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4. Genomic characterization of AML with aberrations of chromosome 7: a multinational cohort of 519 patients

9. Comparison of the 2022 world health organization classification and international consensus classification in myelodysplastic syndromes/neoplasms

10. Dysregulated immune and metabolic pathways are associated with poor survival in adult acute myeloid leukemia with CEBPA bZIP in-frame mutations

15. Management of classical Philadelphia chromosome-negative myeloproliferative neoplasms in Asia: consensus of the Asian Myeloid Working Group

20. Sabatolimab plus hypomethylating agents in previously untreated patients with higher-risk myelodysplastic syndromes (STIMULUS-MDS1): a randomised, double-blind, placebo-controlled, phase 2 trial

21. Validation of the molecular international prognostic scoring system in patients with myelodysplastic syndromes defined by international consensus classification

26. Momelotinib versus danazol in symptomatic patients with anaemia and myelofibrosis (MOMENTUM): results from an international, double-blind, randomised, controlled, phase 3 study

28. Clinical relevance of NFYA splice variants in patients with acute myeloid leukaemia undergoing intensive chemotherapy.

30. Oral Lactobacillus zeae exacerbates the pathological manifestation of periodontitis in a mouse model.

33. Polatuzumab vedotin–based salvage immunochemotherapy as third-line or beyond treatment for patients with diffuse large B-cell lymphoma: a real-world experience

34. Distinct clinico-biological features in AML patients with low allelic ratio FLT3-ITD: role of allogeneic stem cell transplantation in first remission

37. Microbiome of periodontitis and peri‐implantitis before and after therapy: Long‐read 16S rRNA gene amplicon sequencing

40. Genomic characterization of AML with aberrations of chromosome 7:a multinational cohort of 519 patients

41. Gilteritinib as Post-Transplant Maintenance for Acute Myeloid Leukemia With Internal Tandem Duplication Mutation of FLT3

43. TP53 mutations in myelodysplastic syndromes and secondary AML confer an immunosuppressive phenotype

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