The expanding genetic landscape of hereditary motor neuropathies

Source
Brain - ISSN 0006-8950-143:12 (2020) p. 3540-3563
Author(s)

The role of Kv7.2 in neurodevelopment : insights and gaps in our understanding

Source
Frontiers in physiology - ISSN 1664-042X-11 (2020) p.
Author(s)

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy

Source
Brain - ISSN 0006-8950-143:5 (2020) p. 1447-1461
Author(s)
    Nicolas Chatron, Felicitas Becker, Heba Morsy, Miriam Schmidts, Katia Hardies, Beyhan Tuysuz, Sandra Roselli, Maryam Najafi, Dilek Uludag Alkaya, Farah Ashrafzadeh, Amira Nabil, Tarek Omar, Reza Maroofian, Ehsan Ghayoor Karimiani, Haytham Hussien, Fernando Kok, Luiza Ramos, Nilay Gunes, Kaya Bilguvar, Audrey Labalme, Eudeline Alix, Damien Sanlaville, Julitta de Bellescize, Anne-Lise Poulat, Ali-Reza Moslemi, Holger Lerche, Patrick May, Gaetan Lesca, Sarah Weckhuysen, Homa Tajsharghi

Biological concepts in human sodium channel epilepsies and their relevance in clinical practice

Source
Epilepsia - ISSN 0013-9580-61:3 (2020) p. 387-399
Author(s)
    Andreas Brunklaus, Juanjiangmeng Du, Felix Steckler, Ismael I. Ghanty, Katrine M. Johannesen, Christina Dühring Fenger, Stephanie Schorge, David Baez‐Nieto, Hao‐Ran Wang, Andrew Allen, Jen Q. Pan, Holger Lerche, Henrike Heyne, Joseph D. Symonds, Sameer M. Zuberi, Stephan Sanders, Beth R. Sheidley, Dana Craiu, Heather E. Olson, Sarah Weckhuysen, Peter De Jonge, Ingo Helbig, Hilde Van Esch, Tiffany Busa, Matthieu Milh, Bertrand Isidor, Christel Depienne, Annapurna Poduri, Arthur J. Campbell, Jordane Dimidschstein, Rikke S. Møller, Dennis Lal