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Evaluation of valproate effects on acylcarnitine in epileptic children by LC–MS/MS

Brain & development (Tokyo. 1979), 2011-11, Vol.33 (10), p.816-823

2011

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Determination of 3-hydroxyisovalerylcarnitine and other acylcarnitine levels using liquid chromatography–tandem mass spectrometry in serum and urine of a patient with multiple carboxylase deficiency

Journal of chromatography. B, 2008-07, Vol.870 (2), p.154-159

2008

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Simultaneous quantification of acylcarnitine isomers containing dicarboxylic acylcarnitines in human serum and urine by high-performance liquid chromatography/electrospray ionization tandem mass spectrometry

Rapid communications in mass spectrometry, 2007-01, Vol.21 (5), p.799-806

2007

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Detection of Pivaloylcarnitine in Pediatric Patients with Hypocarnitinemia after Long-Term Administration of Pivalate-Containing Antibiotics

The Tohoku Journal of Experimental Medicine, 2010, Vol.221(4), pp.309-313

2010

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A case of holocarboxylase synthetase deficiency with insufficient response to prenatal biotin therapy

Brain & development (Tokyo. 1979), 2009-11, Vol.31 (10), p.775-778

2009

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Acylcarnitine Profiles during Carnitine Loading and Fasting Tests in a Japanese Patient with Medium-Chain Acyl-CoA Dehydrogenase Deficiency

The Tohoku Journal of Experimental Medicine, 2007, Vol.213(4), pp.351-359

2007

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Long follow up of betaine therapy in two Japanese siblings with cystathionine β‐synthase deficiency

Pediatrics international, 2008-10, Vol.50 (5), p.694-695

2008

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Neonatal alkalemia associated with potential hypovolemia in an infant born to a severely dehydrated mother

Pediatrics international, 2007-04, Vol.49 (2), p.245-247

2007

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Kinetic and molecular orbital analyses of dicarboxylic acylcarnitine methylesterification show that derivatization may affect the screening of newborns by tandem mass spectrometry

Bioorganic & medicinal chemistry letters, 2016-01, Vol.26 (1), p.121-125

2016

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Determination of methylmalonyl coenzyme A by ultra high-performance liquid chromatography tandem mass spectrometry for measuring propionyl coenzyme A carboxylase activity in patients with propionic acidemia

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2017-03, Vol.1046, p.195-199

2017

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Assay for methylmalonyl coenzyme A mutase activity based on determination of succinyl coenzyme A by ultrahigh-performance liquid chromatography tandem mass spectrometry

Analytical and bioanalytical chemistry, 2015-07, Vol.407 (18), p.5281-5286

2015

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Recurrence of Cushing's Disease after Long-term Remission due to Pituitary Apoplexy

Endocrine Journal, 2000, Vol.47(6), pp.793-797

2000

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Carnitine-associated encephalopathy caused by long-term treatment with an antibiotic containing pivalic acid

Pediatrics (Evanston), 2007-09, Vol.120 (3), p.e739

2007

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Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency

The Journal of pediatrics, 1999-09, Vol.135 (3), p.375-378

1999

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Long-term treatment and diagnosis of tetrahydrobiopterin-responsive hyperphenylalaninemia with a mutant phenylalanine hydroxylase gene

Pediatric research, 2004-03, Vol.55 (3), p.425-430

2004

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Smoking-induced olfactory dysfunction in chronic sinusitis and assessment of brief University of Pennsylvania Smell Identification Test and T&T methods

American journal of rhinology, 2006-09, Vol.20 (5), p.439-444

2006

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Management of acute metabolic decompensation in maple syrup urine disease: A multi-center study

Pediatrics international, 1999-04, Vol.41 (2), p.132-137

1999

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Unique Electroencephalographic Change of Acute Encephalopathy in Glutaric Aciduria Type 1

The Tohoku Journal of Experimental Medicine, 2000, Vol.191(1), pp.31-38

2000

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Patient Report: Neonatal alkalemia associated with potential hypovolemia in an infant born to a severely dehydrated mother

Pediatrics international, 2007-04, Vol.49 (2), p.245

2007

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Long follow up of betaine therapy in two Japanese siblings with cystathionine [beta]-synthase deficiency

