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Entering a New Era in Protection in Haemophilia A
April 2026
Haemophilia A (HA), defined by factor VIII (FVIII) levels ≤40 IU/dL, is a chronic condition with consequences beyond bleeding…
Read more
2
Mins
18 Sep 2020
European LeukemiaNet 2020 Recommendations for Treating Chronic Myeloid Leukaemia: Implications for Ponatinib
Ponatinib is indicated for the treatment of adults with chronic myeloid leukaemia (CML) who are resistant to dasatinib or nilotinib, are intolerant…
9
Mins
17 Sep 2020
Economic Evaluation of Severe Anaemia
Anaemia is characterised by a decrease in the total amount of red blood cells (RBC) and haemoglobin (Hb) levels, reducing the volume of oxygen transported through the blood…
9
Mins
30 Jul 2020
Doing More for Patients with Immune Thrombocytopenia: Putting New Recommendations into Practice
The American Society of Hematology (ASH) guidelines and the International Consensus Report (ICR) recommendations were first published in 2010 and 2011…
10
Mins
30 Jul 2020
Outcomes for Patients with High-Risk Acute Myeloid Leukaemia: Can We Move from Months to Years?
This symposium focussed on the recognition of, and treatment options for, high-risk AML. Prof Cluzeau considered universal or targeted treatment…
2
Mins
30 Jul 2020
AGILE: Phase III, Double-Blind, Randomised, Placebo-Controlled Study of Ivosidenib in Combination with Azacitidine in Adults with Newly Diagnosed Acute Myeloid Leukaemia and an IDH1 Mutation
Isocitrate dehydrogenase 1 (IDH1) is a metabolic enzyme which catalyses the oxidative decarboxylation of isocitrate to α-ketoglutarate…
3
Mins
30 Jul 2020
Phase Ib/II Study of the IDH1-Mutant Inhibitor Ivosidenib, with the BCL2-Inhibitor Venetoclax +/-Azacitidine in IDH1-Mutated Myeloid Malignancies
Venetoclax is a potent, selective, oral inhibitor of B-cell lymphoma-2. It is approved in the USA in combination with azacitidine, decitabine…
6
Mins
30 Jul 2020
Pregnancy-Related Thromboembolism in Sickle Cell Disease
Haematological disorders are predominant in the tropical and subtropical countries where major problems of sickle-cell disease (SCD) and thalassaemias…
8
Mins
30 Jul 2020
Anticoagulant Management of Deep Vein Thrombosis: Review of Current Approaches
The initial management of deep vein thrombosis is starting to happen in general practice.
6
Mins
30 Jul 2020
Concerns Regarding the Management of β-Thalassaemia Patients in the Era of COVID-19
Many cases of pneumonia clustered in the city of Wuhan, China, were reported in December 2019, and source tracing has showed Huanan Seafood Market, Wuhan, China, as the origin.
8
Mins
30 Jul 2020
Expanding the Role of CAR-T Cell Therapy to Systemic Lupus Erythematosus
Systemic lupus erythematosus (SLE) is a chronic inflammatory autoimmune disorder resulting from autoantibodies produced by B-cell derived plasma cells.
4
Mins
30 Jul 2020
Pancytopenia Secondary to Adult Osteopetrosis
Osteopetrosis (OP) is a rare genetically metabolic bone disorder caused by severe impairment of osteoclast-mediated bone resorption.
5
Mins
30 Jul 2020
Adult-Onset Still’s Disease Complicated with Haemophagocytic Lymphohistiocytosis
Haemophagocytic lymphohistiocytosis (HLH) is a rare but potentially aggressive and life-threatening syndrome of overactive histiocytes and lymphocytes…
6
Mins
23 Jun 2020
The Role of Next-Generation Sequencing and Reduced Time to Diagnosis In Haematological Diseases: Status Quo and Prospective Overview of Promising Molecular Testing Approaches
This review centres on the impact next-generation sequencing (NGS) can have on the current management of haemato-oncological diseases…
10
Mins
13 May 2020
Beyond Clinical Trials in B-Cell Malignancies: What Real-World Experience Tells Us
The Kite, a Gilead company, symposium “Beyond Clinical Trials in B-Cell Malignancies: What Real-World Experience Tells Us” took place as part of the 24th…
10
Mins
13 May 2020
CAR-T: From Bed to Bench and Back Again
The Kite, a Gilead Company, symposium “CAR-T: From bed to bench and back again” took place during the 2019 meeting of the International Conference…
12
Mins
5 May 2020
Antibody Therapies for Patients With Diffuse Large B-cell Lymphoma: What Does the Future Hold?
