Podcasts about epilepsy research

This week, Jonathan sits down with Jacqueline French to explore groundbreaking innovations in epilepsy research, the challenges of misdiagnosis, and the transformative impact of advancements in clinical trial methodologies. French also shares insights into global epilepsy care challenges, and her vision for the future of neurological health.    Timestamps:  (00:00) - Introduction  (01:34) - Career beginnings   (07:38) - The Epilepsy Study Consortium  (14:48) - Ethical considerations in clinical trials  (17:13) - New strategies for designing trials   (25:25) - The evolving landscape of anti-seizure drugs  (27:45) - Innovative treatments  (32:30) - Cases of misdiagnosis   (35:19) - The five S's to identify epilepsy  (39:12) - Educating and tackling stigma  (44:03) - French's three wishes for healthcare  

This month Seizing Life® goes on location at the Joey's Song Freezing Man Festival to speak with Kay Hanley and John Cowsill, two musicians with personal connections to epilepsy who participated in the multiday music festival to raise money for epilepsy research.

Research Fellow Georgia Cook explains the challenges of and positive impacts of positive, effective communication upon patient and family Quality of Life, the importance of qualitative research engagement and how it compliments quantitative research, and strategies to improve patient communication in an epilepsy trial. This is part 2 of 2 with Georgia. ------------------------------------------

Paediatric neurologist, scientist, and PPI Lead Julia Jacobs and Torie Robinson discuss the role of individuals with Lived Experience in research, particularly in the context of the iNeuron project, which focuses on epilepsy, stroke, and dementia. They explore the challenges and opportunities presented by basic science research, the importance of knowledge translation, and the benefits of engaging young researchers. The conversation emphasises the shared experiences across different diseases and the motivation that comes from personal connections in research. ------------------------------------------

James is flying solo in this episode while Mai Ling is traveling and he brings us a fascinating conversation with our guest, Professor Mark Cook, a Melbourne-based Consultant Neurologist who specializes in the treatment of epilepsy. James talks with Mark about what prompted his desire to work in epilepsy research specifically, the impact that epilepsy has on a person's life, the effects of MRI technology in epilepsy treatment, and the value of getting involved with people outside your specialty. This interview is jam-packed with interesting information and valuable takeaways for your own endeavors.

In this episode, we explore the science behind exercise as an adjunct treatment for epilepsy and debunk some common myths (spoiler alert: With very rare exceptions, exercise does NOT increase seizure risk). Dr. Ayushe Sharma talked with Dr. Jane Allendorfer, Dr. Halley Alexander, and Brian Wiedmeyer, who participated in an exercise research study.The episode refers to a 2016 report by the ILAE Task Force on Sports and Epilepsy - that report is freely available online at this link.Some of the other research papers mentioned in the episode are listed below.The relationship between physical activity and cognitive function in people with epilepsy: A systematic review Effects of physical exercise in people with epilepsy: A systematic review and meta-analysis Role of Physical Exercise as Complementary Treatment for Epilepsy and other Brain Disorders Epilepsy and exercise: An experimental study in female rats Effects of an exercise program on health of people with epilepsy: A randomized clinical trialA strength exercise program in rats with epilepsy is protective against seizuresEffectiveness of Yoga Intervention in Reducing Felt Stigma in Adults With Epilepsy Impact of exercise as a complementary management strategy in people with epilepsy: A randomized controlled trial Sharp Waves episodes are meant for informational purposes only, and not as clinical or medical advice.Let us know how we're doing: podcast@ilae.org.The International League Against Epilepsy is the world's preeminent association of health professionals and scientists, working toward a world where no person's life is limited by epilepsy. Visit us on Facebook, X (Twitter), Instagram, and LinkedIn.

Eduardo Pérez Palma, a neurogenetics scientist and bioinformatician, discusses his work in neurogenetics and epilepsy research, emphasising the importance global collaboration in studying the epilepsies in different parts of the world! Eduardo also shares the upcoming Latin American Congress on Genetic Epilepsiesin Jan 2025; which aims to bring together experts from various fields to share knowledge and perspectives! ------------------------------------------

Dr. Abel's clinical interest is in pediatric neurosurgery, epilepsy surgery, and neuromodulation. He completed a fellowship in epilepsy surgery and deep brain stimulation with Philippe Kahane, Dominique Hoffmann, and Stephan Chabardes at University Hospital of Grenoble in Grenoble, France. In Grenoble, Dr. Abel received special training in identification of epileptic foci using stereoelectroencephalography and use of the ROSA robot for epilepsy surgery. Dr. Abel then completed a pediatric neurosurgery fellowship with Jim Drake and Jim Rutka at The Hospital for Sick Children in Toronto, Canada focusing on epilepsy surgery, neuro-oncologic surgery, craniofacial surgery, and endoscopic techniques.

M. Scott Perry explains how Epilepsy Researchers require intros and support to be the best that they can be and initiate, manage, and see results. It's possible through the Pediatric Epilepsy Research Consortium (PERC). ------------------------------------------

Listen back to the full interview.See omnystudio.com/listener for privacy information.

This week on Seizing Life® we speak with Peter Burpee who experienced absence epilepsy in childhood and tonic clonic seizures in his teen years, but has gained seizure control and will be running in the upcoming NYC Marathon to raise money for epilepsy research. The post NYC Marathoner Achieves Seizure Control and Runs for Epilepsy Research appeared first on CURE Epilepsy.

This week on Seizing Life® Peter Burpee shares his experiences with absence and tonic clonic seizures and explains why he's running for Team CURE Epilepsy in the upcoming NYC Marathon. The post NYC Marathoner Achieves Seizure Control and Runs for Epilepsy Research appeared first on CURE Epilepsy.

