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SCI Abstract
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RECOMMENDED
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Impact of Prophylactic Antibacterials on Coagulation Profiles and Bleeding in Patients with Acute Myeloid Leukemia/Myelodysplastic Syndrome
Patients with acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) often receive antibacterial prophylaxis. Ant...
Acta Haematologica
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Recapitulated late-onset inflammatory toxicities and progressive dysautonomia with persistence of central memory CD4+ chimeric antigen receptor T cells in a case of transformed follicular lymphoma: case report
CD19-directed chimeric antigen receptor (CAR) T-cell therapy has been widely used and highly effective for B-cell lymphoid...
Acta Haematologica
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Prediction of Splenectomy Outcomes in Relapsed or Refractory Immune Thrombocytopenia
A recent publication by Kwag et al suggests that first line response to intravenous immunoglobulins in patients with immun...
Acta Haematologica
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Multicentric Castleman disease and concurrent hematological disorders: the occurrence of plasmacytoma and the hypotheses arising from literature’s review
The concomitant presence of Castleman disease with other hematological pathology is an event described in the literature w...
Acta Haematologica
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An Analysis of Dasatinib Treatment Patterns in Patients with Chronic Myeloid Leukemia After Experiencing Pleural Effusion During Dasatinib Therapy
Introduction: Treatment with dasatinib for chronic myeloid leukemia (CML) has been associated with development of pleural ...
Acta Haematologica
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Real-world experience of PD-1 inhibitors for relapsed and refractory Hodgkin lymphoma: A multicenter retrospective analysis of patients in China
Introduction: Despite the promising clinical trial data regarding programmed death 1 (PD-1) inhibitors in relapsed/ refrac...
Acta Haematologica
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CCL3 as possible negative prognostic factor in chronic lymphocytic leukemia.
Introduction: Both microenvironmental signals from surrounding cells and changes in the genome of leukemic cells play esse...
Acta Haematologica
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“The long journey of unexplained erythrocytosis”. Erythrocytosis due to high oxygen affinity hemoglobinopathy - hemoglobin variant Little Rock (HBB: c.432C>A) - A report of a Swiss Family and review of the literature
The differential diagnosis of erythrocytosis is complex, involving a tailored algorithm. Congenital causes are rare and su...
Acta Haematologica
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Waldenström macroglobulinemia and non-IgM-type lymphoplasmacytic lymphoma are genetically similar
Introduction Waldenström macroglobulinemia (WM) represents a subset of lymphoplasmacytic lymphoma (LPL) with the imm...
Acta Haematologica
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The role of follicular regulatory T cells/follicular helper T cells in primary immune thrombocytopenia
Introduction Immune thrombocytopenia (ITP) is an autoimmune disease characterized by thrombocytopenia. Herein, we sought t...
Acta Haematologica
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Successful Multidisciplinary Management of Aortic Valve Repair in Severe Hemophilia B with Extended Half-Life Recombinant Factor IX concentrate
Successful management of surgery in severe coagulation disorders depends on adequate replacement of the deficient factors ...
Acta Haematologica
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Description of an institutional cohort of myeloid neoplasms carrying ETV6-locus deletions or ETV6 rearrangements
The gene encoding for transcription factor ETV6 presents recurrent lesions in hematologic neoplasms, most notably the ETV6...
Acta Haematologica
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Patient-reported Outcomes in Young Adults with Myeloproliferative Neoplasms
Introduction Genetic landscape, disease characteristics and clinical outcomes of young adults with myeloproliferative neop...
Acta Haematologica
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Acquired von Willebrand syndrome following a SARS-CoV2 infection
Acquired von Willebrand syndrome is a rare entity with approximately 700 cases described in the literature. Many etiologie...
Acta Haematologica
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Macrocytosis in Mitochondrial DNA Deletion Syndromes
Large single mtDNA (mitochondrial DNA) deletion syndrome is a rare inborn error of metabolism with variable heteroplasmy l...
