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  1. Pubblicazioni

BLOOD

Rivista
Codice:
E023052
ISSN:
0006-4971
  • Dati Generali

Dati Generali

Pubblicazioni (429)

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3D-Model of Thrombopoiesis
Contributo in Atti di convegno
A Caenorhabditis elegans-based assay recognizes immunoglobulin light chains causing heart amyloidosis
Articolo
A European collaborative study of cyclophosphamide, bortezomib, and dexamethasone in upfront treatment of systemic AL amyloidosis
Articolo
A European collaborative study of treatment outcomes in 346 patients with cardiac stage III AL amyloidosis.
Articolo
A Functional Interplay Between Pyk2 and Src Family Kinases Links Ca2+ Signaling To Protein Tyrosine Phosphorylation In Thrombin-Stimulated Platelets
Abstract
A HOMOZYGOUS POINT MUTATION IN A LEUCINE-RICH MOTIF OF PLATELET GLYCOPROTEIN-IX ASSOCIATED WITH BERNARD-SOULIER SYNDROME (BSS)
Abstract
A Leu40Pro substitution in the leucine rich motif (LRM) of glycoprotein (GP) IX is responsible for dysfunction of a normally expressed GPIB alpha in Bernard-Soulier syndrome (BSS)
Abstract
A WHO classification-based prognostic scoring system (WPSS) for predicting survival in myelodysplastic syndromes
Abstract
A dynamic prognostic model to predict survival in post-polycythemia vera myelofibrosis
Articolo
A dynamic prognostic model to predict survival in primary myelofibrosis: a study by the IWG-MRT (International Working Group for Myeloproliferative Neoplasms Research and Treatment)
Articolo
A modified high-dose dexamethasone regimen for primary systemic amyloidosis
Abstract
A new role for FcgRIIA in the potentiation of human platelet activation induced by weak stimulation.
Contributo in Atti di convegno
A phase 1/2 study of the oral proteasome inhibitor ixazomib in relapsed or refractory light-chain (AL) amyloidosis
Articolo
A phase 2 trial of pomalidomide and dexamethasone rescue treatment in patients with AL amyloidosis
Articolo
A phase 2 trial of pomalidomide and dexamethasone rescue treatment in patients with AL amyloidosis
Articolo
A practical approach to the diagnosis of systemic amyloidoses
Articolo
A prognostic model for predicting the impact of comorbidities on survival of patients with myelodysplastic syndromes
Abstract
A prognostic model to predict survival in 867 WHO-defined essential thrombocythemia at diagnosis: a study by the IWG-MRT.
Articolo
A proportion of patients with lymphoma may harbor mutations of the perforin gene
Articolo
A prospective phase 2 trial of daratumumab in patients with previously treated systemic light-chain amyloidosis
Articolo
A randomized phase 3 study of lenalidomide versus placebo in RBC transfusion-dependent patients with Low-/Intermediate-1-risk myelodysplastic syndromes with del5q
Articolo
A staging system for renal outcome and early markers of renal response to chemotherapy in AL amyloidosis
Articolo
A translational link between Fe and Epo
Articolo
ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization.
Articolo
ALK+ lymphoma: clinico-pathological findings and outcome.
Articolo
ANKRD26-related thrombocytopenia and myeloid malignancies
Articolo
Aberrant mitochondrial iron distribution and maturation arrest characterize early erythroid precursors in low-risk myelodysplastic syndromes
Articolo
Aberrant somatic hypermutation in tumor cells of nodular-lymphocyte-predominant and classic Hodgkin lymphoma.
Articolo
Abnormal regulation of intracellular Ca2+ in human megakaryocytes contributes to the pathophysiology of CALR-mutant myeloproliferative neoplasms.
Contributo in Atti di convegno
Absent phenotypic expression of X-linked sideroblastic anemia in one of 2 brothers with a novel ALAS2 mutation
Articolo
Acquired copy-neutral loss of heterozygosity of chromosome 1p as a molecular event associated with marrow fibrosis in MPL-mutated myeloproliferative neoplasms
Articolo
Activation of the haemostatic process in patients with unruptured aortic aneurysm before and after surgical repair
Abstract
Acute myeloid leukemia (AML) in the elderly: Aggressive versus non-aggressive therapy. A report of the GIMEMA archive of adult acute leukemia
Abstract
Acute promyelocytic leukemia following a previous malignancy. Report of 51 cases
Abstract
Additional chromosomal abnormalities in Ph positive clone: adverse prognostic influence on frontline imatinib therapy, a GIMEMA WP on CML analysis.
Articolo
Adhesion to fibronectin via α5β1 integrin supports expansion of the megakaryocyte lineage in primary myelofibrosis
Articolo
Adult onset and atypical presentation of hemophagocytic lymphohistiocytosis in siblings carrying PRF1 mutations.
Articolo
Allogeneic hematopoietic stem cell transplantation for MDS and CMML: recommendations from an international expert panel.
Articolo
Allogeneic hematopoietic stem cell transplantation in children and adolescents with recurrent and refractory Hodgkin lymphoma: an analysis of the European Group for Blood and Marrow Transplantation.
Articolo
Allogeneic hematopoietic stem cell transplantation in thalassemia major: results of a reduced-toxicity conditioning regimen based on the use of treosulfan.
Articolo
Alteration of BIRC3 and multiple other NF-κB pathway genes in splenic marginal zone lymphoma
Articolo
Altered gene expression in myeloproliferative disorders correlates with activation of signaling by the V617F mutation of Jak2
Articolo
An international consortium proposal of uniform response criteria for myelodysplastic/myeloproliferative neoplasms (MDS/MPN) in adults.
Articolo
Anagrelide in essential thrombocythemia: A retrospective analysis of 220 patients
Abstract
Analysis of Vlambda-Jlambda expression in plasma cells from primary (AL) amyloidosis and normal bone marrow identifies 3r (lambda III) as a new amyloid-associated germline gene segment
Articolo
Analysis of risk factors influencing outcomes after cord blood transplantation in children with juvenile myelomonocytic leukemia: a EUROCORD, EBMT, EWOG-MDS, CIBMTR study.
Articolo
Anti-CD20 monoclonal antibody for the treatment of severe, immune-mediated, pure red cell aplasia and hemolytic anaemia
Articolo
Anti-leukemia activity of alloreactive NK cells in KIR ligand-mismatched haploidentical HSCT for pediatric patients: evaluation of the functional role of activating KIR and redefinition of inhibitory KIR specificity.
Articolo
Antileukemic activity of shepherdin, a novel targeted inhibitor of the survivin-HSP90 complex.
