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The bispecific antibody emicizumab bridges factor IXa and factor X, effectively replacing the function of factor VIII in hemophilia A, but measurement of factor VIII activity is inaccurate in the presence of the drug. © 2020 Springer Nature Switzerland AG. All journal articles featured in Hematology vol 25 issue 1. View all articles Latest articles. Hematology Journals of OMICS group are Open Access with high impact factors publishing advanced research and scientific content in Hematological sciences. This is an open-access journal distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in … Journal Citation Reports (Clarivate Analytics, 2020) 5-Year Impact Factor: 10.910 ℹ Five-Year Impact Factor: 2019: 10.910 Our systems will continue to remind you of the original timelines but we intend to be highly flexible at this time. The bispecific antibody emicizumab bridges factor IXa and factor X, effectively replacing the function of factor VIII in hemophilia A, but measurement of factor VIII activity is inaccurate in the presence of the drug. International Scientific Journal & Country Ranking.

The Impact Factor for the American Journal of Hematology has increased to 6.137 for 2018!

To learn about our use of cookies and how you can manage your cookie settings, please see our Register to receive personalised research and resources by emailAssociation between sickle cell disease and dental caries: a systematic review and meta-analysisIdentification of latent core genes and pathways associated with myelodysplastic syndromes based on integrated bioinformatics analysisThe cut-offs for kappa/lambda ratio in bone marrow immunohistochemistry for the diagnosis of multiple myelomaAnalysis of rare thalassemia caused by HS-40 regulatory site deletionClinical analysis and literature review of a case with the myelodysplastic syndrome/myeloproliferative neoplasm with ring sideroblasts and thrombocytosisVulnerability of sickle cell disease persons to the COVID-19 in sub-Saharan AfricaComprehensive screening for coexisting heterozygous αExpression and clinical significance of phospholipase D1 in Prognostic significance of Twist, ZEB1 and Slug in peripheral T-cell lymphomasMyeloproliferative neoplasms treated with hydroxyurea, pegylated interferon alpha-2A or ruxolitinib: clinicohematologic responses, quality-of-life changes and safety in the real-world settingThe diagnostic and prognostic value of MRI in central nervous system involvement of acute myeloid leukemia: a retrospective cohort of 84 patientsThe effect of rat nerve growth factor combined with vitamin B on peripheral neuropathy in multiple myeloma patientsAssociation between hospital admissions and healthcare provider communication for individuals with sickle cell diseaseThe prognostic impact of abnormally expressed, long noncoding RNAs in acute myeloid leukemia: a meta-analysisMutational landscape of patients with acute myeloid leukemia or myelodysplastic syndromes in the context of RUNX1 mutationA multicentre retrospective study of primary breast diffuse large B-cell and high-grade B-cell lymphoma treatment strategies and survivalFish consumption and risk of non-Hodgkin lymphoma: A meta-analysis of observational studiesIncreased circulating basic fibroblast growth factor levels in acute myeloid leukemia: a meta-analysisImpact of anemia on the outcomes of chronic phase chronic myeloid leukemia in TKI eraCytogenetic abnormalities in patients with newly diagnosed multiple myeloma as a secondary primary malignancy: a retrospective studyDisappearance of monosomy 7 in a patient with aplastic anemia after eltrombopag treatmentIdentification of potential miRNA–mRNA interaction network in bone marrow T cells of acquired aplastic anemiaLncRNA SNHG4 regulates miR-10a/PTEN to inhibit the proliferation of acute myeloid leukemia cellsUp to half of patients diagnosed with chronic lymphocytic leukemia in México may not require treatmentEconomic burden of hemophilia A and B: a case in IranCongenital fibrinogen disorder caused by digenic mutations of the The association between antinuclear antibody and response to rituximab treatment in adult patients with primary immune thrombocytopeniaPre-transplant sTIM-3 levels may have a predictive impact on transplant outcome in acute leukemia patientsExpression of serum BMP6 and hepcidin in cancer-related anemiaEffects of ibrutinib on in vitro platelet aggregation in blood samples from healthy donors and donors with platelet dysfunctionWT1 overexpression predicted good outcomes in adult B-cell acute lymphoblastic leukemia patients receiving chemotherapyThe safety of modern intravenous iron infusions in patients with rheumatoid arthritis – a review of the literaturePhysical exercise is safe and feasible in thrombocytopenic patients with hematologic malignancies: a narrative reviewStudents’ knowledge on sickle cell disease in Kisangani, Democratic Republic of the CongoThe relationship between interferon-gamma (INF-γ) single nucleotide polymorphism +874(T/A) and occurrence risk of aplastic anemia: a meta-analysisClinical features and prognosis of normal karyotype acute myeloid leukemia pediatric patients with WT1 mutations: an analysis based on TCGA databaseThe target hemoglobin content values of reticulocytes for efficient anemia improvement are achieved by low ferritin levels and moderate transferrin saturation: a retrospective observational studyDirect oral anticoagulants for thromboprophylaxis in ambulatory patients with cancerDistribution of sickle cell disease and assessment of risk factors based on transcranial Doppler values in the Gulf regionInvestigation on glucocorticoid receptors within platelets from adult patients with immune thrombocytopeniaDonor CMV-specific cytotoxic T lymphocytes successfully treated drug-resistant cytomegalovirus encephalitis after allogeneic hematopoietic stem cell transplantationEpidemiology of aplastic anemia: a study of 1324 casesAnemia in centenarians: prevalence and association with kidney functionPharmacokinetics and pharmacodynamics of a recombinant fusion protein linking activated coagulation factor VII with human albumin (rVIIa-FP) in patients with congenital FVII deficiencyT-lymphocyte subsets and Th1/Th2 cytokines in convalescent patients with Epstein–Barr virus-associated aplastic anemiaEffect of iron chelation therapy on EPO-STAT5 signalling pathway and EPO resistance in iron-overloaded low-risk myelodysplastic syndrome patients

This official journal of the Japanese Society of Hematology covers all aspects of the field of hematology, namely, erythrocytes, leukocytes and hematopoiesis, hemostasis, thrombosis and vascular biology, hematological malignancies, transplantation, and cell therapy.The journal provides the best of up-to-date information on modern hematology, presenting readers with high-impact, original work focusing on pivotal issues.The Japanese Society of Hematology was founded in 1937.

Make the best use of Researched information from 700+ peer reviewed, Meet Inspiring Speakers and Experts at our 3000+ Global Hematology deals with the processes and production of blood cells and various components of blood like hemoglobin, blood proteins, and blood clotting mechanism. The Journal Impact Quartile of Haematologica is Q1. Please do let us know if you need additional time.

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