Prof Sehn opened the symposium with an overview of diffuse large B-cell lymphoma (DLBCL) focussing on key milestones in treatment developments…
11
Mins
28 Apr 2020
Practical Insights into Managing Follicular Lymphoma: What’s Best for Patients?
The first case focussed on a 56-year-old female economist, who presented with abdominal discomfort that led to a CT scan evaluation where lymph node…
9
Mins
24 Jan 2020
Acute Chest Syndrome in Children with Sickle Cell Disease: Current Perspectives
Acute chest syndrome (ACS) is an acute inflammatory lung injury that usually follows the vaso-occlusive crisis (VOC) seen in sickle cell disease (SCD)…
9
Mins
24 Jan 2020
Therapeutic Options in Myelodysplastic Syndromes Following Hypomethylating Agent Failure
Myelodysplastic syndromes (mds) are a heterogeneous group of disorders defined by ineffective haematopoiesis and clonal instability with risk of…
4
Mins
24 Jan 2020
Reed Sternberg-Like Cells in an Aggressive Lymphoma: Report of a Rare Case and Review of Literature
In low-grade B-cell lymphomas, Reed Sternberg (RS)-like cells can be seen in follicular lymphoma, chronic lymphocytic leukemia/small lymphocytic lymphoma, and marginal zone lymphoma.
11
Mins
24 Jan 2020
Pernicious Anaemia: Mechanisms, Diagnosis, and Management
Pernicious anaemia (PA) is an autoimmune disease of multifactorial aetiology involving environmental and immunological factors. It is the most common cause of cobalamin deficiency anaemia worldwide.
6
Mins
24 Jan 2020
‘Girdle Syndrome’ Progressing to Ischaemic Colitis and Acute Intrahepatic Cholestasis in a Patient with Sickle Cell Disease: A Case Report
Acute vaso-occlusive crisis and haemolysis characterise sickle cell disease. Rarely observed, ‘girdle syndrome’ is a situation in which vaso-occlusion…
3
Mins
12 Dec 2019
Anticipate Your Next Move in Chronic Myeloid Leukaemia Patient Management
Treatment decisions in chronic myeloid leukaemia (CML) are complex and require the evaluation of many factors at each stage of therapy…
8
Mins
12 Sep 2019
Variability of Biologics and its Impact on Biosimilar Development
Biologic drugs are transforming treatment of other hard-to-treat diseases beyond cancer, including multiple sclerosis, heart disease, asthma, and…
8
Mins
1 Aug 2019
Rebooting the Myeloma Treatment Programme
Treatment of MM requires a multifaceted approach using a combination of therapies targeting the several pathophysiological pathways involved in the…
3
Mins
1 Aug 2019
Umbilical Cord Blood Donation: An Evolving Lifeline for the Stem Cell Field
Cord blood can be collected and stored from the placenta and umbilical cord following the birth of a new-born. It is replete with haematopoietic stem…
5
Mins
1 Aug 2019
Editor’s Pick: New Insights in β-Thalassaemia
Thalassaemia is a hereditary cause of hypochromic microcytic anaemia resulting from defects in haemoglobin (Hb) production…
6
Mins
1 Aug 2019
Retrospective Review of the Role of Abdominal Imaging in Evaluation of Cytopenias
Specifically, this study examines the use of abdominal imaging, via an ultrasound or CT scan, to identify the aetiology of haematologic abnormalities…
9
Mins
1 Aug 2019
Eltrombopag-Induced Myelofibrosis in Patients with Adult Immune Thrombocytopenia: Scoping Review
Immune thrombocytopenia (ITP) is an autoimmune bleeding disorder that lessens the production of platelets. Despite treatments being available for ITP…
5
Mins
1 Aug 2019
Resistant Bilateral Chylous Effusion as a Late Adverse Effect of Dasatinib Treatment in Chronic Myeloid Leukaemia
Dasatinib is a potent and efficacious second-generation oral tyrosine kinase inhibitor, frequently used for imatinib-resistant or intolerant BCR-ABL+…
5
Mins
1 Aug 2019
Are Successful Pregnancies an Achievable Goal in Patients with Chronic Myeloid Leukaemia?
