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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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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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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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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Glutarazidurie Typ I: Von der interdisziplinären Forschung zur strukturierten Patientenversorgung von Kölker, S., Sauer, S.W., Okun, J.G., Burgard, P., Hoffmann, G.F.

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Mobility, mood and site of care impact health related quality of life in Parkinson's disease von Nutt, J.G, Siderowf, A.D, Guttman, M, Schmidt, P.N, Zamudio, J.I, Wu, S.S, Okun, M.S, Simuni, T, Parashos, S.A, Dahodwala, N.A, Davis, T.L, Giladi, N, Gurevich, T, Hauser, R.A, Jankovic, J, Lyons, K.E, Marsh, L, Miyasaki, J.M, Morgan, J.C, Santiago, A.J, Tarsy, D, Mari, Z, Malaty, I.A, Nelson, E.C

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