スポンサーリンク
Department Of Molecular Laboratory Medicine Graduate School Of Medical Science Kyoto Prefectural Uni | 論文
- Monosomies 7p and 12p and FLT3 internal tandem duplication : possible markers for diagnosis of T/myeloid biphenotypic acute leukemia and its clonal evolution
- Hyperbaric Oxygen in Addition to Antibiotic Therapy Is Effective for Bisphosphonate-Induced Osteonecrosis of the Jaw in a Patient with Multiple Myeloma
- Human Herpes Virus 8-Negative Primary Effusion Lymphoma in a Patient With a Ventriculoperitoneal Shunt Tube
- Clinical Characteristics of B-cell Lymphoma-associated Hemophagocytic Syndrome (B-LAHS): Comparison of CD5^+ with CD5^- B-LAHS
- Flow cytometric analysis of Thy-1 expression in myelodysplastic syndrome
- Flow cytometric analysis of Thy-1 expression in CD34-positive acute leukemia
- Overexpression of PRAD1/cyclin D1 in plasma cell leukemia with t(11;14)(q13;q32)
- Expression of Adhesion Molecules on Myeloma Cells
- Mutational analysis of the N-ras gene in acute lymphoblastic leukemia: a study of 125 Japanese pediatric cases
- Dexamethasone Reduces the Risk of Bortezomib-Induced Pulmonary Complications in Japanese Myeloma Patients
- Langerhans cell histiocytosis with multifocal bone lesions : comparative clinical features between single and multi-systems
- Monitoring plasma heparin concentration in a patient with antiphospholipid syndrome
- Outcome of pediatric patients with Langerhans cell histiocytosis treated with 2 chlorodeoxyadenosine : a nationwide survey in Japan
- Detection of NOTCH1 Mutations in Adult T-Cell Leukemia/Lymphoma and Peripheral T-Cell Lymphoma
- Scrotal Ulcers Arising during Treatment with All-trans Retinoic Acid for Acute Promyelocytic Leukemia
- Control of hepatic veno-occlusive disease with an antithrombin-III concentrate-based therapy
- Granulocytic Sarcoma Presenting with Severe Adenopathy (Cervical Lymph Nodes, Tonsils, and Adenoids) in a Child with Juvenile Myelomonocytic Leukemia and Successful Treatment with Allogeneic Bone Marrow Transplantation
- Hemophagocytic lymphohistiocytosis during maintenance treatment of precursor B-cell acute lymphoblastic leukemia
- A Novel Perforin Gene Mutation in a Japanese Family with Hemophagocytic Lymphohistiocytosis
- Prognostic significance of the BAALC isoform pattern and CEBPA mutations in pediatric acute myeloid leukemia with normal karyotype : a study by the Japanese Childhood AML Cooperative Study Group