スポンサーリンク
Department Of Pediatrics Osaka University Graduate School Of Medicine | 論文
- SLC2A1 gene analysis of Japanese patients with glucose transporter 1 deficiency syndrome
- Mucolipidosis II and III alpha/beta : mutation analysis of 40 Japanese patients showed genotype-phenotype correlation
- Cross-sectional study of bone metabolism with nutrition in adult classical phenylketonuric patients diagnosed by neonatal screening
- Decrease in serum FGF23 levels after intravenous infusion of pamidronate in patients with osteogenesis imperfecta
- Hypophosphatasia now draws more attention of both clinicians and researchers : A Commentary on prevelance of c. 1559deIT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasias in Japanese and effects of the mutation on he
- Efficacy of pegylated interferon-α2a monotherapy in Japanese children with chronic hepatitis C
- Neuropsychiatric symptoms of progressive supranuclear palsy in a dementia clinic