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Citation: Lem. Niers et al., Prenatal diagnosis of NADH : ubiquinone oxidoreductase deficiency, PRENAT DIAG, 21(10), 2001, pp. 871-880

Authors: Loeffen, JLCM Smeitink, JAM Trijbels, JMF Janssen, AJM Triepels, RH Sengers, RCA van den Heuvel, LP

Citation: Jlcm. Loeffen et al., Isolated complex I deficiency in children: Clinical, biochemical and genetic aspects, HUM MUTAT, 15(2), 2000, pp. 123-134

Authors: Soetekouw, PMMB Wevers, RA Vreken, P Elving, LD Janssen, AJM van der Veen, Y Bleijenberg, G van der Meer, JWM

Citation: Pmmb. Soetekouw et al., Normal carnitine levels in patients with chronic fatigue syndrome, NETH J MED, 57(1), 2000, pp. 20-24

Authors: Rubio-Gozalbo, ME Sengers, RCA Trijbels, JMF Doesburg, WH Janssen, AJM Verbeek, ALM Smeitink, JAM

Citation: Me. Rubio-gozalbo et al., A prognostic index as diagnostic strategy in children suspected of mitochondriocytopathy, NEUROPEDIAT, 31(3), 2000, pp. 114-121

Authors: Scharfe, C Hauschild, M Klopstock, T Janssen, AJM Heidemann, PH Meitinger, T Jaksch, M

Citation: C. Scharfe et al., A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex I, J MED GENET, 37(9), 2000, pp. 669-673