The key to how extraocular muscles are spared in most #MuscularDystrophy ! TL nature.com/articles/s4146…

Registration for WMS 2024 is open! Our 29th annual international annual Congress takes place in Prague, Czechia from 8th-12th October. Topics for #WMS2024 are acquired muscle disorders, neuromuscular disorders around the world, & RNA in NMD. Register now: buff.ly/3v17rzI

Saiu um trabalho muito interessante sobre Ataxia de Friedreich no estado de SP 👏👏👏👏

Delighted to lead new centre for UCL- working in this national partnership -we are finally in a position to translate our science into trials and disease modifying therapies for mito patients! UCLH Robert Pitceathly UCL News The Lily Foundation Muscular Dystrophy UK London Mitochondrial Centre UCL Brain Sciences

Best practice guidelines on genetic diagnostics of FSHD: Update of the 2012 guidelines - Giardina - Clinical Genetics - Wiley Online Library onlinelibrary.wiley.com/doi/10.1111/cg… FSHD Leiden FSHD Society #FSHD ClinGenetNews Dr Pedro J Tomaselli ICGNMD @Gianina_Natoli Ichizo Nishino Silvere vd Maarel

Great to see our collaborative effort on the best practice guidelines on the genetic diagnostics of FSHD published in Clinical Genetics: onlinelibrary.wiley.com/doi/10.1111/cg…

Heather Hilsden was awarded a Leadership in Collaboration award at the Jain Foundation meeting. She has delivered the COS study over 16 sites in 9 countries for 10 years. Longest multicentre Natural History study in #LGMD which brought trial readiness closer to #dysferlinopathy👏

Aaanndd GO! We are now accepting submissions for late breaking abstracts for #WMS2024. Submit your most relevant, exciting, unpublished and recent neuromuscular disorders news. You must be registered to attend #WMS2024. The instructions are on our website: buff.ly/3YbRByg

Venugopalan is an academic neurologist working as additional professor at the All India Institute of Medical Sciences, New Delhi, India. He will talk about neuromuscular disorders in India, where the new world meets the old. buff.ly/4eA8tnn

So excited that our Sarasota friends are hosting a FUNdraiser to celebrate #LGMDAwarenessDay! Join them as they team up with #CureLGMD2i to raise money to drive research toward a cure for #LGMD2A #LGMDR1 #Calpainopathy #LGMD2i #LGMDR9 eventbrite.com/e/891190925047…

Today is LGMD Awareness Day! 💚 Help us Advocate - Educate - Celebrate limb-girdle muscular dystrophy. 💚Please share our post to help raise awareness. To learn more, visit LGMD-Info.org #LgmdAwareness #lgmdday2024 #TogetherWeAreStronger

Today we mark Limb Girdle Muscular Dystrophy Awareness Day with this interview with Bjarne Udd, who has worked in neuromuscular disorders since the 1980s. He describes the early days of identifying family groups and how his team sequenced the Titin gene: buff.ly/4gKFPle

JOB ALERT! MND Accelerator Award funded postdoctoral position in my lab MRC PPU is now LIVE. We will use pooled CRISPR screening of iPSC motor neurons to identify new targets for ALS/MND. To learn more & apply: ppu.mrc.ac.uk/careers/recrui… Please help spread the word! Thank you.

🇪🇺Euromuscular Disorders 43 (2024) 👉#FSHD Poster 630P 🇳🇱🇮🇳🇬🇧 Genetic diversity and clinical implications of #FSHD in the Indian population 💡Need for global FSHD participation in research and the establishment of trial-ready Indian FSHD cohorts

nmd-journal.com/article/S0960-… AIIMS-CNMD Dr Avinash S A @03236316p vishnu v y FSHD Leiden

Congratulations to consultant neurologist and professor of clinical neurology, Mary Reilly, on receiving an honorary MBE for services to #medicine. Her award was published yesterday, recognising those who have made an outstanding contribution to the UK: buff.ly/3CGcBF7

Congratulations to UCL IoN CNMD's Professor Mary Reilly, a globally renowned and award-winning clinical neurologist, who has been awarded an honorary MBE for her services to medicine. link to article here bit.ly/40YPLkb

We're working behind the scenes to get everything ready to open registration for #WMS2025. Expect an announcement in the next couple of weeks. In the meantime, make sure dates, 7th-11th October, are in your calendar!

Since our founding in 1991, we've seen incredible scientific advances & increased support for #FSHDResearch. As we look towards #WorldFSHDDay, let's also remember where we come from & who helped us get where we are today. Read the full story on our blog: fshdsociety.org/2025/05/26/aga…

“This is a deeply significant moment for the FSHD community,” said Mark Stone. “For decades, patients and families have carried the burden of a disease with no treatment that addresses its root cause.” Read the full press release: fshdsociety.org/2025/08/06/epi…