Ozono Keiichi | 大阪大学医学系研究科小児科

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著作論文

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
Endocrinological Analysis of 122 Japanese Childhood Cancer Survivors in a Single Hospital
Pediatric post-transplant diffuse large B cell lymphoma after cardiac transplantation
A case of congenital bone marrow failure with radio-ulnar synostosis
Sleep disordered breathing in childhood-onset acid maltase deficiency
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
Biological Activities of 2α-Substituted Analogues of 1α, 25-Dihydroxyvitamin D_3 in Transcriptional Regulation and Human Promyelocytic Leukemia (HL-60) Cell Proliferation and Differentiation(Medicinal Chemistry)
Application of Signal-Averaged Electrocardiogram to Myocardial Damage in the Late Stage of Kawasaki Disease
A Case of Pediatric Virilizing Adrenocortical Tumor Resulting in Hypothalamic-pituitary Activation and Central Precocious Puberty Following Surgical Removal
Late-onset differentiation syndrome in a child with acute promyelocytic leukemia
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

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