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Last Updated: 01/07/2026
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Found 138 publications
Early postnatal hepatocyte transplantation in a child with molybdenum cofactor deficiency type B.
Journal: Molecular genetics and metabolism
Published: January 14, 2025
A Novel Variant in the SUOX Gene in the Oldest Individual with Late-Onset Isolated Sulfite Oxidase Deficiency.
Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: December 16, 2024
S-Sulfocysteine's toxic effects on HT-22 cells are not triggered by glutamate receptors, nor do they involve apoptotic or genotoxicity mechanisms.
Journal: Cytotechnology
Published: November 20, 2024
Sulfite oxidase deficiency causes persulfidation loss and hydrogen sulfide release.
Journal: The Journal of clinical investigation
Published: April 09, 2024
Consensus guidelines for the diagnosis and management of isolated sulfite oxidase deficiency and molybdenum cofactor deficiencies.
Journal: Journal of inherited metabolic disease
Published: January 05, 2024
A case report of MoCD etiology in a neonate: A novel homozygous MoCS2 variant.
Journal: Clinical case reports
Published: September 24, 2023
Timing of cerebral damage in molybdenum cofactor deficiency: A meta-analysis of case reports.
Journal: Genetics in medicine open
Published: September 18, 2023
The History of Animal and Plant Sulfite Oxidase-A Personal View.
Journal: Molecules (Basel, Switzerland)
Published: September 12, 2023
Analysis of clinical characteristics and genetic variants in a child with Isolated sulfite oxidase deficiency
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 02, 2023
Mechanistic complexities of sulfite oxidase: An enzyme with multiple domains, subunits, and cofactors.
Journal: Journal of inorganic biochemistry
Published: March 21, 2023
Last Updated: 01/07/2026