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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Homocystinuria due to cystathionine β‐synthase deficiency in Ireland: 25 years' experience of a newborn screened and treated population with reference to clinical outcome and bioch... von Yap, S., Naughten, E.

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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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Prevention of cerebral palsy in glutaric aciduria type 1 by dietary management von Monavari, A A, 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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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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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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The role of human demographic history in determining the distribution and frequency of transferase-deficient galactosaemia mutations von Flanagan, J M, McMahon, G, Brendan Chia, S H, Fitzpatrick, P, Tighe, O, O'Neill, C, Briones, P, Gort, L, Kozak, L, Magee, A, Naughten, E, Radomyska, B, Schwartz, M, Shin, J S, Strobl, W M, Tyfield, L A, Waterham, H R, Russell, H, Bertorelle, G, Reichardt, J K V, Mayne, P D, Croke, D T

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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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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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Opt-out testing for blood-borne viruses in primary care: a multicentre, prospective study von O'Kelly, Mark, Byrne, David, Naughten, Edward, Bergin, Colm, Williams, Caroline

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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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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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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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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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Hyperhomocysteinemia: An Independent Risk Factor for Vascular Disease von Clarke, Robert, Daly, Leslie, Robinson, Killian, Naughten, Eileen, Cahalane, Seamus, Fowler, Brian, Graham, Ian

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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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