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Therapy Area
Allergy & Immunology
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Flagship Journal
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Tackling Infectious Diseases
October 2024
This interactive article summarises key discussions from GSK sponsored symposia that took place during the ESCMID Global Congress 2024, held from 27–30th April 2024 in Barcelona, Spain.
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5
Mins
27 Jul 2021
Diagnosis, Treatment, Impact, and Unmet Needs of People with Mycosis Fungoides and Sézary Syndrome
Mycosis fungoides (MF) and Sézary syndrome (SS), two of the most-studied types of cutaneous T-cell lymphoma (CTCL), account for approximately 60% and 10% of CTCL cases, respectively.
8
Mins
27 Jul 2021
Interview: Nikhil Munshi
We are talking about 35 years ago, and some of what drew me to the practice is still true today. There were two major aspects of cancer…
10
Mins
27 Jul 2021
Von Willebrand Factor and ADAMTS13 in COVID-19 and Beyond
von Willebrand factor (VWF) is a large, adhesive, multimeric protein involved in haemostasis. The larger the size (or number of VWF multimers), the greater the functionality of the protein.
11
Mins
27 Jul 2021
Management of Multiple Myeloma in Older Patients
Multiple myeloma is a haematological malignancy predominantly affecting older people and has a median age of onset of 70 years.
10
Mins
27 Jul 2021
Current and Future Therapies for β-Thalassaemia: A Review Article
β-thalassaemias are a clinically heterogenous group of inherited disorders caused by >200 described mutations in the β-globin gene, leading to a decreased or absent production of the β-globin chain.
5
Mins
27 Jul 2021
Recurrent Episodes of Angioedema Consistent with Polycythaemia Vera
Polycythaemia vera (PV) is a condition characterised by an increasing number of the red blood cells in the blood.
4
Mins
27 Jul 2021
Glanzmann Thrombasthenia: A Case Report
Eduard Glanzmann first reported Glanzmann thrombasthenia (GT) in 1918 after he identified a functional abnormality of platelets with defective clot retraction.
9
Mins
23 Jun 2021
FLT3 Mutations in Patients with Acute Myeloid Leukaemia: The Importance of Identification and Monitoring for Prognostic Determination and the Selection of Optimal Treatment Strategies
Mutations in FLT3 are the most common genetic alteration in AML. Patients with a FLT3 internal tandem duplication (ITD) mutation subtype have poor prognosis, especially when there is a high allelic burden.
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