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Browsing by Author Seneca, S.

Full Text	Issue Date	Title	Author(s)
	2012	Fluorescence imaging of mitochondria in cultured skin fibroblasts: a useful method for the detection of oxidative phosphorylation defects.	Paepe, B. De; Smet, J.; Vanlander, A.; Seneca, S.; Lissens, W., et al
	2009	Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects.	Paepe, B. De; Smet, J.; Lammens, M.M.Y.; Seneca, S.; Martin, J.J., et al
	2006	Mitochondrial dysfunction in Brooks-Wisniewski-Brown syndrome.	Morava, E.; Rodenburg, R.J.T.; Hol, F.A.; Meirleir, L. de; Seneca, S., et al
	2005	Aminoacylase I deficiency: a novel inborn error of metabolism.	Coster, R. van; Gerlo, E.A.; Giardina, T.G.; Engelke, U.F.H.; Smet, J.E., et al
	1996	Mutation analysis of the pyruvate dehydrogenase E1-alpha gene in eight patients with a pyruvate dehydrogenase complex deficiency	Lissens, W.; Meirleir, L. de; Seneca, S.; Benelli, C.; Marsac, C., et al