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Department Of Pediatrics Graduate School Of Medicine Kobe University | 論文
- Novel Mutations in 21 Patients with Tuberous Sclerosis Complex and Variation of Tandem Splice-acceptor Sites in TSC1 exon 14
- ベトナム人脊髄性筋萎縮症患者におけるSMN2遺伝子量ならびにNAIP遺伝子量について
- Clinical Types, Molecular Genetic Diagnosis & Genetic : clinical Correlation in Patients with Spinal Muscular Atrophy
- Deletion of the SMN1 and NAIP Genes in Vietnamese Patients with Spinal Muscular Atrophy
- Molecular Genetic Analyses of Five Vietnamese Patients with Spinal Musucular Atrophy
- 全国調査における典型的溶血性尿毒症症候群の重症化因子の検討
- Association of Cumulative Cyclosporine Dose with Its Irreversible Nephrotoxicity in Japanese Patients with Pediatric-Onset Autoimmune Diseases(Biopharmacy)
- 志賀毒素を介さず発症した溶血性尿毒症症候群5症例の予後と腎組織像に関する検討
- A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism
- 小児SLE患者に対する高用量ミゾリビン投与の試み
- Prediction of systemic exposure to cyclosporine in Japanese pediatric patients
- Rituximab treatment for posttransplant lymphoproliferative disorder (PTLD) induces complete remission of recurrent nephrotic syndrome
- The effect of aldosterone blockade in patients with Alport syndrome
- Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation
- Molecular Diagnosis, Correlation of Clinical and Deletion Data in Duchenne Muscular Dystrophy
- Genetic polymorphisms associated with adverse events and elimination of methotrexate in childhood acute lymphoblastic leukemia and malignant lymphoma
- A 2-bp deletion in exon 74 of the dystrophin gene does not clearly induce muscle weakness
- Effects of Polymorphisms of MDR1, MRP1, and MRP2 Genes on Their mRNA Expression Levels in Duodenal Enterocytes of Healthy Japanese Subjects(Biopharmacy)
- The C677T Mutation in the Methylenetetrahydrofolate Reductase Gene among the Indonesian Javanese Population
- HnRNP C1/C2 May Regulate Exon 7 Splicing in the Spinal Muscular Atrophy Gene SMN1