Xanthinuria
Top View
- Phosphorylation and Sequence Dependency of Neurofilament Protein Oxidative
- Identification of a New Mutation in the Human Xanthine Dehydrogenase
- Rare Forms of Nephrolithiasis Rzadkie Postacie Kamicy Nerkowej
- Acetylene Hydratase from Pelobacter Acetylenicus : Functional Studies On
- XDH Gene Mutation Is the Underlying Cause of Classical Xanthinuria: a Second Report
- Purine and Pyrimidine Metabolism Disorders Panel
- The Renal Phenotype of Allopurinol-Treated HPRT-Deficient Mouse
- Family Study of Hereditary Xanthinuria
- Hereditary Xanthinuria with Recurrent Urolithiasis Occurring in Infancy
- The Drosophila Melanogaster Model of Human Uric Acid Nephrolithiasis As a Novel in Vivo Drug Screening Platform
- Silkworm Bombyx Mori
- Family Study of Hereditary Xanthinuria
- Hereditary Xanthinuria. Evidence for Enhanced Hypoxanthine Salvage
- Hereditary Xanthinuria Evidence for Enhanced Hypoxanthine Salvage Felicitas A
- Mutations Associated with Functional Disorder of Xanthine Oxidoreductase and Hereditary Xanthinuria in Humans
- Human Aberrations of Purine Metabolism and Their Significance for Rheumatology
- Allopurinol and Other Inhibitors of Urate Synthesis
- Excretory System