International Journal of Laboratory Hematology

Papers
(The median citation count of International Journal of Laboratory Hematology is 0. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-05-01 to 2025-05-01.)
ArticleCitations
T‐lymphoblastic leukaemia/lymphoma with Burkitt‐like morphology70
International society for laboratory hematology: Focus on education53
Marked polytypic proliferation of immunoblasts, plasmacytoid lymphocytes, and plasma cells in bronchoalveolar lavage fluid in SARS‐CoV‐2 infection44
Alpha Thalassemia Screening in Multiethnic Population in Northern Europe Using Hb Bart's Immunochromatographic Test44
Plasma cell leukemia mimicking erstwhile hairy cell leukemia variant: A case with an intriguing immunophenotype42
Erythroblasts, really?38
Detection of normal B cell precursors in lymph nodes samples38
A case of azathioprine‐induced aplastic anemia36
Early prediction of neutrophil engraftment using manual leukocyte differential count after cord blood transplantation35
Detection of Southern Asian Ovalocytosis with Sysmex XN‐10: A complement to the decision tree previously described29
Applying index of circulating anticoagulant to mixing tests with lupus anticoagulant screen and confirm reagents can distinguish with high specificity between lupus anticoagulants and direct factor Xa28
Reference interval of antithrombin, protein C, and protein S activities in healthy adults in Iran, the effect of age, sex, oral contraceptive intake, and menopause28
The effect of oscillation depolymerization on ethylenediaminetetraacetic acid‐dependent platelet aggregation samples: A cross‐over study28
HDAC3 single‐nucleotide polymorphism rs2530223 is associated with increased susceptibility and severity of primary immune thrombocytopenia27
Verification of a new semi‐automated Von Willebrand factor multimers assay26
Utility of Thromboelastography and velocity curve derivative in diagnosing COVID‐19 associated coagulopathy24
Lineage switch from acute myeloid leukemia with KMT2A‐PTD to mixed phenotype acute leukemia with t(v;11q23)19
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Evaluation of an integrated activated partial thromboplastin time (Cephen LS/Cephen) for the detection of lupus anticoagulant17
Validation of a novel algorithm with a high specificity in ruling out MDS17
Circulating Hodgkin cells: Extending the spectrum of atypical lymphocytes16
Peripheral granular lymphocytopenia and dysmorphic leukocytosis as simple prognostic markers in COVID‐1916
Brief communication: Heparin‐calibrated chromogenic anti‐Xa assay for the detection of threshold‐levels of direct oral anticoagulants16
Invariant finding of non‐clonal bone marrow lymphocytosis, with increased B cell component, in indolent systemic mastocytosis15
Analytical Validation of the High Concentrated Thrombin Time‐To‐Reptilase Time Ratio: A Proposed Assay for Monitoring Unfractionated Heparin in Patients With Low Fibrinogen Levels14
An Unusual Presentation of EATL13
Anaemia can be improved by controlling the disease activity of Takayasu's arteritis without iron administration13
Clinical and genetic characterization of a protein S deficient patient with multiple thrombotic events13
Acute myeloid leukaemia (AML) with KMT2A rearrangement presented with haemophagocytic lymphohistiocytosis (HLH)13
Frozen/Thawed Samples Can Replace Fresh Samples for Assignment of ISI to Secondary Thromboplastin Standards for Multiple Reagent/Instrument Combinations: Data to Support Possible Revision o13
DOAC‐Remove to counteract the interference of anti‐Xa oral anticoagulants on the monitoring of heparin12
Various approaches for accessing the influence of human leukocyte antigens disparity in haploidentical stem cell transplantation12
Effect of DOAC‐Remove on coagulation screening assays in samples from patients receiving oral or parenteral anticoagulation12
Biologic characterization of atypical chronic lymphocytic leukaemia12
Pediatric reference intervals for hematology parameters in healthy infants and young children in Iran12
Inactive T‐cell prolymphocytic leukemia with negative surface CD3: Cytogenetic pitfalls11
Discordant high‐grade B‐cell lymphoma with MYC and BCL6 rearrangements presenting as a pericardial effusion11
Plasmablastic lymphoma with aberrant expression of CD3 and CD411
Investigation of mutations in Fanconi anemia genes and malignancy predisposition in Brazilian patients11
