50 results on '"Magrini, Umberto"'
Search Results
2. Primary myelofibrosis: Older age and high JAK2V617F allele burden are associated with elevated plasma high-sensitivity C-reactive protein levels and a phenotype of progressive disease
3. Spleen endothelial cells from patients with myelofibrosis harbor the JAK2V617F mutation
4. Clonal Megakaryocyte Dysplasia with Isolated Thrombocytosis Is a Distinct Myeloproliferative Neoplasm Phenotype.
5. Clonal Megakaryocyte Dysplasia with Normal Blood Values Is a Distinct Myeloproliferative Neoplasm.
6. Nijmegen Breakage Syndrome-associated T-cell-rich B-cell Lymphoma: Case Report
7. Unique vascular tumor primary arising in the liver and exhibiting histopathological features consistent with so-called polymorphous hemangioendothelioma
8. Aberrant phenotype of plasmacytoid monocytes in acute myeloid leukemia
9. Bone marrow microvessel density in chronic myeloproliferative disorders: a study of 115 patients with clinicopathological and molecular correlations
10. Dyspnea Secondary to Pulmonary Hematopoiesis as Presenting Symptom of Myelofibrosis With Myeloid Metaplasia
11. EBV Positive Primary Cutaneous CD30+ Large T-Cell Lymphoma in a Heart Transplanted Patient: Case Report
12. Incidence of novel N-glycosylation sites in the B-cell receptor of lymphomas associated with immunodeficiency
13. Splenic and Nodal marginal zone lymphomas are indolent disorders at high hipatitis C virus seroprevalence with distinct presenting features but similar Morphologic and Phenotypic profiles
14. MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness
15. Molecular histogenesis of posttransplantation lymphoproliferative disorders
16. Genetics, clinical and pathological features of glomerulonephrites associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)
17. A low serum β2-microglobulin level despite bulky tumor is a characteristic feature of primary mediastinal (thymic) large B-cell lymphoma: implications for serologic staging
18. Deregulated Genes in Hematopoietic Stem Cells Isolated from Spleen of Patients with Myelofibrosis
19. Increased plasma nicotinamide phosphoribosyltransferase is associated with a hyperproliferative phenotype and restrains disease progression in MPN-associated myelofibrosis.
20. V617FJAK2-Positive Endothelial Cells Are Present in Bone Marrow Neovessels of Patients with Myelofibrosis and Could Derive from the Transdifferentiation of Mutated Hematopoietic Cells
21. Somatic and Germ-Line Molecular Characteristics Of Prefibrotic Myelofibrosis
22. Alteration of Liver Enzymes Is a Feature of the Myh9-Related Disease Syndrome.
23. Evidence that Prefibrotic Myelofibrosis Is Aligned along a Clinical and Biological Continuum Featuring Primary Myelofibrosis.
24. High Frequency of Endothelial Colony Forming Cells Marks a Non-Active Myeloproliferative Neoplasm with High Risk of Splanchnic Vein Thrombosis.
25. Clinical, radiological, and biochemical features of a bilateral buttock amyloidoma emerging after 27 years of hemodialysis.
26. B-cell Posttransplant Lymphoproliferative Disorders in Heart and/or Lungs Recipients: Clinical and Molecular-Histogenetic Study of 17 Cases from a Single Institution.
27. research paper Incidence of novel N-glycosylation sites in the B-cell receptor of lymphomas associated with immunodeficiency.
28. Prefibrotic Myelofibrosis (PreMF) Belongs to a Continuum of Epidemiological, Clinical and Histological Characteristics Featuring Primary Myelofibrosis (PMF)
29. Does auto-immunity contribute to anemia in myeloproliferative neoplasms (MPN)-associated myelofibrosis?
30. Primary gastric CD30 (Ki-1)-positive large cell non-Hodgkin's lymphomas. A clinicopathologic analysis of six cases.
31. An atypical myeloproliferative disorder with high thrombotic risk and slow disease progression.
32. Red cell aplasia in myelofibrosis with myeloid metaplasia. A distinct functional and clinical entity.
33. An Enzyme-Histochemical Approach to the Study of the Human Bone-Marrow Stroma.
34. Bone marrow and blood involvement by non-Hodgkin's lymphoma: A study of clinicopathologic correlations and prognostic significance in relationship to the Working Formulation.
35. Pulmonary Arteriovenous Fistulas.
36. Nodular Lymphocyte Predominance Hodgkin's Disease: Long-Term Observation Reveals a Continuous Pattern of Recurrence.
37. Incidence and Clinical Profile of JAK2 V617F Mutation in Myelofibrosis with Myeloid Metaplasia.
38. Angiosarcoma of the heart: Report of a case in a 9-year-old boy.
39. Aberrant phenotype of plasmacytoid monocytesin acute myeloid leukemia.
40. The Role of Human Herpesvirus 8 and Epstein-Barr Virus in the Pathogenesis of Giant Lymph Node Hyperplasia (Castleman's Disease).
41. Ploidy and proliferative activity measurement by flow cytometry in non-hodgkin's lymphomas. Do speculative aspects prevail over clinical ones?
42. ALK Expression Defines a Distinct Group of T/Null Lymphomas (“ALK Lymphomas”) with a Wide Morphological Spectrum
43. Thrombocytopenia, Giant Platelets, and Leukocyte Inclusion Bodies (May-Hegglin Anomaly): Clinical and Laboratory Findings
44. CONGENITAL HEPATIC FIBROSIS
45. Clinical relevance of bone marrow fibrosis and CD34-positive cell clusters in primary myelodysplastic syndromes.
46. Spleen neoangiogenesis in patients with myelofibrosis with myeloid metaplasia.
47. Effects of the R216Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesis.
48. Eber- and LMP-1-expressing pulmonary lymphoepithelioma-like carcinoma in a Caucasian patient.
49. Marginal zone-related neoplasms of splenic and nodal origin.
50. Primary cutaneous large B-cell lymphoma of the leg: histogenetic analysis of a controversial clinicopathologic entity.
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