Webinars

Title; Autoimmune Encephalitis beyond NMDA-R Antibodies, Josep Dalmau, March 27, 2021

Title; Pattern recognition in white matter disorders and leukodystrophies: What have we learned?, Marjo S. van der Knaap, March 13, 2021

Encephalopathic Newborn: It is not HIE, then what?, Linda DeVries, February 27, 2021

Topic; Pediatric Ischemic stroke: Recent practical advances in acute interventions, Mark Mackay (Murdoch Children's Research Institute, Australia), February 13, 2021

FEBSTAT: What have we learned so far?Shlomo Shinnar (Albert Einstein College of Medicine, USA) February 05, 2021

Topic; Precision medicine and Epilepsy GeneticsRikke Steensbjerre Møller (Danish Epilepsy Centre, Dianalund) January 23, 2021

Topic; Neurometabolic disorders: The ones that should not be missed Ingrid Tein (The Hospital for Sick Children, Toronto) January 09, 2021

Are you or someone you know searching for a diagnosis for child with a neurologic condition? Are you searching for the cause of symptoms, such as seizures, because you aren’t confident the current treatment is the best option for the child? You are not alone. Earlier this year, we sent out a survey to our community and heard from over 1,000 families about their diagnostic journey. In response to what we heard from families the Child Neurology Foundation is hosting a webinar on the role of genetic testing to shorten the diagnostic odyssey on November 18. ...