One mutation, three phenotypes: novel metabolic insights on MELAS, MIDD and myopathy caused by the m.3243A > G mutation von Esterhuizen, Karien, Lindeque, J. Zander, Mason, Shayne, van der Westhuizen, Francois H., Rodenburg, Richard J., de Laat, Paul, Smeitink, Jan A. M., Janssen, Mirian C. H., Louw, Roan

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Urinary Metabolites and Their Link with Premature Arterial Stiffness in Black Boys: The ASOS Study von Erasmus, Dalene, Mels, Carina M.C., Louw, Roan, Lindeque, J. Zander, Kruger, Ruan

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A urinary biosignature for mitochondrial myopathy, encephalopathy, lactic acidosis and stroke like episodes (MELAS) von Esterhuizen, Karien, Lindeque, J Zander, Mason, Shayne, van der Westhuizen, Francois H, Suomalainen, Anu, Hakonen, Anna H, Carroll, Christopher J, Rodenburg, Richard J, de Laat, Paul B, Janssen, Mirian C H, Smeitink, Jan A M, Louw, Roan

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