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One or more keywords matched the following items that are connected to Bennett, Michael
Item TypeName
Academic Article Improved stable isotope dilution-gas chromatography-mass spectrometry method for serum or plasma free 3-hydroxy-fatty acids and its utility for the study of disorders of mitochondrial fatty acid beta-oxidation.
Academic Article 3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their children.
Academic Article Glutaric aciduria type I: a common cause of episodic encephalopathy and spastic paralysis in the Amish of Lancaster County, Pennsylvania.
Academic Article CLN3P, the Batten's disease protein, is a novel palmitoyl-protein Delta-9 desaturase.
Academic Article Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease.
Academic Article CLN3P, the Batten disease protein, localizes to membrane lipid rafts (detergent-resistant membranes).
Academic Article Measurement of (C13)arginine incorporation into apolipoprotein B-100 in very low density lipoproteins and low density lipoproteins in normal subjects using (13C)sodium bicarbonate infusion and isotope ratio mass spectrometry.
Academic Article Untargeted metabolomic analysis hits the target.
Academic Article National academy of clinical biochemistry laboratory medicine practice guidelines: follow-up testing for metabolic disease identified by expanded newborn screening using tandem mass spectrometry; executive summary.
Academic Article 3-Hydroxy-fatty acid analysis by gas chromatography-mass spectrometry.
Academic Article Quantitation of methylmalonic acid in serum or plasma using isotope dilution-selected ion gas chromatography-mass spectrometry.
Academic Article Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency.
Academic Article Quantitation of orotic acid in urine using isotope dilution-selected ion gas chromatography-mass spectrometry.
Academic Article Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorder.
Academic Article A rapid ultra performance liquid chromatography tandem mass spectrometric method for measuring amino acids associated with maple syrup urine disease, tyrosinaemia and phenylketonuria.
Academic Article Population screening for medium-chain acyl-CoA dehydrogenase deficiency: analysis of medium-chain fatty acids and acylglycines in blood spots.
Academic Article Identification of urinary metabolites of (+/-)-2-(p-isobutylphenyl)propionic acid (Ibuprofen) by routine organic acid screening.
Academic Article Addition of quantitative 3-hydroxy-octadecanoic acid to the stable isotope gas chromatography-mass spectrometry method for measuring 3-hydroxy fatty acids.
Academic Article Comparison of post-mortem urinary and vitreous humour organic acids.
Academic Article Very long-chain acyl-CoA dehydrogenase deficiency in a patient with normal newborn screening by tandem mass spectrometry.
Academic Article The changing face of newborn screening: diagnosis of inborn errors of metabolism by tandem mass spectrometry.
Academic Article Hydrolethalus syndrome, in contrast to Smith-Lemli-Opitz syndrome, is not due to a defect in post-squalene cholesterol biosynthesis: a case report.
Academic Article 3-Hydroxydicarboxylic and 3-ketodicarboxylic aciduria in three patients: evidence for a new defect in fatty acid oxidation at the level of 3-ketoacyl-CoA thiolase.
Academic Article Inborn errors of metabolism diagnosed in sudden death cases by acylcarnitine analysis of postmortem bile.
Academic Article Simpler liquid-chromatographic screening for organic acid disorders.
Academic Article Urine organic acid analysis for inherited metabolic disease using gas chromatography-mass spectrometry.
Academic Article Tiglylglycine excreted in urine in disorders of isoleucine metabolism and the respiratory chain measured by stable isotope dilution GC-MS.
Academic Article Accumulation of free 3-hydroxy fatty acids in the culture media of fibroblasts from patients deficient in long-chain l-3-hydroxyacyl-CoA dehydrogenase: a useful diagnostic aid.
Concept Spectrometry, Mass, Electrospray Ionization
Concept Gas Chromatography-Mass Spectrometry
Concept Tandem Mass Spectrometry
Concept Mass Spectrometry
Concept Spectrometry, Mass, Fast Atom Bombardment
Academic Article Generalised dicarboxylic aciduria: a common finding in neonates.
Academic Article Clinical applications of 3-hydroxy fatty acid analysis by gas chromatography-mass spectrometry.
Academic Article Flow injection tandem mass spectrometric measurement of ceramides of multiple chain lengths in biological samples.
Academic Article 6-Methyluracil excretion in 2-methylacetoacetyl-CoA thiolase deficiency and in two children with an unexplained recurrent ketoacidaemia.
Academic Article Future directions in metabolic disease testing.
Academic Article Measurement of tissue acyl-CoAs using flow-injection tandem mass spectrometry: acyl-CoA profiles in short-chain fatty acid oxidation defects.
Academic Article Sphingolipid-based drugs selectively kill cancer cells by down-regulating nutrient transporter proteins.
Academic Article In vivo metabolic flux profiling with stable isotopes discriminates sites and quantifies effects of mitochondrial dysfunction in C. elegans.
Academic Article An interference-free two-step enzyme assay with UPLC-tandem mass spectrometric product measurement for the clinical diagnosis of uridine diphosphate galactose-4-epimerase deficiency.
Academic Article Novel biomarkers for diagnosing and understanding pathophysiology of metabolic diseases.
Search Criteria
  • Mass Spectrometry
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.