スポンサーリンク
Department of Pediatrics, Kumamoto University Medical School | 論文
- Tyrosinemia type I-like disease : A possible manifestation of 3-oxo-△^4-steroid 5β-reductase deficiency
- Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency
- CLINICAL PHARMACOLOGICAL STUDIES OF ETHOTOIN IN PEDIATRIC EPILEPTIC PATIENTS
- Production Efficiency and Telomere Length of the Cloned Pigs Following Serial Somatic Cell Nuclear Transfer
- Genetic mutations in exons 3 and 4 of the pancreatic secretory trypsin inhibitor in patients with pancreatitis
- Evaluation of persistence of ductus venosus with Tc-99m DTPA galactosyl human serum albumin liver scintigraphy and I-123 iodoamphetamine per-rectal portal scintigraphy
- Examination of Stability of Anticonvulsants in a Protease Solution and Assay of Anticonvulsants in Hairs
- Mass screening for Wilson's disease : Results and recommendations
- Newborn hearing screening in a single private Japanese obstetric hospital
- AMELIORATION OF PROLIDASE DEFICIENCY IN FIBROBLASTS USING ADENOVIRUS MEDIATED GENE TRANSFER
- 110 A CASE OF INSULIN ALLERGY WITH HIGH LEVEL OF SPECIFIC IGE FOR HUMAN INSULIN
- 44 A CASE OF CONGENITAL HYPOALDOSTERONISM CAUSED BY A MUTATION OF CYP11B2 GENE
- A novel nonsense mutation of the PEPD gene in a Japanese patient with prolidase deficiency
- Apoptosis under hypercytokinemia is a possible pathogenesis in influenza-associated encephalopathy
- Accelerated elimination of phenobarbital by oral activated charcoal suspensions with alkaline diuresis in an overdose patient.