A new simple screening method for the diagnosis of medium chain acyl-CoA dehydrogenase deficiency

Propionylcarnitine physiological variations in vivo

Thomas Bøhmer, Jon Bremer · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · 1968 · 154 citations

Medicine, Pharmacology, Physiology +2

Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups.

Charles R. Roe, Charles L. Hoppel, T. E. Stacey et al. · Archives of Disease in Childhood · 1983 · 122 citations · Full text

Life Sciences, Biochemistry, Pharmacology +12

General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases

N. Gregersen, S. Kelvraa, K. Rasmussen et al. · Clinica Chimica Acta · 1983 · 94 citations

Life Sciences, Biochemistry, Excretion +13

Sex hormone-binding globulin—still many questions

Göran Lindstedt, Per‐Arne Lundberg, Geoffrey L. Hammond et al. · Scandinavian Journal of Clinical and Laboratory Investigation · 1985 · 44 citations

Life Sciences, Biochemistry, Endocrinology +16

The differential diagnosis of dicarboxylic aciduria

M. Durán, J. B. C. de Klerk, S.K. Wadman et al. · Journal of Inherited Metabolic Disease · 1984 · 38 citations

Medicine, Pathology, Renal Pathology +8