Nucleoside supplements as treatments for mitochondrial DNA depletion syndrome von Dombi, Eszter, Marinaki, Tony, Spingardi, Paolo, Millar, Val, Hadjichristou, Nastasia, Carver, Janet, Johnston, Iain G, Fratter, Carl, Poulton, Joanna

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Nomenclature for alleles of the thiopurine methyltransferase gene von Appell, Malin L., Berg, Jonathan, Duley, John, Evans, William E., Kennedy, Martin A., Lennard, Lynne, Marinaki, Tony, McLeod, Howard L., Relling, Mary V., Schaeffeler, Elke, Schwab, Matthias, Weinshilboum, Richard, Yeoh, Allen E.J., McDonagh, Ellen M., Hebert, Joan M., Klein, Teri E., Coulthard, Sally A.

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Nomenclature for alleles of the thiopurine methyltransferase gene von Appell, Malin L, Berg, Jonathan, Duley, John, Evans, William E, Kennedy, Martin A, Lennard, Lynne, Marinaki, Tony, McLeod, Howard L, Relling, Mary V, Schaeffeler, Elke, Schwab, Matthias, Weinshilboum, Richard, Yeoh, Allen E.J, McDonagh, Ellen M, Hebert, Joan M, Klein, Teri E, Coulthard, Sally A

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SuO028GENETIC TESTING REVEALS INCREASED PREVALENCE OF UROMODULIN ASSOCIATED KIDNEY DISEASE von Gast, Christine, Marinaki, Tony, Arenas-Hernandez, Monica, Campbell, Sara, Venkat-Raman, Gopalakrishnan

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Difficulties and possibilities with thiopurine therapy in inflammatory bowel disease—Proceedings of the first Thiopurine Task Force meeting von van Asseldonk, Dirk P, Sanderson, Jeremy, de Boer, Nanne K.H, Sparrow, Miles P, Lémann, Marc, Ansari, Azhar, Almer, Sven H, Florin, Timothy H.J, Gearry, Richard B, Mulder, Chris J, Mantzaris, Gerassimos, van Bodegraven, Ad A

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Adenine phosphoribosyltransferase deficiency in the United Kingdom: two novel mutations and a cross-sectional survey von Balasubramaniam, Gowrie S., Arenas-Hernandez, Monica, Escuredo, Emilia, Fairbanks, Lynette, Marinaki, Tony, Mapplebeck, Sarah, Sheaff, Michael, Almond, Michael K.

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MTHFR C677T Polymorphism Modulates Red Cell TPMT Activity von Arenas, Monica, Marinaki, Tony, Simpson, Gemma, Lewis, Cathryn, Shobowale–Bakre, El-Monsor, Escuredo, Emilia, Fairbanks, Lynette, Duley, John, Sanderson, Jeremy

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Lack of association between VNTR's and TPMT induction in response to azathioprine von Ansari, Azhar R., Yang, Su, Arenas, Monica, Marinaki, Tony, Duley, John, Sanderson, Jeremy

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Polymorphism in the MTHFR gene affects TPMT activity von Ansari, Azhar R., Marinaki, Tony, Arenas, Monica, Shobowale-Bakre, El-Monsor, Lewis, Katherine, Duley, John, Sanderson, Jeremy

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Higher frequency of zero TPMT deficiency: Analysis of 7000 referrals to TPMT reference laboratory von Ansari, Azhar R., Yim, Alistair, Holme, Alex, Arenas, Monica, Shobowale-Bakre, El-Monsor, Marinaki, Tony, Duley, John, Sanderson, Jeremy

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Genetic determinants of the thiopurine methyltransferase intermediate activity phenotype von Ansari, Azhar R., Arenas, Monica, Marinaki, Tony, Lewis, Katherine, Shobowale-Bakre, El-Monsor A., Fairbanks, Lynette, Escuredo, Emila, Duley, John, Sanderson, Jeremy

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Xanthine oxidase/dehydrogenase activity in IBD patients receiving azathioprine von Ansari, Azhar R., De Sica, Anna, Duley, John, Shobowale-Bakre, El-Monsor, Fairbanks, Lynette, Marinaki, Tony, Aslam, Zak, Hirst, Jo, Smith, Catherine, Sanderson, Jeremy

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Mutation in the ITPA gene predicts intolerance to azathioprine von Ansari, Azhar R., Marinaki, Tony, Arenas, Monica, Sumi, Satoshi, Shobowale-Bakre, El-Monsor, Lewis, Katherine, Woodman, Issy, Duley, John, Sanderson, Jeremy

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