Ana Mingorance
@cnsdrughunter
🧠 🧬 Neuroscientist. Looking for new medicines for CDKL5, SCN1A, SHANK3, DHPS and a few others.
ID: 358743576
http://draccon.com 20-08-2011 12:34:58
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Es día internacional del síndrome por deficiencia #CDKL5 #CDKL5AwarenessMonth Un trastorno genético ligado al cromosoma X. Conoce mas gracias a ASOCIACIÓN CDKL5👇 aacdkl5.org Este documental presenta a familias de la comunidad CDKL5 España, cómo es convivir con esta
#Dravet #SCN1A request for grant applications by Dravet Syndrome Foundation is now open! info below
It's #DravetAwarenessDay. Can you share our film to reach more people in need of our support? #LittleMomentsMatter shares what 3 families love about their children, what they don't love about #DravetSyndrome & how DSUK has supported them. Park Lane Stables MeathEpilepsyCharity
Today 6/23 is International #DravetSyndrome Awareness Day! 💜 Today I’m thankful for: 💜Caregivers and their Kids with #Dravet that have taught me so much about caring for this rare #epilepsy 💜Organizations like Dravet Syndrome Foundation that coordinate the relentless pursuit of a cure 🧬
Today we started the #EEC2024 ILAE Epilepsy Congress with a session on #CDKL5 deficiency disorder. It was a great example of collaboration between expert clinicians and parent advocates like Carol-Anne Mum to Amber from Cure CDKL5 💚 it made it worth it to be there at 8am!
Fascinating talk by impressive Gaia Colasante at the #EEC2024 with big implications for #Dravet syndrome treatment! Genetic rescue of #SCN1A in interneurons only works if done pre-symptomatically in Dravet mice. After symptom onset you need to treat all neurons in order to see