Guideline for the diagnosis and management of glutaryl‐CoA dehydrogenase deficiency (glutaric aciduria type I) von Kölker, S., Christensen, E., Leonard, J. V., Greenberg, C. R., Burlina, A. B., Burlina, A. P., Dixon, M., Duran, M., Goodman, S. I., Koeller, D. M., Müller, E., Naughten, E. R., Neumaier‐Probst, E., Okun, J. G., Kyllerman, M., Surtees, R. A., Wilcken, B., Hoffmann, G. F., Burgard, P.

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Glutaric aciduria type I: Outcome in the Republic of Ireland von Naughten, E. R., Mayne, P. D., Monavari, A. A., Goodman, S. I., Sulaiman, G., Croke, D. T.

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Prevention of cerebral palsy in glutaric aciduria type 1 by dietary management von Monavari, A A, Naughten, E R

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The intellectual abilities of early‐treated individuals with pyridoxine‐nonresponsive homocystinuria due to cystathionine β‐synthase deficiency von Yap, S., Rushe, H., Howard, P. M., Naughten, E. R.

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Clinical Course, Early Diagnosis, Treatment, and Prevention of Disease in Glutaryl-CoA Dehydrogenase Deficiency von Hoffmann, G. F., Athanassopoulos, S., Burlina, A. B., Duran, M., Klerk, J. B., Lehnert, W., Leonard, J. V., Monavari, A. A., Müller, E., Muntau, A. C., Naughten, E. R., Plecko-Starting, B., Superti-Furga, A., Zschocke, J., Christensen, E.

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Newborn screening for homocystinuria: Irish and world experience von Naughten, E R, Yap, S, Mayne, P D

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Vascular Complications of Severe Hyperhomocysteinemia in Patients with Homocystinuria Due to Cystathionine β-Synthase Deficiency: Effects of Homocysteine-Lowering Therapy von YAP, SUFIN, NAUGHTEN, EILEEN R., WILCKEN, BRIDGET, WILCKEN, DAVID E.L., BOERS, GODFRIED H.J.

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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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Short-Chain Acyl-CoA Dehydrogenase Deficiency Associated with Early Onset Severe Axonal Neuropathy von Kurian, M. A., Hartley, L., Zolkipli, Z., Little, M. A., Costigan, D., Naughten, E. R., Olpin, S., Muntoni, F., King, M. D.

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Glutaric aciduria and suspected child abuse von MORRIS, A A M, HOFFMANN, G F, NAUGHTEN, E R, MONAVARI, A A, COLLINS, J E, LEONARD, J V

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Emergency treatment in glutaryl‐CoA dehydrogenase deficiency von KÖlker, S., Greenberg, C. R., Lindner, M., Müller, E., Naughten, E. R., Hoffmann, G. F.

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Maintenance treatment of glutaryl‐CoA dehydrogenase deficiency von Mühlhausen, C., Hoffmann, G. F., Strauss, K. A., KÖlker, S., Okun, J. G., Greenberg, C. R., Naughten, E. R., Ullrich, K.

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Abuse or metabolic disorder? von HOFFMANN, GEORG F, NAUGHTEN, EILEEN R

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Multiple origins for phenylketonuria in Europe von EISENSMITH, R. C, OKANO, Y, HAGENFELDT, L, REY, F, MUNNICH, A, LYONNET, S, COCKBURN, F, CONNOR, J. M, PEMBREY, M. E, SMITH, I, GITZELMAN, R, STEINMANN, B, DASOVICH, M, APOLD, J, EIKEN, H. G, GIOVANNINI, M, RIVA, E, LONGHI, R, ROMANO, C, CERONE, R, NAUGHTEN, E. R, MULLINS, C, CAHALANE, S, WANG, T, OZALP, I, FEKETE, G, SCHULER, D, BERENCSI, G. Y, GÜTTLER, F, NASZ, I, BRDICKA, R, KAMARYT, J, PIJACKOVA, A, CABALSKA, B, BOSZKOWA, K, SCHWARTZ, E, KALININ, V. N, JIN, L, CHAKRABORTY, R, LOU, H, WOO, S. L. C, GULDBERG, P, LICHTER-KONECKI, U, KONECKI, D. S, SVENSSON, E

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Ocular complications in homocystinuria--early and late treated von Burke, J. P., O'Keefe, M., Bowell, R., Naughten, E. R.

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Frequency distribution of the Q188R mutation in the Irish galactosaemic population von Murphy, M., Sexton, D., O'Neill, C., Croke, D. T., Mayne, P. D., Naughten, E. R.

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Maternal pyridoxine non‐responsive homocystinuria: the role of dietary treatment and anticoagulation von Yap, S., Barry‐Kinsella, C., Naughten, E.R.

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Ocular findings among patients with late-diagnosed or poorly controlled homocystinuria compared with a screened, well-controlled population von Mulvihill, Alan, Yap, Sufin, O'Keefe, Michael, Howard, Pamela M., Naughten, Eileen R.

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A closer look at the eye in homocystinuria: A screened population von Burke, J. P., O'Keefe, M., Bowell, R., Naughten, E. R.

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Cataracts in children with classical galactosaemia and in their parents von Burke, J. P., O'Keefe, M., Bowell, R., Naughten, E. R.

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