Nasdaq

Biohaven's Taldefgrobep Alfa Receives FDA Fast Track Designation for Spinal Muscular Atrophy

- Taldefgrobep alfa, a myostatin-targeting biologic investigational agent, in Phase 3 development to increase muscle mass for Spinal Muscular Atrophy patients now granted Fast Track in addition to ...
The New England Journal of Medicine

A Case of Progressive Muscular Atrophy Following a Blow on the Head

Read before the Section for Clinical Medicine, Pathology, and Hygiene of the Suffolk District Medical Society, June 9, 1885.
IBTimes UK

What Is SMA Type 1 and Could It Affect You? Jesy Nelson's Twin Daughters Were Just ...

Spinal muscular atrophy is a rare genetic disorder causing progressive muscle weakness, now in focus after Jesy Nelson shared her twins’ diagnosis. Instagram/JesyNelson Spinal muscular atrophy is a ...