Biochemist Matt Gentry shares with us his extensive research into the ultra-rare epilepsy Lafora Disease, his motivation from working with families, the brilliant work of the Lafora Disease charity Chelsea's Hope, and support from both the NIH and the Chan Zuckerberg Initiative. ------------------------------------------

Molecular Neuropathologist & PI Katja Kobow explains her research into unraveling the intricate interplay between epigenetic alterations and the development of epilepsy, specifically in the context of the adult post-mitotic brain. ------------------------------------------

Dr. Bruna Nucera interviewed Dr. Andrea Cheng-Hakimian about a retrospective study that included 28 years of data from women with epilepsy who gave birth in Washington State.This US study compared the relative occurrence of selected pregnancy outcomes and postpartum rehospitalizations among women with and without epilepsy and their infants. It used linked hospital records of women with deliveries in Washington State between 1987 and 2014. Women with epilepsy had increased risks of preeclampsia (RR 1.23; 95 % CI 1.08-1.41) and gestational diabetes (RR 1.18; 95 % CI 1.02-1.36). Their infants had increased risks of malformation (RR 1.23; 95 % C: 1.08-1.42) and small for gestational age (RR 1.39; 95 % CI 1.25-1.54) , and were nearly three times as likely to not be breastfed. Mothers (RR 5.25; 95 % CI 2.46-11.23) and their infants (RR 1.64, 95 % CI 1.41-1.89) required more ICU admissions during hospitalization for delivery and more postpartum rehospitalization, with greatest risk in the first six months. Maternal mortality (up to 2 years after delivery) was increased (RR 7.11; 95 % CI 2.47-20.49). Risks of preterm delivery and low birthweight increased over the study time period (p

Dr. Madeleine Oudin knew she was interested in medicine and biology from a young age. She took a science track of courses in high school in France and went on to do her undergraduate studies at McGill University. Despite a lack of advising, she found that she loved research and continued on to get a Masters and PhD in neuroscience. She shifted gears in her postdoc, studying cancer and tumor biology, and was surprised to learn of some of the overlaps with studying neuroscience. These two fields merged to form her research niche when she founded her own lab at Tufts University. But her research focus would shift once again after she discovered the diagnosis of her daughter Margot, who suffers from a rare form of epilepsy caused by gene mutations in SCN8. Together with her husband, she now also studies these types of disorders in mice and is working towards a cure for her daughter. Join us on this episode of LSP to learn from Dr. Oudin's impressive career journey and her inspiring dedication to help her daughter. Guest links: LinkedIn: https://www.linkedin.com/in/madeleine-oudin-56769529/ Twitter: https://twitter.com/MadeleineOudin Donate to Epilepsy Research: https://give.tufts.edu/campaigns/22193/donations/new?designation=scn8aepilepsyresearchfund Subscribe to our show wherever you listen to podcasts! Thank you for listening.

Hear of Richard Baines and his team use fruit flies in epilepsy research, the discoveries made, and the next steps for epilepsy research! Also hear more about the incredible Fly Facility at Manchester University!r University! ------------------------------------------ More about Richard:

It's that time of the week again. Tommy has found a hidden gem of a bakery, Evo has quite possibly the biggest win of his life. Tommy finds a few surprises at work and Evo gets an email from his agent he doesn't want to reply to. We finish on a high as Evo's bro completes his 12 hour run for Epilepsy Research. Sit back, relax and enjoy some "Good Banter" If you'd like to donate go to -https://www.walkforepilepsy.org.au/fundraisers/heathhocking

Host: Andrew Wilner, MD, Author of "The Locum Life: A Physician's Guide to Locum Tenens" Guest: Sanjay Kumar, PhD Temporal lobe epilepsy (TLE) is the most common form of focal epilepsy. Due to recent research from Florida State University, we might have a better understanding of the potential link between a specific protein and increased vulnerability to neurodegeneration among patients with this disorder. Dr. Andrew Wilner is joined by Dr. Sanjay Kumar, Professor of Biomedical Sciences and Neuroscience at Florida State University, to discuss this new discovery.

Peadiatric neurologist Allan Bayat from the Danish Epilepsy Center speaks of his Ph.D. in genetic epilepsies, his passion for translational medicine for the children and families affected, and future studies into the impact of modified treatments on comorbidities. ------------------------------------------

Drs. Sandi Lam and Joyce Wu, renowned pediatric epilepsy specialists, share news and insight about advances in pediatric epilepsy treatment - surgical and otherwise - and the research they're doing to continue to improve care.

Epilepsy research lead (PI) and lecturer in pharmacy, Cristina Reschke tells us about her work in both her exciting research into how microRNAs and circadian rhythm disruptions lead to epileptogenesis and seizures and educating pharmacists of the future regarding the epilepsies.---More about Cristina:  https://www.torierobinson.com/epilepsy-sparks-insights/cristina-reschke---Glossary:There are many terms used in this recording which you can find in the Epilepsy Sparks Glossary: https://www.epilepsysparks.com/glossary---Follow Torie on:- Twitter: https://twitter.com/torierobinson10- LinkedIn: https://www.linkedin.com/torierobinson- Instagram: https://www.instagram.com/torierobinson10- Facebook: https://www.facebook.com/TorieRobinsonSpeaker- Check out the website: https://www.torierobinson.com

In this episode we interview Daniel Kuebler about his research on the relation between diet and seizures in flies and how it applies to humans. (Radlicz, C., Chamber, A., Olis, E., and Kuebler, D (2019) The addition of a lipid-rich dietary supplement eliminates seizure-like activity and paralysis in the Drosophila Bang sensitive mutants. Epilepsy Research, 155: 106153. doi.org/10.1016/j.eplepsyres.2019.106153 ) We discuss the paper, how they made the discovery, and doing research with students.

We talk to three incredible epilepsy clinicians, geneticists, and researchers from the Danish Epilepsy Center (Rikke Steensbjerre Møller, Guido Rubboli, & Elena Gardella) who are working together with a passion to positively impact the lives of people affected by genetic epilepsies. ---5th Dianalund International Conference,  7-8 April 2022, 4220 Korsør, DenmarkRegister:  https://www.conferencemanager.dk/dice2022 Contact: genetics@filadelfia.dk---More about the team: https://www.torierobinson.com/epilepsy-sparks-insights/danish-epilepsy-center--- Glossary:There are many terms used in this recording which you can find in the Epilepsy Sparks Glossary: https://www.epilepsysparks.com/glossary ---Follow Torie on:Twitter: https://twitter.com/torierobinson10LinkedIn: https://www.linkedin.com/torierobinsonInstagram: https://www.instagram.com/torierobinson10  Facebook: https://www.facebook.com/TorieRobinsonSpeaker Check out the website: https://www.torierobinson.com

