Monogenic Mitochondrial DisordersKOOPMAN, Werner J. H; WILLEMS, Peter H. G. M; SMEITINK, Jan A. M et al.The New England journal of medicine. 2012, Vol 366, Num 12, pp 1132-1141, issn 0028-4793, 10 p.Article

Parenteral medium-chain triglyceride-induced neutrophil activation is not mediated by a Pertussis Toxin sensitive receptorVERSLEIJEN, Michelle W. J; VAN ESTERIK, Joantine C. J; ROELOFS, Hennie M. J et al.Clinical nutrition (Edinburgh). 2009, Vol 28, Num 1, pp 59-64, issn 0261-5614, 6 p.Article

Human NADH:ubiquinone oxidoreductase deficiency : radical changes in mitochondrial morphology?KOOPMAN, Werner J. H; VERKAART, Sjoerd; VISCH, Henk Jan et al.American journal of physiology. Cell physiology. 2007, Vol 62, Num 1, issn 0363-6143, C22-C29Article

Reduction of phospholipase D activity during coxsackievirus infectionDUIJSINGS, Daniël; WESSELS, Els; VAN EMST-DE VRIES, Sjenet E et al.Journal of general virology. 2007, Vol 88, pp 3027-3030, issn 0022-1317, 4 p., 11Article

Isolated Mitochondrial Complex I Deficiency: Explorative Data Analysis of Patient Cell ParametersBLANCHET, Lionel; BUYDENS, Lutgarde M. C; SMEITINK, Jan A. M et al.Current pharmaceutical design (Print). 2011, Vol 17, Num 36, pp 4023-4033, issn 1381-6128, 11 p.Article

Inherited complex I deficiency is associated with faster protein diffusion in the matrix of moving mitochondriaKOOPMAN, Werner J. H; DISTELMAIER, Felix; HINK, Mark A et al.American journal of physiology. Cell physiology. 2008, Vol 63, Num 5, issn 0363-6143, C1124-C1132Article

Inhibition of complex I of the electron transport chain causes O^-2-mediated mitochondrial outgrowthKOOPMAN, Werner J. H; VERKAART, Sjoerd; VISCH, Henk-Jan et al.American journal of physiology. Cell physiology. 2005, Vol 57, Num 6, pp C1440-C1450, issn 0363-6143Article

Upregulation of Ca²⁺ removal in human skeletal muscle: a possible role for Ca²⁺-dependent priming of mitochondrial ATP synthesisKOOPMAN, Werner J. H; RENDERS, Michel; OOSTERHOF, Arie et al.American journal of physiology. Cell physiology. 2003, Vol 54, Num 5, pp C1263-C1269, issn 0363-6143Article

Mitochondrial processes are impaired in hereditary inclusion body myopathyEISENBERG, Iris; NOVERSHTERN, Noa; ITZHAKI, Zohar et al.Human molecular genetics (Print). 2008, Vol 17, Num 23, pp 3663-3674, issn 0964-6906, 12 p.Article

Mitochondrial network complexity and pathological decrease in complex I activity are tightly correlated in isolated human complex I deficiencyKOOPMAN, Werner J. H; VISCH, Henk-Jan; VERKAART, Sjoerd et al.American journal of physiology. Cell physiology. 2005, Vol 58, Num 4, pp C881-C890, issn 0363-6143Article

Effects of chemical chaperones on partially retarded NaCl cotransporter mutants associated with Gitelman's syndrome in a mouse cortical collecting duct cell lineDE JONG, Joke C; WILLEMS, Peter H. G. M; GOOSSENS, Monique et al.Nephrology, dialysis, transplantation (Print). 2004, Vol 19, Num 5, pp 1069-1076, issn 0931-0509, 8 p.Article

Calcitriol controls the epithelial calcium channel in kidneyHOENDEROP, Joost G. J; MÜLLER, Dominik; BINDELS, René J. M et al.Journal of the American Society of Nephrology. 2001, Vol 12, Num 7, pp 1342-1349, issn 1046-6673Article

Modeling mitochondrial dysfunctions in the brain: from mice to menBREUER, Megan E; WILLEMS, Peter H. G. M; RUSSEL, Frans G. M et al.Journal of inherited metabolic disease. 2012, Vol 35, Num 2, pp 193-210, issn 0141-8955, 18 p.Article

COMPLEX I DISORDERS: CAUSES, MECHANISMS, AND DEVELOPMENT OF TREATMENT STRATEGIES AT THE CELLULAR LEVELVALSECCHI, Federica; KOOPMAN, Werner J. H; MANJERI, Ganesh R et al.Developmental disabilities research reviews. 2010, Vol 16, Num 2, pp 175-182, issn 1940-5510, 8 p.Article

The antioxidant Trolox restores mitochondrial membrane potential and Ca²⁺-stimulated ATP production in human complex I deficiencyDISTELMAIER, Felix; VISCH, Henk-Jan; SMEITINK, Jan A. M et al.Journal of molecular medicine (Berlin. Print). 2009, Vol 87, Num 5, pp 515-522, issn 0946-2716, 8 p.Article

Functional expression of mutations in the human NaCl cotransporter: Evidence for impaired routing mechanisms in gitelman's syndromeDE JONG, Joke C; VAN DER VLIET, Walter A; VAN DEN HEUVEL, Lambertus P. W. J et al.Journal of the American Society of Nephrology. 2002, Vol 13, Num 6, pp 1442-1448, issn 1046-6673Article