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Browsing by Author Bentlage, H.A.C.M.

Full Text	Issue Date	Title	Author(s)
	1997	Clinical heterogenity in respiratory chain complex III deficiency in childhood	Mourmans, J.; Wendel, U.A.H.; Bentlage, H.A.C.M.; Trijbels, J.M.F.; Smeitink, J.A.M., et al
	1997	Favourable clinical course in an infant with severe deficiency of complex III of the respiratory chain combined with less severe deficiencies of complexes I, II and IV	Rubio Gozalbo, M.E.; Ruitenbeek, W.; Bentlage, H.A.C.M.; Schägger, H.; Sengers, R.C.A., et al
	1997	New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiency	Dionisi-Vici, C.; Ruitenbeek, W.; Fariello, G.; Bentlage, H.A.C.M.; Wanders, R.J.A., et al
	1996	Electrophoretic separation of multiprotein complexes from blood platelets and cell lines: Technique for the analysis of diseases with defects in oxidative phosphorylation.	Schagger, H.; Bentlage, H.A.C.M.; Ruitenbeek, W.; Pfeiffer, K.; Rotter, S., et al
	1996	Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscle	Bentlage, H.A.C.M.; Wendel, U.; Schägger, H.; Laak, H.J. ter; Janssen, A.J.M., et al
	1995	Neonatal De Toni-Debré-Fanconi syndrome due to a defect in complex III of the respiratory chain	Wendel, U.A.H.; Ruitenbeek, W.; Bentlage, H.A.C.M.; Sengers, R.C.A.; Trijbels, J.M.F.
	1995	Human diseases with defects in oxidative phosphorylation. 1. Decreased amounts of assembled oxidative phosporylation complexes in mitochondrial encephalomyopathies	Bentlage, H.A.C.M.; Coo, I.F.M. de; Laak, H.J. ter; Sengers, R.C.A.; Trijbels, J.M.F., et al
	1995	Multiple deficiencies of mitochondrial DNA- and nuclear-encoded subunits of respiratory NADH dehydrogenase detected with peptide- and subunit-specific antibodies in mitochondrial myopathies	Bentlage, H.A.C.M.; Janssen, A.J.M.; Chomyn, A.; Attardi, G.; Walker, J.E., et al