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Liquid chromatography/mass spectrometry analysis of mixtures of rhamnolipids produced by Pseudomonas aeruginosa strain 57RP grown on mannitol or naphthalene

Biochimica et biophysica acta, 1999-09, Vol.1440 (2), p.244-252

1999

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Trimethylaminuria Is Caused by Mutations of the FMO3 Gene in a North American Cohort

Molecular genetics and metabolism, 1999-09, Vol.68 (1), p.24-31

1999

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Stable isotope dilution techniques

Journal of chromatography. B, Biomedical applications, 1996-06, Vol.682 (1), p.182-183

Mamer, O.A.

1996

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On the mechanisms of the formation of L-alloisoleucine and the 2-hydroxy-3-methylvaleric acid stereoisomers from L-isoleucine in maple syrup urine disease patients and in normal humans

The Journal of biological chemistry, 1992-11, Vol.267 (31), p.22141-22147

1992

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Kinetics and mechanisms of hepatic acute phase response to subtotal partial hepatectomy and cultural impact on environmental hepatic end-stage liver injury in the homeless

Medical hypotheses, 2001-06, Vol.56 (6), p.709-723

2001

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Artefactual pyruvate and 2‐oxobutyrate produced by trimethylsilylation of methylmalonic and ethylmalonic acids in the presence of oxygen

Journal of inherited metabolic disease, 1999-10, Vol.22 (7), p.821-826

1999

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Effects of leucine on whole body leucine, valine, and threonine metabolism in humans

American journal of physiology: endocrinology and metabolism, 1997-06, Vol.272 (6), p.E1037-E1042

1997

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Charged residues in surface-located loops influence voltage gating of porin from Haemophilus influenzae type b

The Journal of membrane biology, 2000-12, Vol.178 (3), p.185-193

2000

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alpha-Keto and alpha-hydroxy branched-chain acid interrelationships in normal humans

The Journal of nutrition, 1993-09, Vol.123 (9), p.1513-1521

1993

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Biogenesis of hepatic acute-phase response to trauma

Medical hypotheses, 1996-08, Vol.47 (2), p.157-177

1996

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Maple syrup urine disease: Interrelations between branched‐chain amino‐, oxo‐ and hydroxyacids; implications for treatment; associations with CNS dysmyelination

Journal of inherited metabolic disease, 1992-01, Vol.15 (1), p.121-135

1992

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Artificial liver support: The pipe dream of today should be the reality of the near future

Medical hypotheses, 1996-08, Vol.47 (2), p.145-155

1996

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Methylmalonic acidemia with a severe chemical but benign clinical phenotype

The Journal of pediatrics, 1993-03, Vol.122 (3), p.428-429

1993

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Measurement of urinary free and acylcarnitines: Quantitative acylcarnitine profiling in normal humans and in several patients with metabolic errors

Analytical biochemistry, 1989, Vol.176 (1), p.85-95

1989

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Kinetics and mechanisms of release of serum proteins of intoxicated rat livers implanted into guinea pigs

Bioorganic & medicinal chemistry letters, 1997-09, Vol.7 (18), p.2337-2342

1997

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Pseudoketogenesis in hepatectomized dogs

American journal of physiology: endocrinology and metabolism, 1990-03, Vol.258 (3), p.E519-E528

1990

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Regioselectivity of the oxygen addition-induced dechlorination of PCBS and DDT metabolites in electron capture mass spectrometry

Journal of the American Society for Mass Spectrometry, 1996, Vol.7 (1), p.66-72

1996

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Brain dysgenesis and congenital intracerebral calcification associated with 3-hydroxyisobutyric aciduria

The Journal of pediatrics, 1992-07, Vol.121 (1), p.86-89

1992

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Synthesis and gas chromatography/mass spectrometry analysis of stereoisomers of 2-hydroxy-3-methylpentanoic acid

Methods in enzymology, 2000, Vol.324, p.3

Mamer, O A

2000

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Chemical and epidemiological aspects of modified butter oil fractions