Today we talk to Samuel Terman; an epileptologist and researcher from the University of Michigan, USA, who specialises in helping people affected by seizures and epilepsy. Samuel tells us about his research into adherence to medications, polypharmacy, deprescribing, and the high rate of multiple disabilities amongst those with epilepsy. Samuel's work focuses on optimising the delivery of medical care for patients with epilepsy, through medication decisions, hospital utilisation and readmissions, and inpatient seizure monitoring quality of care.---Glossary: There are many terms used in this recording which you can find in the Epilepsy Sparks Glossary (useful for clinicians as well as patients/families): here: ww.epilepsysparks.com/glossary ---More about Samuel: www.torierobinson.com/epilepsy-sparks-insights/samuel-terman---Glossary:There are many terms used in this recording which you can find in the Epilepsy Sparks Glossary: https://www.epilepsysparks.com/glossary---Follow Torie on:Twitter: https://twitter.com/torierobinson10LinkedIn: https://www.linkedin.com/torierobinsonInstagram: https://www.instagram.com/torierobinson10Facebook: https://www.facebook.com/TorieRobinsonSpeakerCheck out the website: https://www.torierobinson.com

Christos Lisgaras, a research scientist and post-doctoral fellow at the lab of Prof. Helen Scharfman at the NYU Nathan Kline Institute for Psychiatric Research talks about his epilepsy research, sharing results data, his passion for helping other young people develop their careers in the field of epileptology, and communicating effectively with PWE. Also spoken of are Christos' discoveries linking the epilepsies and Alzheimer's. **CHECK OUT CHRISTOS**LinkedIn: https://www.linkedin.com/in/clisgaras Twitter: https://twitter.com/Chris_Lisgaras  NKI: https://www.nki.rfmh.org/faculty/christos-lisgaras-phd Google Scholar: https://scholar.google.com/citations?hl=en&user=LLrTPmIAAAAJ&view_op=list_works&alert_preview_top_rm=2&sortby=pubdate ORCiD: https://orcid.org/0000-0003-3712-5993 **ILAE-YES (Young Epilepsy Section)**ILAE-YES: https://www.ilae.org/about-ilae/topical-commissions/yes/young-epilepsy-section-yes/about-us  YouTube: https://www.youtube.com/channel/UCm02kiQ3Jd1PrIyJgC0tYMw **CHECK OUT THE PODCAST WITH CHRISTOS**Available on Spotify, Apple, Google, Stitcher, Amazon Music, and Deezer - Type in “Epilepsy Sparks Insights”**CHECK OUT THE YOUTUBE VIDEO WITH CHRISTOS**YouTube: https://youtu.be/_8sYCx96oAQ **CONNECT WITH TORIE**Website: https://www.torierobinson.comTwitter: https://twitter.com/torierobinson10LinkedIn: https://www.linkedin.com/torierobinsonFacebook: https://www.facebook.com/TorieRobinsonSpeakerYouTube: https://www.youtube.com/channel/UCm02kiQ3Jd1PrIyJgC0tYMw **CHECK OUT TORIE'S YOUTUBE**YouTube: https://www.youtube.com/c/TorieRobinson**HIRE TORIE AS A SPEAKER ON EPILEPSY, MENTAL HEALTH, DISABILITY, & DIVERSITY**https://www.torierobinson.com/contact

Business of Cannabis was the Platinum Media Partner for the Lift&Co. Expo in Toronto in November 2021. During the show, the Business of Cannabis team sat down with key leaders in the cannabis sector for conversations about where the industry is right now. This conversation was part of those sessions.Dr. Evan Cole Lewis is a Pediatric Neurologist and Clinical Neurophysiologist with expertise in epilepsy, epilepsy surgery, electroencephalography (EEG), teleneurology and medical cannabis for the treatment of neurologic disorders. Dr. Lewis is the director of the Neurology Centre of Toronto (NCT) which he established in January 2017. At NCT, Dr. Lewis treats children with a variety of neurological disorders and he also treats adults for concussion, headache and epilepsy. Dr. Lewis' interest in medical cannabis began in 2013 while training at Miami Children's Hospital – one of the major sites for the Epidiolex trials. He has significant clinical experience with medical cannabis in adults and children and is a member of the Canadian Consortium for the Investigation of Cannabinoids (CCIC), Canadian Childhood Cannabinoid Clinical Trials (C4T), and the Cannabinoid Research Initiative of Saskatchewan (CRIS).BofC Live is the daily news and interview program of Business of Cannabis. Business of Cannabis highlights the companies, brands, people and trends driving the sector.

WISCONSIN MUSIC PODCAST Episode 57 Joeys Song   Joey's Song was started in 2010 following the death of four-year-old Joey Gomoll, who passed one week shy of his fifth birthday. Joey suffered from a rare and debilitating form of epilepsy known as Dravet Syndrome. Dravet's caused persistent seizures which were never able to be controlled through medications leading to severe learning disabilities. While Dravet's robbed Joey of the ability to speak, Joey remained a happy and fun loving child. He was happiest when music was playing, allowing him to hum, drum and sing in his own way. To be present when music was playing meant only one thing, that Joey would soon have you dancing and enjoying the music with him.   https://www.joeyssong.org/  

Meet Alice Winsor, a research associate at King's College London working on the Integrating Mental & Physical healthcare: Research, Training & Services (IMPARTS) project in epilepsy -  an initiative aiming to bridge together physical and mental healthcare. This is the first time the project shall be rolled out amongst young people with epilepsy.Feel free to contact Alice (see below) to learn more about involvement!alice.winsor@kcl.ac.uk **CHECK OUT THE YOUTUBE VIDEO WITH ALICE**YouTube: https://www.youtube.com/c/TorieRobinson/videos  **CONTACT ALICE**Email: alice.winsor@kcl.ac.uk**CHECK OUT ALICE** Twitter: https://twitter.com/WinsorAlice LinkedIn: https://www.linkedin.com/in/alice-winsor-833b19110 **READ ABOUT ALICE'S WORK**ResearchGate: https://www.researchgate.net/profile/Alice-WinsorPubMed: https://pubmed.ncbi.nlm.nih.gov/?term=Winsor+AA&cauthor_id=33561679Orcid: https://orcid.org/0000-0001-6689-2425IMPARTS: https://imparts.orgKing's Health Partners: https://www.kingshealthpartners.orgKing's College Hospital: https://www.kch.nhs.ukRichards Lab: https://carolinerichards.net/peoplePal Lab: https://childhoodepilepsy.org Richardson Lab: https://epilepsy-london.org Bagshaw Lab: https://www.birmingham.ac.uk/research/centre-for-human-brain-health/labs-groups-networks/MIG/MIG-People.aspx Birmingham Uni: https://research.birmingham.ac.uk/portal/en/publications/sleep-disruption-in-children-and-adolescents-with-epilepsy(9462c710-54c7-4ba6-9f61-2e46e6e614f8).htmlEpilepsy Sparks: https://www.epilepsysparks.com/blog/sleep-disruption-in-childhood-epilepsy-alice-winsor **CONNECT WITH TORIE**Website: https://www.torierobinson.comTwitter: https://twitter.com/torierobinson10LinkedIn: https://www.linkedin.com/torierobinsonFacebook: https://www.facebook.com/TorieRobinsonSpeaker **CHECK OUT TORIE'S YOUTUBE & BLOG**YouTube: https://www.youtube.com/c/TorieRobinsonBlog: https://www.torierobinson.com/blog**HIRE TORIE AS A SPEAKER ON EPILEPSY, MENTAL HEALTH, DISABILITY, & DIVERSITY**https://www.torierobinson.com/contact

