AHC: The Genetic Epilepsy That Doesn’t Yet Make Sense - Alexis Arzimanoglou & Rosaria Vavassori

For the 10-year anniversary of its gene mutation identification, we today learn about the ultra-rare epilepsy: Alternative Hemiplegia of Childhood. Experts Rosaria Vavassoria and Prof. Alexis Arzimanoglou talk about their work to improve the lives of the families affected and indeed how far the understanding of AHC has come over the past decade!
 

**CHECK OUT ROSARIA & ALEXIS**
Rosaria
- LinkedIn: https://www.linkedin.com/in/rosaria-vavassori
- Facebook: https://www.facebook.com/IahcrcDataManager
- EpiCARE: https://epi-care.eu/epicare-patient-representatives
- IAHCRC: http://www.iahcrc.net
- ResearchGate: https://www.researchgate.net/profile/Rosaria-Vavassori

Alexis
- LinkedIn: https://www.linkedin.com/in/alexis-arzimanoglou-ba743729
EpiCARE: https://epi-care.eu/members-of-epicare
- Hospices Civils de Lyon: https://www.chu-lyon.fr/epilepsies-rares-et-complexes-un-reseau-europeen-coordonne-lyon
- Sant Joan de Déu Barcelona Hospital: https://www.sjdhospitalbarcelona.org/en/alexis-arzimanoglouvds
- ResearchGate: https://www.researchgate.net/scientific-contributions/Alexis-Arzimanoglou-2093846668
- ILAE: https://www.ilae.org/files/dmfile/Arzimanoglou--MC-_CV_2021.pdf

**CHECK OUT THE YOUTUBE VIDEO WITH ROSARIA & ALEXIS**
YouTube: https://youtu.be/rRuJim_TWzo

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**HIRE TORIE AS A SPEAKER ON EPILEPSY, MENTAL HEALTH, DISABILITY, & DIVERSITY**
https://www.torierobinson.com/contact