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314 results on '"Kawabata, Hiroshi"'

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5. TAFRO Syndrome: A Disease Requiring Immediate Medical Attention

10. The Usefulness of Machine Learning–Based Evaluation of Clinical and Pretreatment [18F]-FDG-PET/CT Radiomic Features for Predicting Prognosis in Hypopharyngeal Cancer

11. ASXL1 mutations with serum EPO levels predict poor response to darbepoetin alfa in lower-risk MDS: W-JHS MDS01 trial

14. Prognostic impacts of serum levels of C-reactive protein, albumin, and total cholesterol in patients with myelodysplastic syndromes

15. Azacitidine is a potential therapeutic drug for pyridoxine-refractory female X-linked sideroblastic anemia

17. Linking Chemical Heterogeneity to Lithological Heterogeneity of the Samoan Mantle Plume With Fe‐Sr‐Nd‐Pb Isotopes

18. Comprehensive analysis of protein-expression changes specific to immunoglobulin G4-related disease

19. ASXL1 Mutations with Serum EPO Levels Predict a Poor Response to Darbepoetin Alfa in Lower-Risk MDS: W-JHS MDS01 Trial

23. Correction to: Patient’s age and D‑dimer levels predict the prognosis in patients with TAFRO syndrome

24. Patient’s age and d-dimer levels predict the prognosis in patients with TAFRO syndrome

28. ASXL1 Mutations Predict a Poor Response to Darbepoetin Alfa in Anemic Patients with Low-Risk MDS: A Multicenter, Phase II Study

29. Optimal treatments for TAFRO syndrome: a retrospective surveillance study in Japan

32. Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients

37. Successful granulocyte apheresis using medium molecular weight hydroxyethyl starch

38. The potential role of follicular helper T cells in idiopathic multicentric Castleman disease with and without TAFRO syndrome

40. Osteosarcoma Manifesting Systemic Inflammation and Histological Features Mimicking Plasma Cell-type Castleman Disease

41. Is TAFRO syndrome a subtype of idiopathic multicentric Castleman disease?

45. An extranodal histopathological analysis of idiopathic multicentric Castleman disease with and without TAFRO syndrome

46. Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients

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