[…] it funds on one of the most common forms of muscular dystrophy–facioscapulohumeral muscular dystrophy ( FSHD)–while urging the FSHD research community to help the NIH to achieve higher levels of spending […]
From our CEO, a call to FSHD researchers
Unisciti al Registro FSHD
Unisciti al Registro dei contatti per la ricerca sulla FSHD La tua partecipazione è importante La FSHD Society mantiene il più grande registro di contatti al mondo di pazienti e […]
Progress in FSHD Muscular Dystrophy Research Hailed at International Meeting
[…] mysterious disease that causes muscles to weaken throughout the body. Called fascioscapulohumeral muscular dystrophy ( FSHD), this disorder literally robs people of their smiles as their facial muscles fail. The […]
An FSHD Antisense Therapy Primer
[…] Duchenne muscular dystrophy, and spinal muscular atrophy. While antisense therapy for the potential treatment of FSHD is still in the preclinical stage, we do hear occasional encouraging research results involving […]
FSHD Lab Day was empowering for all
Uniting the FSHD Community in Advancing Research by Nizar Saad, PhD, Columbus, Ohio On July 8th, our lab at Nationwide Children’s Hospital (NCH) in Columbus, Ohio, in collaboration with NCH, […]