Y. Inoue

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Pilot study of gas chromatographic-mass spectrometric screening of newborn urine for inborn errors of metabolism after treatment with urease.

I. Yoshida, T. Kuhara, I. Matsumoto, 1999, Journal of chromatography. B, Biomedical sciences and applications.

Application of optical isomer analysis by diastereomer derivatization GC/MS to determine the condition of patients with short bowel syndrome.

T. Kuhara, T. Shinka, Y. Inoue, 2006, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Urinary metabolic profile of phenylketonuria in patients receiving total parenteral nutrition and medication.

K. Omura, T. Miyawaki, H. Shintaku, 2009, Rapid communications in mass spectrometry : RCM.

Abnormal fatty acid metabolism in patients in hopantenate therapy during clinical episodes.

T. Kuhara, I. Matsumoto, T. Shinka, 1991, Journal of chromatography.

Changes in urinary level and configuration ratio of D-lactic acid in patients with short bowel syndrome.

T. Kuhara, T. Shinka, Y. Inoue, 2007, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

GC/MS Analysis of Urine in 3‐Hydroxy‐3‐Methylglutaryl‐CoA Lyase Deficiency

K. Hasumi, T. Kuhara, A. Endo, 1992, Acta paediatrica Japonica : Overseas edition.

Increased urinary excretion of β-hydroxyisovaleric acid in ketotic and nonketotic type II diabetes mellitus

T. Kuhara, R. Iwasaki, S. Morimoto, 1990 .

Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis: a common mutation, R179X

S. Tsujino, K. Takeshita, T. Kuhara, 2001, Journal of Human Genetics.

Gas chromatographic–mass spectrometric newborn screening for propionic acidaemia by targeting methylcitrate in dried filter-paper urine samples

F. Endo, H. Mitsubuchi, N. Sakura, 2002, Journal of Inherited Metabolic Disease.

Biotin Deficiency in an Infant Fed with Amino Acid Formula

M. Inaoki, W. Fujimoto, T. Kuhara, 2005, The Journal of dermatology.

Studies of urinary organic acid profiles of a patient with dihydrolipoyl dehydrogenase deficiency.

T. Kuhara, I. Matsumoto, T. Shinka, 1983, Clinica chimica acta; international journal of clinical chemistry.

Identification of 3-hydroxy-3-ethylglutaric acid in urine of patients with propionic acidaemia.

T. Kuhara, I. Matsumoto, T. Shinka, 1983, Biomedical mass spectrometry.

Five cases of beta-ureidopropionase deficiency detected by GC/MS analysis of urine metabolome.

T. Kuhara, T. Shinka, Y. Inoue, 2009, Journal of mass spectrometry : JMS.

Two cases of benign methylmalonic aciduria detected during a pilot study of neonatal urine screening.

T. Kuhara, T. Shinka, Y. Inoue, 2002, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Benzoylalanine: detection and identification of an alanine conjugate with benzoic acid in hyperammonemic patients treated with sodium benzoate.

T. Kuhara, I. Matsumoto, T. Shinka, 1985, Clinica chimica acta; international journal of clinical chemistry.

Gas chromatographic‐mass spectrometric metabolic profiling of patients with fatal infantile mitochondrial myopathy with de Toni‐Fanconi‐Debré syndrome

T. Kuhara, I. Matsumoto, T. Shinka, 1996, Acta paediatrica Japonica : Overseas edition.

Urinary 2-hydroxy-5-oxoproline, the lactam form of α-ketoglutaramate, is markedly increased in urea cycle disorders

Arthur J. L. Cooper, B. Krasnikov, T. Kuhara, 2011, Analytical and bioanalytical chemistry.

Urinary Acid Profiles in Asymptomatic and Symptomatic Siblings with Propionyl CoA Carboxylase Deficiency

T. Aoyama, M. Matsuo, T. Kuhara, 1989 .

Mass spectrometric identification of 2-hydroxydodecanedioic acid and its homologues in urine from patients with hopantenate therapy during clinical episode.

T. Kuhara, I. Matsumoto, T. Shinka, 1990, Biomedical & environmental mass spectrometry.

Monitoring method for pre- and post-liver transplantation in patients with primary hyperoxaluria type I.

H. Mitsubuchi, T. Kuhara, Y. Inoue, 2003, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

A GC/MS-based metabolomic approach for diagnosing citrin deficiency

Arthur J. L. Cooper, T. Kuhara, Y. Inoue, 2011, Analytical and bioanalytical chemistry.

Asymptomatic alpha-ketoadipic aciduria detected during a pilot study of neonatal urine screening.

H. Mitsubuchi, T. Kuhara, T. Shinka, 1999 .

Markedly Increased ω‐Oxidation of Valproate in Fulminant Hepatic Failure

N. Sakura, T. Kuhara, I. Matsumoto, 1990 .

Altered metabolic profiles of valproic acid in a patient with Reye's syndrome.

N. Sakura, T. Kuhara, I. Matsumoto, 1985, Clinica chimica acta; international journal of clinical chemistry.

Prenatal diagnosis of propionic acidemia by measuring methylcitric acid in dried amniotic fluid on filter paper using GC/MS.

T. Kuhara, T. Shinka, Y. Inoue, 2008, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

An asymptomatic infant with isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency detected by newborn screening for maple syrup urine disease

K. Ihara, R. Kuromaru, T. Kuhara, 1997, European Journal of Pediatrics.

Simple and quantitative analysis of urinary sulfated tauro- and glycodihydroxycholic acids in infant with cholestasis by electrospray ionization mass spectrometry.

T. Kuhara, T. Shinka, Y. Inoue, 2007, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Rapid and sensitive method for prenatal diagnosis of propionic acidemia using stable isotope dilution gas chromatography-mass spectrometry and urease pretreatment.

T. Kuhara, Y. Inoue, 2002, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Asymptomatic a‐ketoadipic aciduria detected during a pilot study of neonatal urine screening

H. Mitsubuchi, T. Kuhara, T. Shinka, 1999, Acta paediatrica.

A study on α-ketoadipic aciduria by gas chromatographic-mass spectrometry

T. Kuhara, T. Shinka, Y. Inoue, 2000 .

Rapid and sensitive detection of urinary 4-hydroxybutyric acid and its related compounds by gas chromatography-mass spectrometry in a patient with succinic semialdehyde dehydrogenase deficiency.

S. Hirose, T. Kuhara, Akira Ito, 2002, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Erythematous skin lesions and partial deficiency of 3-methylcrotonyl-CoA carboxylase in peripheral lymphocytes in a patient with propionic acidaemia

K. Sato, T. Kuhara, I. Matsumoto, 1991, Journal of Inherited Metabolic Disease.

Identification of the N-Acetyl-β-Aryloxyalanines from Rats Treated with 3-(p-Tolyloxy)-1,2-Propanediol and 3-Phenoxy-1,2-Propanediol

T. Kuhara, I. Matsumoto, Y. Inoue, 1977 .