H. R. Scholte - Concepedia

Author

H. R. Scholte

Erasmus University Rotterdam

Also Known As

H R Scholte, H. R. SCHOLTE, H. R. Scholte, H.R. Scholte, HansR. Scholte

Publications

708

Citations

H-Index

Concepts

All Affiliations

Erasmus University Rotterdam Emma Kinderziekenhuis University of Amsterdam Amsterdam UMC Location University of Amsterdam Wilhelmina Children's Hospital

About

H. R. Scholte is an author at Erasmus University Rotterdam specializing in medicine, physiology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	343
2	Health Sciences	2	2	32
3	Clinical Nutrition	2	2	32
4	Biochemistry	1	1	17
5	Hepatology	1	1	10

H. R. Scholte

Publications

540

Citations

H-Index

Page 1

	Year	Citations
X‐linked cardioskeletal myopathy and neutropenia (Barth syndrome): Respiratory‐chain abnormalities in cultured fibroblasts P. G. Barth, Coby Van den Bogert, Pieter A. Bolhuis, Journal of Inherited Metabolic Disease	1996	99
Riboflavin-responsive complex I deficiency H. R. Scholte, H. F. M. Busch, H. D. Bakker, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease PathogenesisPathologyImmunoglobulin EMedicineInborn Error Of Immunity	1995	81
Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiency Frédéric M. Vaz, H. R. Scholte, J. Ruiter, Human Genetics GeneticsInherited Metabolic DiseaseNovel MutationsPathologySystemic Carnitine Deficiency	1999	66
Amelioration of Cardiac Function by L-Carnitine Administration in Patients on Haemodialysis Abdelmonem Esa, F. C. Henny, M. P. Kooistra, Contributions to nephrology Cardiac FunctionHemodialysisHeart FailureRenal FunctionCardiovascular Disease	2015	60
Riboflavin‐responsive lipid‐storage myopathy and glutaric aciduria type II of early adult onset Marianne de Visser, H. R. Scholte, R. B. H. Schutgens, Neurology	1986	56
Cardiomyopathy associated with carnitine loss in kidneys and small intestine Rob Rodrigues Pereira, H. R. Scholte, I. E. M. Luyt‐Houwen, European Journal of Pediatrics CardiomyopathyHeart FailureUrologyMedicinePhysiology	1988	32
Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotype H. R. Scholte, R.N.A. Van Coster, Piet C. De Jonge, Neuromuscular Disorders Cardiac MuscleCardiomyopathyHeart FailureStructural Heart DiseaseCardiovascular Disease	1999	26
L‐2‐Hydroxyglutaric aciduria and lactic acidosis P. G. Barth, Ronald J. A. Wanders, H. R. Scholte, Journal of Inherited Metabolic Disease Lactic AcidosisUrologyChemical PathologyMetabolic AcidosisClinical Chemistry	1998	24
Fatal Malonyl CoA Decarboxylase Deficiency Due to Maternal Uniparental Isodisomy of the Telomeric End of Chromosome 16 Sabrina Malvagia, Laura Papi, Amelia Morrone, Annals of Human Genetics	2007	21
Familial AMP deaminase deficiency with skeletal muscle type I atrophy and fatal cardiomyopathy H. R. Scholte, H. F. M. Busch, I. E. M. Luyt‐Houwen Journal of Inherited Metabolic Disease	1981	21

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