staceywhite, Author at European Medical Journal - Page 58 of 195

Adult Survivors of Childhood Cancer Have Significant Levels of Impaired Cardiorespiratory Fitness, Inflammatory Markers, and Poor Quality of Life Outcomes

Almost two-thirds of the 35,000 children diagnosed with cancer in Europe each year are treated with anthracycline chemotherapy. Despite…

Risk Factors and Patterns of Myocardial Injury in Patients with COVID-19: A Single-Centre Cohort Study

The primary objective was to compare the risk factors and trends of patients with COVID-19 with and without biochemical evidence of…

ESC 2023 Abstract Highlights

The following selected highlights showcase intriguing and relevant abstracts presented at the European Society of Cardiology (ESC)…

PCSK9 Targeting in the Management of Hypercholesterolaemia

In the current era of optimal risk factor modification, proprotein convertase subtilisin/kexin type 9 (PCSK9) targeting has emerged as a…

Lennox–Gastaut Syndrome: Challenges in Diagnosis – Interviews with Two Key Opinion Leaders

Lennox–Gastaut syndrome (LGS) is a severe childhood-onset epilepsy syndrome that can be challenging to identify due to its heterogeneous and..

ECCO 2022 Insights: Treatment developments for inflammatory bowel disease (IBD) and rheumatology

Explore the latest insights from ECCO 2022, which discusses the latest updates and emerging developments in the treatments of irritable bowel disease (IBD) and rheumatic diseases.

Real-World Evidence of Biosimilar Utilisation and Pharmacoeconomics in People Living with Breast or Lung Cancer

As the medical community continues to explore and harness the potential of biosimilars, it is imperative to accumulate robust real-world…

NUVAXOVID™️ COVID-19 Vaccine (Recombinant protein, Adjuvanted) - Canada

Learn about the clinical efficacy and safety data for Nuvaxovid™️ COVID-19 Vaccine (Recombinant protein, Adjuvanted), a protein subunit…

Improving the Effectiveness of Anticoagulant Therapy: The Promise of Factor XI Inhibition

This continuing medical education-accredited symposium, held at the 2023 International Society for Thrombosis and Haemostasis (ISTH)…

The Unspeakable Disease: A Tale of Two Siblings

The deficiency of arylsulfatase A due to the mutations in the ARSA gene is the cause of a rare inherited lysosomal storage disease…