• <em>Chlamydomonas reinhardtii</em>-A Reference Microorganism for Eukaryotic Molybdenum Metabolism
• A case report of MoCD etiology in a neonate: A novel homozygous MoCS2 variant
• A compound heterozygote case of isolated sulfite oxidase deficiency
• A defect in molybdenum cofactor binding causes an attenuated form of sulfite oxidase deficiency
• A mild case of molybdenum cofactor deficiency defines an alternative route of MOCS1 protein maturation
• Analysis of clinical characteristics and genetic variants in a child with Isolated sulfite oxidase deficiency
• Analysis of SUOX gene variants and clinical features in a child with Isolated sulfite oxidase deficiency
• Analysis of the Cellular Roles of MOCS3 Identifies a MOCS3-Independent Localization of NFS1 at the Tips of the Centrosome
• Bezafibrate prevents mitochondrial dysfunction, antioxidant system disturbance, glial reactivity and neuronal damage induced by sulfite administration in striatum of rats: Implications for a possible therapeutic strategy for sulfite oxidase deficiency
• Biological applications of a turn-on bioluminescent probe for monitoring sulfite oxidase deficiency in vivo
• Case Report: Compound Heterozygous Variants in <em>MOCS3</em> Identified in a Chinese Infant With Molybdenum Cofactor Deficiency
• Case Report: Electroencephalography in a neonate with isolated sulfite oxidase deficiency - a case report and literature review
• Cholestatic Jaundice in Sulphite Oxidase Deficiency - An Unusual Association
• Cholestatic Jaundice in Sulphite Oxidase Deficiency - An Unusual Association: Correspondence
• Clinical and neuroimaging features as diagnostic guides in neonatal neurology diseases with cerebellar involvement
• Consensus guidelines for the diagnosis and management of isolated sulfite oxidase deficiency and molybdenum cofactor deficiencies
• Covalent post-synthetic modification of MOFs as a fluorescent sensor for the efficient detection of the biomarker of cystinuria
• Delineating the phenotypic spectrum of sulfite oxidase and molybdenum cofactor deficiency
• Development of a rapid UPLC-MS/MS determination of urine sulfocysteine for diagnosis of sulfocysteinuria and molybdenum co-factor deficiencies
• Diagnostic imaging approach of sulfite oxidase deficiency
• Disturbance of brain energy and redox homeostasis provoked by sulfite and thiosulfate: potential pathomechanisms involved in the neuropathology of sulfite oxidase deficiency
• Epilepsy in inborn errors of metabolism
• Epilepsy in sulfite oxidase deficiency and related disorders: insights from neuroimaging and genetics
• Evidence that Thiosulfate Inhibits Creatine Kinase Activity in Rat Striatum via Thiol Group Oxidation
• Genetics of ectopia lentis
• Hereditary xanthinuria is not so rare disorder of purine metabolism
• HIF-1 Has a Central Role in <em>Caenorhabditis elegans</em> Organismal Response to Selenium
• Higher susceptibility of cerebral cortex and striatum to sulfite neurotoxicity in sulfite oxidase-deficient rats
• Human ultrarare genetic disorders of sulfur metabolism demonstrate redundancies in H₂S homeostasis
• Hydrogen sulfide as an anti-calcification stratagem in human aortic valve: Altered biogenesis and mitochondrial metabolism of H₂S lead to H₂S deficiency in calcific aortic valve disease
• Hypoxia-inducible factor induces cysteine dioxygenase and promotes cysteine homeostasis in <em>Caenorhabditis elegans</em>
• Identification and characterization of the rice pre-harvest sprouting mutants involved in molybdenum cofactor biosynthesis
• Identification of a novel SUOX pathogenic variants as the cause of isolated sulfite oxidase deficiency in a Chinese pedigree
• Identifying potential dietary treatments for inherited metabolic disorders using Drosophila nutrigenomics
• Impaired mitochondrial maturation of sulfite oxidase in a patient with severe sulfite oxidase deficiency
• In vitro evidence that sulfite impairs glutamatergic neurotransmission and inhibits glutathione metabolism-related enzymes in rat cerebral cortex
• Infantile spasms and hyperekplexia associated with isolated sulfite oxidase deficiency
• Internalization of the <em>Aspergillus nidulans</em> AstA Transporter into Mitochondria Depends on Growth Conditions, and Affects ATP Levels and Sulfite Oxidase Activity
• Is There a Connection between the Metabolism of Copper, Sulfur, and Molybdenum in Alzheimer's Disease? New Insights on Disease Etiology
• Isolated sulfite oxidase deficiency
• Isolated sulfite oxidase deficiency
• Isolated sulfite oxidase deficiency: a founder mutation
• Kinetic results for mutations of conserved residues H304 and R309 of human sulfite oxidase point to mechanistic complexities
• Learning from the worm: the effectiveness of protein-bound Moco to treat Moco deficiency
• Lessons Learned from Inherited Metabolic Disorders of Sulfur-Containing Amino Acids Metabolism
• Machine learning-based identification and characterization of 15 novel pathogenic SUOX missense mutations
• Mechanistic complexities of sulfite oxidase: An enzyme with multiple domains, subunits, and cofactors
• Metabolic crisis after trivial head trauma in late-onset isolated sulfite oxidase deficiency: Report of two new cases and review of published patients
• Metabolic stroke in a late-onset form of isolated sulfite oxidase deficiency
