A. Ueta

发表

Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency in the Japanese population.

H. Togari, A. Marinaki, S. Sumi, 2005, Molecular genetics and metabolism.

Urinary uracil in female patients with ornithine transcarbamylase deficiency

H. Togari, S. Sumi, Tetsuya Ito, 2005, Pediatrics international : official journal of the Japan Pediatric Society.

Novel mutations in the cytochrome P450 2C19 gene: a pitfall of the PCR-RFLP method for identifying a common mutation

S. Fujimoto, H. Togari, D. Yamazaki, 2006, Journal of Human Genetics.

Chronic zinc toxicity in an infant who received zinc therapy for atopic dermatitis

S. Fujimoto, H. Togari, Kouichi Ito, 2005 .

Acylcarnitine Profi les during Carnitine Loading and Fasting Tests in a Japanese Patient with Medium-Chain Acyl-CoA Dehydrogenase Defi ciency

H. Togari, I. Kato, Satoshi Suzuki, 2003 .

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.

H. Togari, Tetsuya Ito, Y. Kurono, 2008, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

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

H. Togari, S. Sumi, Tetsuya Ito, 2007, Rapid communications in mass spectrometry : RCM.

Urinary pyrimidine analysis in healthy newborns and newborns with urea cycle disorder

H. Togari, I. Kato, S. Sumi, 2005 .

Vitamin B6-responsive ornithine aminotransferase deficiency with a novel mutation G237D.

H. Togari, S. Sumi, Tetsuya Ito, 2005, The Tohoku journal of experimental medicine.

A simple quantitative assay for urinary adenosine using column-switching high-performance liquid chromatography.

H. Togari, S. Sumi, Tetsuya Ito, 2006, The Tohoku journal of experimental medicine.

A Japanese case with inosine triphosphate pyrophosphohydrolase deficiency attributable to an enzymatic defect in white blood cells

H. Togari, S. Sumi, T. Ito, 2004, Journal of Inherited Metabolic Disease.

Allopurinol challenge tests performed before and after living-related donor liver transplantation in citrullinaemia

H. Togari, Y. Wada, T. Hashimoto, 2003, Journal of Inherited Metabolic Disease.

Acylcarnitine profiles during carnitine loading and fasting tests in a Japanese patient with medium-chain acyl-CoA dehydrogenase deficiency.

H. Togari, I. Kato, Satoshi Suzuki, 2007, The Tohoku journal of experimental medicine.

Allele Frequency of Inosine Triphosphate Pyrophosphatase Gene Polymorphisms in a Japanese Population

J. Duley, L. Fairbanks, A. Marinaki, 2004, Nucleosides, nucleotides & nucleic acids.

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

H. Togari, S. Sumi, Tetsuya Ito, 2008, Pediatrics international : official journal of the Japan Pediatric Society.

SSCP Screening of the Dihydropyrimidine Dehydrogenase Gene Polymorphisms of the Japanese Population Using a Semi-automated Electrophoresis Unit

H. Togari, Y. Okamoto, S. Sumi, 2007, Biochemical Genetics.