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Caterina Ancora presented another very interesting work at the Danish Epilepsy center on transition care in SCN8A

Really amazing and touching talk by Torie Robinson about bridging the gap between professionals, scientists and patients

Cinzia Scarcelli talked about the unmet needs of rare families. Thank you Cinzia and all the families for your great work and collaboration in research

Great work from the SCN8A European Federation presented by Gregory Cabanach

Really interesting to hear from Stefania Dantone, Maaike Studemund and Zhana Chokheli about the different experiences of the SCN2A families associations all over the world

Last talk of a really great conference by Misia Kowanda about Simons Searchlight registry

Thank you very much to everyone for a great conference

Really fantastic to work in a group scientifically at the top, collaborative and humanly warm

Our Rikke talking about epilepsy genetics at the first NorEpiNet. Thank for organizing a so interesting and educating course 😊

Very interesting talk by Elena at the NorEpiNet course. Thank you very much to be my PhD supervisor. I am really very happy to work with you, Rikke, Guido and all the Dianalund group

Proud of our research project about sleep disturbances in SCN8A related disorders that I presented today at the XXXIII Italian Sleep Medicine Congress. Thanks to all my working group at the Danish Epilepsy center

Christmas lunch at the research Department at the Danish Epilepsy Center 🎄

Happy to attend the 6th Dianalund International Conference on Epilepsy. Very interesting and high scientifical level speeches. Thank you to Elena Gardella, Rikke Møller and Guido Rubboli to organize this event and proud to be part of your working group

Thank you very much to the DICE organizing committee for this amazing event with very interesting fantastic talks, stimulating discussions and warm atmosphere

The phenotypic and genotypic spectrum of individuals with mono- or biallelic #ANK3 variants. Our work is now online showing the main clinical features of ANK3: intellectual disability, developmental delay, behavioral issues, hypotonia, sleep disturbances, and epilepsy.

A big thank you to Amanda, Zeynep, Elena, Rikke, and all the co-authors for a very fruitful collaboration.

Honorated to participate to a very interesting STXBP1 summit in Philadelphia and proud to represent the Danish Epilpsy Center with the results of our research on early mortality in STXBP1 disorders