Currently, there is no evidence-based consensus for the management of CML in pregnancy; therefore, clinical observations have become very important…
8
Mins
1 Aug 2019
A Review of the Different Haematological Parameters and Biomarkers Used for Diagnosis of Neonatal Sepsis
Even though there are recent sophisticated biomarkers to diagnose sepsis, it is still challenging to curtail sepsis mortality by timely intervention…
9
Mins
8 Apr 2019
Expectations and Experience: Optimising Efficacy and Maintaining Quality of Life in Follicular Lymphoma
Prof Salles provided an update on the ongoing first-line follicular lymphoma (FL) studies, demonstrating how analysis of the GALLIUM study data regarding…
10
Mins
13 Dec 2018
Editor’s Pick: Newest Approaches in Immunotherapy for Non-Hodgkin’s Lymphoma
Immunotherapy has revolutionised the treatment of haematologic malignancies. Patients with relapsed/refractory non-Hodgkin’s lymphoma have poor response…
8
Mins
4 Sep 2018
Editor’s Pick: Chimeric Antigen Receptor-Engineered T Cell Therapy in Acute Myeloid Leukaemia
Acute myeloid leukaemia (AML) is a disease with a very poor outcome and remains an area of significant unmet need, necessitating novel therapeutic…
12
Mins
4 Sep 2018
Epstein–Barr Virus: A Biological Overview and Clinicopathological Changes of Two Epstein–Barr Virus-Related Lymphoproliferative Disorders in a World Health Organization (WHO) 2017 Report
Epstein–Barr virus (EBV) is one of the most important viral causes for the development of tumours. The global geographical epidemiology of EBV shows…
10
Mins
4 Sep 2018
A Game of Clones: The Complex Interplay of Aplastic Anaemia, Myelodysplastic Syndrome, and Paroxysmal Nocturnal Haemoglobinuria
Although idiopathic aplastic anaemia (AA), myelodysplastic syndrome (MDS), and paroxysmal nocturnal haemoglobinuria (PNH) are all associated with…
6
Mins
2 Aug 2018
Planning Your Next Move in Philadelphia Chromosome Positive Leukaemias
The meeting was arranged as a series of conversations between experts, following a question and answer format with two speakers in each presentation…
9
Mins
2 Aug 2018
Editor's Pick: Allogeneic Haematopoietic Stem Cell Transplantation for Chronic Myeloid Leukaemia in the Era of Tyrosine Kinase Inhibitors
The introduction of tyrosine kinase inhibitors (TKI) has dramatically improved the prognosis of chronic myeloid leukaemia (CML) patients and, therefore…
10
Mins
2 Aug 2018
Therapeutic Options in Myelodysplastic Syndromes: Established and Emerging Therapies
Although hypomethylating agents (HMA) have revolutionised the treatment of myelodysplastic syndromes (MDS), a significant proportion of patients either…
11
Mins
2 Aug 2018
Making Rituximab Directly Cytotoxic for Substantial Improvement in Therapeutic Efficacy
The humanised anti-CD20 antibody (Ab) rituximab (RTX) has significantly improved the prognosis of B cell non-Hodgkin’s lymphomas (BNHL). However, major…
12
Mins
2 Aug 2018
Staging of Mycosis Fungoides and Sézary Syndrome: Time for an Update?
Mycosis fungoides is the most common variant of cutaneous T cell lymphoma and frequently presents as early-stage disease with skin patches and plaques with an indolent course, but patients experience significant morbidity from itch and disfigurement.
