• 2,8-dihydroxyadenine lithiasis. 2 new pediatric cases of this misdiagnosed metabolic abnormality. The value of extracorporeal lithotripsy
• Combined sulfite and xanthine oxidase deficiency due to an anomaly in the metabolism of molybdenum cofactor
• Double deficiency of sulfite and xanthine oxidase causing encephalopathy and due to a hereditary anomaly in the metabolism of molybdenum
• Endothelial dysfunction and hypertensive vasoconstriction
• Hematotoxicity caused by azathioprine genetically determined and aggravated by xanthine oxidase deficiency in a patient following renal transplantation
• Hypouricaemia (author's transl)
• Hypouricemia, an old subject and new concepts
• Neurologic injury in isolated sulfite oxidase deficiency
• Routine urinary oxypurine assays for the detection of xanthine-oxidase deficiency (author's transl)
• Sulfite and xanthine oxidase deficiency: a diagnosis based on 2 simple tests
• Sulfite oxidase deficiency presenting as Leigh syndrome
• The renal lithiasis of a xanthine oxidase-deficient patient
• Three cases of hereditary xanthinuria: review of the literature (author's transl)
• Xanthic lithiasis in the child. A study of one case. Review of the literature (author's transl)
• Xanthine-oxidase deficiency (congenital xanthinuria). Family study