Hematology 2025_ Event Postponement
This is to inform that due to some circumstances beyond the organizer control, "2nd Edition of International Summit on Hematology and Blood Disorders" (Hematology 2025) June 05-07, 2025 | Hybrid Event has been postponed. The updated dates and venue will be displayed shortly.
Your registration can be transferred to the next edition, if you have already confirmed your participation at the event.
For further details, please contact us at hematology@magnusconference.com or call + 1 (702) 988 2320.
HYBRID EVENT: You can participate in person at Rome, Italy or Virtually from your home or work.
2nd Edition of International Summit on Hematology and Blood Disorders
June 05-07, 2025
Hematology 2025
Will be updated soon......
Will be updated soon......
Title : Single cell multi-omics in PBMC’s
Peter J Van Der Spek, Erasmus University Medical Center, Netherlands
Diagnostic monitoring of different states of the Immune system can be done by high throughput imaging of cell morphology or single cell molecular profiling. The relative abundances of cell types across donors highlights the heterogeneity of PBMC samples, even among healthy donors [....] » Read More
Title : Myeloid neoplasms and molecular genetic alterations (Germline vs Somatic) that characterize specific entities in pediatric patients
Aida I Richardson, Ann & Robert H. Lurie Children's Hospital of Chicago, United States
Myeloid neoplasms are less common in pediatric patients than in adults. Some entities preferentially occur in childhood, such as juvenile myelomonocytic leukemia (JMML) or certain types of acute myeloid leukemia (AML). AML is the most frequent in childhood from myeloid neoplasms [....] » Read More
Title : Overview of 2021 guidelines on the diagnosis of Von Willebrand Disease (VWD)
Maryam Asif, University of Washington, United States
Von Willebrand Disease (VWD) is one of the most prevalent bleeding disorders in humans, affecting up to 1% of the general population. It arises from qualitative or quantitative abnormalities of the von Willebrand factor (VWF), a crucial glycoprotein involved in hemostasis. Howeve [....] » Read More
Title : Clinical management of sickle cell disease
Lambros K Bourantas, Larnaca General Hospital, Cyprus
A brief background of disease: epidemiology, genetics, pathophysiology, clinical symptoms and complications. How disease is transmitted, changes in haemoglobin structure and function; how that affects patient health and organ function. Chronic and acute pain and how that affects [....] » Read More
Title : Clonal evolution in children with inherited bone marrow failure syndromes
Raykina Elena, Dmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology, Russian Federation
Inherited bone marrow failure syndromes (IBMFS) are a heterogeneous group of disorders with ineffective haematopoiesis due to underlying germline genetic defects and increased risk of developing of myeloid malignancies. Germline defects impair the fitness of hematopoietic stem ce [....] » Read More
Title : Blood transfusion challenges for one stop perioperative clinic care
Hanadi M Aljedani, King Abdullah Medical City, Saudi Arabia
The one-stop perioperative clinic is a relatively new practice that enhances more integrated multidisciplinary approach for management of prospective surgical patients in outpatient settings. The main benefits of one-stop clinic are minimizing inpatient admission period therefore [....] » Read More
Title : Defining the clinical contribution of platelet-derived FXIII-A to regulation of fibrinolysis
Fahad S Alshehri, King Faisal Medical City for Southern Region, Saudi Arabia
Background: Platelets contain an abundance of cellular FXIII-A in their cytoplasm which is released upon stimulation and participates in extracellular cross-linking reactions. As FXIII-A lacks a signal release peptide, the mechanisms involved in its externalisation remain u [....] » Read More
Title : Multiple alloantibodies: The strategy for identifying antibodies and transfusion management
Ahmed Alharbi, King Abdulaziz Medical City, Saudi Arabia
Patients with multiple alloantibodies exhibit wildly different matching patterns and reaction intensities. Thus, alloantibodies need to have their specificity and clinical importance verified. In the presence of multiple antibodies in the patient’s sample, it is necessary t [....] » Read More
Title : Prevalence of thalassemia and hemoglobinopathy in Eastern India a 10-year high-performance liquid chromatography study of 119,336 cases
Santosh Kumar Mondal, Department of Pathology and Laboratory Medicine AIIMS, India
