Alternating hemiplegia of childhood is a rare disorder caused by de novo mutations in the ATP1A3 gene, expressed in neurons and cardiomyocytes. As affected individuals may survive into adulthood, we use the term 'alternating hemiplegia'. The disorder is characterized by early-onset, recurrent, often alternating, hemiplegic episodes; seizures...
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2015 (v1)PublicationUploaded on: April 14, 2023
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2022 (v1)PublicationA systems-level analysis highlights microglial activation as a modifying factor in common epilepsies
Aims The causes of distinct patterns of reduced cortical thickness in the common human epilepsies, detectable on neuroimaging and with important clinical consequences, are unknown. We investigated the underlying mechanisms of cortical thinning using a systems-level analysis. Methods Imaging-based cortical structural maps from a large-scale...
Uploaded on: February 4, 2024 -
August 2018 (v1)Journal article
International audience
Uploaded on: December 4, 2022