Acta Haematologica
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Therapeutic Efficacy of Platelet Transfusion And Analysis of Influencing Factors in 364 Patients
Introduction: In clinical diagnosis and treatment, we found that PLT counts failed to increase significantly or even decre...
Acta Haematologica
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Erdheim-Chester Disease with BRAF V600E Mutation and a Concomitant Myeloid Malignancy Sharing NRAS and IDH2 Mutations
Erdheim-Chester disease (ECD) is a rare clonal histiocytic process that is characterized by a foamy (xanthomatous) prolife...
Acta Haematologica
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High Expression of CD300A Predicts Poor Survival in Acute Myeloid Leukemia
Introduction: Recent studies have suggested that CD300A was an oncogene in acute myeloid leukemia (AML) development. Howev...
Acta Haematologica
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A Longitudinal Assessment of the Natural Change in Haemoglobin, Haematocrit and Mean Corpuscular Volume with Age
Introduction: We aim to assess the natural annual trends in the levels of haemoglobin, haematocrit and mean corpuscular vo...
Acta Haematologica
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Once Monthly Elotuzumab and Lenalidomide Plus Dexamethasone for Multiple Myeloma: A Multicenter Observation Study
<b><i>Introduction:</i></b> Elotuzumab and lenalidomide plus dexamethasone (ERd) is a standard sal...
Acta Haematologica
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Gene Variants in Two Families with Inherited Coagulation Factor XI Deficiency and Identification of Mutations
<b><i>Introduction:</i></b> Mutations in the <i>F11</i> gene can cause factor XI (FXI)...
Acta Haematologica
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Disparity analysis of clinical features and prognostic evaluation of hemophagocytic lymphohistiocytosis in pediatric and adult patients: a retrospective multicenter study of 525 cases in HHLWG
Introduction: Hemophagocytic lymphohistiocytosis (HLH) is a rare immune disorder with rapid progression and high mortality...
Acta Haematologica
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On behalf of the SFGM-TC: prophylactic donor lymphocyte infusion in patients treated with allogeneic stem-cell transplantation for high-risk myelodysplastic syndrome and acute myeloid leukemia
Introduction: Allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains the best curative option for high-ris...
Acta Haematologica
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Two novel heterozygous mutations (p.γPhe230Val and p.AαAsn839Thr) cause hereditary hypodysfibrinogenemia in two Chinese independent families
The objective of this study was to explore the molecular defects in two Chinese families with hypodysfibrinogenemia. The c...
Acta Haematologica
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High Incidences of Acute and Chronic Graft-Versus-Host Disease after Hematopoietic Cell Transplants for Acute Myeloid Leukemia Using Thiotepa, Busulfan, and Fludarabine Pretransplant Conditioning
...
Acta Haematologica
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Efficacy and incidence of treatment related adverse events of thrombopoietin receptor agonists in adults with immune thrombocytopenia: a systematic review and network meta-analysis of randomized controlled study
Introduction: To conduct a network meta-analysis to assess the efficacy and incidence of treatment related adverse events ...
Acta Haematologica
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Gene Variants in Two Families with Inherited Coagulation Factor Ⅺ Deficiency and Identification of Mutations
Abstract Introduction: Mutations in the F11 gene can cause factor Ⅺ (FⅪ) deficiency, leading to abnormal coagulation activ...
Acta Haematologica
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The effectiveness of the intermediate and therapeutic doses of enoxaparin in COVID-19 patients: A comparative study of factor Xa inhibition
Background: Management of anticoagulant therapy in COVID-19 patients is a critical role. Low Molecular Weight Heparin (LMW...
Acta Haematologica
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Once monthly elotuzumab, lenalidomide plus dexamethasone for multiple myeloma; a multicenter observation study
Introduction: Elotuzumab, lenalidomide plus dexamethasone (ERd) is a standard salvage chemotherapy for multiple myeloma, a...
Acta Haematologica
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Glomerulonephritis Secondary to Acute Promyelocytic Leukemia that Resolved after Induction Therapy.
The association of glomerulonephritis and malignant hematological disease is uncommon, but well known in chronic leukemias...
Acta Haematologica
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