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Therapy Area
Allergy & Immunology
Cardiology
Dermatology
Diabetes
Flagship Journal
Gastroenterology
General Healthcare
Hematology
Hepatology
Innovations
Interventional Cardiology
Microbiology & Infectious Diseases
Nephrology
Neurology
Oncology
Radiology
Reproductive Health
Respiratory
Rheumatology
Urology
Podcasts
Journals
Webinars
Collaborate
Editorial Enquiries – GOLD
Editorial Enquiries – EMJ
Contributors & Authors
Submit a Paper
About
Careers
Partners
Contact Us
EMJ Gold
Subscribe
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Subscribe to EMJ GOLD
Subscribe to EMJ
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Interview: Pier Mannuccio Mannucci
4
Mins
March 2024
I think the beginning was when I graduated in the 1960s; my thesis was on red cell enzymes within haematology, but it had nothing to do…
Read more
11
Mins
2nd August 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
2nd August 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
2nd August 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
7th June 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
22nd September 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
31st August 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
31st August 2017
How I Diagnose Hypereosinophilic Syndromes
Hypereosinophilic syndromes are a group of disorders characterised by significant eosinophilia and organ damage.
9
Mins
31st August 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.
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