Articolo
Antilymphocyte globulin, cyclosporin and granulocyte colony-stimulating factor in patients with acquired severe aplastic anemia (SAA): a pilot study of the EBMT-SAA working party
Articolo
Antilymphocyte globulin, cyclosporine, prednisolone, and granulocyte colony-stimulating factor for severe aplastic anemia: an update of the GITMO/EBMT study on 100 patients
Articolo
Apoptosis and cell cycle status of hematopoietic progenitor cells in patients with severe refractory rheumatoid arthritis candidates to autografting
Abstract
Application of a Diagnostic Algorithm for Inherited Thrombocytopenia Patients in the Setting of a Developing Country.
Abstract
Application of a diagnostic algorithm to 50 consecutive patients with inherited thrombocytopenias
Abstract
Arterial thrombosis in Philadelphia-negative myeloproliferative neoplasms predicts second cancer: a case-control study.
Articolo
Assessment of Proliferation Induced in Fibroblasts and Rabbit Corneal Epithelial Cells by a Platelet Lysate Formulation: A Stability Study
Abstract
Atypical features of familial haemophagocytic lymphohistiocytosis
Articolo
Autologous hematopoietic stem cell transplantation for severe/refractory intestinal Behcet disease
Articolo
Autologous transfusion of thrombosol plus low-dose DMSO cryopreserved platelet concentrates (PCs) for severe thrombocytopenia following high-dose chemotherapy (HDC).
Abstract
Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome.
Articolo
Autosomal dominant thrombocytopenia is most frequently a heterozygous Bernard-Soulier syndrome (BSS).
Abstract
B-cell receptors expressed by lymphomas of hepatitis C virus (HCV)-infected patients rarely react with the viral proteins
Articolo
BDR in newly diagnosed patients with WM: Final analysis of a phase 2 study after a minimum follow-up of 6 years
Articolo
Benefits and risks of JAK inhibition
Articolo
Biologic and clinical significance of red cell ferritin.
Articolo
Biologic and clinical significance of somatic mutations of SF3B1 in myeloid and lymphoid neoplasms
Articolo
Bone marrow stroma CD40 expression correlates with inflammatory mast cell infiltration and disease progression in splenic marginal zone lymphoma.
Articolo
Bone marrow transplantation (BMT) in Europe for primary immunodeficiencies other than severe combined immunodeficieny: a report from the European Group for BMT and the European Group for Immunodeficiency
Articolo
Bridging to transplant with azacitidine in juvenile myelomonocytic leukemia: A retrospective analysis of the EWOG-MDS study group
Articolo
CALR exon 9 mutations are somatically acquired events in familial cases of essential thrombocythemia or primary myelofibrosis
Articolo
CBFA2T3-GLIS2 fusion transcript is a novel common feature in pediatric, cytogenetically normal AML, not restricted to FAB M7 subtype.
Articolo
CD38 expression distinguishies two groups of B cell chronic lymphocytic leukemias with different response to anti IgM antibodies and propensity to apoptosis;
Articolo
Childhood high-risk acute lymphoblastic leukemia in first remission: Results after chemotherapy or transplant from the AIEOP ALL 2000 study
Articolo
Chronic graft-versus-host disease in children: incidence, risk factors and impact on outcome.
Articolo
Chronic myeloid leukemia: a prospective comparison of interphase fluorescence in situ hybridization and chromosome banding analysis for the definition of complete cytogenetic response: a study of the GIMEMA CML WP.
Articolo
Chronic myelomonocytic leukemia in childhood: a retrospective analysis of 110 cases
Articolo
Circulating amyloidogenic free light chains and serum N-terminal natriuretic peptide type B decrease simultaneously in association with improvement of survival in AL amyloidosis
Articolo
Circulating endothelial progenitor cells are increased in patients with myelofibrosis and do not harbor V617FJAK-2 or W515L MPL mutations.
Abstract
Circulating endothelial progenitor cells in patients with myelofibrosis with myeloid metaplasia.
Abstract
Clinical and biological implications of driver mutations in myelodysplastic syndromes
Articolo
Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: A cohort study of 67 patients.
Articolo
Clinical classification of myelofibrosis with myeloid metaplasia (MMM): Cluster analysis of 861 patients enrolled into a nationwide prospective registry (RIMM)
Abstract
Clinical classification of myelofibrosis with myeloid metaplasia (MMM): cluster analysis of 861 patients enrolled into a nationwide prospective registry (RIMM)
Abstract
Clinical effect of driver mutations of JAK2, CALR, or MPL in primary myelofibrosis
Articolo
Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms
Articolo
Clinical significance of somatic mutation in unexplained blood cytopenia
Articolo
Clinicobiological features and outcome of acute promyelocytic leukemia occurring as a second tumor: the GIMEMA experience.
Articolo
Co-transplantation of ex-vivo expanded mesenchymal stem cells accelerates lymphocyte recovery and may reduce the risk of graft failure in haploidentical hematopoietic stem cell transplantation.
Articolo
Comparisons of outcomes of unrelated bone marrow and umbilical cord blood transplants in children with acute leukaemia
Articolo
Congenital erythropoietin-dependent erythrocytosis responsive to theophylline treatment.
Articolo
Cord blood transplantation provides better reconstitution of hematopoietic reservoir as compared to bone marrow transplantation
Articolo
CyBorD: Stellar response rates in AL amyloidosis
Articolo
Cyclosporin A and short-term methotrexate versus cyclosporine A as graft versus host disease prophylaxis in patients with severe aplastic anemia given allogeneic bone marrow transplantation from HLA-identical sibling: results of a GITMO/EBMT randomized trial
Articolo
Cytopenia levels for aiding establishment of the diagnosis of myelodysplastic syndromes.
Articolo
DNA methylation profiling identifies two splenic marginal zone lymphoma subgroups with different clinical and genetic features
Articolo
Dangerous small B-cell clones.
Articolo
Daratumumab Plus CyBorD for Patients With Newly Diagnosed AL Amyloidosis: Safety Run-in Results of ANDROMEDA
Articolo
Defective interaction of mutant calreticulin and SOCE in megakaryocytes from patients with myeloproliferative neoplasms
Articolo
Defective iron supply for erythropoiesis and adequate endogenous erythropoietin production in the anemia associated with systemic-onset juvenile chronic arthritis
Articolo
Definitive radiotherapy for localized follicular lymphoma staged by18F-FDG PET-CT: A collaborative study by ILROG
Articolo
Depletion of alloreactive T cells by a specific anti-interleukin-2 receptor p55 chain immunotoxin does not impair in vitro antileukemia and antiviral activity.
Articolo
Desmopressin and super platelets.