Testing for rare types of Hereditary Hemochromatosis. A genetic study of two Italian families affected by early onset iron overload11
Abstracts11
Aberrant IKZF1 gene as relapse predictor in standard‐risk pediatric patients with B‐cell precursor acute lymphoblastic leukaemia11
Cover Image10
Clinicopathologic features of relapsed CD19(−) B‐ALL in CD19‐targeted immunotherapy: Biological insights into relapse and LILRB1 as a novel B‐cell marker fo10
Recurrent RARG trinary fusion and ligand binding domain truncation in variant acute promyelocytic leukemia resistant to retinoic acid but sensitive to homoharringtonine‐based therapy10
Predictive model of the efficiency of hematopoietic stem cell collection in patients with multiple myeloma and lymphoma based on multiple peripheral blood markers10
Issue Information10
Rare inherited coagulation and fibrinolytic defects that challenge diagnostic laboratories10
Reference intervals for reticulocyte count and derived reticulocyte parameters in a cohort of healthy adults10
The ratio of bone marrow myeloid progenitor cell proportion to mature lymphocytes proportion can effectively differentiate aplastic anemia and hypoplastic myelodysplastic syndrome and evaluate the qua10
Challenging gold standard hematology diagnostics through the introduction of whole genome sequencing and artificial intelligence10
Alectinib‐induced red cell morphological changes in a patient with underlying α‐thalassaemia trait9
Report of the International Council for Standardization in Haematology working group for standardization of reticulocyte parameters9
Cell Population Data Parameters in Dengue—Is There Any Significance? A Single‐Center Study9
Relapsed B‐cell prolymphocytic leukemia (B‐PLL) with distinctive granular inclusion bodies9
Detection of dysplasia in peripheral blood: Proposal of an algorithm to detect myelodysplastic syndromes and chronic myelomonocytic leukemias on a high‐speed technical platform using the Sysmex X9
Supplement Article9
A novel KMT2A::DCP1B rearrangement in chronic neutrophilic leukemia9
Effect of direct thrombin inhibitors on laboratory measurement of fibrinogen: Potential for errors in clinical decision‐making9
Leukocyte deep learning classification assessment using Shapley additive explanations algorithm9
Reference Intervals and Comparative Analysis of Reticulocyte Counts Using the Mindray BC‐6200, Flow Cytometry, and Manual Microscopy9
T cell lymphoblastic lymphoma with uncommon CD20 expression8
The PNH French Working Group Experience: Building a Strong Network of Cytometrists8
Disseminated Intravascular Coagulation in Pediatric Acute Leukemia: Prevalence, Laboratory Features, and Prognostic Significance of ISTH Score8
Prognostic Evaluation of Hemoglobin, Albumin, Lymphocyte, and Platelet (HALP) Score and Hematological Indices in Classic Hodgkin Lymphoma8
Heinz bodies in COVID‐198
Issue Information ‐ TOC8
Issue Information ‐ TOC8
Evaluation of the Sysmex DI‐60 digital morphology analyzer on Wright‐stained samples with a focus on prevalence‐dependent quality indicators8
The Utility of Total Thrombus‐Formation Analysis System (T‐TAS) in the Thrombosis and Hemostasis Field: A Scoping Review8
A novel TNFRSF13B frameshift variant in one family with lymphoid neoplasms8
lnc‐AC145676.2.1‐6‐3 plays an important role in intestinal acute graft‐versus‐host disease through the regulation of interleukin‐1β8
Characteristics of leukemia blasts to differentiate from mature cells by optical diffraction tomography8
Efficiency of lyophilized hemolysate control material in proficiency testing program for G6PD deficiency screening in Thailand8
Atypical presentation of thiamine‐responsive megaloblastic anemia in a Chinese baby boy8
Change in platelet indices in patients with Coronavirus disease‐2019 (COVID‐19): A reflection of platelet activation and contribution to immunothrombosis?8
Issue Information8
Establishing reference intervals for extended red blood cell parameters with the Mindray BC6800Plus hematology analyzer in a Chinese population8
Stability and comparison of complete blood count parameters between capillary and venous blood samples8
Necrotizing herpes simplex lymphadenitis in a patient with chronic lymphocytic leukaemia/small lymphocytic lymphoma, clinically masquerading as Richter transformation8
Digital image analysis of erythroblastic islands in myelodysplastic syndromes7
Monitoring of heparin therapy beyond the anti‐Xa activity assay: Evaluation of a thrombin generation assay7