12
Mins
2 Aug 2018
Iron Deficiency Anaemia in Pregnancy: Developed Versus Developing Countries
Anaemia is the most widespread of the haematological disorders, affecting about one-third of the global population. Despite decades of public health…
12
Mins
7 Jun 2018
Multiple Myeloma: Personalised Medicine Based on Pathogenesis
Multiple myeloma is increasingly being recognised as more than one disease, characterised by marked cytogenetic, molecular, and proliferative heterogeneity.
10
Mins
22 Sep 2017
β-Thalassaemias: Highlights from the European Hematology Association Scientific Working Group (EHA-SWG) Scientific Meeting on Anaemias: Diagnosis and Treatment in the Omics Era
β-thalassaemias are inherited blood disorders caused by a defect in the production of β-globin, giving rise to variable phenotypes.
4
Mins
31 Aug 2017
How I Manage Myelofibrosis
Myelofibrosis (MF), either primary or secondary to polycythaemia vera or essential thrombocythaemia, is the most symptomatic and has the worst prognosis…
7
Mins
31 Aug 2017
How I Diagnose Hypereosinophilic Syndromes
Hypereosinophilic syndromes are a group of disorders characterised by significant eosinophilia and organ damage.
9
Mins
31 Aug 2017
Management of Multiply Relapsed Aggressive Non-Hodgkin Lymphoma: New Perspectives
Patients with refractory/relapsed (R/R) non-Hodgkin lymphoma (NHL) make up a very heterogeneous population with a poor life expectancy.
7
Mins
31 Aug 2017
Redefining Later-Line Therapy in Metastatic Colorectal Cancer
The objective of the symposium was to provide an overview of the current treatment landscape in terms of later-line therapy in metastatic CRC (mCRC) and to discuss the evidence for the various options available.
9
Mins
31 Aug 2017
Management of B-Cell Lymphoma: Where Are We Now and Where Are We Going?
The main objectives of the symposium were to explore the current developments in the diagnosis and treatment of non-Hodgkin lymphoma (NHL).
11
Mins
31 Aug 2017
Inherited Bone Failure Syndromes, Focus on the Haematological Manifestations: A Review
The purpose of this review is to provide the haematologist with a working knowledge of the common inherited bone marrow failure syndromes (iBMFS)…
10
Mins
31 Aug 2017
Non-Classic Myeloproliferative Neoplasms: Are We Really Aware of These Rare Diseases in Daily Practice?
Chronic neutrophilic leukaemia (CNL), chronic eosinophilic leukaemia-not otherwise specified (CEL-NOS), and myeloproliferative neoplasm (MPN)…
8
Mins
31 Aug 2017
Novel Immunotherapy Agents for Acute Lymphoblastic Leukaemia
Acute lymphoblastic leukaemia (ALL) in adults has a survival rate of 40–50% at 5 years, with a high relapse rate after first-line chemotherapy.
3
Mins
9 Aug 2017
Spasmodic Dysphonia: What About It?
Spasmodic dysphonia (SD): what about it? That is the million-dollar question.
9
Mins
8 Aug 2017
Improving Treatment Strategies for Patients with Follicular Lymphoma: How to Translate Novel Study Data into Clinical Practice
Ms Rosmarie Pfau detailed the challenges faced by patients with FL around the world, particularly a desire for improved quality of life (QoL) and…
9
Mins
8 Aug 2017
Shifting Treatment Paradigms in Non-Hodgkin Lymphomas
Despite significant therapeutic advances in the treatment of patients with non-Hodgkin lymphoma (NHL), a significant proportion experience relapse or…
9
Mins
8 Aug 2017
Biosimilars for Haematologic Malignancies: The Path to Sustainable Care
The main objectives of this symposium were to review the value of biosimilars in sustainable treatment for haematologic malignancies and to recognise the…
9
Mins
8 Aug 2017
Patients in Focus: What’s Relevant for Chronic Myeloid Leukaemia and Philadelphia Chromosome-Positive Acute Lymphoblastic Leukaemia?
This symposium was dedicated to discussing BCR-ABL-positive chronic myeloid leukaemia (CML) and Philadelphia-positive acute lymphoblastic leukaemia (Ph+ALL)
8
Mins
8 Aug 2017
Editor’s Pick: The Role and Regulation of Quiescence in Acute Lymphoblastic Leukaemia
There are ˜3,000 children, as well an additional ˜7,000 adults, diagnosed with acute lymphoblastic leukaemia (ALL) each year in the USA.
