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Page 1
Nitisinone causes acquired tyrosinosis in alkaptonuria.
Khedr M, Cooper MS, Hughes AT, Milan AM, Davison AS, Norman BP, Sutherland H, Jarvis JC, Fitzgerald R, Markinson L, Psarelli EE, Ghane P, Deutz NEP, Gallagher JA, Ranganath LR. Khedr M, et al. Among authors: sutherland h. J Inherit Metab Dis. 2020 Sep;43(5):1014-1023. doi: 10.1002/jimd.12229. Epub 2020 Mar 5. J Inherit Metab Dis. 2020. PMID: 32083330
Metabolomic studies in the inborn error of metabolism alkaptonuria reveal new biotransformations in tyrosine metabolism.
Norman BP, Davison AS, Hughes JH, Sutherland H, Wilson PJ, Berry NG, Hughes AT, Milan AM, Jarvis JC, Roberts NB, Ranganath LR, Bou-Gharios G, Gallagher JA. Norman BP, et al. Among authors: sutherland h. Genes Dis. 2021 Feb 22;9(4):1129-1142. doi: 10.1016/j.gendis.2021.02.007. eCollection 2022 Jul. Genes Dis. 2021. PMID: 35685462 Free PMC article.
Comprehensive Biotransformation Analysis of Phenylalanine-Tyrosine Metabolism Reveals Alternative Routes of Metabolite Clearance in Nitisinone-Treated Alkaptonuria.
Norman BP, Davison AS, Hickton B, Ross GA, Milan AM, Hughes AT, Wilson PJM, Sutherland H, Hughes JH, Roberts NB, Bou-Gharios G, Gallagher JA, Ranganath LR. Norman BP, et al. Among authors: sutherland h. Metabolites. 2022 Sep 29;12(10):927. doi: 10.3390/metabo12100927. Metabolites. 2022. PMID: 36295829 Free PMC article.
31 results