Comparison of flow cytometry and next‐generation sequencing in minimal residual disease monitoring of acute myeloid leukemia: One institute’s practical clinical experience7
Hypo‐osmolality and its effect on erythrocyte parameters7
Hb Bart's immunochromatographic test result and Hb F level in normal cord blood and in selected haemoglobinopathy cases7
Prekallikrein deficiency due to homozygous KLKB1(+) mutation c.444_445insT (p.Ser151PhefsTer34)7
Analysis of laboratory blood parameter results for patients diagnosed with COVID‐19, from all ethnic group populations: A single centre study7
Implementation of the new EUR IVD regulation and relation with ISO15189 accreditation: Guidance is urgently required for haemostasis testing7
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Preface7
Next Generation Sequencing Identifies Subgroups of Patients With Triple Negative Primary Thrombocytosis With Different Clinical Thrombotic Outcomes7
Platelet factor 4 triggers thrombo‐inflammation by bridging innate and adaptive immunity7
Modified Giemsa Stain: A solution to improve the quality of hypercellular bone marrow smears7
Performance of direct oral anticoagulant (DOAC) testing by hemostasis laboratories: The Australasian/Asia‐Pacific experience7
Fluorescence‐Based Platelet Count, Blood Smear and Pre‐Analytics Are Decisive in a Case of Fibrin Strand Interference Masking Severe Thrombocytopenia in an ITP Patient6
The utility of hereditary thrombophilia testing among patients with unprovoked venous thromboembolism6
Advantages of patient‐based real‐time quality control applications in modern quality assurance strategies6
A new digital droplet PCR method for looking at epigenetics in diffuse large B‐cell lymphomas: The role of BMI1, EZH2, and USP226
Suffering neutrophils… where is the enemy?6
Early detection of Candida parapsilosis sepsis in peripheral blood as a result of cytografic changes on the Sysmex XN‐3000 hematology analyzer6
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Biological variation of thrombin generation on ST Genesia6
Application of Gene Expression Microarray for the Classification of Ph‐Like B‐Cell Acute Lymphoblastic Leukemia6
Dysfibrinogenemia With the γSer358Cys Variant, Fibrinogen Milano VII, Escapes From the Clauss‐CWA Classification6
Development and Validation of a User‐Friendly Predictive Model Using Demographic and Complete Blood Count Data to Facilitate Early Diagnosis on Suspicion of Myeloproliferative Neoplasms6
Platelet indices and angiogenesis markers in hypertensive disorders of pregnancy6
Issue Information6
Diagnostic utility of the lymphoid screening tube supplemented with TRBC1 for the assessment of T‐cell clonality6
Variability among commercial batches of normal pooled plasma in lupus anticoagulant testing6
Preanalytical Conditions Impact Fibrin Monomers but Not D‐Dimer: A Study With Rigorous Comparisons of a Broad Range of Simulated Conditions6
Editorial 2023 update on the major activities of the International Society for Laboratory Hematology6
Overexpression of lncRNAs HOTAIR and MALAT1 While Downexpression of lncRNA PANDA Predict the Resistance of Diffuse Large B‐Cell Lymphoma to R‐CHOP Chemoimmu6
Th9/IL‐9 may participate in the pathogenesis of multiple myeloma6
The lupus anticoagulant titer is associated with elevated antiphosphatidylserine/prothrombin immunoglobulin‐M isotype antibody levels6
Search for the cause of anaemia and neutropenia in a patient with well‐controlled systemic lupus erythematosus6
Identification of peripheral blood CD26+ leukemic stem cells has a potential role in the rapid diagnosis of chronic myeloid leukemia6
G6PD deficiency in blood donors of Manaus, Amazon Region, northern Brazil5
Variability in combinations of APTT reagent and substrate plasma for a one‐stage clotting assay to measure factor VIII products5
Role of miRNAs in T‐cell activation and Th17/Treg‐cell imbalance in acquired aplastic anemia5
Relapsed Acute Promyelocytic Leukemia With PML: RARA Fusion With Vacuolated Morphology Suggestive of Acute Monocytic/Monoblastic Leukemia5
The role of blood inflammatory markers in the preoperative diagnosis of acute appendicitis5
Additional value of red blood cell parameters in predicting uncommon α‐thalassemia; experience from 10 years of α‐globin gene sequencing and copy number variation analysis5
Interlukin‐27 rs153109 polymorphism confers the susceptibility and prognosis of aplastic anemia in Chinese population5
