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Department Of Pediatrics Osaka University Graduate School Of Medicine | 論文
- Pediatric myeloid/NK cell precursor lymphoma/leukemia expressing T/NK immunophenotype markers
- Allogeneic hematopoietic stem cell transplantation with reduced intensity conditioning for a child with recurrent anaplastic large cell lymphoma
- Analysis of the stable levels of messenger RNA derived from different polymorphic alleles in the vitamin D receptor gene
- Endocrinological Analysis of 122 Japanese Childhood Cancer Survivors in a Single Hospital
- Tacrolimus-Related Encephalopathy following Allogeneic Stem Cell Transplantation in Children
- Establishment of a Monosomy 7 Leukemia Cell Line, MONO-7, With a ras Gene Mutation
- Second Transplantation With CD34^+ Blood Cells From an HLA-Mismatched Related Donor After Engraftment Failure of Transplanted Cord Blood Cells
- Expression of Adhesion Molecules in Childhood B-Lineage-Cell Neoplasms
- Pediatric post-transplant diffuse large B cell lymphoma after cardiac transplantation
- A case of congenital bone marrow failure with radio-ulnar synostosis
- Causes and Differential Diagnosis of Hypocalcemia : Recommendation Proposed by Expert Panel Supported by Ministry of Health, Labour and Welfare, Japan
- Hereditary hypophosphatemic rickets with hypercalciuria : a study for the phosphate transporter gene type IIc and osteoblastic function
- A Case of Persistent Hyperinsulinemic Hypoglycemia of Infancy Successfully Managed with Subcutaneous Octreotide Injection and Nocturnal Intravenous Glucose Supply
- Application of Signal-Averaged Electrocardiogram to Myocardial Damage in the Late Stage of Kawasaki Disease
- Molecular Bases of Diseases Characterized by Hypophosphatemia and Phosphaturia : New Understanding
- Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by Chronic Administration of Furosemide without Alteration of Its Administration and Urinary Calcium Loss
- Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome
- Six novel mutations detected in the GALC gene in 17 Japanese patients with Krabbe disease, and new genotype-phenotype correlation
- A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency
- Novel mutation of gene coding for glial fibrillary acidic protein in a Japanese patient with Alexander disease