Articolo
Determining the significance of MGUS
Articolo
Development Of 3D Models For Studying Megakaryopoiesis In Vitro
Contributo in Atti di convegno
Development and validation of a prognostic scoring system for patients with chronic myelomonocytic leukemia
Articolo
Development and validation of an International Prognostic Score of thrombosis in WHO-Essential Thrombocythemia (IPSET-thrombosis).
Articolo
Development of an allele-specific minimal residual disease assay for patients with juvenile myelomonocytic leukemia
Articolo
Dexamethasone vs prednisone in induction treatment of pediatric ALL: results of the randomized trial AIEOP-BFM ALL 2000
Articolo
Diagnosis and treatment of primary myelodysplastic syndromes in adults: recommendations from the European LeukemiaNet
Articolo
Diagnosis, risk stratification, and response evaluation in classical myeloproliferative neoplasms
Articolo
Diagnostic and clinical relevance of the number of circulating CD34+ cells in myelofibrosis with myeloid metaplasia.
Articolo
Disease anticipation in familial myeloproliferative neoplasms.
Articolo
Disease characteristics and clinical outcome in young adults with essential thrombocythemia versus early /prefibrotic primary myelofibrosis.
Articolo
Distinct clustering of symptomatic burden among myeloproliferative neoplasm patients: retrospective assessment in 1470 patients
Articolo
Donor-recipient incompatibility at CD31-codon 563 is a major risk factor for acute graft-versus-host disease after allogeneic bone marrow transplantation from an HLA-matched donor.
Abstract
Driver somatic mutations identify distinct disease entities within myeloid neoplasms with myelodysplasia.
Articolo
Dynamic International Prognostic Scoring System (DIPSS) predicts progression to acute myeloid leukemia in primary myelofibrosis.
Articolo
EDA Fibronectin-TLR4 Axis Sustains Megakaryocyte Expansion and Inflammation during Bone Marrow Fibrosis Progression.
Contributo in Atti di convegno
EFFECT OF APROTININ ON PLATELET COMPOSITION AND FUNCTION IN PATIENTS UNDERGOING CARDIAC REINTERVENTION UNDER EXTRACORPOREAL-CIRCULATION (ECC)
Abstract
Early Treatment of Acute Graft versus Host disease With High or Low-dose 6 Methylprednisolone: A multicenter Randomized Trial From the Italian Group for Bone Marrow Transplantation (GITMO)
Articolo
Early progression as a predictor of survival in marginal zone lymphomas: An analysis from the FIL-NF10 study
Articolo
Early spontaneous mobilization of hematopoietic and endothelial progenitor cells after acute myocardial infarction.
Abstract
Effect of acidic and basic isoferritins on in vitro growth of human granulocyte-monocyte progenitors.
Articolo
Effect of nucleated marrow cell dose on relapse and survival in identical twin bone marrow transplants for leukemia
Articolo
Effects of recombinant alpha and gamma interferons on the in vitro growth of circulating hematopoietic progenitor cells (CFU-GEMM, CFU-Mk, BFU-E, and CFU-GM) from patients with myelofibrosis with myeloid metaplasia
Articolo
Efficacy and safety of once-weekly and twice-weekly bortezomib in patients with relapsed systemic AL amyloidosis: results of a phase 1/2 study
Articolo
Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations
Abstract
Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations.
Articolo
Emergence of BCR-ABL-specific cytotoxic T cells in the bone marrow of patients with Ph+ acute lymphoblastic leukemia during long-term Imatinib mesylate treatment.
Articolo
Emergence of antitumor cytolytic T cells is associated with maintenance of hematologic remission in children with acute myeloid leukemia.
Articolo
Endothelial colony-forming cells from patients with chronic myeloproliferative disorders lack the disease-specific molecular clonality marker.
Articolo
Enlightening light chain deposition disease
Articolo
Erratum: A phase 1/2 study of the oral proteasome inhibitor ixazomib in relapsed or refractory AL amyloidosis (Blood (2017)130: 5 (597-605)DOI: 10.1182/blood-2017-03-771220)
Articolo
Erythrocyte Adenylate Kinase Deficiency: First In-Depth Biochemical Characterization of the Y164C Mutant Enzyme Causing Hemolytic Anemia
Contributo in Atti di convegno
Erythroid marrow function in anemic patients.
Articolo
Evaluation of cytokines mobilizing hematopoietic progenitor cells in patients with myelofibrosis with myeloid metaplasia (MMM)
Abstract
Evidence that amyloidogenic light chains undergo antigen-driven selection
Articolo
Ex vivo priming for long-term maintenance of antileukemia human cytotoxic T cells suggests a general procedure for adoptive immunotherapy
Articolo
Expression of cyclic ADP-ribose synthetizing CD38 molecule on human platelet membrane
Articolo
Expression, activation and subcellular localization of the Rap1 GTPase in human cord blood-derived megakaryocytes
Contributo in Atti di convegno
Expression, activation, and subcellular localization of the Rap1, GTPase in human cord blood-derived megakaryocytes
Contributo in Atti di convegno
Expression, activation, and subcellular localization of the Rap1, GTPase in human cord blood-derived megakaryocytes.
Abstract
Extracellular matrix structure and nano-mechanics determine megakaryocyte function
Articolo
Factor V Leiden is associated with premature myocardial infarction
Contributo in Atti di convegno
Factors associated with outcome after cord blood transplantation in children with acute leukemia. Eurocord-Cord Blood Transplant Group.
Articolo
Factors influencing outcome and incidence of long-term complications in children who underwent autologous stem cell transplantation for acute myeloid leukemia in first complete remission
Articolo
Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females.
Articolo
FbsA, a fibrinogen-binding protein from Streptococcus agalactiae, mediates platelet aggregation.
Articolo
Fibronectin Is Dispensable for An Efficient Bone Marrow Thrombopoiesis, but Affects Platelet Size in Mice
Contributo in Atti di convegno
Four new mutations in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causing X-linked sideroblastic anemia: increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis.
Articolo
From Janus kinase 2 to calreticulin: the clinically relevant genomic landscape of myeloproliferative neoplasms
Articolo
Functional Analysis of Two Mutants of Pyrimidine 5’ Nucleotidase Causing Nonspherocytic Hemolytic Anemia
Contributo in Atti di convegno
Functional analysis of pyrimidine 5'-nucleotidase mutants causing nonspherocytic hemolytic anemia
Articolo
Functional specialization of human circulating CD16 and CD1c myeloid dendritic-cell subsets.
Articolo
GIMEMA-AIEOP AIDA protocol for the treatment of newly diagnosed acute promyelocytic leukemia (APL) in children
Articolo
Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype
Articolo
Gene expression profiling of megakaryocytes from human cord blood
Abstract
Gene expression profiling of megakaryocytes from human cord blood.
