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Results: 5

Authors: Triepels, RH Van den Heuvel, LP Trijbels, JM Smeitink, JA
Citation: Rh. Triepels et al., Respiratory chain complex I deficiency, AM J MED G, 106(1), 2001, pp. 37-45

Authors: Triepels, RH Hanson, BJ van den Heuvel, LP Sundell, L Marusich, MF Smeitink, JA Capaldi, RA
Citation: Rh. Triepels et al., Human complex I defects can be resolved by monoclonal antibody analysis into distinct subunit assembly patterns, J BIOL CHEM, 276(12), 2001, pp. 8892-8897

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: Triepels, RH van den Heuvel, LP Loeffen, JLCM Buskens, CAF Smeets, RJP Gozalbo, MER Budde, SMS Mariman, EC Wijburg, FA Barth, PG Trijbels, JMF Smeitink, JAM
Citation: Rh. Triepels et al., Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I, ANN NEUROL, 45(6), 1999, pp. 787-790

Authors: Loeffen, JLCM Triepels, RH van den Heuvel, LP Schuelke, M Buskens, CAF Smeets, RJP Trijbels, JMF Smeitink, JAM
Citation: Jlcm. Loeffen et al., cDNA of eight nuclear encoded subunits of NADH : ubiquinone oxidoreductase: Human complex I cDNA characterization completed, BIOC BIOP R, 253(2), 1998, pp. 415-422
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