Maple syrup urine disease in treated patients: Biochemical and oxidative stress profiles
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,General Medicine
Reference28 articles.
1. Maple syrup urine disease (branched-chain ketoaciduria);Chuang,2001
2. Metabolism of branched-chain amino acids in maple syrup urine disease;Schadewaldt;Eur J Pediatr,1997
3. Variant maple syrup urine disease (MSUD)—the entire spectrum;Schadewaldt;J Inherit Metab Dis,2006
4. Dysmyelination in the brain of adolescents and young adults with maple syrup urine disease;Schönberger;Mol Genet Metab,2004
5. Branched-chain ketoacyl dehydrogenase deficiency: maple syrup disease;Strauss;Curr Treat Option Neurol,2003
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2. Pathophysiology of maple syrup urine disease: Focus on the neurotoxic role of the accumulated branched-chain amino acids and branched-chain α-keto acids;Neurochemistry International;2022-07
3. Effective Immobilization of Lactate Dehydrogenase onto Mesoporous Silica;Biotechnology and Applied Biochemistry;2021-12-28
4. Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity;Orphanet Journal of Rare Diseases;2020-11-01
5. Brain Branched-Chain Amino Acids in Maple Syrup Urine Disease: Implications for Neurological Disorders;International Journal of Molecular Sciences;2020-10-11
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