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Topic
Maladaptive Myelination in Pediatric Epilepsy
Description
Maladaptive myelination in epilepsy may represent a novel pathogenic mechanism in neurological diseases that can be targeted in the development of disease-modifying therapeutics. In this talk, Drs. Michelle Monje and Juliet Knowles will speak on a newly-appreciated form of brain plasticity, activity-dependent myelination, and how it may become maladaptive in children with epilepsy.
Dr. Monje is a pediatric neuro-oncologist and neuroscientist whose lab published pioneering work on activity-dependent myelination and neuron-glioma interactions. Dr. Knowles is a neuroscientist and child neurologist specializing in the treatment of children with epilepsy. She will discuss her discovery of a novel pathogenic mechanism in pediatric generalized epilepsy. Activity-dependent myelin plasticity is a newly recognized form of neural network adaptation, which is required for normal function. An unexplored possibility is that seizures may also alter myelin, with deleterious effects. Dr. Knowles’s research demonstrates that seizures induce abnormal myelination which contributes to seizure progression.
Time
Mar 1, 2021 12:00 PM in
Pacific Time (US and Canada)
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Stanford MCHRI
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Hi there, You are invited to a Zoom webinar. When: Mar 1, 2021 12:00 PM Pacific Time (US and Canada) Topic: Maladaptive Myelination in Pediatric Epilepsy Register in advance for this webinar: https://stanford.zoom.us/webinar/register/WN_rrMRPAlKRD2BAhiEDWXW2Q Or an H.323/SIP room system: H.323: 162.255.37.11 (US West) 162.255.36.11 (US East) 115.114.131.7 (India Mumbai) 115.114.115.7 (India Hyderabad) 213.19.144.110 (Amsterdam Netherlands) 213.244.140.110 (Germany) 103.122.166.55 (Australia Sydney) 103.122.167.55 (Australia Melbourne) 149.137.40.110 (Singapore) 64.211.144.160 (Brazil) 69.174.57.160 (Canada Toronto) 65.39.152.160 (Canada Vancouver) 207.226.132.110 (Japan Tokyo) 149.137.24.110 (Japan Osaka) Meeting ID: 925 3657 3977 SIP: 92536573977@zoomcrc.com After registering, you will receive a confirmation email containing information about joining the webinar. ---------- Webinar Speakers Michelle Monje, MD, PhD (Associate Professor of Neurology & Neurological Sciences @Stanford School of Medicine) Michelle Monje, MD, PhD, is an Associate Professor of Neurology & Neurological Sciences at Stanford School of Medicine. Following her undergraduate degree in biology at Vassar College, Dr. Monje received her MD and PhD in Neuroscience from Stanford University. She then completed neurology residency at the Massachusetts General Hospital/Brigham and Women's Hospital/Harvard Medical School program. She subsequently returned to Stanford for a clinical fellowship in pediatric neuro-oncology and a postdoctoral fellowship. The scope of her research program encompasses the molecular determinants of neural precursor cell fate, neuronal-glial interactions, and the role of neural precursor cells in oncogenesis and repair mechanisms. As a practicing neurologist and neuro-oncologist, Dr Monje is dedicated to understanding the neurodevelopmental origins of pediatric brain tumors and the neurological consequences of cancer treatment. Juliet Knowles, MD, PhD (Instructor of Neurology and Neurological Sciences @Stanford School of Medicine) Juliet Knowles, MD, PhD, is an instructor in the department of neurology and neurological sciences at Stanford School of Medicine. Dr. Knowles is a neuroscientist and child neurologist specializing in the treatment of children with epilepsy. She will discuss her discovery of a novel pathogenic mechanism in pediatric generalized epilepsy. Activity-dependent myelin plasticity is a newly recognized form of neural network adaptation, which is required for normal function. An unexplored possibility is that seizures may also alter myelin, with deleterious effects. Dr. Knowles’s research demonstrates that seizures induce abnormal myelination which contributes to seizure progression. Maladaptive myelination in epilepsy may represent a novel pathogenic mechanism that can be targeted in the development of disease-modifying therapeutics.
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