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Measurement of bile acid CoA esters by high-performance liquid chromatography-electrospray ionisation tandem mass spectrometry (HPLC-ESI-MS/MS).
Published in:
Journal of Mass Spectrometry, 2005, v. 40, n. 7, p. 882, doi. 10.1002/jms.864
By:
- Gan-Schreier, H.;
- Okun, J. G.;
- Kohlmueller, D.;
- Langhans, C.-D.;
- Peters, V.;
- ten Brink, H. J.;
- Verhoeven, N. M.;
- Jakobs, C.;
- Voelkl, A.;
- Hoffmann, G. F.
Publication type:
Article
Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndrome.
Published in:
Acta Anaesthesiologica Scandinavica, 2012, v. 56, n. 4, p. 520, doi. 10.1111/j.1399-6576.2011.02628.x
By:
- 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.
Publication type:
Article
In smiles we trust? Smiling in the context of antisocial and borderline personality pathology.
Published in:
PLoS ONE, 2020, v. 15, n. 6, p. 1, doi. 10.1371/journal.pone.0234574
By:
- Reed, Lawrence Ian;
- Meyer, Ashley K.;
- Okun, Sara J.;
- Best, Cheryl K.;
- Hooley, Jill M.
Publication type:
Article
Coenzyme Q<sub>10</sub>is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduria.
Published in:
Journal of Inherited Metabolic Disease, 2009, v. 32, n. 4, p. 570, doi. 10.1007/s10545-009-1150-8
By:
- Haas, D.;
- Niklowitz, P.;
- Hörster, F.;
- Baumgartner, E. R.;
- Prasad, C.;
- Rodenburg, R. J.;
- Hoffmann, G. F.;
- Menke, T.;
- Okun, J. G.
Publication type:
Article
Erratum to: Long-term exposure of human proximal tubule cells to hydroxycobalamin[c-lactam] as a possible model to study renal disease in methylmalonic acidurias.
Published in:
2010
By:
- Sauer, S.;
- Opp, S.;
- Haarmann, A.;
- Okun, J.;
- Kölker, S.;
- Morath, M.
Publication type:
Correction Notice
Long-term exposure of human proximal tubule cells to hydroxycobalamin[c-lactam] as a possible model to study renal disease in methylmalonic acidurias.
Published in:
Journal of Inherited Metabolic Disease, 2009, v. 32, n. 6, p. 720, doi. 10.1007/s10545-009-1197-6
By:
- Sauer, S.;
- Opp, S.;
- Haarmann, A.;
- Okun, J.;
- Kölker, S.;
- Morath, M.
Publication type:
Article
Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism.
Published in:
Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 194, doi. 10.1007/s10545-008-0823-z
By:
- Kölker, S.;
- Sauer, S.;
- Hoffmann, G.;
- Müller, I.;
- Morath, M.;
- Okun, J.
Publication type:
Article
Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I).
Published in:
Journal of Inherited Metabolic Disease, 2007, v. 30, n. 1, p. 5, doi. 10.1007/s10545-006-0451-4
By:
- Kölker, S.;
- Christensen, E.;
- Leonard, J.;
- Greenberg, C.;
- Burlina, A.;
- Dixon, M.;
- Duran, M.;
- Goodman, S.;
- Koeller, D.;
- Müller, E.;
- Naughten, E.;
- Neumaier-Probst, E.;
- Okun, J.;
- Kyllerman, M.;
- Surtees, R.;
- Wilcken, B.;
- Hoffmann, G.;
- Burgard, P.
Publication type:
Article
Maintenance treatment of glutaryl-CoA dehydrogenase deficiency.
Published in:
Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 885, doi. 10.1023/B:BOLI.0000045773.07785.83
By:
- Mühlhausen, C.;
- Hoffmann, G.;
- Strauss, K.;
- KÖlker, S.;
- Okun, J.;
- Greenberg, C.;
- Naughten, E.;
- Ullrich, K.
Publication type:
Article
Looking forward—An evidence-based approach to glutaryl-CoA dehydrogenase deficiency.
Published in:
Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 921, doi. 10.1023/B:BOLI.0000045778.73581.7d
By:
- KÖlker, S.;
- Burgard, P.;
- Okun, J.;
- Schulze-Bergkamen, A.;
- Assmann, B.;
- Greenberg, C.;
- Hoffmann, G.
Publication type:
Article
Animal models for glutaryl-CoA dehydrogenase deficiency.
Published in:
Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 813, doi. 10.1023/B:BOLI.0000045763.52907.5e
By:
- Koeller, D.;
- Sauer, S.;
- Wajner, M.;
- de Mello, C.;
- Goodman, S.;
- Woontner, M.;
- Mühlhausen, C.;
- Okun, J.;
- KÖlker, S.
Publication type:
Article
Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiency.
Published in:
Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 805, doi. 10.1023/B:BOLI.0000045762.37248.28
By:
- KÖlker, S.;
- Koeller, D.;
- Sauer, S.;
- HÖrster, F.;
- Schwab, M.;
- Hoffmann, G.;
- Ullrich, K.;
- Okun, J.
Publication type:
Article
Challenges for basic research in glutaryl-CoA dehydrogenase deficiency.
Published in:
Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 843, doi. 10.1023/B:BOLI.0000045768.38073.22
By:
- KÖlker, S.;
- Strauss, K.;
- Goodman, S.;
- Hoffmann, G.;
- Okun, J.;
- Koeller, D.
Publication type:
Article
S-Acetylglutathione normalizes intracellular glutathione content in cultured fibroblasts from patients with glutathione synthetase deficiency.
Published in:
Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 783, doi. 10.1023/B:BOLI.0000045838.65498.ff
By:
- Okun, J.;
- Sauer, S.;
- Bähr, S.;
- Lenhartz, H.;
- Mayatepek, E.
Publication type:
Article
Molecular and biochemical alterations in tubular epithelial cells of patients with isolated methylmalonic aciduria.
Published in:
Human Molecular Genetics, 2015, v. 24, n. 24, p. 7049, doi. 10.1093/hmg/ddv405
By:
- Ruppert, T.;
- Schumann, A.;
- Gröne, H. J.;
- Okun, J. G.;
- Kölker, S.;
- Morath, M. A.;
- Sauer, S. W.
Publication type:
Article
Trimethylamine‐N‐oxide is elevated in the acute phase after ischaemic stroke and decreases within the first days.
Published in:
European Journal of Neurology, 2020, v. 27, n. 8, p. 1596, doi. 10.1111/ene.14253
By:
- Schneider, C.;
- Okun, J. G.;
- Schwarz, K. V.;
- Hauke, J.;
- Zorn, M.;
- Nürnberg, C.;
- Ungerer, M.;
- Ringleb, P. A.;
- Mundiyanapurath, S.
Publication type:
Article
Methylmalonic acid - an endogenous toxin?
Published in:
Cellular & Molecular Life Sciences, 2005, v. 62, n. 6, p. 621, doi. 10.1007/s00018-005-4463-2
By:
- Kölker, S.;
- Okun, J. G.
Publication type:
Article

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