7
Mins
8 Aug 2017
Thrombocytopenia: A Defect in Actin Dynamics?
The actin cytoskeleton plays many important roles in the lifecycle of platelets, from biogenesis from megakaryocytes, to activation and clearance from…
8
Mins
8 Aug 2017
The Role of Allograft in Acute Lymphoblastic Leukaemia, Including Alternate Donors
The management of acute lymphoblastic leukaemia (ALL) remains challenging.
12
Mins
8 Aug 2017
Double-Hit and Triple-Hit Lymphomas: New Perspectives for Their Classification
In 2016, an update on the classification of lymphoid neoplasm was published, and one of the modifications made focussed on B-cell lymphoma…
9
Mins
8 Aug 2017
Management of Adult Patients with Myelodysplastic Syndromes
The myelodysplastic syndromes form a heterogeneous group of clonal disorders with an increasing incidence in the elderly population and an emerging…
7
Mins
8 Aug 2017
Different Therapeutic Interventions and Mechanisms of Action of Antisickling Agents Currently in Use in Sickle Cell Disease Management
Sickle cell disease is a genetic disorder caused by sickle haemoglobin. In many forms of the disease, the red blood cells can change shape upon…
11
Mins
28 Jul 2017
The Pivotal Role of Proteasome Inhibition in Myeloma Treatment
Prof Munshi opened the presentation with a brief video highlighting the interaction of myeloma cells with the bone microenvironment…
11
Mins
1 Jun 2017
Extension of 2016 World Health Organization (WHO) Classification into a New Set of Clinical, Laboratory, Molecular, and Pathological Criteria for the Diagnosis of Myeloproliferative Neoplasms: From Dameshek to Vainchenker, Green, and Kralovics
Improved Clinical, Laboratory, Molecular, and Pathological (CLMP) 2017 criteria for myeloproliferative neoplasms (MPN) define the JAK2V617F trilinear…
7
Mins
2 Mar 2017
Hide and Seek: The Game Between Chronic Lymphocytic Leukaemia Cells and B Cell Receptor Signalling Inhibitors
The emergence of B cell receptor (BCR) kinase inhibitors has recently changed the treatment landscape in chronic lymphocytic leukaemia (CLL). The…
13 Dec 2016
Non-Transfusion-Dependent Thalassaemia: A Panoramic Survey from Pathophysiology to Treatment
Non-transfusion-dependent thalassaemia (NTDT) is a rather broad term that encompasses a group of thalassaemia syndromes, most commonly β-thalassaemia…
8
Mins
28 Jul 2016
Biosimilars: Shaping the Future of Haematology
Prof Robin Foà opened the symposium by highlighting how improving healthcare and an ageing population are increasing the burden on healthcare resources…
9
Mins
28 Jul 2016
Advances in the Treatment of Non-Hodgkin’s Lymphoma: Exploring New Frontiers
A recent symposium at the European Hematology Association (EHA) congress, chaired by Prof Eva Kimby, explored the changing paradigms in the treatment of…
8
Mins
28 Jul 2016
New Insights in Bone Marrow Failure
Several rare haematological diseases are linked to bone marrow failure (BMF). This symposium provided the latest scientific insights into the different…
9
Mins
28 Jul 2016
Navigating the Changing Multiple Myeloma Treatment Landscape
The treatment landscape for patients with multiple myeloma (MM) is constantly evolving. Over the past decade, the introduction of novel agents including…
9
Mins
28 Jul 2016
Editor’s Pick: Minimisation of Bleeding Risks Due to Direct Oral Anticoagulants
Direct oral anticoagulants (DOAC) are used in several indications for the prevention and treatment of thrombotic events. As highlighted by data from…
9
Mins
28 Jul 2016
Bridging to Transplant in Diffuse Large B Cell Lymphoma
Non-Hodgkin lymphoma (NHL) is the eighth most common malignancy worldwide. Diffuse large B cell lymphoma (DLBCL) is the most frequent subtype, accounting…
9
Mins
28 Jul 2016
Thrombocytopenia Caused By Inherited Haematopoietic Transcription Factor Mutation: Clinical Phenotypes and Diagnostic Considerations
