Precision Medicine For Children With Genetic Epilepsies - Sameer Zuberi, UK
Listen to the podcast:
Hear about precision medicine for children with genetic epilepsies with Sameer Zuberi, Consultant Paediatric Neurologist, Researcher, & Honorary Professor from the Royal Hospital for Children, Glasgow, UK - with a special mention of the rare epilepsies Dravet & CDKL5 (as June happens to be Awareness month for each).
See episode #02 with Sameer here: “Why Have Epilepsy Syndromes Been Reclassified/Renamed?”
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Sameer Zuberi is a Consultant Paediatric Neurologist, Researcher, & Honorary Prof at the Royal Hospital for Children, in Glasgow, UK.
Sameer’s clinical and research interests include epilepsy, movement disorders, neurogenetics, channelopathies and neurological sleep disorders.
In 2005 he established the Glasgow Epilepsy Genetics Service and has been its clinical lead since then. He is Chair of the International League Against Epilepsy Commission on Classification & Terminology, Editor-in-Chief of the European Journal of Paediatric Neurology, Board member of the European Paediatric Neurology Society & Glut1 Deficiency UK, & on the Medical Advisory Board for Dravet Syndrome UK.
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Twitter | University of Glasgow | ILAE | ILAE Award EPNS | Dravet UK | EpiCARE | Glut1 Deficiency UK | Epilepsia | Google Scholar | Wikipedia | EAN Pages |
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Other episodes:
Helplines, email address, and website for Ukrainians seeking anti-seizure medications.