17 results on '"Ueta, Akihito"'
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2. SSCP Screening of the Dihydropyrimidine Dehydrogenase Gene Polymorphisms of the Japanese Population Using a Semi-automated Electrophoresis Unit
3. Novel mutations in the cytochrome P450 2C19 gene: a pitfall of the PCR-RFLP method for identifying a common mutation
4. Long follow up of betaine therapy in two Japanese siblings with cystathionine β-synthase deficiency
5. Chronic zinc toxicity in an infant who received zinc therapy for atopic dermatitis
6. Urinary uracil in female patients with ornithine transcarbamylase deficiency
7. Simultaneous quantification of acylcarnitine isomers containing dicarboxylic acylcarnitines in human serum and urine by high‐performance liquid chromatography/electrospray ionization tandem mass spectrometry
8. Chronic zinc toxicity in an infant who received zinc therapy for atopic dermatitis
9. Acylcarnitine Profiles during Carnitine Loading and Fasting Tests in a Japanese Patient with Medium-Chain Acyl-CoA Dehydrogenase Deficiency
10. A Simple Quantitative Assay for Urinary Adenosine Using Column-Switching High-Performance Liquid Chromatography
11. Novel mutations in the cytochrome P450 2C19 gene: a pitfall of the PCR-RFLP method for identifying a common mutation
12. Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency in the Japanese population
13. Vitamin B6-Responsive Ornithine Aminotransferase Deficiency with a Novel Mutation G237D
14. Urinary pyrimidine analysis in healthy newborns and newborns with urea cycle disorder
15. Gout and Nucleic Acid Metabolism
16. Intra-day variations in urinary pyrimidines in ornithine carbamoyltransferase deficiency and healthy individuals
17. Long follow up of betaine therapy in two Japanese siblings with cystathionine beta-synthase deficiency.
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