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Scott Perry

Showing results (131-140 of 150) with videos related to

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Molecular Cell|November 19, 2021
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brainSanxiong Liu, Kimberly A Aldinger, Chi Vicky Cheng, et al.
Blood Advances|November 8, 2019
Genome editing of HBG1 and HBG2 to induce fetal hemoglobinJean-Yves Métais, Phillip A Doerfler, Thiyagaraj Mayuranathan, et al.
Epilepsia|November 15, 2021
Surgical evaluation in children <3 years of age with drug-resistant epilepsy: Patient characteristics, diagnostic utilization, and potential for treatment delaysMichael Scott Perry, Sabrina Shandley, Max Perelman, et al.
Epilepsia|March 10, 2023
Leveraging expertise and optimizing clinical research: Initial success of a pediatric epilepsy surgery collaborativeMadison M Berl, Jennifer I Koop, Alyssa Ailion, et al.
Pediatric Neurology|March 19, 2026
Corpus Callosotomy or Focal Surgery in Children Presenting With Generalized Tonic Seizures: Findings From the Pediatric Epilepsy Research ConsortiumCemal Karakas, Aaron E L Warren, Juliet K Knowles, et al.
Seizure|January 8, 2024
Epilepsy surgery in children with genetic etiologies: A prospective evaluation of current practices and outcomesJason Coryell, Rani Singh, Adam P Ostendorf, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 29, 2022
Competency-based EEG education: a list of "must-know" EEG findings for adult and child neurology residentsFábio A Nascimento, Jin Jing, Roy Strowd, et al.
Brain : a Journal of Neurology|June 13, 2022
The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implicationsAndreas Brunklaus, Tobias Brünger, Tony Feng, et al.
Pediatric Neurology|June 19, 2024
Pediatric Palliative Epilepsy Surgery: A Report From the Pediatric Epilepsy Research Consortium (PERC) Surgery DatabaseMary Jeno, M Bridget Zimmerman, Sabrina Shandley, et al.
American Journal of Human Genetics|November 4, 2017
Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and OsteopeniaThi Tuyet Mai Nguyen, Yoshiko Murakami, Eamonn Sheridan, et al.
Pageof 15

Showing results (131-140 of 150) with videos related to

Sort By:
Pageof 15
Molecular Cell|November 19, 2021
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brainSanxiong Liu, Kimberly A Aldinger, Chi Vicky Cheng, et al.
Blood Advances|November 8, 2019
Genome editing of HBG1 and HBG2 to induce fetal hemoglobinJean-Yves Métais, Phillip A Doerfler, Thiyagaraj Mayuranathan, et al.
Epilepsia|November 15, 2021
Surgical evaluation in children <3 years of age with drug-resistant epilepsy: Patient characteristics, diagnostic utilization, and potential for treatment delaysMichael Scott Perry, Sabrina Shandley, Max Perelman, et al.
Epilepsia|March 10, 2023
Leveraging expertise and optimizing clinical research: Initial success of a pediatric epilepsy surgery collaborativeMadison M Berl, Jennifer I Koop, Alyssa Ailion, et al.
Pediatric Neurology|March 19, 2026
Corpus Callosotomy or Focal Surgery in Children Presenting With Generalized Tonic Seizures: Findings From the Pediatric Epilepsy Research ConsortiumCemal Karakas, Aaron E L Warren, Juliet K Knowles, et al.
Seizure|January 8, 2024
Epilepsy surgery in children with genetic etiologies: A prospective evaluation of current practices and outcomesJason Coryell, Rani Singh, Adam P Ostendorf, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 29, 2022
Competency-based EEG education: a list of "must-know" EEG findings for adult and child neurology residentsFábio A Nascimento, Jin Jing, Roy Strowd, et al.
Brain : a Journal of Neurology|June 13, 2022
The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implicationsAndreas Brunklaus, Tobias Brünger, Tony Feng, et al.
Pediatric Neurology|June 19, 2024
Pediatric Palliative Epilepsy Surgery: A Report From the Pediatric Epilepsy Research Consortium (PERC) Surgery DatabaseMary Jeno, M Bridget Zimmerman, Sabrina Shandley, et al.
American Journal of Human Genetics|November 4, 2017
Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and OsteopeniaThi Tuyet Mai Nguyen, Yoshiko Murakami, Eamonn Sheridan, et al.
Pageof 15