CD200 Expression by CD4+ T Cells Using Flow Cytometry as a Valuable Marker for Distinguishing Hodgkin Lymphoma From Inflammatory Conditions5
Lupus anticoagulants as a prospective independent predictor in COVID‐19 patients5
Issue Information Covers5
Neutrophil to lymphocyte ratio and systemic immune‐inflammatory index as markers of response to autologous hematopoietic stem cell transplantation in persons with multiple sclerosis5
Issue Information Covers5
Neutrophil Reactivity Intensity and misclassification of immature granulocytes5
Cell population data from Sysmex XN analyzer and myelodysplastic syndrome5
De novo HBB frameshift mutation in a patient with dominant β‐thalassemia major5
Hemophagocytic lymphohistiocytosis‐like presentation of malignant melanoma5
Zopiclone Overdose Is an Important and Under‐Recognized Cause of Drug‐Induced Oxidative Hemolysis: A Case Series Identified by Heinz Body Test Request5
Revealing molecular architecture of FLT3 internal tandem duplication: Development and clinical validation of a web‐based application to generate accurate nomenclature5
Dysplastic eosinophils erroneously counted as neutrophils in the automated analyser5
β‐thalassemia intermedia mimicking β‐thalassemia trait: The importance of family studies and HBB genotyping in phenotypically ambiguous cases5
BCR‐ABL1 p210 screening for chronic myeloid leukemia in patients with peripheral blood cytoses5
The Verifying Accurate Leading‐edge IVCT Development Act: Potential impact on diagnostic testing in the United States5
Quantification of JAK2V617F mutation load by droplet digital PCR can aid in diagnosis of myeloproliferative neoplasms5
Thrombin Generation Assay to Support Hematologists in the Era of New Hemophilia Therapies5
Anti‐factor Xa as the preferred assay to monitor heparin for the treatment of pulmonary embolism4
The combination of emicizumab and recombinant factor VIII in plasma: Which assays can we use for accurate measurement?4
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CD26 expression on circulating CD34+/CD38‐ progenitor population is a specific and reliable tool for the rapid flow cytometric diagnosis of chronic myeloid leukemia—A single‐center validation study4
Value of cerebrospinal fluid white cell count and protein level in predicting leptomeningeal involvement by systemic aggressive B‐cell lymphoma4
FLAER Revealed Normally Expected Non‐PNH FLAER‐Dim Immature Myeloid Cells (CD117+/CD34‐) In Bone Marrow Aspirates and Could Be Utilized as a Marker of Hiera4
Automated Red and White Blood Cell Counting in Capillary Microsamples by Sysmex‐XN Predilution Mode4
Stability of coagulation parameters in plasma samples at room temperature after one freeze/thaw cycle4
Dysregulation of LINC00324 associated with methylation facilitates leukemogenesis in de novo acute myeloid leukemia4
Intracytoplasmic crystalline inclusions in blasts of acute myeloid leukaemia with myelodysplasia‐related changes (AML‐MRC)4
How to assess parallelism in factor assays: coefficient of variation of results with different dilutions or slope ratio?4
Acquired FXI deficiency in a systemic lupus erythematosus patient: Evolution and coagulation phenotypic changed to lupus anticoagulant during immunosuppressive therapy4
Detection of direct oral anticoagulants with the diluted Russel's viper venom time4
Preface4
Changes in peripheral blood in SARS CoV‐2 patients and its clinico‐pathological correlation: A prospective cross‐sectional study4
Hypochromic red blood cells is an independent measure of patient frailty4
Towards Sensitive and Cost‐Effective Chimerism Assays Using FABCASE: A Fast Approach for Estimating Assay Informativity4
ITGAM Upregulation in Acute Myeloid Leukemia Leads to Poor Prognosis Associated With Infiltration of Inhibitory Innate Immune Cells4
Incidence of SARS‐COV‐2 infection in sickle cell patients presenting with a painful crisis: A 12‐month prospective cohort study4
Reference intervals and biological variation in parameters of the thrombin generation test in healthy individuals4
The complicated relationships of heparin‐induced thrombocytopenia and platelet factor 4 antibodies with COVID‐194
Southeast Asian ovalocytosis detected in a critical patient with COVID‐19 pneumonia4
Impact of the 2023 ACR/EULAR Classification Criteria on START2 Antiphospholipid Registry4
Issue Information Covers4
A single‐institution retrospective study of causes of prolonged prothrombin time and activated partial thromboplastin time in the outpatient setting4
Evans syndrome with auto‐immune neutropenia4
