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Department of Pediatrics, Tokyo Jikei University School of Medicine | 論文
- ゴーシェ病での骨リモデリングと造血における特定のサイトカインの役割
- Successful Intrauterine Therapy for Fetal Goitrous Hypothyroidism during Late Gestation
- Enzyme Therapy in Gaucher Disease Type 2 : An Autopsy Case
- Adult-type metachromatic leukodystrophy with a compound heterozygote mutation showing character change and dementia
- 胎児性ゴーシェ病 (fetal Gaucher disease) の一剖検例
- A Novel Mutation of the Arginine Vasopressin Receptor 2 Gene in a Patient with Congenital Nephrogenic Diabetes Insipidus