Global serum glycoform profiling for the investigation of dystroglycanopathies & Congenital Disorders of Glycosylation von Heywood, Wendy E., Bliss, Emily, Mills, Philippa, Yuzugulen, Jale, Carreno, Gabriela, Clayton, Peter T., Muntoni, Francesco, Worthington, Viki C., Torelli, Silvia, Sebire, Neil J., Mills, Kevin, Grunewald, Stephanie

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Protective effects of carnosine against malondialdehyde-induced toxicity towards cultured rat brain endothelial cells von Hipkiss, Alan R, Preston, Jane E, Himswoth, David T.M, Worthington, Viki C, Abbot, N.Joan

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Protective effects of carnosine against protein modification mediated by malondialdehyde and hypochlorite von Hipkiss, Alan R., Worthington, Viki C., Himsworth, David T.J., Herwig, Wolker

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Pre- and postnatal diagnosis of patients with CLN1 and CLN2 by assay of palmitoyl protein thioesterase and tripeptidyl peptidase I activities von Young, Elisabeth P., Worthington, Viki C., Jackson, Marie, Winchester, Bryan G.

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Pre- and postnatal diagnosis of patients withCLN1 and CLN2 by assay of palmitoyl protein thioesterase and tripeptidyl peptidase I activities von Young, Elisabeth P., Worthington, Viki C., Jackson, Marie, Winchester, Bryan G.

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Early-onset fetal hydrops and muscle degeneration in siblings due to a novel variant of type IV glycogenosis von Cox, Phillip M., Brueton, Louise A., Murphy, Karl W., Worthington, Viki C., Bjelogrlic, Predrag, Lazda, Edgar J., Sabire, Neil J., Sewry, Caroline A.

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A novel mutation (G233D) in the glycogen phosphorylase gene in a patient with hepatic glycogen storage disease and residual enzyme activity von Tang, Nelson L.S, Hui, Joannie, Young, Elisabeth, Worthington, Viki, To, Ka-Fai, Cheung, Kam-Lau, Li, Chi-Kong, Fok, Tai-Fai

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