• A case of hereditary xanthinuria type 1 accompanied by bilateral renal calculi
• A case of Xanthinuria in a patient with marked hypouricemia
• A case of xanthinuria type I with a novel mutation in xanthine dehydrogenase
• A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle
• A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation
• A novel mutation in xanthine dehydrogenase in a case with xanthinuria in Hunan province of China
• A Trial of Favipiravir and Hydroxychloroquine combination in Adults Hospitalized with moderate and severe Covid-19: A structured summary of a study protocol for a randomised controlled trial
• Adaptable Xerogel-Layered Amperometric Biosensor Platforms on Wire Electrodes for Clinically Relevant Measurements
• Advances in xanthine biosensors and sensors: A review
• Adverse urinary effects of allopurinol in dogs with leishmaniasis
• Amyloidogenic Propensity of Metabolites in the Uric Acid Pathway and Urea Cycle Critically Impacts the Etiology of Metabolic Disorders
• An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro-Asian stone-forming belt
• An unusual cause of pink diapers in an infant: Questions and Answers
• Analysis of Purine Metabolism to Elucidate the Pathogenesis of Acute Kidney Injury in Renal Hypouricemia
• Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data
• Association of Mutations Identified in Xanthinuria with the Function and Inhibition Mechanism of Xanthine Oxidoreductase
• Asymptomatic classical hereditary xanthinuria type 1
• Beware of the Uric Acid: Severe Azathioprine Myelosuppression in a Patient With Juvenile Idiopathic Arthritis and Hereditary Xanthinuria
• Biosensing methods for xanthine determination: a review
• Candidate causative variant for xanthinuria in a Domestic Shorthair cat
• Classical Xanthinuria in Nine Israeli Families and Two Isolated Cases from Germany: Molecular, Biochemical and Population Genetics Aspects
• Classical xanthinuria: a rare cause of pediatric urolithiasis
• Comparative analysis of nephrolithiasis in otherwise healthy versus medically complex gastrostomy fed children
• Declaration: Novel SLC3A1 mutation in a cystinuria patient with xanthine stones: a case report
• Deletion of <em>Mocos</em> Induces Xanthinuria with Obstructive Nephropathy and Major Metabolic Disorders in Mice
• Deletion of Mocos Induces Xanthinuria with Obstructive Nephropathy and Major Metabolic Disorders in Mice
• Discriminating Susceptibility of Xanthine Oxidoreductase Family to Metals
• Disturbance of uric acid metabolism
• Epidemiology of feline urolithiasis in Mexico (2006-2017)
• Fortuitous Discovery of Hereditary Xanthinuria
• Functional characterization of human xanthine oxidase allelic variants
• Further studies on allopurinol-induced hyperuricaemia and visceral gout in red-tailed hawks (Buteo jamaicensis)
• Genetic and biochemical features of the monogenic hereditary urolithiasis
• Glasgow Early Treatment Arm Favirpiravir (GETAFIX) for adults with early stage COVID-19: A structured summary of a study protocol for a randomised controlled trial
• Hereditary xanthinuria and urolithiasis in a domestic shorthair cat
• Hereditary xanthinuria in a goat
• Hereditary xanthinuria is not so rare disorder of purine metabolism
• High Performance Liquid Chromatography Analysis and Description of Purine Content of Diets Suitable for Dogs with <em>Leishmania</em> Infection during Allopurinol Treatment-A Pilot Trial
• Hypouricaemia in a patient with hereditary xanthinuria type I
• Hypouricemia and Urate Transporters
• Hypouricemia with recurrent nephrolithiasis: an overlooked entity: Answers
• Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria
• Identification of a new mutation in the human xanthine dehydrogenase responsible for xanthinuria type I
• Identification of a xanthinuria type I case with mutations of xanthine dehydrogenase in an Afghan child
• Kidney Failure Secondary to Hereditary Xanthinuria due to a Homozygous Deletion of the XDH Gene in the Absence of Overt Kidney Stone Disease
• Kidney failure secondary to hereditary xanthinuria due to a homozygous deletion of the XDH gene, in the absence of overt kidney stone disease
• Leishmaniosis caused by <em>Leishmania infantum</em> in ferrets: Update review
• Management of urinary stones: state of the art and future perspectives by experts in stone disease