Today's Episode Today Dr. Raj meets with Dr. John Khoury to discuss epilepsy, the different types of seizures, and treatment options available. The second half of today's episode includes a Q&A segment featuring questions you submitted.  Today's Guest  Dr. John S. Khoury attended Cornell University prior to starting his medical degree at Thomas Jefferson University. He remained at Thomas Jefferson University Hospital, where he completed an internship in internal medicine and was then Chief Resident in Neurology. He won numerous awards while at Thomas Jefferson University, including awards for teaching and stroke research. He is a contributor to the book Gray's Clinical Neuroanatomy and has multiple presentations, including publications in Neurology and Epilepsy Research. About Dr. Raj Dr Raj is a quadruple board certified physician and associate professor at the University of Southern California. He was a co-host on the TNT series Chasing the Cure with Ann Curry, a regular on the TV Show The Doctors for the past 7 seasons and has a weekly medical segment on ABC news Los Angeles. Want more Dr. Raj? Check out the Beyond the Pearls lecture series! The Ultimate High Yield Bundle: The complete review of high-yield clinical medicine topics necessary for graduate medical education board exams including NBME, USMLE Steps 1/2/3, ITE and ABIM Boards. You can also listen to the Beyond the Pearls podcast. An InsideTheBoards Podcast. Check out our other shows: Crush Step 1 Step 2 Secrets Physiology by Physeo Step 1 Success Stories The InsideTheBoards Study Smarter Podcast The InsideTheBoards Podcast The Health Beat   Produced by Ars Longa Media To learn more about us and this podcast, visit arslonga.media. You can leave feedback or suggestions at arslonga.media/contact or by emailing info@arslonga.media. Produced by: Christopher Breitigan. Executive Producer: Patrick C. Beeman, MD The information presented in this podcast is intended for educational purposes only and should not be construed as professional or medical advice. Learn more about your ad choices. Visit megaphone.fm/adchoices

Meet Mona Heiland, a final year Ph.D. student from RCSI, Ireland who under the supervision of Prof David Henshall is studying the effects ofcannabidiol (CBD) on microRNA expressions in epilepsy.CBD has shown its potential as an Anti-Seizure Medication; especially for drug-refractory genetic types of epilepsy, however, the underlying molecular mechanisms of CBD's anti-seizure activities are still unknown. Mona investigates whether the anti-seizure effects of CBD are dependent on the regulation of microRNAs. **CONNECT WITH MONA**• Twitter: https://twitter.com/MonaHeiland **READ ABOUT MONA'S WORK**• Website: https://www.futureneurocentre.ie/people/mona-heiland • ResearchGate: https://www.researchgate.net/profile/Mona-Heiland • RCSI: https://repository.rcsi.com/authors/Mona_Heiland/7896944 **CHECK OUT THE YOUTUBE VIDEO WITH MONA**• YouTube: https://www.youtube.com/c/TorieRobinson/videos **CONNECT WITH TORIE**• Website:https://www.torierobinson.com• Twitter:https://twitter.com/torierobinson10• LinkedIn:https://www.linkedin.com/torierobinson• Facebook:https://www.facebook.com/TorieRobinsonSpeaker **CHECK OUT TORIE'S YOUTUBE & BLOG**• YouTube: https://www.youtube.com/c/TorieRobinson• Blog: https://www.torierobinson.com/blog**HIRE TORIE AS A SPEAKER ON EPILEPSY, MENTAL HEALTH, DISABILITY, & DIVERSITY**https://www.torierobinson.com/contact

If you have listened to the Seizing Life podcast you know that it's produced by CURE Epilepsy. But do you know what CURE Epilepsy, the organization, actually does? Are you aware of its mission and how it funds epilepsy research to help accelerate science and find a cure? The post Funding Epilepsy Research: How CURE Epilepsy Advances Science to Find a Cure appeared first on CURE Epilepsy.

CURE Epilepsy CEO Beth Dean explains how the organization funds research, why it remains “patient-focused” in its mission, and what areas of epilepsy research offer the most promise for finding cures. The post Funding Epilepsy Research: How CURE Epilepsy advances science to find a cure appeared first on CURE Epilepsy.

Meet Professor Simon Keller, an imaging neuroscientist from the University of Liverpool. Simon tells us about his neuroimaging work, his passion for helping those affected by epilepsy, and his cool images!  **CONNECT WITH SIMON**Twitter: https://twitter.com/BrainImagingUoL **READ ABOUT SIMON'S WORK**ResearchGate: https://www.researchgate.net/profile/Simon-Keller-2 **The Liverpool BRAIN lab (Brain Research using Advanced Imaging in Neurology)https://www.liverpool.ac.uk/translational-medicine/research/brain-imaging/ University of Liverpool: https://www.liverpool.ac.uk/systems-molecular-and-integrative-biology/staff/simon-keller **CHECK OUT THE YOUTUBE VIDEO WITH SIMON**YouTube:  https://youtu.be/2gxoNo9hmN4**CONNECT WITH TORIE**Website:https://www.torierobinson.comTwitter:https://twitter.com/torierobinson10 LinkedIn:https://www.linkedin.com/torierobinsonFacebook:https://www.facebook.com/TorieRobinsonSpeaker **CHECK OUT TORIE'S YOUTUBE & BLOG**YouTube: https://www.youtube.com/c/TorieRobinsonBlog: https://www.torierobinson.com/blog**HIRE TORIE AS A SPEAKER ON EPILEPSY, MENTAL HEALTH, DISABILITY, & DIVERSITY**https://www.torierobinson.com/contact

