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LEUKEMIA

Rivista
Codice:
E101085
ISSN:
0887-6924
  • Dati Generali

Dati Generali

Pubblicazioni (121)

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A different schedule of zoledronic acid can reduce the risk of the osteonecrosis of the jaw in patients with multiple myeloma.
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A low thymic function is associated with leukemia relapse in children given T-cell-depleted HLA-haploidentical stem cell transplantation.
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A novel t(Y;11) translocation with MLL gene rearrangement in a case of acute myelomonocytic leukemia (AML-M4)
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A prospective study of 338 patients with polycythemia vera: the impact of JAK2 (V617F) allele burden and leukocytosis on fibrotic or leukemic disease transformation and vascular complications.
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A revised international prognostic score system for Waldenstrom's macroglobulinemia
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ACUTE MYELOID LEUKEMIA (AML) HAVING EVOLVED FROM ESSENTIAL THROMBOCYTHEMIA (ET): DISTINCTIVE CHROMOSOME ABNORMALITIES IN PATIENTS TREATED WITH PIPOBROMAN OR HYDROXYUREA
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Aberrant somatic hypermutation in primary mediastinal large B-cell lymphoma.
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Absence of IL-12Rβ2 in CD33(+)CD38(+) pediatric acute myeloid leukemia cells favours progression in NOD/SCID/IL2RγC-deficient mice.
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Allelic imbalance in CALR somatic mutagenesis
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Applicability of a reproducible flow cytometry scoring system in the diagnosis of refractory cytopenia of childhood.
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Assay to rapidly screen for immunoglobulin light chain glycosylation: a potential path to earlier AL diagnosis for a subset of patients
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Assessment of chimerism in sex-mismatched allogeneic bone marrrow transplants (allo-BMT) by in situ hybridization and cytogenetics. Is host cell percentage predictive of relapse?
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Autologous bone marrow transplantation for acute myeloid leukaemia in children using total body irradiation and melphalan as conditioning regimen
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Biological features of the clone involved in primary amyloidosis (AL).
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Burkitt’s lymphoma/leukemia : a clinico-pathologic study on 24 adult patients.
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Busulfan, cyclophosphamide and melphalan as conditioning regimen for bone marrow transplantation in children with myelodysplastic syndromes
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Busulfan, cyclophosphamide and melphalan as conditioning regimen for bone marrow transplantation in children with myelodysplastic syndromes.
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CALR vs JAK2 vs MPL-mutated or triple-negative myelofibrosis: clinical, cytogenetic and molecular comparisons
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Characterization of children with FLT3-ITD acute myeloid leukemia: a report from the AIEOP AML-2002 study group
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Chronic lymphocytic leukemia with 6q- shows distinct hematological features and intermediate prognosis.
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Clinical and cytologic characteristics of blastic phase in Ph-positive chronic myeloid leukemia treated with alfa-interferon
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Clinical characteristics and factors predicting evolution of asymptomatic IgM monoclonal gammopathies and IgM-related disorders.
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Clinical end points for drug treatment trials in BCR-ABL1-negative classic myeloproliferative neoplasms: consensus statements from European LeukemiaNET (ELN) and Internation Working Group-Myeloproliferative Neoplasms Research and Treatment (IWG-MRT)
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Clinical features of childhood acute myeloid leukaemia with specific gene rearrangements
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Clinical importance of interphase cytogenetics detecting occult chromosome lesions in myelodysplastic syndromes with normal karyotype.
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Clinical, histopathological and molecular characterization of hypoplastic myelodysplastic syndrome
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Co-mutation pattern, clonal hierarchy, and clone size concur to determine disease phenotype of SRSF2 P95-mutated neoplasms
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Consensus guidelines for the conduct and reporting of clinical trials in systemic light-chain amyloidosis
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Correction: Outcomes in first relapsed-refractory younger patients with mantle cell lymphoma: results from the MANTLE-FIRST study (Leukemia, (2021), 35, 3, (787-795), 10.1038/s41375-020-01013-3)
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Correction: “The 5th edition of The World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms” Leukemia. 2022 Jul;36(7):1720–1748 (Leukemia, (2022), 36, 7, (1720-1748), 10.1038/s41375-022-01620-2)
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Cytogenetic and FISH analyses in five patients with hypoplastic bone marrow.
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Deletions of the transcription factor Ikaros in myeloproliferative neoplasms
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Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells.
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Diagnostic approach to the myelodysplastic syndromes.
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Differential clinical effects of different mutation subtypes in CALR-mutant myeloproliferative neoplasms
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Disruption of SF3B1 results in deregulated expression and splicing of key genes and pathways in myelodysplastic syndrome hematopoietic stem and progenitor cells
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Driver mutations' effect in secondary myelofibrosis: an international multicenter study based on 781 patients
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Dysregulation of global microRNA expression in splenic marginal zone lymphoma and influence of chronic hepatitis C virus infection.