Inherited thrombocytopenias comprise a heterogeneous group of blood disorders with abnormalities in genes related to glycoproteins and adhesion molecules…
9
Mins
28 Jul 2016
The Relative Contributions of Germline Variation, Epimutation, and Somatic Mutation to Paediatric Leukaemia Predisposition
The next-generation sequencing era has repeatedly demonstrated that the amount of acquired somatic mutations in paediatric cancers can rarely account for…
16
Mins
28 Jul 2016
Current Management of Adult Acute Lymphoblastic Leukaemia: Emerging Insights and Outstanding Questions
Less than 50% of patients with adult acute lymphoblastic leukaemia (ALL) experience long-term survival and for those adults >60 years old, long-term…
7
Mins
28 Jul 2016
Management of Children With Sickle Cell Disease in Europe: Current Situation and Future Perspectives
Sickle cell disease (SCD) is the most common haemoglobinopathy worldwide and its frequency has steadily increased in Europe in the past decades. SCD is a…
3
Mins
12 Jul 2016
A Call from a Patient to Openly Discuss Body Image in the Treatment of Type 1 Diabetes
Diabetes is a non-communicable disease (NCD) meaning that it often cannot be seen. After 20 years of living with Type 1 diabetes I am lucky to have no…
16 Jun 2016
Advancing Our Clinical Perspectives in Haematology: What Is Your Approach?
The 11th New Horizons in Haematology (NHH11) conference was moderated by Dr Sarah Jarvis, healthcare reporter and television presenter, and was delivered…
30 Jul 2015
Thrombosis in Haematological Disorders: Tailored Management Approaches
The meeting commenced with a talk from Prof Anna Falanga on the management of thrombosis in both onco-haematological and non-oncological diseases.
30 Jul 2015
Why Biosimilars Matter: An Innovative Solution to Improve Patient Access
The meeting was introduced by Prof Robin Foà who spoke about the difficulties for patients Prof Foà opened the symposium by highlighting…
30 Jul 2015
Perspectives on the Treatment of Mantle Cell Lymphoma and Follicular Lymphoma in 2015 and Beyond
Prof Martin Dreyling opened the symposium by providing an overview of the current status of mantle cell lymphoma (MCL) and the current guidelines…
30 Jul 2015
Relapsed/Refractory Multiple Myeloma: The Current State of Play
Multiple myeloma (MM) usually responds to treatment but is incurable. The clinical course is characterised, in most patients, by a series of remissions…
3
Mins
7 May 2015
Subclinical Hypothyroidism and its Impact on Reproductive Health
Subclinical hypothyroidism (SCH) is defined by elevated thyroid-stimulating hormone (TSH) levels in the presence of normal thyroxine (T4) levels.
3
Mins
10 Mar 2015
Below the Belt, Experiences with Prostate Cancer
There is a new guy on the block. A new guy in the guise of a book written by new-age men talking about their very own personal experiences of their…
12 Dec 2014
Iron Overload: Causes, Consequences, And Control
The endeavours of physicians taxed with the problem of iron deficiency over the last 100 years have successfully eliminated this as an issue of…
11 Dec 2014
Inherited Thrombocytopaenias: Beyond the Bleeding
The improvement of molecular biology technologies and the increasing number of researchers interested in inherited thrombocytopaenias (ITs) has led…
1 Dec 2014
Inherited Bone Marrow Failure Syndromes with Pancytopaenia
Bone marrow failure (BMF) is characterised by a reduction in the effective production of mature erythrocytes, granulocytes, and platelets by the bone…
31 Jul 2014
Biosimilars in Hematology: Increasing Choice, Expanding Access
Biologicals have revolutionised modern medicine by offering vital therapeutic options to treat or prevent complex, disabling, and life-threatening diseases.
