R. A. Chalmers

Natural History, Outcome, and Treatment Efficacy in Children and Adults with Glutaryl-CoA Dehydrogenase Deficiency

Stefan Kölker, Sven F. Garbade, Cheryl R. Greenberg et al. · Pediatric Research · 2006 · 266 citations · Full text

Nutrition, Metabolic Disorder, Pediatric Hematology +8

Urinary Excretion of l-Carnitine and Acylcarnitines by Patients with Disorders of Organic Acid Metabolism: Evidence for Secondary Insufficiency of l-Carnitine

R. A. Chalmers, Charles R. Roe, T. E. Stacey et al. · Pediatric Research · 1984 · 248 citations · Full text

Secondary Insufficiency, Urology, Urinary Excretion +4

Deconvolution gas chromatography/mass spectrometry of urinary organic acids - potential for pattern recognition and automated identification of metabolic disorders

John M. Halket, A. Przyborowska, Stephen E. Stein et al. · Rapid Communications in Mass Spectrometry · 1999 · 241 citations

Engineering, Urinary Organic Acids, Metabolomic Profiling +19

D‐2‐hydroxyglutaric aciduria: Case report and biochemical studies

R. A. Chalmers, A. M. Lawson, R. W. E. Watts et al. · Journal of Inherited Metabolic Disease · 1980 · 132 citations

Diagnostic and Therapeutic Implications of Medium-Chain Acylcarnitines in the Medium-Chain Acyl-CoA Dehydrogenase Deficiency

Charles R. Roe, David S. Millington, David Maltby et al. · Pediatric Research · 1985 · 128 citations · Full text

Biosynthesis, Aldo-keto Reductase, Aldehyde Dehydrogenase +9