20 results on '"Loghavi, Sanam"'
Search Results
2. The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms
3. Publisher Correction: Clonal evolution of acute myeloid leukemia revealed by high-throughput single-cell genomics
4. Additional file 1 of Outcomes with sequential FLT3-inhibitor-based therapies in patients with AML
5. Myeloid Neoplasms with Concurrent BCR-ABL1 and CBFB-MYH11 Rearrangements: Clinicopathologic Features and Treatment Implications
6. Distinct Genetic Features of Myelodysplastic Syndromes as Defined in the Revised 2016 World Health Organization Classification
7. Familial Platelet Disorder with Propensity to Myeloid Malignancy (FPDMM) Associated with Germline RUNX1 Mutation Shows Characteristic Morphologic Features
8. Dealing With the Incidental: Experiences Implementing the ACMG Guidelines for Reporting Germline Findings in a Comprehensive Somatic Mutation Assay
9. Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma with Prominent Proliferation Centers in Bone Marrow Is Associated with High Tumor Burden and TP53 Deletion
10. CD5-Negative and CD10-Positive Mantle Cell Lymphoma: A Clinicopathologic Study of 10 Cases
11. Aberrant Cytokeratin Expression in Acute Myeloid Leukemia is Associated with Complex Karyotype and TP53 Alterations
12. CD5 Positive De Novo Diffuse Large B Cell Lymphoma: Clinicopathologic Findings and Correlation With Outcome
13. Differential Proteomic Signatures in Chronic Myelomonocytic Leukemia Subsets Identified by Reverse Phase Protein Array Analysis
14. De Novo Acute Myeloid Leukemia (AML) with RUNX1 Mutations Shows Characteristic Clinicopathologic Features
15. Bone Marrow and Extramedullary Lesions in Patients with Myeloproliferative Neoplasms Exhibit Similar miRNA Profiles
16. Clinicopathologic and Molecular Characteristics of Myeloid Neoplasms with Non-Canonical MPL Mutations
17. Evaluation of Myelodysplastic Features and Correlation With Cytogenetic Findings in Hepatosplenic T-Cell Lymphoma: Analysis of 28 Patients
18. JAK2 p.V617F Mutations Are Common in Chronic Myelomonocytic Leukemia with Fibrosis
19. DDX41 Mutations in Myeloid Neoplasms Are Associated with Male Predominance, TP53 mutation and a High Risk of Progression to AML
20. De Novo Myelodysplastic Syndromes With Fibrosis Exhibit an Increased Frequency of TP53 Mutations and p53 Overexpression
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.