Rohit Sharma(@piandro3142) 's Twitter Profile Photo

Very interesting 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 🧵

Very interesting #MitochondrialDisease upload to @Radiopaedia 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 🧵
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Marcell Harhai(@MarcellHarhai) 's Twitter Profile Photo

March milestones:
✅ Finished my 1st year of PhD.
⭐️ I had the honour to give a short talk about new approaches to identifying new genes during the conference at Hinxton Hall Conference Centre, Cambridge (UK).

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 @HinxtonHall, Cambridge (UK). 
#MitochondrialResearch #PhDVoice
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Carly Davey 💜(@carlystroke) 's Twitter Profile Photo

Today is 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 called but it will give him the best quality of life 🩵💜Rare Disease Day

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Tensodaz(@tensodaz1) 's Twitter Profile Photo

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!

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
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United Mitochondrial Disease Foundation(@UMDF) 's Twitter Profile Photo

10-year-old Vera loves the outdoors. But, when Vera is low on energy she sometimes rides in a stroller. This is life for the thousands of patients living with chondrialdisease . Help us go the distance and fund research for treatments. Give Hope umdf.org/24hope

10-year-old Vera loves the outdoors. But, when Vera is low on energy she sometimes rides in a stroller. This is life for the thousands of patients living with #mitochondrialdisease. Help us go the distance and fund research for #mito treatments. Give Hope umdf.org/24hope
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Mitochondrial Medicine(@Mito_Therapy) 's Twitter Profile Photo

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!

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
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NeuRA (Neuroscience Research Australia)(@neuraustralia) 's Twitter Profile Photo

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

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MRC MitoCluster(@MRCMitoCluster) 's Twitter Profile Photo

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 & mouse mtDNA knockouts

Really great get together at the @MRCMouseNetwork Science Day in York yesterday MitoCluster PI @CarloViscomi & ECR Pedro Silva-Pinheiro presented their recent research on AAV-based gene therapy for #mitochondrialdisease & mouse mtDNA knockouts
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tisentotx(@tisentotx) 's Twitter Profile Photo

The 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…

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 @UMDF website: umdf.org/voice-of-the-p…
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Angela Topping 💜💚(@AngelaTopping74) 's Twitter Profile Photo

Today's 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

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
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My Mito Mission(@MyMitoMission) 's Twitter Profile Photo

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…

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
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