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Goetz, M., Schröter, J., Dattner, T., Brennenstuhl, H., Lenz, D., Opladen, T., Hörster, F., Okun, J.G., Hoffmann, G.F., Kölker, S., Staufner, C.
Published in Molecular genetics and metabolism (01.09.2022)
Published in Molecular genetics and metabolism (01.09.2022)
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Molecular and biochemical alterations in tubular epithelial cells of patients with isolated methylmalonic aciduria
Ruppert, T, Schumann, A, Gröne, H J, Okun, J G, Kölker, S, Morath, M A, Sauer, S W
Published in Human molecular genetics (15.12.2015)
Published in Human molecular genetics (15.12.2015)
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Pretreatment d-2-hydroxyglutarate serum levels negatively impact on outcome in IDH1-mutated acute myeloid leukemia
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
Published in Leukemia (01.04.2016)
Published in Leukemia (01.04.2016)
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Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency ( Aldh5a1 −/− mice)
Sauer, S.W., Kölker, S., Hoffmann, G.F., ten Brink, H.J., Jakobs, C., Gibson, K.M., Okun, J.G.
Published in Neurochemistry international (01.03.2007)
Published in Neurochemistry international (01.03.2007)
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Glutarazidurie Typ I: Von der interdisziplinären Forschung zur strukturierten Patientenversorgung
Kölker, S., Sauer, S.W., Okun, J.G., Burgard, P., Hoffmann, G.F.
Published in Monatsschrift Kinderheilkunde (01.09.2011)
Published in Monatsschrift Kinderheilkunde (01.09.2011)
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