Contributo in Atti di convegno
Gene mutations and treatment outcome in chronic lymphocytic leukemia: results from the CLL8 trial
Articolo
Genetic evidence for a predominant role of PI3Kbeta catalytic activity in ITAM- and integrin-mediated signaling in platelets.
Articolo
Genome integrity of myeloproliferative neoplasms in chronic phase and during disease progression
Articolo
Genome-wide DNA profiling of marginal zone lymphomas identifies subtype-specific lesions with an impact on the clinical outcome
Articolo
Genotype-phenotype correlation in cases of juvenile myelomonocytic leukemia with clonal RAS mutations.
Articolo
Germline RBBP6 mutations in familial myeloproliferative neoplasms.
Articolo
Graft rejection after unrelated donor hematopoietic stem cell transplantation for thalassemia is associated with nonpermissive HLA-DPB1 disparity in host-versus-graft direction
Articolo
Graft versus host disease prophylaxis with low-dose cyclosporine-A reduces the risk of relapse in children with acute leukemia given HLA-identical sibling bpne marrow transplantation: results of a randomized trial
Articolo
Granulocyte/macrophage-colony-stimulating factor autoantibodies and myeloid cell immune functions in healthy subjects.
Articolo
Growth Differentiation Factor 15 Is a New Biomarker for Survival and Renal Outcomes in Light Chain (AL) Amyloidosis
Articolo
Growth differentiation factor-15 is a new biomarker for survival and renal outcomes in light chain amyloidosis
Articolo
HAP1 loss in L-asparaginase resistance
Articolo
HLA-haploidentical stem cell transplantation after removal of αβ+ T and B cells in children with nonmalignant disorders
Articolo
HSCT corrects primary immunodeficiency and immune dysregulation in patients with POMP-related auto-inflammatory disease
Articolo
Hematopoietic stem cell transplantation (HSCT) in children with juvenile myelomonocytic leukemia (JMML): results of the EWOG-MDS/EBMT trial.
Articolo
Hemophagocytic lymphohistiocytosis due to germline mutations in SH2D1A, the X-linked lymphoproliferative disease gene
Articolo
Hepatitis C virus RNA dynamics during antiretroviral therapy
Articolo
Hepatitis C virus infection in children treated for acute lymhoblastic leukemia
Articolo
Hereditary hyperferritinemia-cataract syndrome: relationship between phenotypes and specific mutations in the iron-responsive element of ferritin light-chain mRNA.
Articolo
Heterogeneous cytogenetic subgroups and outcomes in childhood acute megakaryoblastic leukemia: A retrospective international study
Articolo
Heterozygous Ala156Val Mutation in the GPIb Alpha (Heterozygous Bernard-Soulier Syndrome Type Bolzano) Induces Macrothrombocytopenia by Hampering Proplatelet Formation
Contributo in Atti di convegno
Heterozygous Ala156Val Mutation in the GPIb Alpha (Heterozygous Bernard-Soulier Syndrome Type Bolzano)InducesMacrothrombocytopenia by Hampering Proplatelet Formation.
Abstract
High incidence of symptomatic cytomegalovirus infection in multiple myeloma patients undergoing autologous peripheral blood stm cell transplantation.
Articolo
How I Treat AL Amyloidosis
Articolo
How I treat enteropathy-associated T-cell lymphoma
Articolo
How I treat essential thrombocythemia.
Articolo
How I treat juvenile myelomonocytic leukemia
Articolo
How I treat myelodysplastic syndromes of childhood
Articolo
How I treat polycythemia vera.
Articolo
How I treat relapsed childhood acute lymphoblastic leukemia.
Articolo
Human CD4+CD25+ regulatory T cells selectively express tyrosine hydroxylase and contain endogenous catecholamines subserving an autocrine/paracrine inhibitory functional loop
Articolo
Human cytomegalovirus immediate-early mRNAemia versus pp65 antigenemia for guiding pre-emptive therapy in children and young adults undergoing hematopoietic stem cell transplantation: a prospective, randomized, open-label trial
Articolo
Human cytomegalovirus immediate-early mRNAemia versus pp65 antigenemia for guiding pre-emptive therapy in children and young adults undergoing hematopoietic stem cell transplantation: a prospective, randomized, open-label trial.
Articolo
Human erythrocyte pyruvate kinase:characterization of the recombinant enzyme and a mutant form(R510Q))causing nonspherocytic hemolytic anemia.
Articolo
Human metapneumovirus infection in adult patients after allogenic hemopoietic stem cell transplantion
Abstract
Imatinib for refractory chronic graft-versus-host-disease with fibrotic features.
Articolo
Immunosuppression for acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2).
Articolo
Impact of allele-level HLA matching on outcomes after myeloablative single unit umbilical cord blood transplantation for hematologic malignancy
Articolo
Impact of mutational status on outcomes in myelofibrosis patients treated with ruxolitinib in the COMFORT-II study
Articolo
Impact of ruxolitinib on the natural history of primary myelofibrosis: a comparison of the DIPSS and the COMFORT-2 cohorts
Articolo
Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associations.
Articolo
Impaired thrombin-induced platelet activation and thrombus formation in mice lacking the Ca2+-dependent tyrosine kinase Pyk2
Articolo
Improved outcome in high-risk childhood acute lymphoblastic leukemia defined by prednisone-poor response treated with double Berlin-Frankfurt-Muenster protocol II
Articolo
In contemporary patients with polycythemia vera, rates of thrombosis and risk factors delineate a new clinical epidemiology.
Articolo
In utero transplantation of adult bone marrow decreases perinatal lethality and rescues the bone phenotype in the knock-in murine model for classical, dominant osteogenesis imperfecta
Articolo
In vitro and in vivo effect of desmopressin on platelet function
Abstract
Incidence and clinical profile of JAK2 V617F mutation in myelofibrosis with myeloid metaplasia
Abstract
Increased B4GALT1 expression is associated with platelet surface galactosylation and thrombopoietin plasma levels in MPNs
Articolo
Increased circulating hematopoietic and endothelial progenitor cells in the early phase of acute myocardial infarction.
Articolo
Increased risk of pregnancy complications in patients with essential thrombocythemia carrying the JAK2 (617V>F) mutation
Articolo
Induction of alloantigen-specific anergy does not impair cytolytic activity of leukemia-reactive human T cells
Abstract
Induction of p53 and up-regulation of the p53 pathway in the human 5q- syndrome.
Articolo
Induction therapy with idarubicin alone significantly influences event-free survival duration in patients with newly diagnosed hypergranular acute promyelocytic leukemia: final results of the GIMEMA randomized study LAP 0389 with 7 years of minimal follow-up
Articolo
Infusion of autologous Epstein-Barr (EBV)-specific cytotoxic T cells for prevention of EBV-related lymphoproliferative disorder in solid organ transplant recipients with evidence of active virus replication.