31 Jul 2014
Next Steps in Front-Line Treatment of Lymphoma: The Road Ahead
Prof Zelenetz opened the symposium on the evolving front-line treatment options for follicular lymphoma (FL) and discussed the potential of novel agents…
31 Jul 2014
The Multiple Facets of Thrombotic Microangiopathies
The Alexion satellite symposium was introduced by Prof Pier Mannuccio Mannucci who provided an introduction to the history of thrombotic…
31 Jul 2014
The Standard of Care in Relapsed Refractory CD30+ Lymphoma
CD30-positive (CD30+) lymphomas are a heterogeneous group of hematological malignancies that share the same antigen. Over recent decades, advances…
31 Jul 2014
Overcoming Immunodeficiency in Chronic Lymphocytic Leukaemia: Current Knowledge and Perspectives
While the standard of care for chronic lymphocytic leukaemia (CLL) leads to high overall response rates and a long progression-free survival, it can be…
31 Jul 2014
The Role of CD49d in Chronic Lymphocytic Leukaemia: Microenvironmental Interactions and Clinical Relevance
Chronic lymphocytic leukaemia (CLL) is a clinically heterogeneous disease characterised by the accumulation/expansion of a clonal population of…
31 Jul 2014
Current Developments and Perspectives in Multiple Myeloma
In the last decades, advances in the therapeutic management of multiple myeloma (MM) with new drug armamentarium and strategies have significantly…
31 Jul 2014
Autologous Stem Cell Transplantation In Multiple Myeloma: Is It Still The Right Choice?
Autologous stem cell transplantation (ASCT) is considered the standard of care for multiple myeloma patients aged <65 years with no relevant…
31 Jul 2014
The Role of JAK2 Mutation in Thrombotic Complications of Chronic Myeloproliferative Neoplasms
Patients diagnosed with myeloproliferative neoplasms (MPNs) often develop thrombotic events as an onset of symptoms or in evolution. The pathogenesis of…
31 Jul 2014
Calreticulin in Myeloproliferative Neoplasms: The Other Side of the Alice Mirror
Calreticulin (CALR), a Ca2+ binding protein mostly localised in the endoplasmic reticulum, regulates Ca2+ homeostasis, chaperones, and other proteins to…
31 Jul 2014
Iron Supplementation for Perioperative Anaemia in Patient Blood Management
In patients undergoing major surgical procedures, preoperative anaemia and perioperative allogeneic blood transfusion (ABT) have been linked to increased…
31 Jul 2014
Looking Back To Our Roots: 80 Years of Wintrobe’s Indices
This year (2014) we are celebrating the 80th anniversary of Dr Maxwell Myer Wintrobe’s pioneer works, one of the most important contributions in clinical…
1 Aug 2013
Delayed Erythroid and Platelet Response to Eculizumab in Paroxysmal Nocturnal Haemoglobinuria - A Case Report and Literature Review
Paroxysmal nocturnal haemoglobinuria (PNH) is an acquired clonal disorder of haemopoiesis characterised by haemolytic anaemia, thrombophilia and variable…
1 Aug 2013
The Chemokine CCL17/TARC as a Biomarker in Hodgkin Lymphoma
Classical Hodgkin lymphoma (cHL) is a lymphoproliferative disorder hallmarked by a distinctive type of neoplastic cells, the Hodgkin and Reed/Sternberg…
1 Aug 2013
Pain Management in Patients with Sickle Cell Disease - A Review
Pain is defined, by the International Association for the Study of Pain (IASP), as an ‘unpleasant sensitive and emotional experience, associated with or…
1 Aug 2013
Treatment of HIV-Associated Burkitt Lymphoma
Burkitt lymphoma (BL) is a highly aggressive B-cell malignancy, occurring with increased frequency among patients infected with HIV. For several years…
1 Aug 2013
RNA Interference (RNAi): An Effective Way to Develop Rational Combination Therapies with Hypomethylating Agents in Acute Leukaemias and Myelodysplastic Syndrome
Therapeutic progress in aggressive myeloid malignancies such as acute myeloid leukaemia (AML), myelodysplastic syndrome (MDS) and advanced…
1 Aug 2013
Preventing Infections in Higher-Risk Myelodysplastic Syndrome Patients Treated with Hypomethylation Agents
Hypomethylation agents became the standard of care for patients with high-risk myelodysplastic syndrome (MDS). While long-term benefits of azacitidine…
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