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Ranganath, L, Khedr, M, Milan, AM, Davison, AS, Norman, BP, Janssen, MCH, Lock, EA, Bou-Gharios, G and Gallagher, JA (2023) Increased prevalence of Parkinson's disease in alkaptonuria. JIMD reports, 64 (4). pp. 282-292. ISSN 2192-8304

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 and Ranganath, LR (2022) Comprehensive Biotransformation Analysis of Phenylalanine-Tyrosine Metabolism Reveals Alternative Routes of Metabolite Clearance in Nitisinone-Treated Alkaptonuria. Metabolites, 12 (10). ISSN 2218-1989

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 and Gallagher, JA (2021) Metabolomic studies in the inborn error of metabolism alkaptonuria reveal new biotransformations in tyrosine metabolism. Genes and Diseases, 9 (4). pp. 1129-1142. ISSN 2352-3042

Hughes, JH, Keenan, CM, Sutherland, H, Edwards, HR, Wilson, PJM, Ranganath, LR, Jarvis, JC, Bou-Gharios, G and Gallagher, JA (2020) Anatomical Distribution of Ochronotic Pigment in Alkaptonuric Mice is Associated with Calcified Cartilage Chondrocytes at Osteochondral Interfaces. Calcified Tissue International. ISSN 0171-967X

Hughes, JH, Wilson, PJM, Sutherland, H, Judd, S, Hughes, AT, Milan, AM, Jarvis, JC, Bou-Gharios, G, Ranganath, LR and Gallagher, JA (2020) Dietary restriction of tyrosine and phenylalanine lowers tyrosinaemia associated with nitisinone therapy of alkaptonuria. Journal of Inherited Metabolic Disease. pp. 1-10. ISSN 0141-8955