Katrien
@katriendeckers
Rare disease Mum working to find a cure for her son, Bear @cureSYNGAP1 #Syngap1 #epilepsy #autism #ID
ID: 1328112598596935681
https://www.syngapresearchfund.org/home/our-team/team-srf-eu#googtrans(en|en) 15-11-2020 23:08:23
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We are grateful to Lundbeckfonden for a very substantial support for our collaborative project on protein dynamics and brain diseases with Mingjie Zhang SUSTech 南方科技大学 lundbeckfonden.com/en/proteiners-…
RegEl Therapeutics announces T3 Platform & development pipeline as well as expanding BoD & SAB. CNS Pipe: 🧬 #SCN1A 🧬 #SCN2A 🧬 #SYNGAP1 💥 Bravo Orrin Devinsky Nadav Ahituv Navneet Matharu & team! prnewswire.com/news-releases/…
Thanks to a $25 million gift from an anonymous donor, our researchers and those from Penn Medicine will establish the Center for Epilepsy and Neurodevelopmental Disorders (ENDD), accelerating research for neurodevelopmental disorders. Learn more here: bit.ly/3YBOUmJ.
4th grade assignment near MLK day: What’s your dream. See photo for answer from sister to a girl with SYNGAP1, a rare genetic NDD. #SYNGAP1 CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3) #RareDiseases #Rdd
Interesting session on #IEC2023. Interesting and slightly "provoking" statements from #RodScott advocating that we need therapies that improve the network and overall excitability rather than #Genetherapy for single genes. International League Against Epilepsy IBE Epilepsy Torie Robinson 🇺🇦 Dennis Lal
#SYNGAP1 knowledge dissemination at #IEC2023 👇 International League Against Epilepsy AGE Program - Adult Genetic Epilespy Quratulain Zulfiqar Ali (she/her) Torie Robinson 🇺🇦 CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3)
Always great to connect with these two and talk syngap1! #IEC2023 CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3) SYNGAP Elternhilfe e.V.
Visit us at our posters today on #surgicalgenomics and #genes and #encephalitis Ready for some poster tour rapid fire sessions! #IEC2023 yesILAE AGE Program - Adult Genetic Epilespy @Paulatmarques Allan Bayat, associated professor Ángel Aledo-Serrano CAIHONG JI @this_is_farah Victor @marlenerong Pat Moloney @DrValiante
Wow! There are 925 confirmed epilepsy genes 🧬 with 825 producing DEEs! Just learnt that from Prof Ingrid Scheffer at the #IEC2023
Giving hope that disease modifying treatments are on the horizon for parents struggling with the many comorbidities of DEEs. 🙏CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3) The Notorious EEG (M. Scott Perry MD) Stoke Therapeutics #IEC2023
Stoke presents data from ongoing clinical studies of STK-001 for the treatment of Dravet syndrome at the 35th International Epilepsy Congress. Learn more here: investor.stoketherapeutics.com/news-releases/… International League Against Epilepsy #IEC2023 #ILAE
So please to meet Quratulain Zulfiqar Ali (she/her) live at #IEC2023 and talk syngap1 and adults! Thank for all your work so far 🙏 CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3) AGE Program - Adult Genetic Epilespy
Hi Syngap Europe - apparently the EpiCARE patient & caregiver leaflet on syngap1 is only available in 3 languages 😳 We can do better, let’s get this translated! CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3) SYNGAP1 Global Network (SGN) Syngap1 Italia overcome syngap1 SYNGAP Elternhilfe e.V.
Join us for a platform presentation where we talk about the adult phenotype of #SYNGAP1 #IEC2023 CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3) International League Against Epilepsy AGE Program - Adult Genetic Epilespy @marlenerong
Here is my summary of the highlights for DEEs from the #IEC2023 meeting. Don't miss Dennis Lal summaries on the genetics front, and also the general updates through the hashtag #IEC2023 draccon.com/dracaena-repor…
What happens when they grow up? Thanks to this wonderful collaboration we can tell! CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3) @marlenerong Ángel Aledo-Serrano Allan Bayat, associated professor Orrin Devinsky Alfonso Fasano Alessandra Rossi #AES2023
Learning from @SulserGonzalez that #syngap1 deficiency steals half of the children’s dream time 😢 Also about using deep learning to develop EEG Biomarkers together with Melissa Fasol at the #SyngapConf
International 🌍 collaboration is key to improve the life of people living with a rare genetic #epilepsy ‼️ #StrongerTogether #EpilepsyAwareness 💜 #Genetics 🧬 #KCNA2 #RareDisease KCNA2 Epilepsy EpiCARE Torie Robinson 🇺🇦 @MatjasDW