🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

Andy Berglund The RNA Institute presenting to the dmcrn on natural products that rescue splicing.

Cynthia Gagnon and Guillaume Bassez presenting on the classification of myotonic dystrophy at our dmcrn meeting

GRASP LGMD meeting underway!

Peter Kang discusses the challenges of genetic diagnosis in lgmd.

If you or a family member have myotonic dystrophy, the #1 thing you can do to help researchers develop an effective treatment is to enroll in the END-DM1 natural history study. Details here: clinicaltrials.gov/ct2/show/NCT03…

Moving research forward in myotonic dystrophy at CIMR! #internationalmyotonicdystrophyday #myotonicstrong VCU Neurology & Neurosurgery

The CIMR team celebrates Beckers awareness and helps move research forward.

Great MDCRN meeting to advance treatments for myotonic dystrophy, limb girdle muscular dystrophy and facioscapulohumeral muscular dystrophy! Children's Hospital of Richmond at VCU VCU Neurology & Neurosurgery MyoStrong CureCalpain3 FSHD Society

For more information: curecalpain3.org/trial-readines…

You’re never too young to be an advocate for a better healthcare system! #AANadvocacy #NOH24 American Academy of Neurology Nicholas Johnson Women Neurologists Group THGR Neurology Residency THGR Vascular Neurology Fellowship

Aileen Antonio, MD, FAAN American Academy of Neurology Nicholas Johnson Women Neurologists Group THGR Neurology Residency THGR Vascular Neurology Fellowship Look out 👀💪🧠

Myotonic dystrophy is an autosomal dominant form of muscular dystrophy characterized by progressive muscle weakness and wasting. JAMA Insights discusses the signs and symptoms, diagnosis, and treatment of myotonic dystrophy type 1. ja.ma/49Okvav

CHLA Neuroimmunology expert Jonathan Santoro, MD shares breakthrough discovery in Down Syndrome Regression Disorder with The Washington Post. chla.org/blog/hospital-…

The Splice Index as a prognostic biomarker of strength and function in myotonic dystrophy type 1 biorxiv.org/content/10.110…

Deletion of miR-146a enhances therapeutic protein restoration in model of dystrophin exon skipping biorxiv.org/content/10.110…

Deletion of miR-146a enhances therapeutic protein restoration in model of dystrophin exon skipping ncbi.nlm.nih.gov/pmc/articles/P…

Learn more about one of MDF's 2024 Research Fellows, Ms. Alexandra Marrero Quinones! Her long-term goal is to identify genetic modifiers of disease severity in #myotonicDystrophy. Learn more at: myotonic.org/research-fello…

We're hiring! We are excited to be in our new home VCU in Richmond, VA and are actively recruiting lab members at all levels! If you're interested in basic or translational science in dystrophic muscle 💪 or heart ❤️, contact us!

The MDCRN meeting was a success! Thanks to all for working towards treatments for myotonic dystrophy, Charcot Marie tooth disease, facioscapulohumeral muscular dystrophy, and limb girdle muscular dystrophy!

Virginia delegation at #NOH25