Trimethylamine‐N‐oxide is elevated in the acute phase after ischaemic stroke and decreases within the first days von Schneider, C., Okun, J. G., Schwarz, K. V., Hauke, J., Zorn, M., Nürnberg, C., Ungerer, M., Ringleb, P. A., Mundiyanapurath, S.

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In smiles we trust? Smiling in the context of antisocial and borderline personality pathology von Reed, Lawrence Ian, Meyer, Ashley K, Okun, Sara J, Best, Cheryl K, Hooley, Jill M, Didden, Robert

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Genotypic and phenotypic spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency von Goetz, M., Schröter, J., Dattner, T., Brennenstuhl, H., Lenz, D., Opladen, T., Hörster, F., Okun, J.G., Hoffmann, G.F., Kölker, S., Staufner, C.

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The branched-chain amino acid transaminase 1 sustains growth of antiestrogen-resistant and ERα-negative breast cancer von Thewes, V, Simon, R, Hlevnjak, M, Schlotter, M, Schroeter, P, Schmidt, K, Wu, Y, Anzeneder, T, Wang, W, Windisch, P, Kirchgäßner, M, Melling, N, Kneisel, N, Büttner, R, Deuschle, U, Sinn, H P, Schneeweiss, A, Heck, S, Kaulfuss, S, Hess-Stumpp, H, Okun, J G, Sauter, G, Lykkesfeldt, A E, Zapatka, M, Radlwimmer, B, Lichter, P, Tönjes, M

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Molecular and biochemical alterations in tubular epithelial cells of patients with isolated methylmalonic aciduria von Ruppert, T, Schumann, A, Gröne, H J, Okun, J G, Kölker, S, Morath, M A, Sauer, S W

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Pretreatment d-2-hydroxyglutarate serum levels negatively impact on outcome in IDH1-mutated acute myeloid leukemia von Balss, J, Thiede, C, Bochtler, T, Okun, J G, Saadati, M, Benner, A, Pusch, S, Ehninger, G, Schaich, M, Ho, A D, von Deimling, A, Krämer, A, Heilig, C E

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Guideline for the diagnosis and management of glutaryl‐CoA dehydrogenase deficiency (glutaric aciduria type I) von Kölker, S., Christensen, E., Leonard, J. V., Greenberg, C. R., Burlina, A. B., Burlina, A. P., Dixon, M., Duran, M., Goodman, S. I., Koeller, D. M., Müller, E., Naughten, E. R., Neumaier‐Probst, E., Okun, J. G., Kyllerman, M., Surtees, R. A., Wilcken, B., Hoffmann, G. F., Burgard, P.

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Three classes of inhibitors share a common binding domain in mitochondrial complex I (NADH:ubiquinone oxidoreductase) von Okun, J.G. (Universitatsklinikum Frankfurt, Germany.), Lummen, P, Brandt, U

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Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndrome von VANLANDER, A. V., JORENS, P. G., SMET, J., DE PAEPE, B., VERBRUGGHE, W., VAN DEN EYNDEN, G. G., MEIRE, F., PAUWELS, P., VAN DER AA, N., SENECA, S., LISSENS, W., OKUN, J. G., VAN COSTER, R.

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Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency ( Aldh5a1 −/− mice) von Sauer, S.W., Kölker, S., Hoffmann, G.F., ten Brink, H.J., Jakobs, C., Gibson, K.M., Okun, J.G.

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Neurodegeneration and chronic renal failure in methylmalonic aciduria—A pathophysiological approach von Morath, M. A., Okun, J. G., Müller, I. B., Sauer, S. W., Hörster, F., Hoffmann, G. F., Kölker, S.

