A homozygous nonsense mutation in the methylmalonyl-CoA epimerase gene (MCEE) results in mild methylmalonic aciduria by Bikker, H., Bakker, H.D., Abeling, N.G.G.M., Poll-The, B.T., Kleijer, W.J., Rosenblatt, D.S., Waterham, H.R., Wanders, R.J.A., Duran, M.

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3-Methoxytyramine: An independent prognostic biomarker that associates with high-risk disease and poor clinical outcome in neuroblastoma patients by Verly, I.R.N., van Kuilenburg, A.B.P., Abeling, N.G.G.M., Goorden, S.M.I., Fiocco, M., Vaz, F.M., van Noesel, M.M., Zwaan, C.M., Kaspers, G.J.L., Merks, J.H.M., Caron, H.N., Tytgat, G.A.M.

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Molecular and clinical characterization of a Moroccan Cog7 deficient patient by Ng, Bobby G., Kranz, Christian, Hagebeuk, E.E.O., Duran, M., Abeling, N.G.G.M., Wuyts, B., Ungar, Daniel, Lupashin, Vladimir, Hartdorff, C.M., Poll-The, B.T., Freeze, Hudson H.

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Fatty acids and homocysteine levels in patients with recurrent depression: an explorative pilot study by Assies, J, Lok, A, Bockting, C.L, Weverling, G.J, Lieverse, R, Visser, I, Abeling, N.G.G.M, Duran, M, Schene, A.H

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X-linked borderline mental retardation with prominent behavioral disturbance : phenotype, genetic localization, and evidence for disturbed monoamine metabolism by BRUNNER, H. G, NELEN, M. R, VAN ZANDVOORT, P, ABELING, N. G. G. M, VAN GENNIP, A. H, WOLTERS, E. C, KUIPER, M. A, ROPERS, H. H, VAN OOST, B. A

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Inborn errors of pyrimidine degradation: Clinical, biochemical and molecular aspects by Gennip, A.H., Abeling, N.G.G.M., Vreken, P., Kuilenburg, A.B.P.

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Inhibition of pyrimidine degradation to β-alanine by propionate may contribute to the neurologic complications in patients with propionic acidemia by van Gennip, A.H., Abeling, N.G.G.M., Vreken, P., van Lenthe, H., Scholten, E.G., van Kuilenburg, A.B.P.

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