who are living with Spinal Muscular Atrophy (SMA) with the support of her mother, sister and teacher. Ms. Keya was felicitated by the Visakha Rasagna Vedika, a cultural organisation, at the Public ...

in response to a contempt of court petition by a 25-year-old woman from Ernakulam suffering from Type 2 Spinal Muscular Atrophy. She was previously treated at SAT Hospital in Thiruvananthapuram ...

The Princess of Wales, 43, is undertaking two engagements in south Wales today, including a moving visit to Tŷ Hafan children ...

The 18-month-old, suffering from a rare genetic disease called Spinal Muscular Atrophy (SMA ... union launches Touch Me Not drive for women The Mumbai Autorickshamen's Union on Sunday announced ...

A Boston-area biopharmaceutical firm has submitted a biologics license application to the FDA for its investigational, fully ...

A new drug-free, minimally invasive intervention targets the root cause of progressive loss of neural function in spinal muscle atrophy (SMA), an inherited neuromuscular disease.

Three patients with spinal muscular atrophy had improved muscle strength and could walk farther after a month of daily spinal ...

Three people with a muscle-destroying disease destined to worsen got a little stronger – able to stand and walk more easily – ...

Seeking urgent Union government intervention to overcome the lack of affordable access to medicines for treating Spinal Muscular Atrophy (SMA) and the need to allow local manufacturers to make ...

How a tiny spinal implant could help those with muscle-wasting disease - Three people with a muscle-destroying disease got ...