Articolo
Initial bone marrow reticulin fibrosis in polycythemia vera exerts an impact on clinical outcome.
Articolo
Integrating clinical features and genetic lesions in the risk assessment of patients with chronic myelomonocytic leukemia
Articolo
Interferon alpha 2B (IFN2B) in the treatment of Ph1 negative chronic myeloproliferative syndromes with excessive thrombocytosis
Contributo in Atti di convegno
Interferon alpha-2b as therapy for Ph1-positive chronic myelogenous leukemia: a study of 82 patients treated with intermittent or daily administration
Articolo
International prognostic scoring system (IPSS) and other prognostic systems for myelodysplastic syndromes (MDS).
Abstract
International prognostic scoring system and other prognostic systems for myelodysplastic syndromes.
Articolo
International prognostic scoring system for Waldenstrom macroglobulinemia
Articolo
International prognostic scoring system for Waldenstrom macroglobulinemia.
Articolo
Investigating the Molecular Bases of the Phosphoglycerate Kinase Deficiency: Characterization ofG158V, R206P, V266M and D285V Pathological Variants.
Contributo in Atti di convegno
Is thiazole orange fluorescence of human platelets directly related to their age?
Abstract
JAK inhibitors and risk of B-cell lymphomas.
Articolo
JAK2 or CALR mutation status defines subtypes of essential thrombocythemia with substantially different clinical course and outcomes.
Articolo
KIR B haplotype donors confer a reduced risk for relapse after haploidentical transplantation in children with all
Articolo
Killer Ig-like receptor-mediated control of natural killer cell alloreactivity in haploidentical hematopoietic stem cell transplantation.
Articolo
LNK mutations in familial myeloproliferative neoplasms.
Articolo
Late MRD response determines relapse risk overall and in subsets of childhood T-cell ALL: results of the AIEOP-BFM-ALL 2000 study.
Articolo
Long term outcomes of 107 patients with myelofibrosis receiving JAK1/JAK2 inhibitor ruxolitinib: survival advantage in comparison to matched historical controls.
Articolo
Long-term follow-up from a phase 1/2 study of single-agent bortezomib in relapsed systemic AL amyloidosis
Articolo
Loss of non-muscle myosin heavy chain iia function does not restrict megakaryocyte maturation and spontaneous platelet release and likely affects non-cell-autonomous aspects of thrombopoiesis.
Contributo in Atti di convegno
MLL-AF6 fusion oncogene sequesters AF6 into the nucleus to trigger RAS activation in myeloid leukemia
Articolo
MUNC13-4 mutations in patients with hemophagocytic lymphohistiocytosis are scattered over the functional domains of the protein.
Contributo in Atti di convegno
MYD88 (L265P) mutation is an independent risk factor for progression in patients with IgM monoclonal gammopathy of undetermined significance
Articolo
MYD88 L265P in Waldenström macroglobulinemia, immunoglobulin M monoclonal gammopathy, and other B-cell lymphoproliferative disorders using conventional and quantitative allele-specific polymerase chain reaction
Articolo
Management of AL amyloidosis in 2020
Articolo
Management of AL amyloidosis in 2020
Articolo
Management of bleeding in acquired hemophilia A: results from the European Acquired Haemophilia (EACH2) Registry.
Articolo
Manipulations of cellular iron metabolism for modulating normal and malignant cell proliferation: achievements and prospects.
Articolo
Max(a), a new low-frequency platelet-specific antigen localized on glycoprotein IIb, is associated with neonatal alloimmune thrombocytopenia.
Articolo
May-Hegglin anomaly: Clinical and laboratory investigation of 14 cases
Abstract
Megakaryocyte-matrix interaction within bone marrow: new roles for fibronectin and factor XIII-A.
Articolo
Megakaryocytic progenitors can be generated ex vivo and safely administered to autologous peripheral blood progenitor cell transplant recipients
Articolo
Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia
Articolo
Molecular Basis of Hemolytic Anemia: First Biochemical Characterization of Wild-Type and N190S Mutant Human Erythrocyte Pyrimidine 5'-Nucleotidase.
Contributo in Atti di convegno
Molecular Characterization of Three New Mutant Enzymes of Pyrimidine 5-Nucleotidase Causing Hereditary Hemolytic Anemia.
Contributo in Atti di convegno
Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis.
Articolo
Molecular and clinical features of the myeloproliferative neoplasm associated with JAK2 exon 12 mutations.
Articolo
Molecular and clinical presentation of UBA1-mutated myelodysplastic syndromes
Articolo
Molecular histogenesis of posttransplantation lymphoproliferative disorders.
Articolo
Monitoring of minimal residual disease after CHOP and rituximab in previously untreated patients with follicular lymphoma
Articolo
Monoclonal gammopathy of clinical significance: a novel concept with therapeutic implications
Articolo
Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia:An international retrospective study
Articolo
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.
Articolo
Multivariate analysis of eight possible risk factors for acute graft versus host disease in HLA-matched bone marrow transplantation.
Abstract
Mutational landscape of the transcriptome offers putative targets for immunotherapy of myeloproliferative neoplasms.
Articolo
Mutations Identified in Thrombocytopenia THC2 Are Likely to Dysregulate ANKRD26 Expression.
Abstract
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.
Articolo
Mutations in CBL occur frequently in juvenile myelomonocytic leukemia.
Articolo
Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemia
Articolo
Myelodysplastic Syndrome (MDS)-Specific Comorbidity Index for Predicting the Impact of Extra-Hematological Comorbidities on Survival of Patients with MDS
Abstract
NEONATAL ALLOIMMUNE THROMBOCYTOPENIA (NATP) CAUSED BY A NEW LOW-FREQUENCY PLATELET-SPECIFIC ALLOANTIGEN, MAXA, LOCATED ON GPIIB
Abstract
NOTCH1, SF3B1, and TP53 mutations in fludarabine-refractory CLL patients treated with alemtuzumab: results from the CLL2H trial of the GCLLSG
Articolo
Natural history of idiopathic refractory sideroblastic anemia.
Articolo
New Mechanisms of Megakaryocyte-Matrix Interaction within Bone Marrow Environment
Contributo in Atti di convegno
New and old integral proteins of the human erythrocyte membrane
Articolo
New aspects of Filamin A versatility
Articolo
New drug therapy of amyloidoses: resorption of AL-type deposits with 4'-iodo-4'-deoxydoxorubicin.
Articolo
New prognostic scoring system for primary myelofibrosis based on a study of the International Working Group for Myelofibrosis Research and Treatment
Articolo
No difference in outcome between children and adolescents transplanted for acute lymphoblastic leukemia in second remission.
