Differential diagnosis of hemophagocytic syndrome: underlying disorders and selection of the most effective treatment
スポンサーリンク
概要
著者
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Imashuku Shinsaku
Division Of Pediatrics Takasago-seibu Hospital
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Imashuku Shinsaku
Division Of Pediatrics And Hematology Takasago-seibu Hospital
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Imashuku Shinsaku
Division Of Pediatrics Children's Research Hospital Kyoto Prefectural University Of Medicine
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Imashuku Shinsaku
Division Of Hematology Takasago-seibu Hospital
関連論文
- Fatal Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis With Clonal Karyotype Abnormality
- Risk of Etoposide-Related Acute Myeloid Leukemia in the Treatment of Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis
- M-protein-positive chronic active Epstein-Barr virus infection: features mimicking HIV-1 infection
- Langerhans cell histiocytosis with multifocal bone lesions : comparative clinical features between single and multi-systems
- Treatment of infant acute lymphoblastic leukemia in Japan
- Nationwide Survey of Hemophagocytic Lymphohistiocytosis 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
- Sudden death of a 21-year-old female with Williams syndrome showing rare complications
- 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
- 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
- Hemophagocytosis by leukemic blasts in a case a of acute megakaryoblastic leukemia with t(16 ; 21) (p11 ; q22)
- Hypercalcemia in children presenting with acute lymphoblastic leukemia
- Bone Marrow Changes Mimicking Myelodysplasia in Patients With Hemophagocytic Lymphohistiocytosis
- Differential diagnosis of hemophagocytic syndrome: underlying disorders and selection of the most effective treatment
- Fatal hemophagocytic lymphohistiocytosis in an extremely-low-birthweight infant
- 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
- Persistent thrombocytosis in elderly patients with rare hyposplenias that mimic essential thrombocythemia
- Therapeutic outcome of multifocal Langerhans cell histiocytosis in adults treated with the Special C regimen formulated by the Japan LCH Study Group