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Recruiting CASTLE Advisory Group Members

Would you like to contribute to research about rolandic epilepsy? Do you have rolandic epilepsy and are aged between 5 and 18? Are you a parent or carer of a child with rolandic epilepsy? Do you want to make a difference to the rolandic epilepsy community? If so, we need your help. We are looking […]

A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy

Rolandic epilepsy is a common genetic focal epilepsy of childhood characterized by centrotemporal sharp waves on electroencephalogram. In previous genome-wide analysis, we had reported linkage of centrotemporal sharp waves to chromosome 11p13, and fine mapping with 44 SNPs identified the ELP4-PAX6 locus in two independent US and Canadian case–control samples. Here, we aimed to find […]

What every parent should know about Rolandic Epilepsy

Rolandic epilepsy is the most common type of epilepsy – affecting about one-sixth of all children with epilepsy in the UK – that means over 10,000 people! So you are definitely not alone. We will use the simple term “rolandic epilepsy” (RE) throughout this book, although you will also find it labelled elsewhere as “benign […]

Register for Symposium on Idiopathic Focal Epilepsies

Please complete the form below to register your interest in the upcoming symposium. For questions and further details please contact amber.collingwood@kcl.ac.uk.

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