Campaign to Persuade States to Screen Newborns for SMA to Be Key Topic at Conference
A revved-up campaign to persuade the U.S. government to ask states to screen newborns for spinal muscular atrophy will be…
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A revved-up campaign to persuade the U.S. government to ask states to screen newborns for spinal muscular atrophy will be…
One way Cure SMA’s Annual SMA Conference encourages collaboration among academics, industry executives, government officials and families is through its Family…
Cure SMA has awarded a $75,000 basic research grant to Dr. Stephen J. Kolb of Ohio State University (OSU) for…
As part of a $1.03 million basic research funding initiative, Cure SMA has awarded a $75,000 grant to University…
Cure SMA has announced two additional grants to its current round of basic funding for research into spinal muscular…
Dr. Jocelyn Côté, an RNA metabolism expert at the University of Ottawa, has received $140,000 in basic research funding from …
Spinal muscular atrophy (SMA) is a step closer to being on a list of diseases that the U.S. government recommends…
A new saliva-based screening test for the two most commonly inherited genetic disorders, cystic fibrosis (CF) and spinal muscular atrophy…
Cure SMA has created a series of educational modules to address the topics, issues, and questions that are critical…
The 2016 SMA Researcher Meeting, the largest gathering specifically dedicated to spinal muscular atrophy (SMA), set a record with 350 attendees who…
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