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Methylmalonic acid--an endogenous toxin? von Kölker, S, Okun, J G

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Neurodegeneration in Methylmalonic Aciduria Involves Inhibition of Complex II and the Tricarboxylic Acid Cycle, and Synergistically Acting Excitotoxicity von Okun, Jürgen G., Hörster, Friederike, Farkas, Lilla M., Feyh, Patrik, Hinz, Angela, Sauer, Sven, Hoffmann, Georg F., Unsicker, Klaus, Mayatepek, Ertan, Kölker, Stefan

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High pre-transplant serum nitrate levels predict risk of acute steroid-refractory graft-versus-host disease in the absence of statin therapy von Dietrich, Sascha, Okun, Jürgen G, Schmidt, Kathrin, Falk, Christine S, Wagner, Andreas H, Karamustafa, Suzan, Radujkovic, Aleksandar, Hegenbart, Ute, Ho, Anthony D, Dreger, Peter, Luft, Thomas

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Newborn screening for homocystinurias: recent recommendations versus current practice von Keller, R, Chrastina, P, Pavlíková, M, Gouveia, S, Ribes, A, Kölker, S, Blom, H J, Baumgartner, M R, Bártl, J, Dionisi Vici, C, Gleich, F, Morris, A A, Kožich, V, Huemer, M, Barić, I, Ben-Omran, T, Blasco-Alonso, J, Bueno Delgado, M A, Carducci, C, Cassanello, M, Cerone, R, Couce, M L, Crushell, E, Delgado Pecellin, C, Dulin, E, Espada, M, Ferino, G, Fingerhut, R, Garcia Jimenez, I, Gonzalez Gallego, I, González-Irazabal, Y, Gramer, G, Juan Fita, M J, Karg, E, Klein, J, Konstantopoulou, V, la Marca, G, Leão Teles, E, Leuzzi, V, Lilliu, F, Lopez, R M, Lund, A M, Mayne, P, Meavilla, S, Moat, S J, Okun, J G, Pasquini, E, Pedron-Giner, C, Racz, G Z, Ruiz Gomez, M A, Vilarinho, L, Yahyaoui, R, Zerjav Tansek, M, Zetterström, R H, Zeyda, M

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Long-term exposure of human proximal tubule cells to hydroxycobalamin[c-lactam] as a possible model to study renal disease in methylmalonic acidurias von Sauer, S. W, Opp, S, Haarmann, A, Okun, J. G, Kölker, S, Morath, M. A

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Abnormal sterol metabolism in holoprosencephaly: studies in cultured lymphoblasts von Haas, D, Morgenthaler, J, Lacbawan, F, Long, B, Runz, H, Garbade, S F, Zschocke, J, Kelley, R I, Okun, J G, Hoffmann, G F, Muenke, M

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Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism von Kölker, S., Sauer, S. W., Hoffmann, G. F., Müller, I., Morath, M. A., Okun, J. G.

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Coenzyme Q₁₀ is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduria von Haas, D, Niklowitz, P, Hörster, F, Baumgartner, E. R, Prasad, C, Rodenburg, R. J, Hoffmann, G. F, Menke, T, Okun, J. G

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Recommendations for diagnosing and managing individuals with glutaric aciduria type 1: Third revision von Boy, Nikolas, Mühlhausen, Chris, Maier, Esther M., Ballhausen, Diana, Baumgartner, Matthias R., Beblo, Skadi, Burgard, Peter, Chapman, Kimberly A., Dobbelaere, Dries, Heringer‐Seifert, Jana, Fleissner, Sandra, Grohmann‐Held, Karina, Hahn, Gabriele, Harting, Inga, Hoffmann, Georg F., Jochum, Frank, Karall, Daniela, Konstantopoulous, Vassiliki, Krawinkel, Michael B., Lindner, Martin, Märtner, E. M. Charlotte, Nuoffer, Jean‐Marc, Okun, Jürgen G., Plecko, Barbara, Posset, Roland, Sahm, Katja, Scholl‐Bürgi, Sabine, Thimm, Eva, Walter, Magdalena, Williams, Monique, vom Dahl, Stephan, Ziagaki, Athanasia, Zschocke, Johannes, Kölker, Stefan

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