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  1. Pubblicazioni

AMERICAN JOURNAL OF HEMATOLOGY

Rivista
Codice:
E007636
ISSN:
0361-8609
  • Dati Generali

Dati Generali

Pubblicazioni (75)

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5' Nucleotidase in chronic B cell leukemias: a cytochemical and ultrastructural study
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A novel germline JAK2 mutation in familial myeloproliferative neoplasms.
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A novel missense variant in ATP11C is associated with reduced red blood cell phosphatidylserine flippase activity and mild hereditary hemolytic anemia
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Aberrant phenotype of plasmacytoid monocytesin acute myeloid leukemia.
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Aberrant phenotype of plasmocytoid monocytes in acute myeloid leukemia.
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Age and dPCR can predict relapse in CML patients who discontinued imatinib: The ISAV study
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Ataluren-driven restoration of Shwachman-Bodian-Diamond syndrome protein function in Shwachman-Diamond syndrome bone marrow cells
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Autologous stem cell transplantation with in vivo purged progenitor cells shows long-term efficacy in relapsed/refractory follicular lymphoma
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Blast phase of essential thrombocythemia: A single center study.
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CHEK2 Germline Variants in Early-Onset and Familial Myeloproliferative Neoplasms
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Cellular properties of human erythrocytes preserved in saline-adenine-glucose-mannitol in the presence of L-carnitine
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Characteristics and outcome of therapy-related myeloid neoplasms: Report from the Italian network on secondary leukemias.
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Characterization of a Newly Discovered Non-Coding Variant in the EPO Gene Identified in Two Unrelated Italian Pedigrees With Erythrocytosis
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Circulating endothelial cells in COVID-19
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Clinical and molecular characteristics of lymphoplasmacytic lymphoma not associated with an IgM monoclonal protein: A multicentric study of the Rete Ematologica Lombarda (REL) network
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Clinical presentation and management practice of systemic mastocytosis. A survey on 460 Italian patients
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Coexisting Myeloproliferative and Lymphoid Neoplasms: A European Multicenter Retrospective Study
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Common germline variation at the TERT locus contributes to familial clustering of myeloproliferative neoplasms
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Cutaneous involvement by post-polycythemia vera myelofibrosis.
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Cutaneous septic emboli from Candida glabrata in a haematological patient
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Distinct and convergent consequences of splice factor mutations in myelodysplastic syndromes
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Dyspnea secondary to pulmonary hematopoiesis as presenting symptom of myelofibrosis with myeloid metaplasia
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Eltrombopag in preparation for surgery in patients with severe MYH9-related thrombocytopenia
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Essential thrombocythemia and pregnancy: Observations from recent studies and management recommendations.
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Frequent deletions of JARID2 in leukemic transformation of chronic myeloid malignancies.
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Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis
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Good clinical activity and favorable toxicity profile of once weekly bortezomib, fotemustine, and dexamethasone (B-MuD) for the treatment of relapsed multiple myeloma
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Gray platelet syndrome: Novel mutations of the NBEAL2 gene
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High rate of profound clonal and renal responses with daratumumab treatment in heavily pre-treated patients with light chain (AL) amyloidosis and high bone marrow plasma cell infiltrate
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High sensitivity M-protein detection in a case of light-chain cardiac amyloidosis without evidence of plasma cell dyscrasia
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High-dose human immunoglobulins in thrombotic thrombocytopenic purpura
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Identification of genomic aberrations associated with disease transformation by means of high-resolution SNP array analysis in patients with myeloproliferative neoplasm
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Impact of comorbidities and body mass index on the outcomes of allogeneic hematopoietic cell transplantation in myelofibrosis: A study on behalf of the Chronic Malignancies Working Party of EBMT
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Impact of treatment-related liver toxicity on the outcome of HCV-positive non-Hodgkin's lymphomas.
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Iron overload and iron chelation therapy in patients with myelodysplastic syndrome treated by allogeneic stem-cell transplantation: report from the working conference on iron chelation of the Gruppo Italiano Trapianto di Midollo Osseo.
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Karyotype in myelodysplastic syndromes: relations to morphology, clinical evolution and survival
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Looking for familial nodular lymphocyte-predominant Hodgkin lymphoma
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MASS-FIX may allow identification of patients at risk for light chain amyloidosis before the onset of symptoms
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MYH9-related disease mutations cause abnormal red blood cell morphology through increased myosin-actin binding at the membrane