Articolo
Nongenomic effects of 17beta-estradiol in human platelets: potentiation of thrombin-induced aggregation through estrogen receptor beta and Src kinase
Articolo
Nonlymphoplasmacytic lymphomas associated with light-chain amyloidosis
Articolo
Nonpermissive HLA-DPB1 disparity is a significant independent risk factor for mortality after unrelated hematopoietic stem cell transplantation.
Articolo
Normalization of homocysteine plasma levels improves the physiological anticoagulation in patients with thromboembolic diseases
Articolo
Novel drivers and modifiers of MPL-dependent oncogenic transformation identified by deep mutational scanning.
Articolo
Novel variants in GALE cause syndromic macrothrombocytopenia by disrupting glycosylation and thrombopoiesis
Articolo
Nucleophosmin mutations in childhood acute myelogenous leukemia with normal karyotype
Articolo
Oligodeoxynucleotides antisense to c-abl specifically inhibit entry into S phase of CD34-positive hematopoietic cells and their differentation to granulocyte-macrophage progenitors
Articolo
Oligodeoxynucleotides antisense to c-abl specifically inhibit entry into S-phase of CD34+ hematopoietic cells and their differentiation to granulocyte-macrophage progenitors.
Articolo
Oncogene-induced maladaptive activation of trained immunity in the pathogenesis and treatment of Erdheim-Chester disease
Articolo
Only genuine CD4+CD25+ Tregs may be friends or foes
Articolo
Outcome of 69 allogeneic stem cell transplantations for Fanconi anemia using HLA-matched unrelated donors: a study on behalf of the European Group for Blood and Marrow Transplantation
Articolo
Outcome of children with ALL who started a search for matched donor.
Abstract
Outcome of children with acute leukemia given HLA-haploidentical HSCT after αβ T-cell and B-cell depletion
Articolo
Outcome of patients with hemoglobinopathies given either cord blood or bone marrow transplantation from an HLA-identical sibling.
Articolo
PDGFRB disease: right diagnosis to prolong survival
Articolo
PHILADELPHIA-CHROMOSOME (PH-1) POSITIVE ACUTE LYMPHOBLASTIC-LEUKEMIA (ALL) IN ADULT - INTERIM RESULTS OF GIMEMA ALL 0288 PILOT-STUDY
Abstract
PI3Kβ inhibition: All that glitters is not gold
Recensione
Patients with light-chain amyloidosis and low free light-chain burden have distinct clinical features and outcome
Articolo
Phenotypic and functional heterogeneity of human NK cells developing after umbilical cord blood transplantation: a role for human cytomegalovirus?
Articolo
Phosphoglycerate Kinase Deficiency: Characterization of the Wild-Type Enzyme and Three Pathological Variants Generated from C.140T>a, C.491A>T and C.959G>a Mutations
Contributo in Atti di convegno
Phosphorylation of the myosin IIA tailpiece regulates single myosin IIA molecule association with lytic granules to promote NK-cell cytotoxicity.
Articolo
Platelet Derived Growth Factors in a Mucoadhesive Vehicle for Treatment of Patients with Oral Mucositis in Graft Versus Host Disease
Abstract
Platelet amyloid precursor protein is a modulator of venous thromboembolism in mice
Articolo
Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders.
Articolo
Platelet predeposit and transfusion in patients receiving high-dose chemotherapy and autologous transplant for breast cancer
Abstract
Possible Role of Rap1B in the Cross-Talk between Integrins {alpha}2ß1 and {alpha}IIbß3
Contributo in Atti di convegno
Post-transplant emergence and persistence of leukemia-specific CTLp is associated with a lower risk of relapse.
Abstract
Pre-Treatment with Bendamustine Does Not Affect Stem Cell Mobilization in Patients with Indolent Non-Hodgkin Lymphomas: A Multicenter Study on Behalf of the Fondazione Italiana Linfomi
Articolo
Pre-transplant CYA. Preliminary results of a randomized study in pediatric recipients of unrelated-donor BMT.
Abstract
Predictive factors for the outcome of allogeneic transplantation in patients with MDS stratified according to the revised IPSS-R.
Articolo
Presentation and outcome of patients with 2016 WHO diagnosis of prefibrotic and overt primary myelofibrosis
Articolo
Presentation and outcome with second-line treatment in AL amyloidosis previously sensitive to nontransplant therapies
Articolo
Prevalence and clinical significance of the MYD88 (L265P) somatic mutation in Waldenstrom's macroglobulinemia and related lymphoid neoplasms
Articolo
Prevalence, clinical characteristics and prognosis of GATA2-related myelodysplastic syndromes (MDS) in children and adolescents
Articolo
Primary therapy of Waldenstrom macroglobulinemia (WM) with weekly bortezomib, low-dose dexamethasone, and rituximab (BDR): long-term results of a phase 2 study of the European Myeloma Network (EMN).
Articolo
Prognostic impact of c-KIT mutations in core binding factor leukemias: an Italian retrospective study
Articolo
Prognostic impact of t(16;21)(p11;q22) and t(16;21)(q24;q22) in pediatric AML: a retrospective study by the I-BFM Study Group
Articolo
Programmable 3D silk bone marrow niche for platelet generation ex vivo and modeling of megakaryopoiesis pathologies
Articolo
Proposals for revised IWG 2018 hematological response criteria in patients with MDS included in clinical trials.
Articolo
Prospective simultaneous quantification of human cytomegalovirus-specific CD4+ and CD8+ T-cell reconstitution in young recipients of allogeneic hematopoietic stem cell transplantation
Articolo
Protocol II versus protocol III given twice during reinduction therapy in children with medium risk ALL
Articolo
Pyrimidine 5' Nucleotidase Deficiency: Clinical and Molecular Characterization of Two New Italian Patients
Contributo in Atti di convegno
Quantitative PCR of bone marrow BCL2/IgH positive cells at diagnosis predicts treatment response and long-term outcome in follicular non Hodgkin's lymphoma
Articolo
Recombinant human erythropoietin in the anemia associated with multiple myeloma or non-Hodgkin's lymphoma: dose finding and identification of predictors of response.
Articolo
Reconstitution dynamics of plasmacytoid and myeloid dendritic cell precursors after allogeneic myeloablative hematopoietic stem cell transplantation
Articolo
Recurrent ETNK1 mutations in atypical chronic myeloid leukemia
Articolo
Recurrent abnormalities can be used for risk group stratification in pediatric AMKL: A retrospective intergroup study
Articolo
Red blood cell precursor mass as an independent determinant of serum erythropoietin level.