Bone marrow necrosis in childhood: The hunt for blasts4
VEXAS syndrome: Vacuoles in myeloid, erythroid, and lymphoid lineages4
Genotype and phenotype characteristics of homozygous and compound heterozygous β‐thalassemia with 3.4 kb deletion4
Performance evaluation of the new platelet measurement channel on the BC‐6800 Plus automated hematology analyzer4
An intriguing case of childhood primary bone marrow histiocytic sarcoma: A diagnostic challenge4
Performance analysis of the compact haematology analyser Sight OLO4
Pitfalls in molecular standardization for detection of FLT3‐ITD in acute myeloid leukemia4
Comparative analysis of automated cell counts in oncological patients: Reliable results of point of care blood impedance measurements and pitfalls in myelodysplastic neoplasias and acute myeloid 3
Molecular characterization and prognosis of mutant TP53 acute myeloid leukemia and myelodysplastic syndrome with excess blasts3
Molecular analysis of severe hemophilia B in Indian families: Identification of mutational hotspot and novel variants3
Significance of WT1 and multiparameter flow cytometry assessment in patients with chronic myelomonocytic leukemia receiving allogeneic hematopoietic stem cell transplantation3
Serious consequences of Epstein‐Barr virus infection: Hemophagocytic lymphohistocytosis3
Detection of unstable haemoglobin variants with Sysmex XN‐103
Interchangeability of multiple Sysmex XN10 and XN20 modules for six types of leukocytes3
Comparative Analysis of the Performance of Automated Digital Cell Morphology Analyzers for Leukocyte Differentiation in Hematologic Malignancies: Mindray MC‐80 Versus West Medical Vision He3
The value of bone marrow examinations performed in the investigation of HIV infected patients with cytopenias3
Mature plasmacytoid dendritic cell proliferation associated with acute myeloid leukemia3
Lymphocytes screening on admission is essential for predicting in‐hospital clinical outcome in COVID‐19 patients: A retrospective cohort study3
Interpretation of clot‐based lupus anticoagulant assays—Normalizing clotting time against different denominators3
Intensive Care Infection Score (ICIS) is an Early Marker for Infection in Time of Admission to Intensive Care Units3
Spurious Lymphocyte Differential Counts: An Unusual Cytomorphometric Interference of Target Cells—A Tale of Two Automated Hematology Analyzers3
Solitary central nervous system relapse in acute promyelocytic leukemia3
Blue‐green cytoplasmic inclusions in neutrophils/monocytes of patients with yellow fever3
Practical application of mathematical calculations and statistical methods for the routine haematology laboratory3
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Whole blood clotting time: Current practices among Thailand National External Quality Assessment Scheme for blood coagulation member laboratories3
A case of a primary myelofibrosis with progression and related literature review of progression phase genetics3
Diagnostic Implications of CD63 and CD64 Expression Levels and FcγRIIIA 158 V/F Gene Polymorphism in Primary Immune Thrombocytopenia Adult Patients3
The new way to identify Leishmania amastigotes in peripheral blood smear using digital cell morphology instrument3
Isolated erythrocytosis: A consequence of COVID‐19 induced hypoxia3
Issue Information Covers3
Osmotic gradient ektacytometry: A tool for more than just hereditary haemolytic anaemia3
Plasmablastic lymphoma: An update3
A rare case of bone marrow infiltration by Langerhans cell with bilobed and folded lobulated nuclei3
Is monitoring of antiplatelet therapy by light transmission aggregometry dependent on instrument and reagent used?3
The structural parameters and flags of the Sysmex XN™ analyser: Are they discriminative between reactive and malignant lymphocytosis in the context of lymphocyte counts above 5 × 109/L in a3
Neonatal diagnosis of congenital dyserythropoietic anemia type II3
ADAMTS13 testing update: Focus on laboratory aspects of difficult thrombotic thrombocytopenic purpura diagnoses and effects of new therapies3
Performance comparison of Westergren modified SRS 100/II and alternate iSED® method for erythrocyte sedimentation rate3
Plasma long noncoding RNAs lncDC and THRIL as potential diagnostic markers of adult primary immune thrombocytopenia3
Sex‐associated differences in genomic profile of chronic myelomonocytic leukemia involving differential representation of SRSF2 gene mutation3
