Urinary copper/zinc ratio: a promising parameter for replacement of 24-hour urinary copper excretion for diagnosis of Wilson’s disease in children
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s12519-010-0023-4.pdf
Reference23 articles.
1. Bull PC, Thomas GR, Rommens JM, Forbes JR, Cox DW. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nat Genet 1993;5:327–337.
2. Petrukhin K, Fischer SG, Pirastu M, Tanzi RE, Chernov I, Devoto M, et al. Mapping, cloning and genetic characterization of the region containing the Wilson disease gene. Nat Genet 1993;5:338–343.
3. Ala A, Schilsky ML. Wilson disease: pathophysiology, diagnosis, treatment, and screening. Clin Liver Dis 2004;8:787–805.
4. Brewer GJ, Askari FK. Wilson’s disease: clinical management and therapy. J Hepatol 2005;42:S13–S21.
5. Schilsky ML. Diagnosis and treatment of Wilson’s disease. Pediatr Transplantation 2002;6:15–19.
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1. Could Urinary Copper/Zinc Ratio Be a Newer Tool to Replace 24-Hour Urinary Copper Excretion for Diagnosing Wilson Disease in Children?;Pediatric Gastroenterology, Hepatology & Nutrition;2024
2. Ideal serum non-ceruloplasmin bound copper prediction for long-term treated patients with Wilson disease: a nomogram model;Frontiers in Medicine;2023-11-03
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4. Ratio of aspartate aminotransferase to alanine aminotransferase and alkaline phosphatase to total bilirubin in Wilsonian acute liver failure in children;Indian Journal of Gastroenterology;2022-06
5. Actualización en el diagnóstico bioquímico de la enfermedad de Wilson;Advances in Laboratory Medicine / Avances en Medicina de Laboratorio;2022-05-09
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