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Our 🧬team is heading to International League Against Epilepsy's 15th European #Epilepsy Congress❗️ We are looking forward to seeing friends and colleagues from around the world 🌎, to raise awareness of genetic epilepsies and to share our latest research results 👇 Hope to see you in Rome 🇮🇹 #EEC2024

Looking forward to our session! We hope to see carers, people with epilepsy, scientists, clinicians and allied health professionals. yesILAE International League Against Epilepsy Lucy Vivash IBE Epilepsy The Epilepsy Society of Australia Luca de Palma Dravet Italia Onlus

Check out the prize winning poster @sopio_gverd #EEC2024

Key point: "CACNA1E variant p.(Gly352Arg) is associated with early-onset DEE, dystonia/dyskinesia and contractures." Epileptic Disorders: doi.org/10.1002/epd2.2…

Start of the break out sessions on #epilepsy Francesca Furia on #STXBP1 . Registries and natural history studies are necessary for Trial readiness. #EPNSresearchmeeting2024 #Ljubliana

Next, another Rikke S. Møller disciple. Alessandra Rossi on #SYNGAP1 #EPNSresearchmeeting2024 #Ljubliana

Here comes diagnostic strategies in genetic epilepsy International League Against Epilepsy - current practices in a nutshell - represented pictorially in these beautiful infographics by YESer Matheus Gallas-Lopes . A Thread 🧵

The Education Task Force of yesILAE would like to assess the educational needs of the young people working in #epilepsy across all #ILAE regions. Participate by the 31 December deadline: l8r.it/B1XO

New paper! Our team developed a new missense variant pathogenicity and function predictor for #GRIN1, #GRIN2A, #GRIN2B & #GRIN2D genes, linked to severe neurodevelopmental disorders (NDDs). 🔗to Study: academic.oup.com/hmg/advance-ar… #bioinformatics #precisionmedicine #genetics

Instead of listing my publications, as the year draws to an end, I want to put pressure on the commonplace assumption that productivity must always increase. Good research is disruptive and thinking time is central to high quality scholarship and necessary for disruptive research

Explore the phenotypes of RORA-related NDD. #epilepsy #geneticsinmedicine. sciencedirect.com/science/articl…

We are very happy to share the newest achievement of Sarah Weckhuysen lab VIB Center for Molecular Neurology on Fibroblast transcriptomics. Congrats to Noor Smal #clinicalimplications #geneticepilepsy onlinelibrary.wiley.com/share/author/K…

Join me on this interesting journal club about treatment of #EESWAS. thelancet.com/journals/laneu…. Register on epns.us20.list-manage.com/track/click?u=…

Have you looked at these Collaborative Genetic Research Calls? ⭐Find out more about these collaborative research calls: lnkd.in/epZRBtWy

Happy to present you our latest work on #KCNQ2 and #KCNQ3. Amitriptyline has beneficial effects in some individuals with gain of function variants. Sarah Weckhuysen Charissa Millevert Rikke S. Møller Stéphane Auvin Allan Bayat, associated professor onlinelibrary.wiley.com/doi/10.1111/ep…

Read our latest work on amitriptyline in #KCNQ2 and #KCNQ3 in Epilepsia #OpenAccess onlinelibrary.wiley.com/doi/10.1111/ep…

Let's talk about #epilepsy #notonlyseizures. UZA Epilepsy Sparks.

The importance of precision medicine in #epilepsy. Check out our paper in Epilepsia! onlinelibrary.wiley.com/doi/10.1111/ep…