Meet Asst. Prof. Gabriele Lignani: the Principal Investigator, Senior Research Fellow, & Biotechnologist at the University for Neurology and Neurosurgery, Queen Square, London, and recent winner of the Harinarayan Young Neuroscientist Award 2021 for his research into Activity-dependent Gene Therapy for Intractable Epilepsy! Gabriele speaks with Torie about researching gene therapy for epilepsy and his journey into epilepsy research.CONNECT WITH GABRIELELinkedIn: https://www.linkedin.com/in/gabriele-lignani-288b9023Twitter: https://twitter.com/LignaniLab_UCL & https://twitter.com/gabrilignani READ ABOUT GABRIELE'S WORKWebsite: https://www.lignanilab.comResearchGate: https://www.researchgate.net/profile/Gabriele-Lignani Rare Revolution interview: https://bit.ly/3reUJacREAD THE INTERVIEW WITH GABRIELEhttps://www.torierobinson.com/blog/gabriele-lignani-gene-therapy CONNECT WITH TORIEWebsite: https://www.torierobinson.comTwitter: https://twitter.com/torierobinson10LinkedIn: https://www.linkedin.com/torierobinsonFacebook: https://www.facebook.com/TorieRobinsonSpeaker CHECK OUT TORIE'S YOUTUBE & BLOGYouTube: https://youtube.com/c/TorieRobinsonBlog: https://www.torierobinson.com/blog

Meet Dr. Gareth Morris, a neuroscientist at FutureNeuro, honorary lecturer at RCSI, and Editor of Epilepsy In English. We talk about his research into temporal lobe epilepsy, how he first got into and what attracted him to epilepsy research, and how much it means to him to hear from people with epilepsy! You'll also hear a bit about his cool website and blog.**CONNECT WITH GARETH MORRIS**• LinkedIn: https://www.linkedin.com/in/gareth-morris • Twitter: https://twitter.com/GarethMorris5 **READ ABOUT GARETH'S WORK**• Website: https://www.epilepsyinenglish.ie • ResearchGate: https://www.researchgate.net/profile/Gareth-Morris-3 • FutureNeuro: https://www.futureneurocentre.ie/people/gareth-morris **CHECK OUT THE YOUTUBE VIDEO WITH GARETH**• YouTube: https://www.youtube.com/c/TorieRobinson**CONNECT WITH TORIE**• Website:https://www.torierobinson.com• Twitter:https://twitter.com/torierobinson10• LinkedIn:https://www.linkedin.com/torierobinson• Facebook: https://www.facebook.com/TorieRobinsonSpeaker **CHECK OUT TORIE'S YOUTUBE & BLOG**• YouTube: https://www.youtube.com/c/TorieRobinson• Blog: https://www.torierobinson.com/blog**HIRE TORIE AS A SPEAKER ON EPILEPSY, MENTAL HEALTH, DISABILITY, & DIVERSITY & INCLUSION**https://www.torierobinson.com/contact

Dear Friends Family Revolutionaries, and the UninitiatedIt is our privilege to take a dive behind the scenes and speak to one of the individuals affecting real change. PhD candiditate Patrick Milder helps get a better understanding of our interconnectedness to the Tree of Life. Taking a peek at life, from a non-human perspective to  begin to see the beauty of Life. RNA strands floating freely in the deep basins of the sea, explosive geosphere altering volcanoes; the boom of life that always accompanies a mass extinction event, and it occuring all around us. Missing links much? Times flies like a banana, Mojave flies like alcohol. Everything drinks alcohol, and how some animals survive in the "exotic" environments. Inducing epilipectic seizures in fish, to help treat medication resistant Epilepsy. No fish can't feel pain, can; Well we discussed it- consensus ???Science the truth in our continued errors, and why that; makes science more trustworthy. Thank you Asett for taking the time to edit the voices and make them shine like ebony. Art by Jesse Owins for the "Firs & Desire" to the podcast message https://www.jesseowinsart.com/ Music by Erky  twitter: https://twitter.com/ErkyPlaysyoutube: Erky PlaysThank you Dear friends, family, revolutionaries, & the uninitiated; thank you for taking the time to lend an ear, as we hold conversations with these soapbox revolutionaries. It starts with a conversation, and it helps to have ears; be blessed.Be revolutionary, Thoughts are free; Revolution takes action.Donations: https://ko-fi.com/freethoughtrevolutionContact: freethoughtrev@gmail.com

Jay and Eric talk with Autumn Karen on a challenging subject – A rare chromosome disorder of her daughter Hermione. Sadly, they lost her at the age of 3.5 years, but those years were blessed with loved and empathy. Episode Highlights: 03:01: Autumn narrates about her tragedy. She states that at first, all looked good, but there was a slight clue that something was wrong which the doctors were not able to put a pin.05:18: There are markers for normal or commonly known syndromes or congenital disabilities, but everything was new and unheard of in Hermione’s case. She had plastic surgery at the age of 3 months.06:29: Interestingly, during the same time, Autumn was doing a psychological dissertation on the topic “How families are told about diagnosis.”07:00: Jay empathizes and supports Autumn saying that it might have been confusing and challenging as a nail already hits you in the head.07:28: At the hospital when Autumn was informed of her daughter’s condition. The doctor coldly asks her to google it.07:40: Jay and Eric discuss how some people don’t understand or communicate with you about your pain during tough times. Eric shares a personal experience about how he felt when doctors don’t show any empathy.09:54: Jay points out mental health crisis is not just for the parents or children; doctors also deal with the same situation. There should be an awareness about the same.13:23: Hermione had a 10% chance of survival when she was born. Autumn discusses the privileges that they got from the government and family members.14:54: Eric puts an important question “What are the options available to those people who don’t have such kind of privileges?”16:58: Jay stresses that the issue should be addressed so that, privileged or not, no child should be left out to get proper care and service.17:56: Autumn shares about Hermione’s seizures; at times, they were for 2 hours.19.24: Autumn confesses that before this tragic incident, she had no idea about Sudden Unexpected Death in Epilepsy (SUDEP).22:30: Autumn takes the listeners to an emotional ride when she narrates Hermione’s last moments.25:01: Jay respected the fact that Autumn did not put Hermione under heavy medication but instead tried her best to give her a normal childhood.28:27: Eric talks about his personal experience with epilepsy and how he jokes about it.32:18: Autumn jokes about how her other two kids took things lightly and made seizure faces.35:20: To help parents who have special needs children, Autumn points out that it is essential to talk about it. There is nothing to be afraid of about it.37:24: Funding is also missing for special needs child welfare.48:00: Eric and Jay discuss that “The importance of discussing how it feels to go back to the house post a tragic loss. This discussion is something that has to happen.”49:32: Jay talks about the importance of meditation.53:57: Family with special needs child tends to isolate from the society, it is important to invite them and make them feel welcome.55:15: Jay asks, “Do you think society is becoming more understanding towards special needs children?”58.31: Jay and Eric motivate Autumn and appreciates that she talks about Hermione. They acknowledge that she is making a change.59:55: Jay points out that the entire situation is more about miscommunication; hence it is crucial to talk about it.01:01:06: Autumns stresses that she is not ashamed to talk about Hermione or her disability.3 Key Points:Autumn knows about life with and without a child with a disability, and she shares how life was like Hermione.Autumn explains the difference between controlled and uncontrolled seizures. She also shares about the percentage of survival. Autumn shares the challenges she faced as a single mom of 3 kids and how society, friends, family, or neighbors can help take the pressure off.Resources Mentioned:www.c22c.org | https://www.purpleday.org/C22C Videohttps://autumnkaren.compurpleday.org

