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Journal of Inherited Metabolic Disease|January 1, 1987
Normal dolichol concentration in urine sediments from four patients with neuronal ceroid lipofuscinosis (Batten's disease)B C Paton, A PoulosClinica Chimica Acta; International Journal of Clinical Chemistry|December 31, 1993
Excretion of 3,6-epoxydicarboxylic acids in peroxisomal disordersJ J Pitt, A PoulosJournal of Inherited Metabolic Disease|January 1, 1984
Dolichol metabolism in cultured skin fibroblasts from patients with "neuronal" ceroid lipofuscinosis (Batten's disease)B C Paton, A PoulosLipids|August 14, 2016
Ether-containing lipids of the slime mold,Physarum polycephalum: II. Rates of biosynthesisA Poulos, G A ThompsonJournal of Inherited Metabolic Disease|January 1, 1985
Identification of 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestan-26-oic acid, an intermediate in cholic acid synthesis, in the plasma of patients with infantile Refsum's diseaseA Poulos, M J WhitingLaboratory Medicine|May 9, 2019
Prospective Investigation of an Automated PCR/Nucleic Acid Microarray-Based Platform for Enteric Pathogen TestingAmy K Beckman, Patricia FerrieriThe Biochemical Journal|February 1, 1986
Preliminary evidence for a processing error in the biosynthesis of Gaucher activator in mucolipidosis disease types II and IIIE Ranieri, B Paton, A PoulosClinical Genetics|October 1, 1983
Sphingomyelinase in cultured skin fibroblasts from normal and Niemann-Pick type C patientsA Poulos, N Hudson, E RanieriArchives of Biochemistry and Biophysics|February 1, 1989
Dihydroxyacetone phosphate acyltransferase and alkyldihydroxyacetone phosphate synthase activities in rat liver subcellular fractions and human skin fibroblastsH Singh, S Usher, A PoulosJournal of Neurochemistry|January 1, 1991
Molecular species of phosphatidylcholine containing very long chain fatty acids in human brain: enrichment in X-linked adrenoleukodystrophy brain and diseases of peroxisome biogenesis brainP Sharp, D Johnson, A PoulosPageof 22