Morimoto Akira | Jichi Medical Univ. Shimotsuke Jpn

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著作論文

Risk of Etoposide-Related Acute Myeloid Leukemia in the Treatment of Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis
Mosaic Down syndrome-associated acute myeloid leukemia does not require high-dose cytarabine treatment for induction and consolidation therapy
Langerhans cell histiocytosis with multifocal bone lesions : comparative clinical features between single and multi-systems
Outcome of pediatric patients with Langerhans cell histiocytosis treated with 2 chlorodeoxyadenosine : a nationwide survey in Japan
Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese people
Control of hepatic veno-occlusive disease with an antithrombin-III concentrate-based therapy
Prognostic Value of Early Response to Treatment Combined with Conventional Risk Factors in Pediatric Acute Lymphoblastic Leukemia
Risk Factors for Cytomegalovirus Retinitis Following Bone Marrow Transplantation From Unrelated Donors in Patients With Severe Aplastic Anemia or Myelodysplasia
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
Response to Imatinib Mesylate in a Patient with Idiopathic Hypereosinophilic Syndrome Associated with Cyclic Eosinophil Oscillations
Hb Bristol-Alesha Presenting Thalassemia-Type Hyperunstable Hemoglobinopathy
Hemophagocytic Syndrome Associated with Severe Adenoviral Pneumonia : Usefulness of Real-Time Polymerase Chain Reaction for Diagnosis
Low Frequency of KIT Gene Mutation in Pediatric Acute Myeloid Leukemia with inv(16)(p13q22) : A Study of the Japanese Childhood AML Cooperative Study Group
Treatment of patients with hypothalamic-pituitary lesions as adult-onset Langerhans cell histiocytosis
Analysis of 43 cases of Langerhans cell histiocytosis (LCH)-induced central diabetes insipidus registered in the JLSG-96 and JLSG-02 studies in Japan

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