Physical Activity Is the Key Determinant of Skeletal Muscle Mitochondrial Function in Type 2 Diabetes von van Tienen, F. H. J, Praet, S. F. E, de Feyter, H. M, van den Broek, N. M, Lindsey, P. J, Schoonderwoerd, K. G. C, de Coo, I. F. M, Nicolay, K, Prompers, J. J, Smeets, H. J. M, van Loon, L. J. C

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The interactive animated e-book as a word learning device for kindergartners von SMEETS, D. J. H., BUS, A. G.

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Interactive electronic storybooks for kindergartners to promote vocabulary growth von Smeets, Daisy J.H., Bus, Adriana G.

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A 5-year natural history study in LAMA2-related muscular dystrophy and SELENON-related myopathy: the Extended LAST STRONG study von de Laat, E C M, Houwen-van Opstal, S L S, Bouman, K, van Doorn, J L M, Cameron, D, van Alfen, N, Dittrich, A T M, Kamsteeg, E J, Smeets, H J M, Groothuis, J T, Erasmus, C E, Voermans, N C, Voermans, Nicol C

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Using Electronic Storybooks to Support Word Learning in Children With Severe Language Impairments von Smeets, Daisy J. H., van Dijken, Marianne J., Bus, Adriana G.

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The unfolding clinical spectrum of POLG mutations von Blok, M J, van den Bosch, B J, Jongen, E, Hendrickx, A, de Die-Smulders, C E, Hoogendijk, J E, Brusse, E, de Visser, M, Poll-The, B T, Bierau, J, de Coo, I F, Smeets, H J

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Novel pathogenic SLC25A46 splice‐site mutation causes an optic atrophy spectrum disorder von Nguyen, M., Boesten, I., Hellebrekers, D. M. E. I., Mulder‐den Hartog, N. M., de Coo, I. F. M., Smeets, H. J. M., Gerards, M.

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Added Value of Dialogic Parent-Child Book Readings: A Meta-Analysis von Mol, Suzanne E., Bus, Adriana G., de Jong, Maria T., Smeets, Daisy J. H.

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How do changes in the mtDNA and mitochondrial dysfunction influence cancer and cancer therapy? Challenges, opportunities and models von van Gisbergen, M.W., Voets, A.M., Starmans, M.H.W., de Coo, I.F.M., Yadak, R., Hoffmann, R.F., Boutros, P.C., Smeets, H.J.M., Dubois, L., Lambin, P.

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Defective NDUFA9 as a novel cause of neonatally fatal complex I disease von van den Bosch, B J C, Gerards, M, Sluiter, W, Stegmann, A P A, Jongen, E L C, Hellebrekers, D M E I, Oegema, R, Lambrichs, E H, Prokisch, H, Danhauser, K, Schoonderwoerd, K, de Coo, I F M, Smeets, H J M

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Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion von Poelmans, G., Engelen, J.J.M., Van Lent-Albrechts, J., Smeets, H.J., Schoenmakers, E., Franke, B., Buitelaar, J.K., Wuisman-Frerker, M., Erens, W., Steyaert, J., Schrander-Stumpel, C.

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Common SNPs in LEP and LEPR associated with birth weight and type 2 diabetes-related metabolic risk factors in twins [Erratum: 2008, v. 32, no. 8 p. 1335-1336.] [Erratum: 2008 Nov.... von Souren, N.Y, Paulussen, A.D, Steyls, A, Loos, R.J, Stassen, A.P, Gielen, M, Smeets, H.J, Beunen, G, Fagard, R, Derom, C

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Blood biomarkers for assessment of mitochondrial dysfunction: An expert review von Hubens, W.H.G., Vallbona-Garcia, A., de Coo, I.F.M., van Tienen, F.H.J., Webers, C.A.B., Smeets, H.J.M., Gorgels, T.G.M.F.

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RRM1 variants cause a mitochondrial DNA maintenance disorder via impaired de novo nucleotide synthesis von Shintaku, Jonathan, Pernice, Wolfgang M, Eyaid, Wafaa, Gc, Jeevan B, Brown, Zuben P, Juanola-Falgarona, Marti, Torres-Torronteras, Javier, Sommerville, Ewen W, Hellebrekers, Debby Mei, Blakely, Emma L, Donaldson, Alan, van de Laar, Ingrid Mbh, Leu, Cheng-Shiun, Marti, Ramon, Frank, Joachim, Tanji, Kurenai, Koolen, David A, Rodenburg, Richard J, Chinnery, Patrick F, Smeets, H J M, Gorman, Gráinne S, Bonnen, Penelope E, Taylor, Robert W, Hirano, Michio

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Glenohumeral joint injection: a comparative study of ultrasound and fluoroscopically guided techniques before MR arthrography von Rutten, Matthieu J. C. M., Collins, James M. P., Maresch, Bas J., Smeets, Jacques H. J. M., Janssen, Caroline M. M., Kiemeney, Lambertus A. L. M., Jager, Gerrit J.

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Treatment preferences for medication or surgery in patients with deep endometriosis and bowel involvement – a discrete choice experiment von Metzemaekers, Jeroen, Akker‐van Marle, M. Elske, Sampat, Jonathan, Smeets, Mathilde J. G. H., English, James, Thijs, Elke, Maas, Jacques W. M., Willem Jansen, Frank, Essers, Brigitte

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Dealing with uncertainties: ethics of prenatal diagnosis and preimplantation genetic diagnosis to prevent mitochondrial disorders von Bredenoord, A.L., Pennings, G., Smeets, H.J., de Wert, G.

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Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease von Blok, M J, Spruijt, L, de Coo, I F M, Schoonderwoerd, K, Hendrickx, A, Smeets, H J

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Modeling Genetic and Environmental Factors to Increase Heritability and Ease the Identification of Candidate Genes for Birth Weight: A Twin Study von Gielen, M., Lindsey, P. J., Derom, C., Smeets, H. J. M., Souren, N. Y., Paulussen, A. D. C., Derom, R., Nijhuis, J. G.

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Cardiac hypertrophy is enhanced in PPARα−/− mice in response to chronic pressure overload von Smeets, Pascal J.H., Teunissen, Birgit E.J., Willemsen, Peter H.M., van Nieuwenhoven, Frans A., Brouns, Agnieszka E., Janssen, Ben J.A., Cleutjens, Jack P.M., Staels, Bart, van der Vusse, Ger J., van Bilsen, Marc

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