Evolution of Dihydropyrimidine Dehydrogenase (DPD) Diagnostics in A Single Center in A Time-Period of Seven Years by van den Bosch, B.J.C, Paulussen, A.D.C, Breuer, M, Lindhout, M, Tserpelis, D.C.J, Steyls, A, Bierau, J, Coenen, M.J.H

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Early and transient gene expression changes in pressure overload-induced cardiac hypertrophy in mice by van den Bosch, B.J.C., Lindsey, P.J., van den Burg, C.M.M., van der Vlies, S.A., Lips, D.J., van der Vusse, G.J., Ayoubi, T.A., Doevendans, P.A., Smeets, H.J.M.

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P311 Defective Complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome by de Coo, I.F.M, Gerards, M, Sluiter, W, van den Bosch, B.J.C, Frentzen, M, Akbari, H, Schoonderwoerd, K.C, Scholte, H.R, Smeets, H.J.M

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Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distribution by Voets, A M, van den Bosch, B J C, Stassen, A P, Hendrickx, A T, Hellebrekers, D M, Van Laer, L, Van Eyken, E, Van Camp, G, Pyle, A, Baudouin, S V, Chinnery, P F, Smeets, H J M

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Altered myocardial gene expression reveals possible maladaptive processes in heterozygous and homozygous cardiac myosin-binding protein C knockout mice by Eijssen, L.M.T., van den Bosch, B.J.C., Vignier, N., Lindsey, P.J., van den Burg, C.M.M., Carrier, L., Doevendans, P.A., van der Vusse, G.J., Smeets, H.J.M.

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Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNA Leu(UUR) gene by van den Bosch, B.J.C., de Coo, I.F.M., Hendrickx, A.T.M., Busch, H.F.M., de Jong, G., Scholte, H.R., Smeets, H.J.M.

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Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNALeu(UUR) gene by van den Bosch, B J C, de Coo, I F M, Hendrickx, A T M, Busch, H F M, de Jong, G, Scholte, H R, Smeets, H J M

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