Kawabata Hiroshi | Department of Electronic Science and Engineering, Kyoto University, Kyoto 606-8501, Japan

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著作論文

Reversible Cardiomyopathy Associated with Multicentric Castleman Disease : Successful Treatment with Tocilizumab, an Anti-Interleukin 6 Receptor Antibody
Oncostatin M and leukemia inhibitory factor increase hepcidin expression in hepatoma cell lines
Mycophenolate mofetil combined with tacrolimus and minidose methotrexate after unrelated donor bone marrow transplantation with reduced-intensity conditioning
Intravascular large B cell lymphoma : proposed of the strategy for early diagnosis and treatment of patients with rapid deteriorating condition
A case of Mikulicz's disease complicated with interstitial nephritis successfully treated by high-dose corticosteroid
Incidence of Diffuse Large B-Cell Lymphoma of Germinal Center B-Cell Origin in Whole Diffuse Large B-Cell Lymphoma : Tissue Fluorescence In Situ Hybridization Using t(14 ; 18) Compared with Immunohistochemistry
Distribution of endogenous endonuclease activities capable of producing internucleosomal DNA cleavage in hematopoietic cells
Density Functional Theory and Direct Molecular Dynamics Study of the Hydrogen Atom on a Finite-Sized Graphene
Intra-molecular Carrier Pathway Analysis in One-Dimensional Fused Furan Polymer
PD20 DNA STRAND SCISSION BY NEOCARZINOSTATIN : REACTION OF SELF-COMPLEMENTARY OLIGONUCLOETIDE
Interaction of Hydroxyl OH Radical with Graphene Surface: A Density Functional Theory Study
Regression of Hodgkin Lymphoma in Response to Antiviral Therapy for Hepatitis C Virus Infection
Molecular Design of High Performance Molecular Devices Based on Direct Ab-initio Molecular Dynamics Method: Diffusion of Lithium Ion on Fluorinated Amorphous Carbon
A Density Functional Theory Study on the Hole Transfer in Fullerene Hydride C60H2
Castleman-Kojima Disease (TAFRO Syndrome) : A Novel Systemic Inflammatory Disease Characterized by a Constellation of Symptoms, Namely, Thrombocytopenia, Ascites (Anasarca), Microcytic Anemia, Myelofibrosis, Renal Dysfunction, and Organomegaly : A Statu
Successful Treatment of a Patient with Multicentric Castleman's Disease who Presented with Thrombocytopenia, Ascites, Renal Failure and Myelofibrosis Using Tocilizumab, an Anti-Interleukin-6 Receptor Antibody
Clinical Features and Treatment of Multicentric Castleman's Disease : A Retrospective Study of 21 Japanese Patients at a Single Institute
Effects of Fluorine Atom Substitution of Graphene Edge Site on the Diffusion of Lithium Ion
Absent or Extremely Low Neutrophil Alkaline Phosphatase Activity Levels in Patients with Myelodysplastic Syndromes
A Case of Congenital Dyserythropoietic Anemia Type 1 in a Japanese Adult with a CDAN1 Gene Mutation and an Inappropriately Low Serum Hepcidin-25 Level
Splenic Irradiation as a Component of a Reduced-Intensity Conditioning Regimen for Hematopoietic Stem Cell Transplantation in Myelofibrosis with Massive Splenomegaly
Differing impacts of pretransplant serum ferritin and C-reactive protein levels on the incidence of chronic graft-versus-host disease after allogeneic hematopoietic stem cell transplantation
Acidic milieu augments the expression of hepcidin, the central regulator of iron homeostasis
Molecular Design of High Performance Poly-Fused Thiophene Radical Cations: A Density Functional Theory Study
Clinical Features and Treatment of Multicentric Castleman's Disease : A Retrospective Study of 21 Japanese Patients at a Single Institute

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