H.R. Scholte

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

P. G. Barth, H.R. Scholte, J.A. Berden et al. · Journal of the Neurological Sciences · 1983 · 701 citations

Medicine, Cardiology, Molecular Genetics +17

Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency

Brage Storstein Andresen, S. E. Olpin, Ben J. H. M. Poorthuis et al. · The American Journal of Human Genetics · 1999 · 302 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Fatty Acid Activation: Specificity, Localization, and Function

Pieter H.E. Groot, H.R. Scholte, W.C. Hülsmann · Advances in lipid research · 1976 · 213 citations

Life Sciences, Biochemistry, Physiology +12

Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.

Daniëlle de Vries, L.N. Went, G.W. Bruyn et al. · PubMed · 1996 · 192 citations

Life Sciences, Genetics, Molecular Genetics +16

Patients with chronic fatigue syndrome performed worse than controls in a controlled repeated exercise study despite a normal oxidative phosphorylation capacity

Ruud CW Vermeulen, Ruud M Kurk, Frans C. Visser et al. · Journal of Translational Medicine · 2010 · 148 citations · Full text

Life Sciences, Biochemistry, Physiology +17