Pediatrics international, 2008-10, Vol.50 (5), p.694

2008

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A pediatric patient with classical citrullinemia who underwent living-related partial liver transplantation

Transplantation, 2001-05, Vol.71 (10), p.1495

2001

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Two cases of NADH-coenzyme Q reductase deficiency: Relationship to MELAS syndrome

The Journal of pediatrics, 1987-02, Vol.110 (2), p.223-227

1987

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Effect of Carnitine Administration on Glycine Metabolism in Patients with Isovaleric Acidemia: Significance of Acetylcarnitine Determination to Estimate the Proper Carnitine Dose

The Tohoku Journal of Experimental Medicine, 1996, Vol.179(2), pp.101-109

1996

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Alteration of Ammonia and Carnitine Levels in Short-Term Treatment with Pivalic Acid-Containing Prodrug

The Tohoku Journal of Experimental Medicine, 1995, Vol.175(1), pp.43-53

1995

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Carnitine determination by an enzymatic cycling method with carnitine dehydrogenase

Clinical chemistry (Baltimore, Md.), 1994-05, Vol.40 (5), p.817

1994

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Evaluation of valproate effects on acylcarnitine in epileptic children by LC–MS/MS

Determination of 3-hydroxyisovalerylcarnitine and other acylcarnitine levels using liquid chromatography–tandem mass spectrometry in serum and urine of a patient with multiple carboxylase deficiency

Simultaneous quantification of acylcarnitine isomers containing dicarboxylic acylcarnitines in human serum and urine by high-performance liquid chromatography/electrospray ionization tandem mass spectrometry

Detection of Pivaloylcarnitine in Pediatric Patients with Hypocarnitinemia after Long-Term Administration of Pivalate-Containing Antibiotics

A case of holocarboxylase synthetase deficiency with insufficient response to prenatal biotin therapy

Acylcarnitine Profiles during Carnitine Loading and Fasting Tests in a Japanese Patient with Medium-Chain Acyl-CoA Dehydrogenase Deficiency

Long follow up of betaine therapy in two Japanese siblings with cystathionine β‐synthase deficiency

Neonatal alkalemia associated with potential hypovolemia in an infant born to a severely dehydrated mother

Kinetic and molecular orbital analyses of dicarboxylic acylcarnitine methylesterification show that derivatization may affect the screening of newborns by tandem mass spectrometry

Determination of methylmalonyl coenzyme A by ultra high-performance liquid chromatography tandem mass spectrometry for measuring propionyl coenzyme A carboxylase activity in patients with propionic acidemia

Assay for methylmalonyl coenzyme A mutase activity based on determination of succinyl coenzyme A by ultrahigh-performance liquid chromatography tandem mass spectrometry

Recurrence of Cushing's Disease after Long-term Remission due to Pituitary Apoplexy

Carnitine-associated encephalopathy caused by long-term treatment with an antibiotic containing pivalic acid

Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency

Long-term treatment and diagnosis of tetrahydrobiopterin-responsive hyperphenylalaninemia with a mutant phenylalanine hydroxylase gene

Smoking-induced olfactory dysfunction in chronic sinusitis and assessment of brief University of Pennsylvania Smell Identification Test and T&T methods

Management of acute metabolic decompensation in maple syrup urine disease: A multi-center study

Unique Electroencephalographic Change of Acute Encephalopathy in Glutaric Aciduria Type 1

Patient Report: Neonatal alkalemia associated with potential hypovolemia in an infant born to a severely dehydrated mother

Long follow up of betaine therapy in two Japanese siblings with cystathionine [beta]-synthase deficiency

A pediatric patient with classical citrullinemia who underwent living-related partial liver transplantation

Two cases of NADH-coenzyme Q reductase deficiency: Relationship to MELAS syndrome

Effect of Carnitine Administration on Glycine Metabolism in Patients with Isovaleric Acidemia: Significance of Acetylcarnitine Determination to Estimate the Proper Carnitine Dose

Alteration of Ammonia and Carnitine Levels in Short-Term Treatment with Pivalic Acid-Containing Prodrug

Carnitine determination by an enzymatic cycling method with carnitine dehydrogenase

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