Background: Hereditary hemoglobin (Hb) disorders are the most commonly encountered single gene disorders in India. Proper timely identification of these disorders is of paramount importance to prevent thalassemia major and clinically severe hemoglobinopathy as well as for epidemi [....] » Read More
Title : The important role of hematopoietic stem cell in myelodysplastic syndrome
Ahmad Reza Rahnemoon, Iran University of Medical Sciences, Iran (Islamic Republic of)
Hematopoietic stem cells (HSCs) are multi-potent stem cells that defined by their ability to selfrenewal, clifferentiation and maintenance of all blood cell types in the hematological system during the entire lifetime of the organism. In fact, in stem cell niche unit, we have two [....] » Read More
Title : Chitosan/gallic acid-grafted-alginate based hydrogel for the controlled release of platelet derived exosomes in cutaneous wound healing
Shaban Alizadeh, Tehran University of Medical Sciences, Iran (Islamic Republic of)
The intricate process of full-thickness skin regeneration is susceptible to oxidative stress, bacterial infection, excessive swelling, poor blood flow, to name a few. One suitable candidate for dressing materials to enhance the wound healing process is hydrogel, which is characte [....] » Read More
Title : Immune system exhaustion and immune evasion mechanisms in leukemic cells: A focus on key signaling pathways
Saeid Taghiloo, Mazandaran University of Medical Sciences, Iran (Islamic Republic of)
The immune system plays a vital role in recognizing and eliminating malignant cells, including those in leukemia. However, leukemic cells develop various mechanisms to evade immune detection and induce immune exhaustion, promoting disease progression. Understanding these mechanis [....] » Read More
Title : Age-dependent trends in the expression of major haemoglobin types among infants of African descent in the first twenty-four months of life
Zaccheaus Awortu Jeremiah, Rivers State University, Nigeria
Haemoglobin is the principal protein in red blood cells and is responsible for delivering oxygen from the lungs to other body parts. Understanding the haemoglobin type profile of infants and the patterns of expression in the first twenty-four months of life is a significant area [....] » Read More
Title : Four principles of hemodynamic monitoring: Early, optimal, combined, and sequential
Wang Hui, China-Japan Friendship Hospital, China
In recent years, hemodynamic monitoring technology has developedfromincoherentto continuous, from noninvasive to invasive, and then back to minimally invasive, fromsimplearterial blood pressure monitoring to accurate monitoring of cardiac output (CO), extravascularlung water (EVL [....] » Read More
Title : Clinical case of thrombotic thrombocytopenia purpura
Nguyen Dang Duc, Bach Mai Hospital, Vietnam
Thrombotic thrombocytopenic purpura (TTP) is one of the rare autoimmune diseases, with an incidence of about 3 per million each year [1]. Symptoms of the disease are quite different, it can be purpura from mild to severe level, with classic symptoms are intravascular hemolytic an [....] » Read More
Title : Repurposing of atovaqoune for treatment of FLT3-ITD quizartinib sensitive and resistant acute myeloid leukemia
Fatma Rabia, University of Liverpool, United Kingdom
FLT3-ITD is the most common mutation in acute myeloid leukemia (AML). Despite the clinical availability of some targeted agents against AML, including a recently approved FLT3 inhibitor, quizartinib, the poor survival rate and drug resistance remain a problem. Here, we explore th [....] » Read More
Title : Hemophagocitic lymphocitosis, first presentation of hodgin lympoma - Case report and literature review
Marsela Shani, Mother Teresa University Hospital Center, Albania
Hemophagocytic lymphohistiocytosis (HLH) is described as a hyperferritinemic? ? hyperin-inflammatory syndrome, in the pathogenesis of which ,an important role is played by the uncontrolled activation of cells with an important role in the body's immune mechanisms, such as mac [....] » Read More
Title : ABO, RH, and Kell blood group antigens frequencies among Saudi population in Qurayyat City, Saudi Arabia
Shahad Naif Hussain ALanazi, Al Jouf University, Saudi Arabia
Background: Understanding the distribution of blood group antigens is crucial for optimizing transfusion practices and managing hemolytic disorders. This study aims to analyze the frequencies of ABO, Rh, and Kell blood group antigens in the Saudi population of Qurayyat city, Saud [....] » Read More