• Microarray analysis unmasked paternal uniparental disomy of chromosome 12 in a patient with isolated sulfite oxidase deficiency
• Mild phenotype in Molybdenum cofactor deficiency: A new patient and review of the literature
• Molybdenum cofactor and isolated sulphite oxidase deficiencies: Clinical and molecular spectrum among Egyptian patients
• Molybdenum cofactor deficiency
• Molybdenum Cofactor Deficiency in Humans
• Molybdenum cofactor deficiency: A natural history
• Molybdenum cofactor deficiency: a new HPLC method for fast quantification of s-sulfocysteine in urine and serum
• Molybdenum Cofactor Deficiency: Mega Cisterna Magna in Two Consecutive Pregnancies and Review of the Literature
• Molybdenum cofactor deficiency: metabolic link between taurine and S-sulfocysteine
• Molybdenum cofactor transfer from bacteria to nematode mediates sulfite detoxification
• Molybdenum trioxide nanoparticles with intrinsic sulfite oxidase activity
• Mutation analysis of SUOX in isolated sulfite oxidase deficiency with ectopia lentis as the presenting feature: insights into genotype-phenotype correlation
• Myelin Disruption, Neuroinflammation, and Oxidative Stress Induced by Sulfite in the Striatum of Rats Are Mitigated by the pan-PPAR agonist Bezafibrate
• Neonatal epilepsies: Clinical management
• Neurologic injury in isolated sulfite oxidase deficiency
• New insights into the molecular physiology of sulfoxide reduction in bacteria
• Novel Compound Heterozygous Pathogenic Variants in <em>SUOX</em> Cause Isolated Sulfite Oxidase Deficiency in a Chinese Han Family
• Novel Compound Heterozygous Pathogenic Variants in SUOX Cause Isolated Sulfite Oxidase Deficiency in a Chinese Han Family
• Obtaining the necessary molybdenum cofactor for sulfite oxidase activity in the nematode Caenorhabditis elegans surprisingly involves a dietary source
• Oxygen and nitrite reduction by heme-deficient sulphite oxidase in a patient with mild sulphite oxidase deficiency
• Oxygen reactivity of mammalian sulfite oxidase provides a concept for the treatment of sulfite oxidase deficiency
• Oxygen Vacancy-Engineered PEGylated MoO₃_-x Nanoparticles with Superior Sulfite Oxidase Mimetic Activity for Vitamin B1 Detection
• Postmortem whole-genome sequencing on a dried blood spot identifies a novel homozygous SUOX variant causing isolated sulfite oxidase deficiency
• Preimplantation genetic diagnosis in isolated sulfite oxidase deficiency
• Prenatal brain disruption in isolated sulfite oxidase deficiency
• Prenatal multicystic encephalopathy in isolated sulfite oxidase deficiency with a novel mutaion
• Prenatal symptoms and diagnosis of inherited metabolic diseases
• Protein-bound molybdenum cofactor is bioavailable and rescues molybdenum cofactor-deficient <em>C. elegans</em>
• S-Sulfocysteine Induces Seizure-Like Behaviors in Zebrafish
• Severe isolated sulfide oxidase deficiency with a novel mutation
• Stable clinical course in three siblings with late-onset isolated sulfite oxidase deficiency: a case series and literature review
• Strong anion determination in biological fluids by capillary electrophoresis for clinical diagnostics
• Sulfite Alters the Mitochondrial Network in Molybdenum Cofactor Deficiency
• Sulfite disrupts brain mitochondrial energy homeostasis and induces mitochondrial permeability transition pore opening via thiol group modification
• Sulfite Impairs Bioenergetics and Redox Status in Neonatal Rat Brain: Insights into the Early Neuropathophysiology of Isolated Sulfite Oxidase and Molybdenum Cofactor Deficiencies
• Sulfite leads to neuron loss in the hippocampus of both normal and SOX-deficient rats
• Sulfite oxidase activity deficiency caused by cofactor molybdenum deficiency: A case of early severe encephalopathy
• Sulfite oxidase deficiency in a newborn
• Sulfite oxidase deficiency--an unusual late and mild presentation
• Sulfite-induced protein radical formation in LPS aerosol-challenged mice: Implications for sulfite sensitivity in human lung disease
• Teaching NeuroImages: Early imaging of sulfite oxidase deficiency mimics severe hypoxic ischemic encephalopathy
• The central active site arginine in sulfite oxidizing enzymes alters kinetic properties by controlling electron transfer and redox interactions
• The effect of ingested sulfite on active avoidance in normal and sulfite oxidase-deficient aged rats
• The effect of ingested sulfite on visual evoked potentials, lipid peroxidation, and antioxidant status of brain in normal and sulfite oxidase-deficient aged rats
• The History of Animal and Plant Sulfite Oxidase-A Personal View
• The mitochondrial-targeted reactive species scavenger JP4-039 prevents sulfite-induced alterations in antioxidant defenses, energy transfer, and cell death signaling in striatum of rats
• The role of glutamate oxaloacetate transaminases in sulfite biosynthesis and H₂S metabolism
• The Role of Oxidative Stress and Bioenergetic Dysfunction in Sulfite Oxidase Deficiency: Insights from Animal Models
• The Role of Sulfide Oxidation Impairment in the Pathogenesis of Primary CoQ Deficiency
• Very early neuroimages of sulfite oxidase deficiency mimicing severe hypoxic ischemic encephalopathy in a neonate
• Whole exome sequencing identified a homozygous novel mutation in SUOX gene causes extremely rare autosomal recessive isolated sulfite oxidase deficiency