H.R. Scholte - Concepedia

Author

H.R. Scholte

Also Known As

H R Scholte, H SCHOLTE, H. R. SCHOLTE, H. R. Scholte, H. Scholte, H.R. SCHOLTE, H.R. Scholte, HANS R. SCHOLTE, Hans R Scholte, Hans R. Scholte

124

Publications

5.1K

Citations

H-Index

109

Concepts

All Affiliations

Erasmus University Rotterdam University of Amsterdam Erasmus MC Maastricht University Radboud University Nijmegen

About

H.R. Scholte is an author at Erasmus University Rotterdam specializing in medicine, mitochondrial function, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	27	46	3.1K
2	Health Sciences	11	12	305
3	Natural Sciences	7	7	407
4	Engineering	1	1	40
5	Public Health	1	1	16

H.R. Scholte

Publications

4.4K

Citations

H-Index

Page 1

	Year	Citations
An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes P. G. Barth, H.R. Scholte, J.A. Berden, Journal of the Neurological Sciences Mitochondrial MyopathyCardiac MuscleCardiomyopathyHeart FailureX-linked Mitochondrial Disease	1983	695
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, The American Journal of Human Genetics Genetic DiseasesDisease PhenotypeGenetic DeterminantGenetic DisorderGenetics	1999	300
Fatty Acid Activation: Specificity, Localization, and Function Pieter H.E. Groot, H.R. Scholte, W.C. Hülsmann Advances in lipid research BiochemistryLipid MetabolismOmega-3 Fatty AcidPhysiologyLipids	1976	212
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, PubMed	1996	192
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, Journal of Translational Medicine	2010	146
A rapid and simple procedure to deplete rat-liver mitochondria of lysosomal activity Joseph E. Loewenstein, H.R. Scholte, E.M. Wit-Peeters Biochimica et Biophysica Acta (BBA) - Bioenergetics MitophagyBiochemistryMitochondrial FunctionMedicineLiver Physiology	1970	129
Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene Mike Gerards, B.J.C. van den Bosch, Katharina Danhauser, Brain Old GeneGeneticsMolecular BiologyMolecular GeneticsMitochondrial Biology	2010	126
The localization of mitochondrial creatine kinase, and its use for the determination of the sidedness of submitochondrial particles H.R. Scholte, P.J. Weijers, E.M. Wit-Peeters Biochimica et Biophysica Acta (BBA) - Biomembranes MitophagyBiochemistryMitochondrial FunctionSubmitochondrial ParticlesNatural Sciences	1973	118
On the triple localization of creatine kinase in heart and skeletal muscle cells of the rat: Evidence for the existence of myofibrillar and mitochondrial isoenzymes H.R. Scholte Biochimica et Biophysica Acta (BBA) - Bioenergetics MechanobiologySkeletal Muscle CellsCardiac MuscleMuscle FunctionMitochondrial Function	1973	105
Exome sequencing reveals a novel Moroccan founder mutation in<i>SLC19A3</i>as a new cause of early-childhood fatal Leigh syndrome Mike Gerards, Rick Kamps, Jo van Oevelen, Brain	2013	93

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