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大阪大学 医学系研究科小児科 | 論文
- Long-term hospitalization during pregnancy is a risk factor for vitamin D deficiency in neonates
- Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome
- A Patient with Sotos Syndrome Who Reached Final Height
- 136 Excessive Growth in a Japanese Girl with Weaver Syndrome
- A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia
- A Case of Primary Hyperparathyroidism in Childhood Found by a Chance Hematuria
- Pediatric post-transplant lymphoproliferative disorder after cardiac transplantation
- Clinical aspects and adrenal functions in eleven Japanese children with X-linked adrenoleukodystrophy
- Anthracyclines for acute lymphoblastic leukemia in a child with congenital long QT syndrome
- Hematopoietic stem cell transplantation with reduced intensity conditioning from a family haploidentical donor in an infant with familial hemophagocytic lymphohistocytosis
- 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
- Decrease in serum FGF23 levels after intravenous infusion of pamidronate in patients with osteogenesis imperfecta