With terms like vaccine trials and research currently being floated and discussed in the media right now, it makes you wonder how does the research get done? Dr. Richard Marn’s guest for today’s episode is Onome Eka, a Clinical Research Coordinator for the Epilepsy Program of the Department of Neurology at Mount Sinai Health System. Onome discusses how they’re doing research studies to understand seizures and the brain at Mount Sinai. She also explains the importance of their role in making sure the studies' information and the coordination of such research are done in the right and proper way, especially as it applies to clinical research and healthcare.

Today on Seizing Life, we speak with Mike Coburn, Executive Vice President and Chief Operating Officer of Research!America, an organization that advocates for science, discovery and innovation to achieve better health for all.  The post The Impact of COVID-19 on Epilepsy Research appeared first on CURE Epilepsy.

Mike Coburn of Research!America shares insights on the near- and long-term impacts of the COVID-19 pandemic on epilepsy research and the research community at large. The post The Impact of COVID-19 on Epilepsy Research appeared first on CURE Epilepsy.

As a child growing up with epilepsy, Christin Godale experienced stigma and exclusion by her peers, driving her to hide her condition from friends and classmates. But a neurologist's encouragement sparked Christin's interest in understanding her own epilepsy and eventually brought her to acceptance, advocacy, and the pursuit of her PhD in neuroscience with the ultimate the goal of becoming an epilepsy researcher. The post It's Personal: Christin Godale's Path to Epilepsy Research appeared first on CURE Epilepsy.

PhD candidate and aspiring epilepsy researcher Christin Godale shares her journey from hiding her epilepsy to becoming an advocate and pursuing a career in neuroscience. The post It’s Personal: Christin Godale’s Path to Epilepsy Research appeared first on CURE Epilepsy.

PhD candidate and aspiring epilepsy researcher Christin Godale shares her journey from hiding her epilepsy to becoming an advocate and pursuing a career in neuroscience. The post It’s Personal: Christin Godale’s Path to Epilepsy Research appeared first on CURE Epilepsy.

“The thing about it, she said, ‘Why are they destroying our city?'  And I said, ‘What if you were trying to get mommy and daddy's attention and we weren't paying attention to you? What would you do?'  She was like, ‘Well, I would talk louder.'  I'm like, ‘What if we still didn't listen to you?'  She was like, ‘I would scream!'  And I was like, ‘What if we STILL didn't listen?'  She was like, ‘I would be really sad. I would start crying.'  And I was like, ‘I know! And what if we STILL didn't listen?  What if it went on all day long and we just didn't listen to you?'  She was like, ‘I would be so upset. I would… I don't know.'  And I was like, ‘Would you throw a fit? A tantrum?'  And she was like, ‘Yeah, I probably would. I'd probably throw my toys at you.'  And I was like ‘That's kind of what happened, and then we would notice you because you would be making a mess, and we'd say ‘Sydney, Sydney, what's wrong?'  And we would stand with you and try to calm you down and listen to you.'  So I said, ‘That's kind of what happened with black people around the city.'  Definitely the first night. And people I think have realized what was going on, finally, and what black lives matters means and they were like, ‘Alright. You're right.  We stand with you.'” - Deborah Cordner Carson   The CrossFit community may best recognize and remember Deborah Cordner Carson as the gutsy athlete who gave an inspirational performance at the 2012 CrossFit Games, overcoming a fear of open water swimming in the triathlon event and going on to win the 2012 Spirit of the Games award.  Deb could also be distinguished by the compression sleeve she wears on her left leg, and by the color of her skin.  Deb is one of the few black competitors in the sport of CrossFit. Growing up, Deborah was inspired by great athletes in her family.  Her father came to America from Trinidad and Tobago on a track and field scholarship and her grandfather was the heavy weight lifting champion of the British Empire.  As a young girl she competed in gymnastics, and as a teenager she excelled in track and field, eventually earning a full scholarship to the University of Northern Iowa as a 400-meter sprinter. When Deb developed lymphedema, a condition where fluid is retained in certain parts of the body and can cause dangerous swelling, she was forced to retire from her track and field career, but in time, she discovered ways to manage her condition- including that recognizable compression sleeve- while still being active.  She took up CrossFit and quickly rose to elite status in the sport, placing as high as 5th in the 2013 CrossFit Open and 13th at the 2012 CrossFit Games. Since retiring, Deborah continues to do CrossFit for health, but she has also struggled with the heartbreak of multiple miscarriages, and most recently, a diagnosis of gestational trophoblastic disease, a type of pregnancy-related cancer. Throughout her life, Deborah has been aware that the color of her skin means she's had to work harder for opportunities than others.  As a mother to two mixed-race little girls and a resident of the Minneapolis area, she also has a unique perspective on the recent events that have highlighted the ongoing systemic racism in our society. I am grateful to Deb for taking a moment to share her perspective amidst all the other challenges she is currently taking on.  These conversations can be uncomfortable, but they're also important as we all strive to stand together and learn from each other.  In this episode, we chat about her experiences as a minority CrossFit Games athlete, the mentality she's using to fight her cancer diagnosis, the lessons she strives to teach her daughters, and how we should all speak up to overcome injustice and racial bias.   In this episode we discuss: Deborah's struggles with multiple miscarriages How she is coping with the diagnosis of gestational trophoblastic disease, a type of pregnancy-related cancer How Deborah's experience competing in CrossFit helps her focus on the task at hand when it comes to tackling challenges Her initial reactions to hearing about George Floyd's death and the outrage in Minneapolis Explaining the looting and rioting to her daughter Deborah's personal experiences with systemic racism and unconscious racism How Deborah needed to be the best of the best to have the same opportunities as her white classmates Deborah's thoughts on why there's a disconnect in people understanding the additional challenges a black person has to overcome The lack of sponsorship opportunities available for a black CrossFit athlete Her disappointment with CrossFit HQ's silence What it's like to be a black athlete in the predominantly white sport of CrossFit Ways that Deb approaches the topic of racism with her children The importance of speaking up and making an effort to understand other cultures Three things Deborah does on a regular basis that have the biggest positive impact on her health One thing she thinks could have a big impact on her health, but she has a hard time implementing What a healthy life looks like to Deborah   You can follow Deborah on Instagram Links: 2012 CrossFit Games - Spirit of The Games Winner: Deborah Cordner Carson CrossFit Games Regionals 2012 - Proud: Deborah Cordner Carson CrossFit - 'I'll Do It All' LymphCare: Deborah's Story Related episodes: Ep 10 - Jenny LaBaw on Running 500 Miles for Epilepsy Research and Education Ep 15 - Lewis Howes on Chasing Greatness Ep 70 - USA Track & Field Heptathlete Tiffeny Parker on Beating the Odds Ep 137 - Rich & Hillary Froning on Putting Family First If you like this episode, please subscribe to Pursuing Health on iTunes and give it a rating. I'd love to hear your feedback in the comments below and on social media using the hashtag #PursuingHealth. I look forward to bringing you future episodes with inspiring individuals and ideas about health every other Tuesday. Disclaimer: This podcast is for general information only, and does not provide medical advice. We recommend that you seek assistance from your personal physician for any health conditions or concerns. This post was originally published on June 8, 2020.