Concurrent contracted cells, bite cells, hemighost cells, ghost cells, doughnut cells, and Heinz body in a 16 months‐old boy3
Clinicopathologic and Molecular Characterization of NUP98‐Rearranged Acute Leukemias3
Immune reconstitution in children after haploidentical haematopoietic stem cell transplantation3
Exploiting adaptive immune receptor recombination read recoveries from exome files to identify subsets of ALL and to establish TCR features that correlate with better outcomes3
Italian Cytometry Society (GIC) endorsement of consensus recommendations for measurable residual disease in chronic lymphocytic leukemia3
Arterial blood as an alternative specimen source for complete blood cell count: More human studies are needed3
Molecular diagnosis of hereditary hemolytic anemias: Recent updates3
Issue Information ‐ TOC3
Diagnosing heparin‐induced thrombocytopenia: The need for accuracy and speed3
Effects of CD34+ cell dose on haematopoietic recovery in acute lymphoblastic leukaemia patients with positive pretransplant measurable residual disease3
Immature platelet fraction as a systemic inflammation marker in patients with chronic obstructive pulmonary disease3
Concurrent carcinocythemia, pleural and pericardial involvement in metastatic clear cell sarcoma3
An automated method for thrombocyte counting in capillary microsamples3
Issue Information ‐ TOC3
The role of cystatin C in multiple myeloma3
Discordance in the morphologic diagnosis of lymphocytes in HTLV‐1‐infected individuals3
Thrombin generation assay in platelet‐poor plasma in children with iron deficiency anemia3
Evaluation of measurable residual disease in multiple myeloma by multiparametric flow cytometry: Current paradigm, guidelines, and future applications3
Automated measurement of coagulation and fibrinolytic activation markers: Outcomes in coronavirus disease 2019 (COVID‐19) patients3
Diagnosis of disseminated Talaromycesmarneffei infection by examination of a peripheral blood smear3
Thrombolysis in the recovery of coagulated bone marrow aspirate samples3
Issue Information ‐ TOC3
The dose–response of direct oral anticoagulants is non‐linear at plasma levels below 100 ng/ml2
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Minimizing cost associated with management of heparin‐induced thrombocytopenia: A cost analysis of various laboratory testing models2
The effect of haemoglobin, albumin, lymphocyte and platelet score on the prognosis in patients with multiple myeloma2
An observation of a potential metastatic mimic in bone marrow aspirate smears2
A comparative evaluation of three consecutive artificial intelligence algorithms released by Techcyte for identification of blasts and white blood cells in abnormal peripheral blood films2
Potential modifications of the PLASMIC scoring system for predicting thrombotic thrombocytopenic purpura: Sometimes, less is more2
Differential diagnosis of lymphocytosis in routine laboratory practice: Contribution of lymphocyte parameters using the Sysmex‐XN9000 haematology analyzer2
The activated partial thromboplastin time‐clot waveform analysis in hemophilia: Does it help in differentiation?2
A rare occurrence of haemophilia A in a female due to compound heterozygosity of a de novo missense variant (presenting as pseudohomozygous) in F8 gene with Xq28 deletion inherited from 2
High‐Speed Centrifugation Fails to Mitigate Severe Lipemic Interference in D‐dimer Measurement2
Ectopic band 3 expression as a cause of mature ovarian teratoma‐associated secondary autoimmune hemolytic anemia2
A novel α0‐thalassemia deletion in a Brazilian child with Hb H disease: −−Mococa2
Comment on “Platelet Reactivity to Zika and Dengue Non‐Structural Protein 1 (NS1) Assessed by Flow Cytometry, Atomic Force Microscopy, and Quartz Crystal Microbalance”2
First reported co‐occurrence of “GATA1‐mutated X‐linked thrombocytopenia with thalassemia (XLTT)” with heterozygous β‐thalassemia2
Use of total thrombus‐formation analysis system in detecting acquired platelet function defects: A case report2
Role of Preoperative Inflammatory Blood Cell Indexes as a Postoperative Risk Predictor Among Patients Undergoing On‐Pump Cardiac Surgery2
Plasma levels do not predict thrombin generation in patients taking direct oral anticoagulants2
White blood cells scattergram as a valuable tool for COVID‐19 screening: A multicentric study2
Hematopoietic cells vacuolation, not always a reactive event. The VEXAS syndrome2
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