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Effects of desferrrioxamine on normal and leukemic human hematopoietic cell growth: in vitro and in vivo studies
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Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance
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Epigenetic heterogeneity affects the risk of relapse in children with t(8;21)RUNX1-RUNX1T1-rearranged AML
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European myeloma network recommendations on diagnosis and management of patients with rare plasma cell dyscrasias
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Factors influencing post-transfusional platelet increment in pediatric patients given hematopoietic stem cell transplantation.
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Flow cytometry evaluation of erythroid and myeloid dysplasia in patients with myelodysplastic syndrome
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Flow cytometry evaluation of erythroid dysplasia in patients with myelodysplastic syndrome.
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Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia.
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Functional and genetic aberrations of in vitro cultured marrow-derived mesenchymal stromal cells of patients with classical Philedelphia-negative myeloproliferative neoplasms
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Gene expression profiling of isolated tumour cells from anaplastic large cell lymphomas: insights into its cellular origin, pathogenesis and relation to Hodgkin lymphoma.
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Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma
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Growth of human hematopoietic colonies from patients with myelodysplastic syndromes in response to recombinant human granulocyte-macrophage colony-stimulating factor.
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Growth of human hemopoietic colonies from patients with myelodysplastic syndromes in response to recombinant human granulocyte-macrophage colony-stimulating factor
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Hematopoietic stem cell transplantation for advanced myelodysplastic syndrome in children: results of the EWOG-MDS 98 study.
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High mortality rate in COVID-19 patients with myeloproliferative neoplasms after abrupt withdrawal of ruxolitinib
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How to manage polycythemia vera
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Idarubicin-containing regimen and G-CSF are capable of recruiting CD34+/DR- cells with high proliferative potential which sustain Ph-negative polyclonal hematopoiesis.
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Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia
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Immunophenotypic, cytogenetic and functional characterization of circulating endothelial cells in myelodysplastic syndromes.
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Impact of pretransplant minimal residual disease after cord blood transplantation for childhood acute lymphoblastic leukemia in remission: an Eurocord, PDWP-EBMT analysis.
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Improvement over time in outcome for children with acute lymphoblastic leukemia in second remission given hematopoietic stem cell transplantation from unrelated donors
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Incidence and prognostic significance of karyotype abnormalities in de novo primari myelodysplastic syndromes: a study on 331 patients from a single institution.
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Incidence and risk factors for bleeding in 1104 patients with essential thrombocythemia or prefibrotic myelofibrosis diagnosed according to the 2008 WHO criteria.
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Infusion of donor-derived peripheral blood leukocytes after transplantation of cord blood progenitor cells can increase the graft-versus-leukemia effect
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Inhibitors of tyrosine phosphorylation induce apoptosis in human leukemic cell lines.
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Interferon-free compared to interferon-based antiviral regimens as first-line therapy for B-cell lymphoproliferative disorders associated with hepatitis C virus infection
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International Myeloma Working Group guidelines for serum-free light chain analysis in multiple myeloma and related disorders
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International Myeloma Working Group guidelines for serum-free light chain analysis in multiple myeloma and related disorders.
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International myeloma working group (IMWG) consensus statement and guidelines regarding the current status of stem cell collection and high-dose therapy for multiple myeloma and the role of plerixafor (AMD 3100).
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Is FISH a relevant prognostic tool in myelodysplastic syndromes with a normal chromosome pattern on conventional cytogenetics? A study on fifty-seven patients
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JAK inhibitor therapy for myelofibrosis: critical assessment of value and limitations.
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JAK2 V617F mutation is a rare event in juvenile myelomonocytic leukemia
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KRAS and CREBBP mutations: A relapse-linked malicious liaison in childhood high hyperdiploid acute lymphoblastic leukemia
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Leukemia risk models in primary myelofibrosis: an International Working Group study.
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Life expectancy and prognostic factors in the classic BCR/ABL-negative myeloproliferative disorders
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Long-term results of the Italian Association of Pediatric Hematology and Oncology (AIEOP) Studies 82, 87, 88, 91 and 95 for childhood acute lymphoblastic leukemia
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Looking for CALR mutations in familial myeloproliferative neoplasms
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Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia
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Melphalan and dexamethasone with or without bortezomib in newly diagnosed AL amyloidosis: a matched case-control study on 174 patients
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Minimal morphological criteria for defining bone marrow dysplasia: a basis for clinical implementation of WHO classification of myelodysplastic syndromes
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Minimal residual disease is an important predictive factor of outcome in children with relapsed 'high-risk' acute lymphoblastic leukemia.
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Molecular profiling of blastic plasmacytoid dendritic cell neoplasm reveals a unique pattern and suggests selective sensitivity to NF-kB pathway inhibition
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Monoclonal gammopathy of undetermined significance (MGUS) and smoldering (asymptomatic) multiple myeloma: IMWG consensus perspectives risk factors for progression and guidelines for monitoring and management.
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Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR.
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Multilineage dysplasia without increased blasts identifies a poor prognosis subset of myelodysplastic syndromes.
