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Issue Date	Title	Author(s)
2011	Cell biological consequences of Leigh disease.	Distelmaier, F.; Willems, P.H.; Smeitink, J.A.; Koopman, W.J.; Mayatepek, E.
2010	Blue native electrophoresis to study mitochondrial complex I in C. elegans.	Ecker, D. van den; Brand, M.A.M. van den; Bossinger, O.; Mayatepek, E.; Nijtmans, L.G.J.; Distelmaier, F.
2010	Clinical spectrum of the pseudotumor cerebri complex in children.	Tibussek, D.; Schneider, D.T.; Meulebroecke, N. van de; Turowski, B.; Messing-Juenger, M.; Willems, P.H.G.M.; Mayatepek, E.; Distelmaier, F.
2009	C. elegans ATAD-3 is essential for mitochondrial activity and development.	Hoffmann, M.; Bellance, N.; Rossignol, R.; Koopman, W.J.H.; Willems, P.H.G.M.; Mayatepek, E.; Bossinger, O.; Distelmaier, F.
2009	Human Golgi antiapoptotic protein modulates intracellular calcium fluxes.	Mattia, F.P. de; Gubser, C.; Dommelen, M.M.T. van; Visch, H.J.; Distelmaier, F.; Postigo, A.; Luyten, T.; Parys, J.B.; Smedt, H. de; Smith, G.L.; Willems, P.H.G.M.; Kuppeveld, F.J.M. van
2009	The antioxidant Trolox restores mitochondrial membrane potential and Ca2+ -stimulated ATP production in human complex I deficiency.	Distelmaier, F.; Visch, H.J.; Smeitink, J.A.M.; Mayatepek, E.; Koopman, W.J.H.; Willems, P.H.G.M.
2009	Mitochondrial complex I deficiency: from organelle dysfunction to clinical disease.	Distelmaier, F.; Koopman, W.J.H.; Heuvel, L.P.W.J. van den; Rodenburg, R.J.T.; Mayatepek, E.; Willems, P.H.G.M.; Smeitink, J.A.M.
2009	Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorder.	Janssen, R.J.R.J.; Distelmaier, F.; Smeets, R.J.P.; Wijnhoven, T.J.M.; Ostergaard, E.; Jaspers, N.G.; Raams, A.; Kemp, S.; Rodenburg, R.J.T.; Willems, P.H.G.M.; Heuvel, L.P.W.J. van den; Smeitink, J.A.M.; Nijtmans, L.G.J.
2008	Probable idiopathic intracranial hypertension in pre-pubertal children.	Distelmaier, F.; Mayatepek, E.; Tibussek, D.
2008	Mitochondrial Ca2+ homeostasis in human NADH:ubiquinone oxidoreductase deficiency.	Willems, P.H.G.M.; Valsecchi, F.; Distelmaier, F.; Verkaart, S.; Visch, H.J.; Smeitink, J.A.M.; Koopman, W.J.H.
2008	Life cell quantification of mitochondrial membrane potential at the single organelle level.	Distelmaier, F.; Koopman, W.J.; Testa, E.R.; Jong, AS de; Swarts, H.G.P.; Mayatepek, E.; Smeitink, J.A.M.; Willems, P.H.G.M.
2008	Computer-assisted live cell analysis of mitochondrial membrane potential, morphology and calcium handling.	Koopman, W.J.H.; Distelmaier, F.; Esseling, J.J.; Smeitink, J.A.M.; Willems, P.H.G.M.
2008	NDUFA2 complex I mutation leads to Leigh disease.	Hoefs, S.J.; Dieteren, C.E.; Distelmaier, F.; Janssen, R.J.; Epplen, A.; Swarts, H.G.P.; Forkink, M.; Rodenburg, R.J.; Nijtmans, L.G.J.; Willems, P.H.G.M.; Smeitink, J.A.M.; Heuvel, L.P.v.d.
2008	Inherited complex I deficiency is associated with faster protein diffusion in the matrix of moving mitochondria	Koopman, W.J.H.; Distelmaier, F.; Hink, M.A.; Verkaart, S.; Wijers, M.; Fransen, J.; Smeitink, J.A.M.; Willems, P.H.G.M.
2007	Fatal hypertensive crisis as presentation of mitochondrial complex I deficiency.	Lohmeier, K.; Distelmaier, F.; Heuvel, L.P.W.J. van den; Rodenburg, R.J.T.; Smeitink, J.A.M.; Mayatepek, E.; Hoehn, T.
2007	Cystic renal dysplasia as a leading sign of inherited metabolic disease.	Distelmaier, F.; Vogel, M.; Spiekerkotter, U.; Gempel, K.; Klee, D.; Braunstein, S.; Groneck, H.P.; Mayatepek, E.; Wendel, U.A.H.; Schwahn, B.
2007	Secondary pseudotumor cerebri in pediatric oncology and hematology: an unpredictable condition of varying etiology.	Distelmaier, F.; Gobel, U.; Meulebroecke, N. van de; Mayatepek, E.; Rosenbaum, T.; Laws, H.J.
2007	Seasonal variation and atypical presentation of idiopathic intracranial hypertension in pre-pubertal children.	Distelmaier, F.; Tibussek, D.; Schneider, D.T.; Mayatepek, E.
2007	"How much brain is really necessary?" A case of complex cerebral malformation and its clinical course.	Distelmaier, F.; Richter-Werkle, R.; Schaper, J.; Messing-Juenger, M.; Mayatepek, E.; Rosenbaum, T.
2007	Fatal glioblastoma multiforme in a patient with neurofibromatosis type I: the dilemma of systematic medical follow-up.	Distelmaier, F.; Fahsold, R.; Reifenberger, G.; Messing-Juenger, M.; Schaper, J.; Schneider, D.T.; Gobel, U.; Mayatepek, E.; Rosenbaum, T.
2007	Phytanic acid impairs mitochondrial respiration through protonophoric action.	Komen, J.C.; Distelmaier, F.; Koopman, W.J.H.; Wanders, R.J.A.; Smeitink, J.A.M.; Willems, P.H.G.M.
2006	Disseminated pilocytic astrocytoma involving brain stem and diencephalon: a history of atypical eating disorder and diagnostic delay.	Distelmaier, F.; Janssen, G.; Mayatepek, E.; Schaper, J.; Gobel, U.; Rosenbaum, T.
2006	Ovarian small cell carcinoma of the hypercalcemic type in children and adolescents: a prognostically unfavorable but curable disease.	Distelmaier, F.; Calaminus, G.; Harms, D.; Strater, R.; Kordes, U.; Fleischhack, G.; Gobel, U.; Schneider, D.
2006	Antiepileptic treatment in paediatric oncology--an interdisciplinary challenge.	Tibussek, D.; Distelmaier, F.; Schonberger, H.J.; Gobel, U.; Mayatepek, E.
2006	Pseudotumor cerebri as an important differential diagnosis of papilledema in children.	Distelmaier, F.; Sengler, U.; Messing-Juenger, M.; Assmann, B.; Mayatepek, E.; Rosenbaum, T.
2006	Status epilepticus due to attempted suicide with isoniazid.	Tibussek, D.; Mayatepek, E.; Distelmaier, F.; Rosenbaum, T.