H. R. Scholte

X‐linked cardioskeletal myopathy and neutropenia (Barth syndrome): Respiratory‐chain abnormalities in cultured fibroblasts

P. G. Barth, Coby Van den Bogert, Pieter A. Bolhuis et al. · Journal of Inherited Metabolic Disease · 1996 · 99 citations · Full text

Riboflavin-responsive complex I deficiency

H. R. Scholte, H. F. M. Busch, H. D. Bakker et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 1995 · 81 citations · Full text

Pathogenesis, Pathology, Immunoglobulin E +3

Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiency

Frédéric M. Vaz, H. R. Scholte, J. Ruiter et al. · Human Genetics · 1999 · 66 citations

Genetics, Inherited Metabolic Disease, Novel Mutations +4

Amelioration of Cardiac Function by L-Carnitine Administration in Patients on Haemodialysis

Abdelmonem Esa, F. C. Henny, M. P. Kooistra et al. · Contributions to nephrology · 2015 · 60 citations

Cardiac Function, Hemodialysis, Heart Failure +11

Riboflavin‐responsive lipid‐storage myopathy and glutaric aciduria type II of early adult onset

Marianne de Visser, H. R. Scholte, R. B. H. Schutgens et al. · Neurology · 1986 · 56 citations