Articolo
Reduced expression of CXCR4 on circulating CD34+ cells is associated with hematopoietic progenitor cells (HPC) mobilization in patients with myelofibrosis with myeloid metaplasia (MMM).
Abstract
Refractory anemia in childhood: a retrospective analysis of 67 patients with particular reference to monosomy 7
Articolo
Regulation of protein kinase C by the platelet P2Y12 receptor.
Contributo in Atti di convegno
Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease
Articolo
Relation between JAK2 (V617F) mutation status, granulocyte activation, and constitutive mobilization of CD34+ cells into peripheral blood in myeloproliferative disorders
Articolo
Relationship between JAK2 V617F Mutation Status, Granulocyte CD177 mRNA Expression and CD177 Soluble Protein Level in Patients with Polycythemia Vera
Contributo in Atti di convegno
Reliable typing of systemic amyloidoses through proteomic analysis of subcutaneous adipose tissue
Articolo
Response criteria for essential thrombocythemia and polycythemia vera: result of a European LeukemiaNet consensus conference.
Articolo
Results and factors influencing outcome after fully haploidentical hematopoietic stem cell transplantation in children with very high-risk acute lymphoblastic leukemia: impact of center size: an analysis on behalf of the Acute Leukemia and Pediatric Disease Working Parties of the European Blood and Marrow Transplant group.
Articolo
Results of the AIEOP AML 2002/01 multicenter prospective trial for the treatment of children with acute myeloid leukemia.
Articolo
Retrospective comparison of bone marrow and granulocyte colony-stimulating factor-mobilized peripheral blood progenitor cells for allogeneic stem cell transplantation using HLA identical sibling donors in myelodysplastic syndromes.
Articolo
Retrospective survival analysis of elderly patients with acute myeloid leukemia (AML) treated with aggressive or non aggressive therapy
Abstract
Revised international prognostic scoring system for myelodysplastic syndromes
Articolo
Revised response criteria for myelofibrosis: International Working Group-Myeloproliferative Neoplasms Research and Treatment (IWG-MRT) and European LeukemiaNet (ELN) consensus report
Articolo
Revised response criteria for polycythemia vera and essential thrombocythemia: an ELN and IWG-MRT consensus project
Articolo
Risk factors for arterial and venous thrombosis in WHO-defined essential thrombocythemia: an international study of 891 patients.
Articolo
Risk of HBV reactivation in patients with B-cell lymphomas receiving obinutuzumab or rituximab immunochemotherapy
Articolo
Risk-adapted treatment of acute promyelocytic leukemia: Results from the international consortium for childhood APL
Articolo
Rituximab for the treatment of refractory autoimmune hemolytic anemia in children
Articolo
Role and regulation of phosphatidylinositol 3-kinase β in platelet integrin α2β1 signaling.
Articolo
Role of Busulfan and Total Body Irradiation on Growth of Prepubertal Children Receiving Bone Marrow Transplantation and Results of Treatment With Recombinant Human Growth Hormone
Articolo
Role of KIR ligand incompatibility in hematopoietic stem cell transplantation using unrelated donors
Articolo
Role of splenectomy in inherited thrombocytopenias.
Articolo
Ruxolitinib for essential thrombocythemia refractory to or intolerant of hydroxyurea: long-term phase 2 study results.
Articolo
SAP controls the cytolytic activity of CD8+ T cells against EBV-infected cells
Articolo
SF3B1 mutation identifies a distinct subset of myelodysplastic syndrome with ring sideroblasts
Articolo
SF3B1-mutant MDS as a distinct disease subtype: A proposal from the International Working Group for the Prognosis of MDS
Articolo
Screening hepcidin for mutations in juvenile hemochromatosis: identification of a new mutation (C70R)
Articolo
Secreted mutant calreticulins as rogue cytokines in myeloproliferative neoplasms
Articolo
Should pregnant women be screened for factor V Leiden? Acost-effectiveness analysis.
Articolo
Significant Activity of Bortezomib-Based Therapy in Patients with Primary Systemic (AL) Amyloidosis
Articolo
Simple, reliable detection of amyloid in fat aspirates using the fluorescent dye FSB: Prospective study in 206 patients
Articolo
Small red blood cells mimicking platelets.
Articolo
Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders
Articolo
Specific targeting of the KRAS mutational landscape in myeloma as a tool to unveil the elicited antitumor activity
Articolo
Spectrum of ASXL1 mutations in primary myelofibrosis: prognostic impact of the ASXL1 p.G646Wfs*12 mutation.
Articolo
Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis
Articolo
Spleen endothelial cells from patients with myelofibrosisharbor the JAK2V617F mutation
Articolo
Splenic marginal zone lymphoma: a prognostic model for clinical use
Articolo
Splenic marginal zone lymphoma: from genetics to management
Articolo
Stem cell transplantation for chronic myeloid leukemia in children.
Articolo
Study of Megakaryopoiesis and Proplatelet Formation In Myeloproliferative Disorders
Contributo in Atti di convegno
Study of prognosis in Waldenström's macroglobulinemia: a proposal for a simple binary classification with clinical and investigational utility
Articolo
Subcutaneous erythropoietin for treatment of refractory anemia in hematologic disorders. Results of a phase I/II clinical trial.
Articolo
Subcutaneous panniculitis-like T-cell lymphoma: definition, classification and prognostic factors. An EORTC Cutaneous Lymphoma Group study of 83 cases.
Articolo
Survival Advantage with KIR Ligand Incompatibility in Hematopoietic Stem Cell Transplantation from Unrelated Donors
Articolo
Survival after T-cell depleted haploidentical stem cell transplantation is improved using the mother as donor
Articolo
Synergistic antiproliferative effect of recombinant interferon-gamma with recombinant interferon-alpha on chronic myelogenous leukemia hematopoietic progenitor cells (CFU-GEMM, CFU-Mk, BFU-E, and CFU-GM).
Articolo
Systemic light chain amyloidosis: an update for treating physicians.
Articolo
T cell epitope encoded by a subset of HLA-DPB1 alleles determines non-permissive mismatches for hematological stem cell transplantation
Articolo
T lymphocytes of recipient origin may contribute to the recovery of specific immune response toward viruses and fungi in children undergoing cord blood transplantation.
Articolo
Thalidomide plus intermediate-dose dexametasone is an effective but toxic treatment for patients with AL (primary) amyloydosis
Articolo
The BRAF V600E mutation in hairy cell leukemia and other mature B-cell neoplasms
Articolo
The Effects of Mitochondrial Ferritin Expression in Normal and Sideroblastic Erythropoiesis
Abstract
The May-Hegglin anomaly gene Myh9 is a negative regulator of platelet biogenesis modulated by the Rho-ROCK pathway
Articolo
The Myeloproliferative Neoplasm Symptom Assessment Form (MPN-SAF): international prospective validation and reliability trial in 402 patients.
