The Fabry disease-associated lipid Lyso-Gb3 enhances voltage-gated calcium currents in sensory neurons and causes pain von Choi, L., Vernon, J., Kopach, O., Minett, M.S., Mills, K., Clayton, P.T., Meert, T., Wood, J.N.

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A New Method for the Analysis of Urinary Vitamin E Metabolites and the Tentative Identification of a Novel Group of Compounds von Pope, S.A.S., Clayton, P.T., Muller, D.P.R.

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The significance of elevated CSF lactate von Chow, S L, Rooney, Z J, Cleary, M A, Clayton, P T, Leonard, J V

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The significance of a high plasma ammonia value von Chow, S L, Gandhi, V, Krywawych, S, Clayton, P T, Leonard, J V, Morris, A A M

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Diagnosis of metabolic liver disease in infancy von Clayton, P.T.

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Molecular studies in Portuguese patients with Smith–Lemli–Opitz syndrome and report of three new mutations in DHCR7 von Cardoso, M.L., Balreira, A., Martins, E., Nunes, L., Cabral, A., Marques, M., Lima, M. Reis, Marques, J.S., Medeira, A., Cordeiro, I., Pedro, S., Mota, M.C., Dionisi-Vici, C., Santorelli, F.M., Jakobs, C., Clayton, P.T., Vilarinho, L.

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Diagnostic difficulties in a case of primary systemic carnitine deficiency with idiopathic dilated cardiomyopathy von Kinali, M, Olpin, S.E, Clayton, P.T, Daubeney, P.E.F, Mercuri, E, Manzur, A.Y, Tein, I, Leonard, J, Muntoni, F

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Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome von Horslen, S P, Clayton, P T, Harding, B N, Hall, N A, Keir, G, Winchester, B

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Rapid diagnosis of Zellweger syndrome and infantile Refsum's disease by fast atom bombardment—mass spectrometry of urine bile salts von Lawson, A.M., Madigan, M.J., Shortland, D., Clayton, P.T.

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3-OXO-Δ4 BILE ACIDS IN LIVER DISEASE von Clayton, P.T., Patel, E., Lawson, A.M., Carruthers, R.A., Tanner, M.S., Strandvik, B., Egestad, B., Sjövall, J.

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3-OXO-Δ 4 BILE ACIDS IN LIVER DISEASE von Clayton, P.T., Patel, E., Lawson, A.M., Carruthers, R.A., Tanner, M.S., Strandvik, B., Egestad, B., Sjövall, J.

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A simplified gas-liquid chromatographic method for the estimation of non-sulphated plasma bile acids von Clayton, P.T., Muller, D.P.R.

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ULTRASTRUCTURE OF LIVER IN INHERITED DISORDERS OF FAT OXIDATION von Lake, B.D., Clayton, P.T., Leonard, J.V., Bhuiyan, A.K.M.J., Bartlett, K., Aynsley Green, A.

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Peroxisomal disorders von Champion, M.P., Clayton, P.T.

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MUNCHAUSEN SYNDROME BY PROXY von Clayton, P.T., Counahan, R., Chantler, C.

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Increased first trimester nuchal translucency as a prenatal manifestation of Smith-Lemli-Opitz syndrome von Hyett, Jon A., Clayton, Peter T., Moscoso, Gonzalo, Nicolaides, Kypros H.

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Impact of blinding on estimated treatment effects in randomised clinical trials: meta-epidemiological study von Moustgaard, Helene, Clayton, Gemma L, Jones, Hayley E, Boutron, Isabelle, Jørgensen, Lars, Laursen, David R T, Olsen, Mette F, Paludan-Müller, Asger, Ravaud, Philippe, Savović, Jelena, Sterne, Jonathan A C, Higgins, Julian P T, Hróbjartsson, Asbjørn

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Empirical Evidence of Study Design Biases in Randomized Trials: Systematic Review of Meta-Epidemiological Studies von Page, Matthew J, Higgins, Julian P T, Clayton, Gemma, Sterne, Jonathan A C, Hróbjartsson, Asbjørn, Savović, Jelena

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Development of de novo HLA donor specific antibodies (HLA-DSA), HLA antibodies (HLA-Ab) and allograft rejection post blood transfusion in kidney transplant recipients von Jalalonmuhali, M., Carroll, R.P., Tsiopelas, E., Clayton, P., Coates, P.T.

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Use of external evidence for design and Bayesian analysis of clinical trials: a qualitative study of trialists' views von Clayton, Gemma L., Elliott, Daisy, Higgins, Julian P. T., Jones, Hayley E.

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