Journal of toxicology and environmental health. Part B, Critical reviews, 1998-04, Vol.1 (2), p.149-179

1998

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gamma.-Irradiation-Induced Degradation of DDT and its Metabolites in Organic Solvents

Journal of agricultural and food chemistry, 1994-09, Vol.42 (9), p.2012-2018

1994

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Collision-induced oxygen addition to chloroaromatic compounds

Journal of the American Society for Mass Spectrometry, 1996-11, Vol.7 (11), p.1144-1150

1996

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Plasma reduced homocysteine concentrations are increased in end-stage renal disease

Kidney international, 2001-01, Vol.59 (1), p.372-377

2001

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Measurement of Phenyllactate, Phenylacetate, and Phenylpyruvate by Negative Ion Chemical Ionization–Gas Chromatography/Mass Spectrometry in Brain of Mouse Genetic Models of Phenylketonuria and Non-Phenylketonuria Hyperphenylalaninemia

Analytical biochemistry, 2000-05, Vol.280 (2), p.242-249

2000

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3‐Methylglutaconic aciduria: A marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a ‘new’ type (‘type 4’)

Journal of inherited metabolic disease, 1992-01, Vol.15 (2), p.204-212

1992

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Liquid chromatography/mass spectrometry analysis of mixtures of rhamnolipids produced by Pseudomonas aeruginosa strain 57RP grown on mannitol or naphthalene

Trimethylaminuria Is Caused by Mutations of the FMO3 Gene in a North American Cohort

Stable isotope dilution techniques

On the mechanisms of the formation of L-alloisoleucine and the 2-hydroxy-3-methylvaleric acid stereoisomers from L-isoleucine in maple syrup urine disease patients and in normal humans

Kinetics and mechanisms of hepatic acute phase response to subtotal partial hepatectomy and cultural impact on environmental hepatic end-stage liver injury in the homeless

Artefactual pyruvate and 2‐oxobutyrate produced by trimethylsilylation of methylmalonic and ethylmalonic acids in the presence of oxygen

Effects of leucine on whole body leucine, valine, and threonine metabolism in humans

Charged residues in surface-located loops influence voltage gating of porin from Haemophilus influenzae type b

alpha-Keto and alpha-hydroxy branched-chain acid interrelationships in normal humans

Biogenesis of hepatic acute-phase response to trauma

Maple syrup urine disease: Interrelations between branched‐chain amino‐, oxo‐ and hydroxyacids; implications for treatment; associations with CNS dysmyelination

Artificial liver support: The pipe dream of today should be the reality of the near future

Methylmalonic acidemia with a severe chemical but benign clinical phenotype

Measurement of urinary free and acylcarnitines: Quantitative acylcarnitine profiling in normal humans and in several patients with metabolic errors

Kinetics and mechanisms of release of serum proteins of intoxicated rat livers implanted into guinea pigs

Pseudoketogenesis in hepatectomized dogs

Regioselectivity of the oxygen addition-induced dechlorination of PCBS and DDT metabolites in electron capture mass spectrometry

Brain dysgenesis and congenital intracerebral calcification associated with 3-hydroxyisobutyric aciduria

Synthesis and gas chromatography/mass spectrometry analysis of stereoisomers of 2-hydroxy-3-methylpentanoic acid

Chemical and epidemiological aspects of modified butter oil fractions

gamma.-Irradiation-Induced Degradation of DDT and its Metabolites in Organic Solvents

Collision-induced oxygen addition to chloroaromatic compounds

Plasma reduced homocysteine concentrations are increased in end-stage renal disease

Measurement of Phenyllactate, Phenylacetate, and Phenylpyruvate by Negative Ion Chemical Ionization–Gas Chromatography/Mass Spectrometry in Brain of Mouse Genetic Models of Phenylketonuria and Non-Phenylketonuria Hyperphenylalaninemia

3‐Methylglutaconic aciduria: A marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a ‘new’ type (‘type 4’)

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