ereprof. dr. Rudy Van Coster
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Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12
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Analysis of the mitochondrial encoded subunits of complex 1 in 20 patients with a complex 1 deficiency
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Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L gene
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Homozygous Gly555Glu mutation in the nuclear-encoded 70 kDa flavoprotein gene causes instability of the respiratory chain complex II
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Automated nanoflow Liquid chromatography/tandem mass spectrometric identification of liver mitochondrial proteins
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Timing a catch in children with and without DCD
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Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease
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Combination of proteomic techniques as powerful tool in the search for the underlying defect in OXPROS complex deficiencies
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eIF2B-related disorders: Antenatal onset and involvement of multiple organs
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A new leukodystrophy with brainstem and spinal cord involvement and high lactate