Hemoglobin precipitation greatly improves 4-methylumbelliferone-based diagnostic assays for lysosomal storage diseases in dried blood spots by Oemardien, L.F., Boer, A.M., Ruijter, G.J.G., van der Ploeg, A.T., de Klerk, J.B.C., Reuser, A.J.J., Verheijen, F.W.

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Brain abnormalities in a case of malonyl-CoA decarboxylase deficiency by de Wit, M.C.Y., de Coo, I.F.M., Verbeek, E., Schot, R., Schoonderwoerd, G.C., Duran, M., de Klerk, J.B.C., Huijmans, J.G.M., Lequin, M.H., Verheijen, F.W., Mancini, G.M.S.

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Severe acute necrotizing pancreatitis associated with lipoprotein lipase deficiency in childhood by van Walraven, L.A, de Klerk, J.B.C, Postema, R.R

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Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiency by Vaz, F.M., Scholte, H.R., Ruiter, J., Hussaarts-Odijk, L.M., Rodrigues Pereira, R., Schweitzer, S., de Klerk, J.B.C., Waterham, H.R., Wanders, R.J.A.

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Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotype by Scholte, H.R., Van Coster, R.N.A., de Jonge, P.C., Poorthuis, B.J.H.M., Jeneson, J.A.L., Andresen, B.S., Gregersen, N., de Klerk, J.B.C., Busch, H.F.M.

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L‐2‐Hydroxyglutaric aciduria: Normal L‐2‐hydroxyglutarate dehydrogenase activity in liver from two new patients by Wanders, R.J.A., Vilarinho, L., Hartung, H.P., Hoffmann, G.F., Mooijer, P.A.W., Jansen, G.A., Huijmans, J.G.M., Klerk, J.B.C., Brink, H.J., Jakobs, C., Duran, M.

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Tetrahydrobiopterin Loading Test in Xanthine Dehydrogenase and Molybdenum Cofactor Deficiencies by Blau, N., de Klerk, J.B.C., Thöny, B., Heizmann, C.W., Kierat, L., Smeitink, J.A.M., Duran, M.

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Aberrant aversive learning signals in the habenula in remitted unmedicated patients with recurrent depression by De Klerk-Sluis, J., Geugies, H., Mocking, R.T., Figueroa, C.A., Marsman, J.B.C., Van Eijndhoven, P.F.P., Geurts, D.E.M., Ruhé, H.G.

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