Dr. Abel’s clinical interest is in pediatric neurosurgery, epilepsy surgery, and neuromodulation. He completed a fellowship in epilepsy surgery and deep brain stimulation with Philippe Kahane, Dominique Hoffmann, and Stephan Chabardes at University Hospital of Grenoble in Grenoble, France. In Grenoble, Dr. Abel received special training in identification of epileptic foci using stereoelectroencephalography and use of the ROSA robot for epilepsy surgery. Dr. Abel then completed a pediatric neurosurgery fellowship with Jim Drake and Jim Rutka at The Hospital for Sick Children in Toronto, Canada focusing on epilepsy surgery, neuro-oncologic surgery, craniofacial surgery, and endoscopic techniques.

On this episode of Seizing Life, Dr. Vicky Whittemore, Program Director for Epilepsy and Epileptogenesis at NINDS and CURE Scientific Advisory Council member, explains how NINDS sets priorities, funds research, and collaborates with non-profits to move science forward in pursuit of new treatments for epilepsy. The post NINDS Its Role in Epilepsy Research appeared first on CURE Epilepsy.

Discover how NINDS funds epilepsy research and fosters collaboration towards cures from Program Director Dr. Vicky Whittemore. The post NINDS and Its Role in Epilepsy Research appeared first on CURE Epilepsy.

Discover how NINDS funds epilepsy research and fosters collaboration towards cures from Program Director Dr. Vicky Whittemore. The post NINDS and Its Role in Epilepsy Research appeared first on CURE Epilepsy.

A lot of people think that if you have epilepsy, you were born with it or developed it as a child. But the truth is, 1 in 26 people will be diagnosed with epilepsy in their lifetime. Anyone can develop epilepsy - at any point, at any age. And as the population grows older, more and more adults will develop epilepsy. Nancy Goldfarb is one of those people. Nancy explains what it feels like for her to have a seizure, how her super power is something called an aura, and why the last thing she wants you to do is put a stick in her mouth. To help tell her story, Nancy is joined by her Neurologist and Jefferson University Physician, Dr. Christopher Skidmore. Thank you to our sponsors: Sunovion - A committed partner of the Epilepsy Foundation and TalkAboutIt.org To learn more about Epilepsy Research and how to join a clinical trial, Visit efepa.org/research Credits: Produced by The Epilepsy Foundation Eastern Pennsylvania Post Production by Studio D Podcast Production Additional Resources: https://www.beyondceliac.org/celiac-disease/facts-and-figures/ https://www.joslin.org/info/genetics_and_diabetes.html

On this episode of Seizing Life®, we take our show on the road to Epilepsy Awareness Day to speak with several experts from around the United States on a variety of epilepsy topics including genetic testing, new epilepsy devices, advances in epilepsy surgery and promising new treatments for Dravet Syndrome. The post Hot Topics in Epilepsy Research appeared first on CURE Epilepsy.

The post Hot Topics in Epilepsy Research appeared first on CURE Epilepsy.

The post Hot Topics in Epilepsy Research appeared first on CURE Epilepsy.

In the eighth episode of TSC Now, host Dan Klein catches up with TS Alliance partners at the annual American Epilepsy Society Meeting (AES), the largest gathering on epilepsy in the world, which was held December 6-10 in Baltimore. Seizures remain one of the most common neurological features of TSC, occurring in 85% of individuals … Continue reading Episode 8: Excerpts from AES and the Current State of Epilepsy Research →

You don't have to be a neuroscientist to understand epilepsy research. CURE's Board Chair and former Head of the Research Committee, Stacey Pigott, explains how even those without a science background can develop the skills they need to dive into research findings, using them to better communicate with physicians and empower advocacy. The post You Don't Have to Be a Brain Surgeon to Understand Epilepsy Research appeared first on CURE Epilepsy.

You don’t have to be a neuroscientist to understand epilepsy research.  Learn how people without a science background can be empowered by research. The post You Don’t Have to Be a Brain Surgeon to Understand Epilepsy Research appeared first on CURE Epilepsy.

You don’t have to be a neuroscientist to understand epilepsy research.  Learn how people without a science background can be empowered by research. The post You Don’t Have to Be a Brain Surgeon to Understand Epilepsy Research appeared first on CURE Epilepsy.

Recorded on Anchor.fm with use of Audacity 0 I made it on Monday `6mm 2019. This episode blends epilepsy with paranormal activity in a question. My Skype ID is Dusty Road and my facebook group is Gary Murphy presents = Dusty Road.