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Masked polycythemia Vera (mPV): Results of an international study.
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Masked polycythemia vera diagnosed according to WHO and BCSH classification
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Mutational and immunogenetic landscape of HCV-associated B-cell lymphoproliferative disorders
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Mutations of RUNX1 in families with inherited thrombocytopenia
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N-terminal fragment of the type-B natriuretic peptide (NT-proBNP) contributes to a simple new frailty score in patients with newly diagnosed multiple myeloma
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Newly identified roles for PIEZO1 mechanosensor in controlling normal megakaryocyte development and in primary myelofibrosis
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Optimal timing of allogeneic hematopoietic stem cell transplantation in patients with myelodysplastic syndrome
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Outcome of patients activating an unrelated donor search for severe acquired aplastic anemia.
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Patterns of presentation and thrombosis outcome in patients with polycythemia vera strictly defined by WHO-criteria and stratified by calendar period of diagnosis
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Pregnancy complications predict thrombotic events in young women with essential thrombocythemia
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Prognostic impact of somatic mutations on time to first treatment: Results of targeted next-generation sequencing in 211 patients with early stage chronic lymphocytic leukemia
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Prognostic relevance of anemia in myelodysplastic syndromes.
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Relative iron deficiency in hereditary spherocytosis.
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Response-adjusted ISS (RaISS) is a simple and reliable prognostic scoring system for predicting progression-free survival in transplanted patients with multiple myeloma.
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Reversal of nephrotic syndrome due to reactive amyloidosis (AA-type) after excision of localized Castleman's disease.
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Sequential next generation sequencing analysis in homogeneously treated low risk NPM1-mutated acute myeloid leukemia with an adverse clinical outcome
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Space anemia unexplained: Red blood cells seem to be space-proof
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Successful bone marrow transplantation in children with severe aplastic anemia using HLA-partially matched family donors
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Successful treatment with Rituximab and Bendamustine in a patient with newly diagnosed Waldenström's Macroglobulinemia complicated by Bing-Neel syndrome
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Survival in young patients with intermediate-/high-risk myelofibrosis: Estimates derived from databases for non transplant patients
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The 2024 Three-Strata Baseline Anemia Definition of the Revised IWG-ELN Criteria Dissects Survival in Ruxolitinib-Treated Myelofibrosis Patients
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The effect of arterial hypertension on thrombosis in low-risk polycythemia vera.
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The relevance of transfusion-dependency in the prognostic assessment of patients with myeloid neoplasms
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The spleen of patients with myelofibrosis harbors defective mesenchymal stromal cells
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The use of anthracycline at first-line compared to alkylating agents or nucleoside analogs improves the outcome of salvage treatments after relapse in follicular lymphoma The REFOLL study by the Fondazione Italiana Linfomi.
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The utility of MASS-FIX to detect and monitor monoclonal proteins in the clinic
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Thrombotic thrombocytopenic purpura and relapses: why do case series differ? The Italian Cooperative Group for TTP
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Total Metabolic Tumor Volume Is a Strong Independent Prognostic Factor in Follicular Lymphomas: Results From a Sub-Study of the FOLL12 Trial
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Transfusion-dependency at presentation and its acquisition in the first year of diagnosis are both equally detrimental for survival in primary myelofibrosis--prognostic relevance is independent of IPSS or karyotype.
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Treatment options in skeletal localizations of hairy cell leukemia: A systematic review on the role of radiation therapy
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Type 1 versus Type 2 calreticulin mutations in essential thrombocythemia: A collaborative study of 1027 patients
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Ultrasound-guided fine needle biopsy of the spleen: high clinical efficacy and low risk in a multicenter Italian study
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Unlocking Sanctuary Sites: The Efficacy of Brexucabtagene Autoleucel in Ocular B-ALL Relapse
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Unraveling the genetic underpinnings of myeloproliferative neoplasms and understanding their effect on disease course and response to therapy: proceedings from the 6th International Post-ASH Symposium.
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Validation of the new comprehensive cytogenetic scoring system (NCCSS) on 630 consecutive de novo MDS patients from a single institution.
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Younger patients with Waldenström Macroglobulinemia exhibit low risk profile and excellent outcomes in the era of immunotherapy and targeted therapies
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No Results Found
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