Day 1: Picture Collage on Facebook for 10 Years AHC & ATP1A3 Symposium (Edinburgh) 19th Oct 2022
We would like to thank Malcolm Cochrane for all the amazing professional pictures he has taken for the symposium.
10-YEAR ANNIVERSARY CONFERENCE
10-YEAR ANNIVERSARY CONFERENCE COMMEMORATING THE GENE DISCOVERY ‘DEFINING THE FUTURE FOR AHC & ATP1A3 DISEASES’
Alternating Hemiplegia of Childhood in Korea: a Case Report
Alternating Hemiplegia of Childhood in Korea: a Case Report Chaewon Shin,1,2 Dallah Yoo,3 Han-Joon Kim,4 and Beomseok Jeon4 Abstract Alternating hemiplegia of childhood (AHC) is a rare neurodevelopmental disorder characterized…
SAVE the DATE (19th to 21st of Oct 2022): 10 years Anniversary Conference
Do you want to connect with the international AHC and ATP1A3 community? Are you interested in learning more about current research and future plans in AHC and ATP1A3? Would you…
Alternating Hemiplegia of Childhood (AHC) Patient Journey Leaflet
The news of the publication of the leaflet and patient journey for AHC has been included in the newsletter of EpiCARE-ERN, the European Reference Network for Rare and Complex Epilepsies.…
Newsletter January 2022
Dear AHC families, researchers and supporters, As we come to the end of the first week of 2022, we hope you and your family have had a good Christmas and…
Andrea’s Long Covid Static Cycle for Anya & All AHC Champions
For the past 7 months, I have been one of the estimated 2 million people in the UK with Long Covid. It has prevented me from doing most of the…
Revision of the Diagnostic Criteria of Alternating Hemiplegia of Childhood
EDITORIAL | ARTICLES IN PRESS Revision of the Diagnostic Criteria of Alternating Hemiplegia of Childhood Mohamad A. Mikati, Eleni Panagiotakaki, Alexis Arzimanoglou Published: May 03, 2021 DOI: https://doi.org/10.1016/j.ejpn.2021.05.004 Article Info:…
De novo ATP1A3 variants cause polymicrogyria
Satoko Miyatake, Mitsuhiro Kato, Takuma Kumamoto, Tomonori Hirose, Eriko Koshimizu, Takaaki Matsui, Hideyuki Takeuchi, Hiroshi Doi, Keisuke Hamada, Mitsuko Nakashima, Kazunori Sasaki, Akio Yamashita, Atsushi Takata, Kohei Hamanaka, Mai Satoh,…
Distinct neurological disorders with ATP1A3 mutations
Erin L Heinzen, Alexis Arzimanoglou, Allison Brashear, Steven J Clapcote, Fiorella Gurrieri, David B Goldstein, Sigurður H Jóhannesson, Mohamad A Mikati, Brian Neville, Sophie Nicole, Laurie J Ozelius, Hanne Poulsen,…
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