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📢Next #euronmd WEBINAR ! 📅Sept 1st, 2022, 16:00 Paris time 💻Mitochondrial Epilepsy 🗣️Delivered by Prof Michelangelo Mancuso ℹ️1st webinar in the World Mitochondrial Awareness Week 2022 💚 series. Don't miss it ‼️ Read more and register 👉bit.ly/3d7yTCr

Just finished Filadelfia Epilepsy Hospital's 125 Year Anniversary 5 km relay. Go Team Genetic Epilepsy! 🥳 What a fun way to end the day 🤩

Welcome to the team @BeneKassabian, we are delighted to have you on-board🤩 Benedetta is a neurologist from 🇮🇹 and during her stay in 🇩🇰 she will be working on #DLG4 and #SLC6A1 related disorders😊 Give her a follow😀 #Epilepsy #Genetics #RareDisease @ShineSyndrome @SLC6A1_Mom

🚨 EJP RD is delighted to announce an upcoming webinar on “The Statistical Evaluation of Surrogate Endpoints in Clinical Trials” 🗓️ November 18, 2022 ⏰ 16:00 CEST 👉 More info here: ejprarediseases.org/ejprd-webinar-…

Jump start Monday at Filadelfia with the resident species 🐸🐸🐸🐸#lifeatFiladelfia #geneticsdept #researchisfun #FiladelfiaIT

Farewell lunch for Vivian Liao and Alessandra Rossi 🤩 It has been a great pleasure having you in the dept. 🤗 Ale and Vivi have been super productive 💪. Watch out for their upcoming papers on #GABRA1, #GABRG2, #SYNGAP1, #POU3F3 ‼️ 🇮🇹🇦🇺🇩🇰 dream team 💪 #FriendsInScience 💜

Excellent educational talk on the phenotypic spectrum of #SCN2A and #SCN8A related disorders by my dear colleague Elena Gardella 🧬🧠 A spectrum of conditions ranging from self-limiting epilepsies to severe DEEs have been reported. Both GOF and LOF variants can cause #epilepsy ‼️

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Huge thanks to Morten Lossius and Guido Rubboli for organizing the 4th Annual Meeting between Epilepsihospitalet, Filadelfia 🇩🇰 and the Norwegian 🇳🇴 #Epilepsy Center 👏 Excellent presentations, friendly atmosphere and nice discussions on epilepsy syndromes, genetics and #PrecisionMedicine 🧬🧠

Farewell lunch for caterina ancora 🤩 It has been a great pleasure having you in the dept. 🤗 For the past months Caterina has been working extremely hard to describe the long-term evolution of #SCN8A related disorders with a special focus on transition age 💜 #epilepsy 🧬🧠

Today is #SCN8A awareness day 💜 SCN8A has been associated with a broad spectrum of neurodevelopmental disorders, epilepsies and movement disorders ‼️ Learn more about the upcoming #SCN2A and SCN8A network conference here: scn8a.eu

Today is #SCN8A awareness day 💜 We love supporting #SCN8A research ‼️ This is our SCN8A team: Elena Gardella, Roberto Previtali Francesca Furia Alessandra Rossi caterina ancora. Give them a follow to learn more about #SCN8A-related disorders 😊

Incredibly honored to be part of this amazing international community 💜

Beyond grateful for having this opportunity 😍

🔊What makes an appointment with a neurologist "good" 🤔? Find out now on the Epilepsy Sparks Insights podcast🎧👇 with Álvaro Beltrán of NeurologiaHRI 🇪🇸! 📹 YouTube - shorturl.at/jqD16 🎧 Podcast - shorturl.at/hwMXY 🔗 Website - shorturl.at/iswRZ #epilepsy

Filadelfia alumni reunion at #IEC2023. Fantastic to see that our #epilepsy #genetics family keeps growing 😍 Incredibly grateful to keep working with these amazing people, and to see them growing into becomming independent researchers 😍 #FriendsInScience #ProudPI Elena Gardella

For those who missed the #IEC2023 platform session '#Genetics'; here is a short summary of our session. It's amazing to see that most talks were focused on clinical care with strong examples for the ion channels. Congrats Katrine M Johannesen Allan Bayat, associated professor Caterina Ancora & Ne He.

The transfer from paediatric to adult care can be a problematic process in many rare genetic epilepsies‼️ Our fellow caterina ancora gave an excellent presentation about the relevance of a tailored and well-planned transition in #SCN8A-related disorders💪 Elena Gardella #IEC2023

What a time! 🤩