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Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia
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Mutations and prognosis in primary myelofibrosis
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New drugs and novel mechanisms of action in multiple myeloma in 2013: a report from the International Myeloma Working Group (IMWG)
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Osteoprotegerin serum levels in multiple myeloma and MGUS patients compared with age- and sex-matched healthy controls
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Outcomes in first relapsed-refractory younger patients with mantle cell lymphoma: results from the MANTLE-FIRST study
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PRV-1 and its correlation with treatments and disease status in 210 patients with polycythemia vera and essential thrombocythemia
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Platelet count predicts driver mutations’ co-occurrence in low JAK2 mutated essential thrombocythemia and myelofibrosis
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Prediction of thrombosis in post-polycythemia vera and post-essential thrombocythemia myelofibrosis: a study on 1258 patients
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Proposed criteria for the diagnosis of post-polycythemia vera and post-essential thrombocythemia myelofibrosis: a consensus statement from the international working group for myelofibrosis research and treatment
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Rationale, application and clinical qualification for NT-proBNP as a surrogate end point in pivotal clinical trials in patients with AL amyloidosis
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Recombinant gamma-interferon induces in vitro monocytic differentiation of blast cells from patients with acute nonlymphocytic leukemia and myelodysplastic syndromes.
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Recommendations for the management of COVID-19 in patients with haematological malignancies or haematopoietic cell transplantation, from the 2021 European Conference on Infections in Leukaemia (ECIL 9)
Recensione
Redirecting proteoxicity
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Retrospective comparison of qualitative and quantitative reverse transcriptase polymerase chain reaction in diagnosing and monitoring the ALL1-AF4 fusion transcript in patients with acute lymphoblastic leukaemia
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Revisiting guidelines for integration of flow cytometry results in the WHO classification of myelodysplastic syndromes-proposal from the International/European LeukemiaNet Working Group for Flow Cytometry in MDS.
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Ruxolitinib and survival improvement in patients with myelofibrosis
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Second cancer in Philadelphia negative myeloproliferative neoplasms (MPN-K). A nested case-control study.
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Sirolimus-based graft-versus-host disease prophylaxis promotes the in vivo expansion of regulatory T cells and permits peripheral blood stem cell transplantation from haploidentical donors
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Splenectomy for patients with myelofibrosis with myeloid metaplasia: pretreatment variables and outcome prediction.
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Standardization of flow cytometry in myelodysplastic syndromes: a report from an international consortium and the European LeukemiaNet Working Group.
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Survival and prognosis among 1545 patients with contemporary polycythemia vera: an international study.
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TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups
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The 'GGCC' haplotype of JAK2 confers susceptibility to JAK2 exon 12 mutation-positive polycythemia vera.
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The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome.
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The krüppel-like factor 2 transcription factor gene is recurrently mutated in splenic marginal zone lymphoma.
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The number of prognostically detrimental mutations and prognosis in primary myelofibrosis: an international study of 797 patients
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The prognostic value of cytogenetics is reinforced by the kind of induction/consolidation therapy in influencing the outcome of acute myeloid leukemia—analysis of 848 patients
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The transporter ABCB7 is a mediator of the phenotype of acquired refractory anemia with ring sideroblasts
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Treatment and Long-term Results in Children with Acute Myeloid Leukaemia (AML) Treated According to the AIEOP AML Protocols
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Tumor necrosis factor alpha down-regulates c-myc mRNA expression and induces in vitro monocytic differentiation in fresh blast cells from patients with acute myeloblastic leukemia.
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Tumor necrosis factor alpha modulates the messenger RNA expression of hematopoietic growth factor genes in fresh blast cells from patients with acute myeloblastic leukemia.
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Unrelated cord blood transplantation for childhood acute myelogenous leukemia: The influence of cytogenetic risk group stratification
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Validation of WHO classification-based Prognostic Scoring System (WPSS) for myelodysplastic syndromes and comparison with the revised International Prognostic Scoring System (IPSS-R). A study of the International Working Group for Prognosis in Myelodysplasia (IWG-PM)
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c-abl function in normal and chronic myelogenous leukemia hematopoiesis: in vitro studies with antisense oligomers.
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for the European Working Group on childhood MDS (EWOG-MDS).The international prognostic scoring system (IPSS) for childhood myelodysplastic syndrome (MDS) and juvenile myelomonocytic leukemia (JMML)
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on behalf of European Working Group of MDS in Childhood (EWOG-MDS). Donor leukocyte infusion after hematopoietic stem cell transplantation in patients with juvenile myelomonocytic leukemia
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on behalf of GITMO. Second allogeneic bone marrow transplantation in acute leukemia: a multicenter study from the Gruppo Italiano Trapianto di Midollo Osseo (GITMO)
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on behalf of the European Working Group of MDS in Childhood (EWOG-MDS). Second allogeneic hematopoietic stem cell transplantation (HSCT) results in outcome similar to that of first HSCT for patients with juvenile myelomonocytic leukemia
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No Results Found
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