Emma Matthews 💙
@EmmaM_Channels
Neurologist and Neuromuscular Specialist @StGeorgesTrust, Reader @StGeorgesUni, Director Genomics CAG, Rare Disease Lead @SEgenomics #neuromuscular #channels
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Aware of the increased access to genetic testing offered by NHSE but unsure how to order tests or discuss the implications and results? Our new short course could be just for you! sgul.ac.uk/genetics @StGeorgesUni @geshNHS @SEgenomics
Nayana and Meriel superstar clinical geneticists! Not only did they develop a great module but they deliver a fantastic clinical service supporting our neurology patients and helping with all our difficult questions! @StGeorgesUni @geshNHS
The amazing St George’s Team launched a brilliant module on Genomics of Neurological Disorders. To find out more, please follow the link below. genomicseducation.hee.nhs.uk/education/taug…
Absolute pleasure Tootie. So encouraging to see such engagement and enthusiasm for cardiologists and neuromuscular specialists working together in neuromuscular disease. #AICCUK
Thank you @EmmaM_Channels for a comprehensive talk on Neuromuscular dse rel to #cardiogen! 💪🫀🧬 @SEgenomics @AiccUk @markmencias @rach_bastiaenen @robert_leema
Standing room only for the channelopathy session at #ICNMD2024. Thanks to Jaya and Jeff for great talks, and to the organisers. Perth was beautiful. Had great fun with friends old and new 😊
This meeting is always so informative and inspiring and such a nice opportunity to connect with colleagues #MDCRN
A brilliant day at the #MDCRN meeting to advance treatments in #myotonicdystrophy #FSHD #LGMD #CMT 🇬🇧 UK team representing @UCLIoN @UCL_QS_CNMD @sheffielduni @neuroshef @StGeorgesUni
We have made a four year funding commitment to an MND Care and Research Network across SW London and Surrey to improve support, in partnership with the NHS. Kuai, who cares for her husband KT, shared "To have this support is brilliant and I hope it will benefit many families."
Congrats to our neuromuscular team who received a Centre of Excellence award for patient care. The team treats patients with genetic condition Charcot-Marie-Tooth disease at St George's Atkinson Morley Neuromuscular Centre. The centre is the 2nd in the UK to receive the award.
Really proud of this award recognising the input of St George’s’ neuromuscular team as well as our community colleagues and allied specialists in providing excellent care to those with CMT @cmtausa @StGeorgesTrust cmtausa.org/news/cmta-anno…
Neuromuscular clinical trials team @StGeorgesTrust had a great visit to Washington meeting new colleagues and bumping into old ones!
Today we announced that the U.S. FDA has granted Breakthrough Therapy designation to our lead clinical development program for the treatment of myotonic dystrophy type 1 (#DM1). Learn more in our press release: aviditybiosciences.investorroom.com/2024-05-08-Avi…
Delighted to see END DM1 trial now open @StGeorgesTrust. Thanks to all those taking part in this international study. First participant enrolled last week. #myotonicdystrophy #DMCRN @StGeorgesUni
So we haven’t done this in a while. Feels good to catch up with old friends 😊
Great work Pam and team! @StGeorgesTrust
We had a great time @SMAEurope Proud to share my MSc research highlighting the impact of DMT on quality of life of adults with SMA - pleased to find like minded HCP from across the globe! With thanks to @SMA_UK_ and @MunfordDanielle
I even snuck in a zebra like dress 🦓😉#rarediseaseday @Medics4RareDiseases
We marked #RareDiseaseDay2024 with an excellent Symposium @StGeorgesUni organised by @EmmaM_Channels with talks from @EllaFWhittle and others…and of course we wore our stripes.
Really inspiring talks at St George’s Genomics CAG rare disease workshop for #rarediseaseday and we had to bring the socks 🦓! @SEgenomics @StGeorgesTrust @StGeorgesUni @EllaFWhittle @MaurerConstance @Carroll_C_J @alan_michael_p
Really looking forward to this with @markmencias @PamAppletonNMC @drmaryodisco Raising awareness of DM1 and ensuring patients get appropriate care is so important and it’s amazing to see such interest #myotonicdystrophy
EventBrite tickets are sold out but there’s more available on TicketSource. We have an amazing lineup of great speakers: Dr. @EmmaM_Channels @PamAppletonNMC Dr. Mary O’Driscoll! ticketsource.co.uk/whats-on/onlin… @SEgenomics
Nurses, midwives, doctors and everyone in between: please join us in exploring the genetics of myotonic dystrophy in the @SEgenomics lunch & learn on 26/Jan/2024. It is free!!! eventbrite.co.uk/e/lunch-and-le…
Raj you are a star. Thank you for bringing us all together!
Introducing the FSHD UK Research Team #research #fshd #uk #md #musculardystrophy #clinicaltrials #fshduk
What lovely feedback - thank you! We hope others find it useful too
These people deserve 🏅🏅🏅Clear concise useful 👏👏wow @EmmaM_Channels @drmaryodisco thank you!
Really proud to have been part of this with the fab, funny and very wise @drmaryodisco GeNotes Neurology now live. Check it out!
Our new #neurology #GeNotes resources have been developed in collaboration with #neurologists across the #NHS. From concise summaries based on example clinical scenarios to more in-depth learning, we’ve got your #genomics needs covered. Find out more: orlo.uk/43F0v
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