F. J. van Sprang

Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acid<i>β</i>‐oxidation

R. J. A. Wanders, Lodewijk IJlst, A. H. van Gennip et al. · Journal of Inherited Metabolic Disease · 1990 · 121 citations

Metabolic Syndrome, Aldehyde Dehydrogenase, Metabolic Disorder +10

3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment

M. Durán, Ronald J. A. Wanders, J. P. de Jager et al. · European Journal of Pediatrics · 1991 · 77 citations

Metabolic Syndrome, Metabolic Disorder, Diabetes +11

<i>β</i>‐Mannosidosis in two brothers with hearing loss

L. Dorland, M. Durán, F. E. T. Hoefnagels et al. · Journal of Inherited Metabolic Disease · 1988 · 58 citations

Pediatric Otolaryngology, Audiology, Otorhinolaryngology +5

β-Mannosidosis in Two Brothers with Hearing Loss

L. Dorland, M. Durán, F. E. T. Hoefnagels et al. · 1988 · 55 citations

Auditory Processing, Pediatric Otolaryngology, Pediatric Audiology +7

Abnormal tyrosine and phenylalanine metabolism in patients with tyrosyluria and phenylketonuria; gas-liquid chromatographic analysis of urinary metabolites

S.K. Wadman, Colin van der Heiden, D. Ketting et al. · Clinica Chimica Acta · 1971 · 50 citations

Gas-liquid Chromatographic Analysis, Abnormal Tyrosine, Urology +8