Duchenne Muscular Dystrophy (DMD) is the most common form of muscular dystrophy characterised by progressive skeletal muscle degeneration and weakness....
Spinal Muscular Atrophy (SMA) is a genetic neurodegenerative disease that leads to progressive muscle weakness and paralysis and if left...
Alagille syndrome (ALGS) is a rare genetic disorder that affects around one in every 30,000 live births. It results from...
In 2018, the estimated incidence of prostate cancer was high, with Japan accounting for 6% (78,400 people) of the total...
The global pandemic, COVID-19, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is ongoing. Although numerous effective vaccines have...
Myasthenia gravis (MG) is a rare neuromuscular disorder that affects the transmission of signals between nerves and muscles. It is...
Pompe disease, also known as glycogen storage disease type II, is a rare genetic disorder that affects approximately 1 in...
INTRODUCTION Dr. Ahmed Farrag is a hematology and internal medicine specialist at the Thalassemia Centre at Latifa Women and Children...
The Food and Drug Administration (FDA) approved AstraZeneca's tremelimumab in combination with durvalumab and platinum-based chemotherapy for adult patients with...
GE Healthcare received FDA 510(k) clearance to add 3D imaging capabilities and PROPELLER technology as extensions to their AIR Recon...