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Interview: Niamh O'Connell
5
Mins
April 2024
When I was a medical student in the small university city of Cork, in Ireland, there was one female consultant, and she was a haematologist…
Read more
9
Mins
8th August 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
8th August 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
8th August 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
8th August 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
8th August 2017
The Role of Allograft in Acute Lymphoblastic Leukaemia, Including Alternate Donors
The management of acute lymphoblastic leukaemia (ALL) remains challenging.
12
Mins
8th August 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
8th August 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
8th August 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…
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