Ohcanbohtosat - Wevers, Ron A

Neurometabolic disorders: Five new things Dahkki Willemsen, Michèl A., Harting, Inga, Wevers, Ron A.

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Autosomal recessive cutis laxa syndrome revisited Dahkki Morava, Éva, Guillard, Maïlys, Lefeber, Dirk J, Wevers, Ron A

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Reply to Leao-Teles et al Dahkki Morava, Eva, Guillard, Maïlys, Lefeber, Dirk J, Wevers, Ron A

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Response to “Leigh-like syndrome with mild mtDNA depletion due to the SUCLG1 variant c.626C>A” Dahkki Chinopoulos, Christos, Wevers, Ron A., Waterham, Hans R., Zafeiriou, Dimitrios

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Cerebrospinal Fluid Glucose and Lactate: Age-Specific Reference Values and Implications for Clinical Practice Dahkki Leen, Wilhelmina G., Willemsen, Michèl A., Wevers, Ron A., Verbeek, Marcel M.

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Metabolic cutis laxa syndromes Dahkki Mohamed, Miski, Kouwenberg, Dorus, Gardeitchik, Thatjana, Kornak, Uwe, Wevers, Ron A., Morava, Eva

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Leucine Loading Test is Only Discriminative for 3-Methylglutaconic Aciduria Due to AUH Defect Dahkki Wortmann, Saskia B., Kluijtmans, Leo A. J., Sequeira, Silvia, Wevers, Ron A., Morava, Eva

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Normal glycosylation screening does not rule out SRD5A3-CDG Dahkki Mohamed, Miski, Cantagrel, Vincent, Al-Gazali, Lihadh, Wevers, Ron A, Lefeber, Dirk J, Morava, Eva

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The 3-methylglutaconic acidurias: what’s new? Dahkki Wortmann, Saskia B., Kluijtmans, Leo A., Engelke, Udo F. H., Wevers, Ron A., Morava, Eva

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Towards the Disease Biomarker in an Individual Patient Using Statistical Health Monitoring Dahkki Engel, Jasper, Blanchet, Lionel, Engelke, Udo F. H., Wevers, Ron A., Buydens, Lutgarde M. C.

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A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic Dahkki Imbach, Timo, Burda, Patricie, Kuhnert, Peter, Wevers, Ron A., Aebi, Markus, Berger, Eric G., Hennet, Thierry

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Monitoring creatine and phosphocreatine by (13)C MR spectroscopic imaging during and after (13)C4 creatine loading: a feasibility study Dahkki Janssen, Barbara H., Lassche, Saskia, Hopman, Maria T., Wevers, Ron A., van Engelen, Baziel G. M., Heerschap, Arend

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Blood, urine and cerebrospinal fluid analysis in TH and AADC deficiency and the effect of treatment Dahkki Wassenberg, Tessa, Geurtz, Ben P.H., Monnens, Leo, Wevers, Ron A., Willemsen, Michèl A., Verbeek, Marcel M.

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Lactate infusion as therapeutical intervention: a scoping review Dahkki van Gemert, Loes A., de Galan, Bastiaan E., Wevers, Ron A., ter Heine, Rob, Willemsen, Michèl A.

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GC–MS-based urinary organic acid profiling reveals multiple dysregulated metabolic pathways following experimental acute alcohol consumption Dahkki Irwin, Cindy, Mienie, Lodewyk J., Wevers, Ron A., Mason, Shayne, Westerhuis, Johan A., van Reenen, Mari, Reinecke, Carolus J.

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The (1)H-NMR-based metabolite profile of acute alcohol consumption: A metabolomics intervention study Dahkki Irwin, Cindy, van Reenen, Mari, Mason, Shayne, Mienie, Lodewyk J., Wevers, Ron A., Westerhuis, Johan A., Reinecke, Carolus J.

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Ovarian Cyst Fluid of Serous Ovarian Tumors Contains Large Quantities of the Brain Amino Acid N-acetylaspartate Dahkki Kolwijck, Eva, Wevers, Ron A., Engelke, Udo F., Woudenberg, Jannes, Bulten, Johan, Blom, Henk J., Massuger, Leon F. A. G.

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SUCLA2 Deficiency: A Deafness-Dystonia Syndrome with Distinctive Metabolic Findings (Report of a New Patient and Review of the Literature) Dahkki Maas, Roeltje R., Marina, Adela Della, de Brouwer, Arjan P. M., Wevers, Ron A., Rodenburg, Richard J, Wortmann, Saskia B.

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A diagnostic biomarker profile for fibromyalgia syndrome based on an NMR metabolomics study of selected patients and controls Dahkki Malatji, Bontle G., Meyer, Helgard, Mason, Shayne, Engelke, Udo F.H., Wevers, Ron A., van Reenen, Mari, Reinecke, Carolus J.

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A hypothetical astrocyte–microglia lactate shuttle derived from a (1)H NMR metabolomics analysis of cerebrospinal fluid from a cohort of South African children with tuberculous men... Dahkki Mason, Shayne, van Furth, A. Marceline, Mienie, Lodewyk J., Engelke, Udo F. H., Wevers, Ron A., Solomons, Regan, Reinecke, Carolus J.

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