• Metabolic and Genetic Evaluation in Children with Nephrolithiasis
• MOCOS-associated renal syndrome in a Brown Swiss cattle
• Modern diagnostic approach to hereditary xanthinuria
• Modified forearm ischemic test in hypouricemic patients
• Molybdenum cofactor deficiency type B manifested as Leigh-like syndrome: a case report and literature review
• Molybdenum in human health and disease
• Monogenic urinary lithiasis in Tunisian children: 25 years' experience of a referral center
• Multi-exon deletion in the XDH gene as a cause of classical xanthinuria
• Multiple variants in <em>XDH</em> and <em>MOCOS</em> underlie xanthine urolithiasis in dogs
• Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans
• Next-generation metabolic screening: targeted and untargeted metabolomics for the diagnosis of inborn errors of metabolism in individual patients
• Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: biochemical and molecular genetic analysis in two Czech families with xanthinuria type I
• Nutritional aspect of nephrolithiasis
• Plasma metabolomic profiles enhance precision medicine for volunteers of normal health
• Pure xanthine pediatric urolithiasis: A cause of acute renal failure
• Purine disorders with hypouricemia
• Randomized, allopurinol-controlled trial of the effects of dietary nucleotides and active hexose correlated compound in the treatment of canine leishmaniosis
• Rare cause of xanthinuria: a pediatric case of molybdenum cofactor deficiency B
• Rare causes of emesis
• Recent progress in nanomaterial-based electrochemical and optical sensors for hypoxanthine and xanthine. A review
• Recurrent urinary lithiasis revealing hereditary xanthinuria
• Renal stone and chronic kidney failure associated with hypouricemia: Answers
• Renal stone and chronic kidney failure associated with hypouricemia: Questions
• Research progress on renal calculus associate with inborn error of metabolism
• Review of childhood genetic nephrolithiasis and nephrocalcinosis
• Successful Kidney Transplantation in a Young Male with Type 2 Xanthinuria
• Targeted renal knockdown of Na⁺/H⁺ exchanger regulatory factor <em>Sip1</em> produces uric acid nephrolithiasis in <em>Drosophila</em>
• The lowest uric acid in kidney transplant and review of literature
• Thiopurine-induced toxicity is associated with dysfunction variant of the human molybdenum cofactor sulfurase gene (xanthinuria type II)
• Three cases of xanthinuria identified by gas chromatography/mass spectrometry-based urine metabolomics
• Type 1 xanthinuria: Report on three cases
• Uric acid accumulation in an Arabidopsis urate oxidase mutant impairs seedling establishment by blocking peroxisome maintenance
• Uric Acid Metabolism, Uric Acid Transporters and Dysuricemia
• Urine concentrations of xanthine, hypoxanthine and uric acid in UK Cavalier King Charles spaniels
• Urolithiasis due to Hereditary Xanthinuria Type II: A Long-term Follow-up report
• Using Next-Generation Sequencing to Identify a Mutation in Human MCSU that is Responsible for Type II Xanthinuria
• Xanthine dehydrogenase deficiency with novel sequence variations presenting as rheumatoid arthritis in a 78-year-old patient
• Xanthine nephrolithiasis in a galician blond beef calf
• XANTHINE NEPHROLITHIASIS IN JUVENILE CAPTIVE GIANT OTTERS (<em>PTERONURA BRASILIENSIS</em>)
• Xanthine oxidoreductase knockout mice with high HPRT activity were not rescued by NAD⁺ replenishment
• Xanthine urolithiasis
• Xanthine urolithiasis causing bilateral ureteral obstruction in a 10-month-old cat
• Xanthine urolithiasis in a cat: a case report and evaluation of a candidate gene for xanthine dehydrogenase
• Xanthine urolithiasis: Inhibitors of xanthine crystallization
• Xanthinuria in a domestic shorthair cat
• Xanthinuria in a familial group of Munchkin cats and an unrelated domestic shorthair cat
• Xanthinuria secondary to allopurinol treatment in dogs with leishmaniosis: Current perspectives of the Iberian veterinary community
• Xanthinuria type 1 in a woman with arthralgias: a combined clinical and molecular genetic investigation
• Xanthinuria Type 1 with a Novel Mutation in Xanthine Dehydrogenase and a Normal Endothelial Function
• Xanthinuria type I as the cause of nephrolithiasis in 17-years old girl
• Xanthinuria type I with a novel mutation of xanthine dehydrogenase
• Xanthinuria type I: a rare cause of urolithiasis