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Items where Author is "Hughes, JH"

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Article

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

Ranganath, LR, Milan, AM, Hughes, AT, Khedr, M, Davison, AS, Shweihdi, E, Norman, BP, Hughes, JH, Bygott, H, Luangrath, E, Fitzgerald, R, Psarelli, EE, van Kan, C, Laan, D, Olsson, B, Rudebeck, M, Mankowitz, L, Sireau, N, Arnoux, J-B, Le Quan Sang, K-H , Jarvis, JC, Genovese, F, Braconi, D, Santucci, A, Zatkova, A, Glasova, H, Stančík, R, Imrich, R, Rhodes, NP and Gallagher, JA (2019) Homogentisic acid is not only eliminated by glomerular filtration and tubular secretion but also produced in the kidney in alkaptonuria. Journal of Inherited Metabolic Disease. ISSN 0141-8955

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