Articolo
The amyloidogenic light chain is a stressor that sensitizes plasma cells to proteasome inhibitor toxicity
Articolo
The association of melphalan and high-dose dexamethasone is effective and well tolerated in patients with AL (primary) amyloidosis ineligible for stem cell transplantation
Articolo
The combination of high-sensitivity cardiac troponin T (hs-cTnT) at presentation and changes in N-terminal natriuretic peptide type B (NT-proBNP) after chemotherapy best predicts survival in AL amyloidosis
Articolo
The combination of high-sensitivity cardiac troponin T (hs-cTnT) at presentation and changes in N-terminal natriuretic peptide type B (NT-proBNP) after chemotherapy best predicts survival in AL amyloidosis.
Articolo
The combination of thalidomide and intermediate-dose dexamethasone is an effective but toxic treatment for patients with primary amyloidosis (AL).
Articolo
The effect of transfusion dependency and secondary iron overload on survival of patients with myelodysplastic syndrome
Abstract
The elusive pathogenesis of schnitzler syndrome
Articolo
The genetic basis of myelodysplasia and its clinical relevance
Articolo
The genetics of Richter syndrome reveals disease heterogeneity and predicts survival post-transformation.
Articolo
The genetics of nodal marginal zone lymphoma
Articolo
The graft-versus-leukemia effect using matched unrelated donors is not superior to HLA-identical siblings for hematopoietic stem cell transplantation.
Articolo
The incidence of heparin-induced thrombocytopenia in medical patients treated with low molecular weigh heparin. A prospective cohort study
Articolo
The low-molecular-weight phosphotyrosine phosphatase is a negative regulator of FcgammaRIIA-mediated cell activation
Articolo
The proteasome load vs. capacity balance determines apoptotic sensitivity of multiple myeloma cells to proteasome inhibition
Articolo
The repertoire of λ light chains causing predominant amyloid heart involvement and identification of a preferentially involved germline gene, IGLV1-44
Articolo
The small GTPase Rap1b regulates the cross talk between platelet integrin alpha2beta1 and integrin alphaIIbbeta3
Articolo
The small proteoglycan decorin supports adhesion and activation of human platelets
Articolo
The sumoylation pathway is dysregulated in multiple myeloma and is associated with adverse patient outcome
Articolo
The thrombospondin-1 N700S polymorphism is associated with early myocardial infarction without altering von Willebrand factor multimer size
Articolo
Three cases of hereditary spherocytosis associated with a post-translational defect of band 3 glycosylation
Contributo in Atti di convegno
Three-year efficacy, safety, and survival findings from COMFORT-II, a phase 3 study comparing ruxolitinib with best available therapy for myelofibrosis
Articolo
Thrombopoietin (TPO) levels in inflammatory disorders with or without reactive thrombocytosis.
Abstract
Time-dependent changes in mortality and transformation risk in MDS
Articolo
Tolerance: pregnancy matters
Articolo
Transferrin saturation, plasma iron turnover, and transferrin uptake in normal humans.
Articolo
Translational pathophysiology: a novel molecular mechanism of human disease
Articolo
Treatment of AL amyloidosis with 4'-lodo-4'-deoxydoxorubicin: an update.
Articolo
Treatment of AL amyloidosis with bendamustine: A study of 122 patients
Articolo
Treatment of Ph1 positive chronic myelogenous leukemia with interferon alpha-2b (IFN 2b)
Contributo in Atti di convegno
Treatment of adult acute lymphoblastic leukemia (ALL): long-term follow-up of the GIMEMA ALL 0288 randomized study.
Articolo
Treatment recommendations for patients with Waldenstrom macroglobulinemia (WM) and related disorders: IWWM-7 consensus
Articolo
Treatment recommendations from the Eighth International Workshop on Waldenstrom's Macroglobulinemia
Articolo
Treatment with erythropoietin and G-CSF improves survival in MDS patients with low transfusion need
Abstract
Treatment with oral melphalan plus dexamethasone produces long-term remissions in AL amyloidosis
Articolo
Twenty-one cases of blastic plasmacytoid dendritic cell neoplasm: focus on biallelic locus 9p21.3 deletion.
Articolo
Two main genetic pathways lead to the transformation of chronic lymphocytic leukemia to Richter syndrome
Articolo
Two-hit strategy for treating AL amyloidosis?
Articolo
Unrelated cord blood transplantation for childhood acute myeloid leukemia: a Eurocord group analysis
Articolo
Unrelated donor bone marrow transplantation for thalassemia: the effect of extended haplotypes
Articolo
Upregulation of lysyl oxidase and adhesion to collagen of human megakaryocytes and platelets in primary myelofibrosis
Articolo
Use of a DNAemia cut-off for monitoring human cytomegalovirus infection reduces the number of preemptively treated children and young adults receiving hematopoietic stem-cell transplantation compared with qualitative pp65 antigenemia.
Articolo
Use of recombinant human erythropoietin outside the setting of uremia.
Articolo
Validation of cytogenetic-based risk stratification in primary myelofibrosis.
Articolo
Variations of the perforin gene in patients with autoimmunity/lymphoproliferation and defective fas function
Articolo
WHO classification and WPSS predict posttransplantation outcome in patients with myelodysplastic syndrome: a study from the Gruppo Italiano Trapianto di Midollo Osseo (GITMO)
Articolo
WHO classification and WPSS predict posttransplantation outcome in patients with myelodysplastic syndrome: a study from the Gruppo Italiano Trapianto di Midollo Osseo (GITMO).
Articolo
Weekly and twice-weekly bortezomib in patients with systemic AL-amyloidosis: results of a phase 1 dose-escalation study
Articolo
What is new in diagnosis and management of light chain amyloidosis?
Articolo
Whole-exome sequencing identifies novel MPL and JAK2 mutations in triple-negative myeloproliferative neoplasms.
Articolo
Whole-genome CRISPR screening identifies N-glycosylation as a genetic and therapeutic vulnerability in CALR-mutant MPNs
Articolo
Why the disorder induced by GATA1 Arg216Gln mutation should be called X-linked thrombocytopenia with thalassemia rather than X-linked gray platelet syndrome
Articolo
X-linked thrombocytopenia with thalassemia: Clinical and biological features of a second family
Abstract
miRNA-mRNA integrative analysis in primary myelofibrosis CD34+ cells: role of miR-155/JARID2 axis in abnormal megakaryopoiesis
Articolo
γδ T-cell reconstitution after HLA-haploidentical hematopoietic transplantation depleted of TCR-αβ+/CD19+ lymphocytes
Articolo
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