24 results on '"Martini, Maurizio"'
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2. Thrombocythemia and polycythemia in patients younger than 20 years at diagnosis: clinical and biologic features, treatment, and long-term outcome
3. Endothelial progenitor cells are clonal and exhibit the JAK2V617F mutation in a subset of thrombotic patients with Ph-negative myeloproliferative neoplasms
4. Genotyping of Classical Hodgkin Lymphoma on the Liquid Biopsy
5. Prognostic Role of the CD68+ Cell Count and Early Response Evaluation with Interim-PET and Levels of Plasma Thymus and Activation-Regulated Chemokine (TARC) in ABVD-Treated Classical Hodgkin Lymphoma
6. Primary Trombocythemia in Children and Adolescents Includes Different Subtypes Compared to Adult Essential Thrombocythemia
7. Abnormal Mirna Expression Profile and Cytokine Production in Myelodysplastic Vascular Niche
8. CALR mutations in patients with essential thrombocythemia diagnosed in childhood and adolescence
9. EBV-DNA In Peripheral Blood Of Patients With Diffuse Large B Cell Lymphoma: Associations With Patient Characteristics and Outcome
10. Defective WNT Signaling and Genetic Profile Of Endothelial Cells In Patients With Low Risk Myelodysplastic Syndromes Suggest a Contribution Of Vascular Niches To Myelodysplasia
11. The Contact with MDS Endothelial Cells Alters the Pattern of Lineage-Specific Gene Expression During Normal Hematopoietic Differentiation
12. Quantitation of EBV-DNA In Peripheral Blood In Hodgkin Lymphoma: Associations with Other Biomarkers and Patient Characteristics
13. Molecular History of Richter Syndrome: Origin From a Common Ancestor Cell Already Present at Chronic Lymphocytic Leukemia Diagnosis
14. Hereditary Thrombocythemia: Clinical Characteristics, Biological Markers and Long-Term Follow-up in 4 Families Observed in a Single Hematologic Pediatric Center
15. Usage of IGHV4-39 with Stereotypic B Cell Receptor Is An Independent Risk Factor of Chronic Lymphocytic Leukemia Transformation to Richter Syndrome
16. The revised WHO diagnostic criteria for Ph-negative myeloproliferative diseases are not appropriate for the diagnostic screening of childhood polycythemia vera and essential thrombocythemia
17. Different STAT-3 and STAT-5 phosphorylation discriminates among Ph-negative chronic myeloproliferative diseases and is independent of the V617F JAK-2 mutation
18. Combined Muliparameter Approach to the Diagnosis of Polycythemia Vera and Essential Thrombocythemia.
19. Polymorphism in Cytokine Genes as Prognostic Marker in Hodgkin’s Lymphoma.
20. The PRV-1 gene expression in essential thrombocythemia
21. Expression of p15ink4b gene during megakaryocytic differentiation of normal and myelodysplastic hematopoietic progenitors
22. Endothelial progenitor cells are clonal and exhibit the JAK2V617Fmutation in a subset of thrombotic patients with Ph-negative myeloproliferative neoplasms
23. CALRmutations in patients with essential thrombocythemia diagnosed in childhood and adolescence
24. Expression of p15ink4bgene during megakaryocytic differentiation of normal and myelodysplastic hematopoietic progenitors
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