In part 2 of Epilepsy & Research, Dr. Kate Davis shows what research and funding can do in the field of Epilepsy. She also talks about why she joined the field and what we can do to support the next generation of doctors and researchers. Luke Debevec continues his story about how he was diagnosed with Epilepsy in the middle of his career as a lawyer. He also shares how he his helping other professionals with disabilities. Thank you to our sponsors: Walk to End Epilepsy – Pennsylvania Series Penn Medicine To learn more about Epilepsy Research and how to join a clinical trial, Visit efepa.org/research EFEPA Young Adult Retreat Credits: Produced by The Epilepsy Foundation Eastern Pennsylvania Post Production by Studio D Podcast Production

Epilepsy can be hard to diagnose and people commonly mistake it for something else. Luke Debevec shares his story of being diagnosed with Epilepsy in the middle of his career as an attorney. Host Missy Dolaway also talks to Dr. Kate Davis about new technology and treatment being researched at Penn Medicine. Thank you to our sponsors: Penn Medicine To learn more about Epilepsy Research and how to join a clinical trial, Visit efepa.org/research The 2019 Mardi Gras Gala Produced by The Epilepsy Foundation Eastern Pennsylvania Post Production by Studio D Podcast Production

Measles cases in Europe have tripled between 2017 and 2018, the highest number recorded this decade according to the World Health Organisation. We discuss parental attitudes to vaccinating children and what parents should know with Helen Bedford, Professor of Children's Health at University College London's Great Ormond Street Institute of Child Health and Samantha Vanderslott, social sciences researcher at Oxford Vaccine Group. There are 600,000 people in the UK with epilepsy and one third of them find that current treatment options do not fully help them to control their seizures. Many of those are women who find that their condition worsens in pregnancy or experience increased seizure frequency around their menstrual cycle. Jane talks to Fran Thomas who has epilepsy and to Dr Simona Balestrini who is undertaking research into improved diagnosis and treatment options that may benefit women. President Trump has attracted regular criticism from left of centre women, not least at last month's women's marches across the US. But what of those women who already back his party, the Republicans? We hear about the many women who support him and his policies. And, what's the secret to hosting and delivering a great speech, presentation or event? We hear from Mariella Frostrup and Viv Groskop.

Dr. Cass Ingram is a nutritional physician who received a B.S. in biology and chemistry from the University of Northern Iowa (1979) and a D.O. from the University of Osteopathic Medicine and Health Sciences in Des Moines, IA (1984). Dr. Ingram has since written over 20 books on natural healing and is recognized as one of North America's leading experts on the health benefits and disease fighting properties of wild medicinal spice extracts. A popular media personality, he has appeared on over 5,000 radio and TV shows. He now travels the world promoting perfect health – the natural way. An interview with medicinal herb and spice expert Dr. Cass Ingram author of The Cannabis Cure Study: Neurologist uses cannabis to stop or reduce seizures in 261 epileptic kids Researchers are burning the midnight oil to discover the many wonderful medicinal properties of the cannabis plant – a rich source of important chemical compounds called cannabinoids which are linked to the healthy function of virtually every organ and system in the human body. In a clinical study recently presented to members of the American Epilepsy Society, Dr. Orrin Devinski, Professor of Neurology, Neurosurgery, and Psychiatry at New York University School of Medicine, was able to demonstrate how one powerful cannabinoid known as CBD (short for cannabidiol) was able to significantly reduce or halt seizures and convulsions more than two hundred epileptic children. “The study involved some 313 epilepsy victims, all children, who were given a medically purified form of the CBD cannabinoid and monitored over a 90-day period. Of the 261 children who remained in the study, virtually all had a response that was astounding: a 50% reduction in seizures or convulsions. Furthermore, 10% of the children became seizure-free during the treatment period,” says Dr. Cass Ingram, author of the book The Cannabis Cure. Dr. Ingram, an expert in the medicinal properties of cannabis and other plants, says the historical evidence supporting the use of cannabinoid-rich herbs such as cannabis, holy basil, wild sage, wild rosemary, and wild oregano to treat epilepsy and nervous disorders is vast. “A wide range of infectious agents can be involved in the causation of seizure syndromes, including viruses, molds, fungi, worms, protozoa, and other parasites, and all are capable of invading brain tissue where they lay eggs or create cysts which place pressure on brain centers, leading to seizures,” says Dr. Ingram. “The cannabinoid rich-plants and their oils are especially suited to attack these hidden invaders and quickly inactivate them.” In terms of pure antiseptic properties, Dr. Ingram says wild oregano oil has been documented as the most potent natural germ and parasite killer known. “It is particularly effective against viruses, bacteria, molds, and yeasts,” says Dr. Ingram. “As published in the scientific literature, oregano’s main action is against protozoans: amoebas, blastocysts, cryptosporidium, the malarial parasite, and giardia. It is also an ideal agent for brain infections of any type, as many of its components penetrate the blood-brain barrier.” Is there any evidence that wild oregano by itself is a remedy for seizures? “Historically, it was used precisely for precisely that purpose,” says Dr. Ingram. “It was the ancient Greeks who used it successfully for treating seizure syndromes, but they also used it as a cure for other head-related syndromes such as migraines. In an animal study published in Epilepsy Research and Treatment, researchers found that the essential oil of wild oregano, rich in the active ingredient carvacrol, prevented seizures significantly. So did other essential oils, including oils of mint, peppermint, basil, rosemary, and lavender.” #insomnia #epilepsy #autism #depression #stress #pain #cancer #heart #medical #marihuana #medicalmarihuana #hemp #hempanol

This month, Mark Richardson, professor of epilepsy, Kings College London, relates his vision for the future of epilepsy research (1.07).Alexander Leff, consultant neurologist, Institute of Cognitive Neuroscience, University College London, discusses his online tool for diagnosing and providing treatment for hemianopia, the visual impairment which can follow stroke or brain injury (14.07).And measuring sensory nerve conduction. Tom Sears, emeritus professor of neurophysiology, King’s College London, recalls the beginnings of the technique (22.39).See also:Large scale brain models of epilepsy: dynamics meets connectomics http://tinyurl.com/ab6ggfhA ‘web app’ for diagnosing hemianopia http://tinyurl.com/ahca28xRead-Right http://tinyurl.com/37f3y3kEye-Search http://tinyurl.com/af3fsz2Sensory nerve action potentials in patients with peripheral lesions http://tinyurl.com/a7rsj4s

Solomon Moshe, M.D., director of the division of pediatric neurology, and Shlomo Shinnar, M.D., Ph.D., professor of neurology and pediatrics, discuss three decades of epilepsy research. Their collaboration bridges the gap between basic and clinical research. Interviewed by Einstein’s Karen Gardner.