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Case Report of a Patient Presenting with Acute Flank Pain
April 2025
A female in her 40s, with a history of heavy smoking presented to the emergency department with a 6-hour history of paraesthesia and…
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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
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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…
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