Francesca Magrinelli (@framagrinelli) 's Twitter Profile
Francesca Magrinelli

@framagrinelli

MD, PhD. Consultant Neurologist, National Hospital for Neurology & Neurosurgery. Senior Clinical Research Fellow, Dept Clinical & Movement Neurosciences @UCLIoN

ID: 1276233433891721218

calendar_today25-06-2020 19:19:04

389 Tweet

852 Followers

510 Following

Genetic Alliance UK (@geneticall_uk) 's Twitter Profile Photo

Fahr's disease is a rare neurodegenerative condition, characterised by calcification in the brain. FahrBeyond is the only registered charity in the world that supports the Fahr’s community in the UK and globally. Please join us in welcoming them as our newest member.

Fahr's disease is a rare neurodegenerative condition, characterised by calcification in the brain. <a href="/FahrBeyond/">FahrBeyond</a> is the only registered charity in the world that supports the Fahr’s community in the UK and globally. Please join us in welcoming them as our newest member.
FahrBeyond (@fahrbeyond) 's Twitter Profile Photo

We are delighted to join Genetic Alliance UK, adding the voice of the Fahr's community to the collective action to support the 3.5 million people in the UK with genetic, rare, and undiagnosed conditions. #Wearestrongertogether #Fahrs #PFBC #RareDisease

Francesca Magrinelli (@framagrinelli) 's Twitter Profile Photo

It’s been all very dark, but you, #ChrisMartin, make my night full of stars #FixYou #ColdplayLondon #WembleyStadium #Unforgettable

Francesca Magrinelli (@framagrinelli) 's Twitter Profile Photo

Enjoyed the “September vibes” at the UCL Queen Square Institute of Neurology MSc Clinical Neuroscience induction this morning — that fresh start-of-year purpose and enthusiasm never fade. Grateful to Dr Dr Valeria Iodice for bringing me on board as a module co-convenor and showing me the path. Let’s go! 🧠✨

Francesca Magrinelli (@framagrinelli) 's Twitter Profile Photo

🧬By tripling the number of reported cases, we strengthen and expand the evidence that biallelic NDUFA9 variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency academic.oup.com/braincomms/art… The Neurogenetics Lab UCL ION Clinical and Movement Neurosciences @ UCL IoN UCL Queen Square Institute of Neurology

🧬By tripling the number of reported cases, we strengthen and expand the evidence that biallelic NDUFA9 variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency academic.oup.com/braincomms/art… <a href="/IonSynapse/">The Neurogenetics Lab UCL ION</a> <a href="/UCLIoN_DCMN/">Clinical and Movement Neurosciences @ UCL IoN</a> <a href="/UCLIoN/">UCL Queen Square Institute of Neurology</a>
Anna Latorre (@annalatorre14) 's Twitter Profile Photo

We developed a new PSD-based approach to characterize tremor & cortical myoclonus. OT, ET, DT & myoclonus form a spectrum of movement regularity. Combined PSD features differentiate conditions and distinguish ET from DT. Clinical and Movement Neurosciences @ UCL IoN UCL Queen Square Institute of Neurology Movement Disorders Journal …mentdisorders.onlinelibrary.wiley.com/doi/full/10.10…

Simon Mead (@smead2) 's Twitter Profile Photo

Agree. Two superb colleagues at UCL/UCLH. It’s a shame clinical academic careers are being made so unnecessarily difficult. The next Professor Wild and Tabrizi are doing the general medical take and mulling over whether they can really still fit everything in…