A. Arzimanoglou

Methodology of a Natural History Study of a Rare Neurodevelopmental Disorder: Alternating Hemiplegia of Childhood as a Prototype Disease

Maria Papadopoulou, E. Panagiotakaki, R. Vavassori, 2023, Journal of child neurology.

Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene.

E. Heinzen, L. Vijfhuizen, A. M. van den Maagdenberg, 2023, European journal of human genetics : EJHG.

Alternating hemiplegia of childhood: metabolic studies in the largest European series of patients.

S. Nevsimalova, R. Artuch, A. Arzimanoglou, 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Absence of Mutation in the SLC2A1 Gene in a Cohort of Patients with Alternating Hemiplegia of Childhood (AHC)

A. Arzimanoglou, B. Fontaine, S. Nicole, 2010, Neuropediatrics.