Acute presentations of inherited metabolic disorders: investigation and initial management by Morris, A.A.M, Leonard, J.V

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The investigation and the initial management of children with suspected metabolic disease presenting acutely by Leonard, J.V, Morris, A.A.M

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G.P.3.03 Recurrent mutations in the NDUFS2 gene causing isolated complex I deficiency in skeletal muscle by McFarland, R, Tuppen, H, He, L, Blakely, E.L, Morris, A.A.M, Clarke, M, Jones, S, Devlin, A.M, Taylor, R.W

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Cataract in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) by Russell-Eggitt, I.M., Leonard, J.V., Lund, A.M., Manoj, B., Thompson, D.A., Morris, A.A.M.

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Cerebral edema associated with betaine treatment in classical homocystinuria by Devlin, A.M, Hajipour, L, Gholkar, A, Fernandes, H, Ramesh, V, Morris, A.A.M

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Are tablets a practical source of protein substitute in phenylketonuria? by MacDonald, A, Ferguson, C, Rylance, G, Morris, A A M, Asplin, D, Hall, S K, Booth, I W

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A patient with carnitine-acylcarnitine translocase deficiency with a mild phenotype by Morris, A.A.M., Olpin, S.E., Brivet, M., Turnbull, D.M., Jones, R.A.K., Leonard, J.V.

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Urea cycle disorders by Leonard, J.V., Morris, A.A.M.

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Medium chain acyl-CoA dehydrogenase deficiency caused by a deletion of exons 11 and 12 by Morris, A.A.M., Taylor, R.W., Lightowlers, R.N., Aynsley-Green, A., Bartlett, K., Turnbull, D.M.

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A novel biomarker panel for irritable bowel syndrome and the application in the general population by Mujagic, Zlatan, Tigchelaar, Ettje F., Zhernakova, Alexandra, Ludwig, Thomas, Ramiro-Garcia, Javier, Baranska, Agnieszka, Swertz, Morris A., Masclee, Ad A. M., Wijmenga, Cisca, van Schooten, Frederik J., Smolinska, Agnieszka, Jonkers, Daisy M. A. E.

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