold: A contribution to molecular therapies for primary hyperoxalurias
• Late diagnosis of primary hyperoxaluria type 2 in the adult: effect of a novel mutation in GRHPR gene on enzymatic activity and molecular modeling
• Lessons for the clinical nephrologist: lumasiran as the future cornerstone treatment for patients with primary hyperoxaluria type 1?
• Long-term outcome after combined or sequential liver and kidney transplantation in children with infantile and juvenile primary hyperoxaluria type 1
• Long-term outcomes after pre-emptive liver transplantation in primary hyperoxaluria type 1
• Lumasiran for Advanced Primary Hyperoxaluria Type 1: Phase 3 ILLUMINATE-C Trial
• Lumasiran: a potential therapy for the management of primary hyperoxaluria type 1? An editorial
• Massive hyperoxaluria
• Modification of primers for GRHPR genotyping: avoiding allele dropout by single nucleotide polymorphisms and homology sequence
• Molecular analysis of the glyoxylate reductase (GRHPR) gene and description of mutations underlying primary hyperoxaluria type 2
• Monogenic urinary lithiasis in Tunisian children: 25 years' experience of a referral center
• Natural history of urine and plasma oxalate in children with primary hyperoxaluria type 1
• Nephrocalcinosis in a patient with primary hyperoxaluria type 2
• Nephrocalcinosis in a patient with primary hyperoxaluria type 2
• Nephrocalcinosis is a risk factor for kidney failure in primary hyperoxaluria
• Novel mutation in the GRHPR gene in a Chinese patient with primary hyperoxaluria type 2 requiring renal transplantation from a living related donor
• Patients with primary hyperoxaluria type 2 have significant morbidity and require careful follow-up
• Pediatric combined living donor liver and kidney transplantation for primary hyperoxaluria type 2
• PHYOX2: a pivotal randomized study of nedosiran in primary hyperoxaluria type 1 or 2
• Preemptive liver transplant in two patients with primary hyperoxaluria type 1: Clinical significance of nephrolithiasis and nephrocalcinosis
• Primary hyperoxaluria type 1 in children: clinical and laboratory manifestations and outcome
• Primary Hyperoxaluria Type 1: Clinical, Paraclinical, and Evolutionary Aspects in Adults from One Nephrology Center
• Primary Hyperoxaluria Type 2
• Primary hyperoxaluria type 2
• Primary hyperoxaluria type 2
• Primary hyperoxaluria type 2 in children
• Primary hyperoxaluria type 2 successfully treated with combined liver-kidney transplantation after failure of isolated kidney transplantation
• Primary hyperoxaluria type 2 without L-glycericaciduria: is the disease under-diagnosed?
• Primary hyperoxaluria type 2: enzymology
• Primary hyperoxaluria type 2(PH2)
• Primary hyperoxaluria: A review
• Progress with RNA Interference for the Treatment of Primary Hyperoxaluria
• Promoter rearrangements cause species-specific hepatic regulation of the glyoxylate reductase/hydroxypyruvate reductase gene by the peroxisome proliferator-activated receptor alpha
• Pruritic eruption in a patient with end-stage renal disease
• Quantification of oxalate by novel LC-MS/MS: assay development, validation and application in lumasiran clinical trials
• Recent developments in our understanding of primary hyperoxaluria type 2
• Recurrence of oxalate nephropathy after isolated kidney transplantation for primary hyperoxaluria type 2
• Recurrent Nephrolithiasis Causing Kidney Failure
• Recurrent primary hyperoxaluria type 2 leads to early post-transplant renal function loss: A case report
• Reduced Electroretinogram Responses in Morphologically Normal Retina in Patients with Primary Hyperoxaluria Type 1
• Searching glycolate oxidase inhibitors based on QSAR, molecular docking, and molecular dynamic simulation approaches
• Severe child form of primary hyperoxaluria type 2 - a case report revealing consequence of GRHPR deficiency on metabolism
• Severe infantile epileptic encephalopathy associated with D-glyceric aciduria: report of a novel case and review
• Simultaneous Liver Kidney Transplantation in a Primary Type 2 Hyperoxaluria With Corrected TOF and Severe Cardiomyopathy: A Case Report
• Structural basis of substrate specificity in human glyoxylate reductase/hydroxypyruvate reductase
• Successful Treatment of Primary Hyperoxaluria Type 2 with a Combined Liver and Kidney Transplant
• Synthesis and <em>h</em>LDH Inhibitory Activity of Analogues to Natural Products with 2,8-Dioxabicyclo[3.3.1]nonane Scaffold
• The appearance of oxalate crystals in a kidney biopsy is no proof of post-transplant oxalate nephropathy in primary hyperoxaluria type 1
• The real world experience of pediatric primary hyperoxaluria patients in the PEDSnet clinical research network
• The retinal phenotype in primary hyperoxaluria type 2 and 3
• Three Tesla magnetic resonance imaging detects oxalate osteopathy in patients with primary hyperoxaluria type I
• Tissue differences in the expression of mutations and polymorphisms in the GRHPR gene and implications for diagnosis of primary hyperoxaluria type 2
• Up regulation of glyoxylate reductase/hydroxypyruvate reductase (GRHPR) is associated with intestinal epithelial cells apoptosis in TNBS-induced experimental colitis
• Updated genetic testing of Italian patients referred with a clinical diagnosis of primary hyperoxaluria
• Verkalkte Knoten an allen Fingerspitzen
• Young Male With End-Stage Renal Disease Due to Primary Hyperoxaluria Type 2: A Rare Presentation