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1
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0024290589
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Xenobiotic metabolism in motorneuron disease
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Steventon G, Williams AC, Waring RH, Pall HS, Adams D. Xenobiotic metabolism in motorneuron disease. Lancet 1988; ii: 644-647.
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4
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0025833504
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Hereditary variation of liver enzymes involved with detoxification and neurodegenerative disease
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Williams AC, Steventon GB, Sturman S, Waring RH. Hereditary variation of liver enzymes involved with detoxification and neurodegenerative disease. J Inherit Metab Dis 1991; 14: 431-435.
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Phenotypic variation in xenobiotic metabolism and adverse environmental response: Focus on sulfur-dependent detoxification pathways
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McFadden SA. Phenotypic variation in xenobiotic metabolism and adverse environmental response: focus on sulfur-dependent detoxification pathways. Toxicology 1996; 111: 43-65.
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Toxicology
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McFadden, S.A.1
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6
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0025637516
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Monoamine oxidase substrates in Parkinson's disease
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Humfrey CDN, Steventon GB, Sturman SG, Waring RH, Williams AC. Monoamine oxidase substrates in Parkinson's disease. Biochem Pharmacol 1990; 40: 2562-2564.
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Biochem Pharmacol
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Humfrey, C.D.N.1
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Williams, A.C.5
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7
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0025822293
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N-Methylation of pyridines in Parkinson's disease
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Green S, Buttrum S, Molloy H, Steventon G, Sturman S, Waring R, Pall H, Williams A. N-Methylation of pyridines in Parkinson's disease. Lancet 1991; 338: 120-121.
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Green, S.1
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Pall, H.7
Williams, A.8
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8
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0024353389
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S-Methylation in motorneuron disease and Parkinson's disease
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Waring RH, Steventon GB, Sturman SG, Heafield MTE, Smith MCG, Williams AC. S-Methylation in motorneuron disease and Parkinson's disease. Lancet 1989; ii: 356-357.
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Williams, A.C.6
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9
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0025020452
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Metabolism of low-dose paracetamol in patients with chronic neurological disease
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Steventon GB, Heafield MTE, Sturman S, Waring RH, Williams AC. Metabolism of low-dose paracetamol in patients with chronic neurological disease. Xenobiotica 1990; 20: 2562-2564.
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Xenobiotica
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11
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Thiopurine phannacogenetics: Clinical and molecular studies of thiopurine methyltransferase
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Weinshilboum RM. Thiopurine phannacogenetics: clinical and molecular studies of thiopurine methyltransferase. Drug Metab Disp 2001; 29: 601-605.
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Determination of S-carboxymethyl-L-cysteine and some of its metabolites in urine and serum by high-performance liquid chromatography using fluorescent pre-column labelling
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Staffeldt B, Brockmoller J, Roots I. Determination of S-carboxymethyl-L-cysteine and some of its metabolites in urine and serum by high-performance liquid chromatography using fluorescent pre-column labelling. J Chromatogr 1991; 571: 133-147.
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15
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0018668152
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Human erythrocyte thiol methyltransferase: Radiochemical microassay and biochemical properties
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Weinshilboum RM, Sladek S, Klumpp S. Human erythrocyte thiol methyltransferase: radiochemical microassay and biochemical properties. Clin Chim Acta 1979; 97: 59-71.
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Genetic aspects of the polymodally distributed sulphoxidation of S-carboxymethyl-L-cysteine in man
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Mitchell SC, Waring RH, Haley CS, Idle JR, Smith RL. Genetic aspects of the polymodally distributed sulphoxidation of S-carboxymethyl-L-cysteine in man. Br J Clin Pharmacol 1984; 18: 507-521.
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17
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0020521957
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Thiol methylation pharmacogenetics: Heritability of human erythrocyte thiol methyltransferase activity
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Keith RA, Van Loon J, Wusson LF, Weinshilboum RM. Thiol methylation pharmacogenetics: heritability of human erythrocyte thiol methyltransferase activity. Clin Pharm Ther 1983; 34: 521-528.
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Keith, R.A.1
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18
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0033056792
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The metabolism of S-carboxymethyl-L-cysteine in man. A neurodegenerative disease study
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Steventon G, Waring R, Sturman S, Heafield MTE, Williams AC. The metabolism of S-carboxymethyl-L-cysteine in man. A neurodegenerative disease study. Med Sci Res 1999; 27: 119-120.
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19
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0028172367
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D-Penicillamine metabolism in neurodegenerative disease: An in vivo/in vitro sulphydryl methylation study
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Peters L, Steventon GB, Green S, Sturman S, Waring RH, Williams AC. D-Penicillamine metabolism in neurodegenerative disease: an in vivo/in vitro sulphydryl methylation study. Xenobiotica 1994; 24: 1013-1020.
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Peters, L.1
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Williams, A.C.6
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