Vascular Outcome in Patients With Homocystinuria due to Cystathionine β-Synthase Deficiency Treated Chronically: A Multicenter Observational Study von Yap, Sufin, Boers, Godfried H.J, Wilcken, Bridget, Wilcken, David E.L, Brenton, David P, Lee, Philip J, Walter, John H, Howard, Pamela M, Naughten, Eileen R

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Adult care in phenylketonuria and hyperphenylalaninaemia: the relevance of neurological abnormalities von Brenton, D P, Pietz, J

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The adult and adolescent clinic for inborn errors of metabolism von Brenton, D. P.

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Brain MRI changes in phenylketonuria: Associations with dietary status von Thompson, Alan J., Tillotson, Sarah, Smith, Isabel, Kendall, Brian, Moore, Susan G., Brenton, David P.

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Cutis verticis gyrata of the scalp in a patient with autosomal dominant insulin resistance syndrome von WOOLLONS, A, DARLEY, C. R, LEE, P. J, BRENTON, D. P, SONKSEN, P. H, BLACK, M. M

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Inhibition of L-{18F}fluorodopa uptake into human brain by amino acids demonstrated by positron emission tomography von Leenders, K. L., Poewe, W. H., Palmer, A. J., Brenton, D. P., Frackowiak, R. S. J.

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Maternal phenylketonuria. A study from the United Kingdom von Brenton, D P, Lilburn, M

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Progressive osseous heteroplasia: A case report von Athanasou, N.A., Benson, M.K.D'A., Brenton, D.P., Smith, R.

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Cardiac defects in the children of mothers with high concentrations of plasma phenylalanine von Brenton, D P

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Recommendations on the dietary management of phenylketonuria

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Pancreatitis and homocystinuria von Collins, J. E., Brenton, D. P.

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Phenylketonuria: treatment in adolescence and adult life von Brenton, D P, Tarn, A C, Cabrera-Abreu, J C, Lilburn, M

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Transport of L-phenylalanine and related amino acids at the ovine blood-brain barrier von Brenton, D P, Gardiner, R M

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Dystonia in homocystinuria von Kempster, P A, Brenton, D P, Gale, A N, Stern, G M

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Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis von READ, A. P, THAKKER, R. V, MCGLADE, S, PEACOCK, C. J, SMITH, R, O'RIORDAN, J. L. H, DAVIES, K. E, MOUNTFORD, R. C, BRENTON, D. P, DAVIES, M, GLORIEUX, F, HARRIS, R, HENDY, G. N, KING, A

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Neurological involvement in X-linked hypophosphataemic rickets von Bradbury, P G, Brenton, D P, Stern, G M

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Glycerol‐3‐phosphate excretion in fructose‐1,6‐diphosphatase deficiency von Krywawych, S., Katz, G., Lawson, A. M., Wyatt, S., Brenton, D. P.

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Myoglobinuria: the importance of reaching a firm diagnosis--a patient with defective fatty acid oxidation von Ellis, C. J., Dewhurst, A. G., Cooper, M., Brenton, D. P., Dathan, J. R.

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Skeletal abnormalities in homocystinuria von Brenton, D. P.

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3‐Methyladipate excretion in animals fed a phytol supplement with reference to Refsum's disease von Krywawych, S., Brenton, D. P., Jackson, M. J., Forte, C., Walker, D. K., Lawson, A. M.

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