Congratulations to our 2023 Young Bioenergeticist Award winner, Shanna Hamilton, PhD! #mitochondria #mitochondria ldisease #Ryanodinereceptorhyperactivity #youngtalent #2023BPS
Very interesting #MitochondrialDisease upload to Radiopaedia.org by Dr Glick: mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
Case: radiopaedia.org/cases/mitochon…
Extremely rare condition with non-specific imaging, but some very unique learning points, more in 🧵
March milestones:
✅ Finished my 1st year of PhD.
⭐️ I had the honour to give a short talk about new approaches to identifying new #mitochondrialdisease genes during the #MitoMed24 conference at Hinxton Hall Conference Centre, Cambridge (UK).
#MitochondrialResearch #PhDVoice
Today is #RareDiseaseDay2024 this is my gorgeous nephew Michael💙 he is being facilitated by physios to take steps for the 1st time 🥹 Therapy won't cure his very rare #MitochondrialDisease called #MegdelSyndrome but it will give him the best quality of life 🩵💜Rare Disease Day
#WhatIf we didn't have the #roundworm ( #CElegans ) in research?
#AnimalResearch #ParkinsonsDisease #MitochondrialDisease #ImmuneSystem
#RareDeseaseDay #LeighsSyndrome #dystonia #mitochondrialdisease alone we are rare, collectively we are stronger, together supported we are heard 💪🏽
Just In! All proceeds going to The Liam Foundation The Raw Knuckles Podcast #mitochondrialdisease #shop #support #donate #give
knucklesnilan.com/shop/p/knuckle…
Brilliant opening talk by Professor Carolyn Sue at Euromit 2023 today on the improving the diagnosis of #mitochondrialdisease with public funding for WGS NeuRA (Neuroscience Research Australia) University of Sydney Kolling Institute Mito Research
#StrongerTogether 💚
An exciting two days ahead for the team at UCL_QS_CNMD for the
Neuromuscular Translational Research
Conference alongside Sarah Pickett Valeria Di Leo and Prof Bobby McFarland #NMD #Mitochondrialdisease
Tomorrow is the day for the fundraiser! It'll most likely start around 1pm CST. Retweets appreciated I need help spreading the word. Remember every donation puts you in the running for a NINTENDO SWITCH!
#charity #fundraising #awareness #gaming #twitch #mitochondrialdisease
Another exciting congress begins.... this year the gurus of Fetal Medicine gather in Valencia! I hope to develop the right ideas for the prevention and prenatal treatment of mitochondrial diseases! #fetalmedicine #mitochondrialdisease
A new report by Mito Foundation has shown that mitochondrial disease costs the Australian economy $1B+ each year. Amber Laidler of @7newsydney spoke with Professor Carolyn Sue, Kinghorn Chair, Neurodegeneration at NeuRA, about the impact of the disease on patients #MitochondrialDisease
Really great get together at the MRC National Mouse Genetics Network Science Day in York yesterday MitoCluster PI Carlo Viscomi & ECR Pedro Silva-Pinheiro presented their recent research on AAV-based gene therapy for #mitochondrialdisease & mouse mtDNA knockouts
Officially Doctor in Philosophy of ocular genomics! It was such an interesting journey (with ups and downs) to study mitochondrial eye diseases UCL Institute of Ophthalmology and Moorfields Eye Hospital NHS Foundation Trust.
#mitochondria #mitochondria ldisease #inheritedopticneuropathy
UCL Portico was lit up green to mark World Mitochondrial Disease WMDW Week!
#WorldMitoWeek #lightupformito #mito chondrialdisease #mito
The #MitochondrialDisease Voice of the Patient report is a valuable resource highlighting the perspectives of patients and families on the burden of disease and what matters most in potential new treatments. Check it out on United Mitochondrial Disease Foundation website: umdf.org/voice-of-the-p…
Today's #parkruntourism took us to The Town Moor parkrun which was taken over by the Newcastle University Mitochondrial Research Team. Raising awareness as part of World Mitochondrial Disease Research Week #mitochondrialdisease #projectpearl
We're absolutely delighted to welcome our newest mission on board: John, from Batley, West Yorkshire! ⚡
Head to our website to read about John's story with mito!
mymitomission.uk/johns-mito-mis…
#livingwithmito #smallcharity #mitoaware #mitochondrialdisease #yorkshire #westyorkshire