Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Jeffrey L Neul

Showing results (111-120 of 122) with videos related to

Pageof 13
Sort By:
Trials|December 21, 2024
International workshop: what is needed to ensure outcome measures for Rett syndrome are fit-for-purpose for clinical trials? June 7, 2023, Nashville, USAJenny Downs, Dominique C Pichard, Walter E Kaufmann, et al.
Human Molecular Genetics|July 2, 2016
Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndromeSurabi Veeraragavan, Ying-Wooi Wan, Daniel R Connolly, et al.
Journal of Neurodevelopmental Disorders|September 17, 2021
Current neurologic treatment and emerging therapies in CDKL5 deficiency disorderHeather E Olson, Carolyn I Daniels, Isabel Haviland, et al.
Therapeutic Advances in Rare Disease|July 14, 2025
Finding buried genetic test results in the electronic health record is inefficient and variable across institutionsOlivia J Veatch, Jomol Mathew, Shira Rockowitz, et al.
Disease Models & Mechanisms|November 2, 2012
Preclinical research in Rett syndrome: setting the foundation for translational successDavid M Katz, Joanne E Berger-Sweeney, James H Eubanks, et al.
Journal of Neurodevelopmental Disorders|May 15, 2022
Anxiety-like behavior and anxiolytic treatment in the Rett syndrome natural history studyCaroline B Buchanan, Jennifer L Stallworth, Aubin E Joy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 19, 2006
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed malesDaniela del Gaudio, Ping Fang, Fernando Scaglia, et al.
Pediatric Neurology|August 13, 2021
Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental SyndromesOlivia J Veatch, Beth A Malow, Hye-Seung Lee, et al.
Neuroscience and Biobehavioral Reviews|August 24, 2019
Towards a consensus on developmental regressionDajie Zhang, Francesco Bedogni, Sofie Boterberg, et al.
Nature|May 22, 2015
Wild-type microglia do not reverse pathology in mouse models of Rett syndromeJieqi Wang, Jan Eike Wegener, Teng-Wei Huang, et al.
Pageof 13

Showing results (111-120 of 122) with videos related to

Sort By:
Pageof 13
Trials|December 21, 2024
International workshop: what is needed to ensure outcome measures for Rett syndrome are fit-for-purpose for clinical trials? June 7, 2023, Nashville, USAJenny Downs, Dominique C Pichard, Walter E Kaufmann, et al.
Human Molecular Genetics|July 2, 2016
Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndromeSurabi Veeraragavan, Ying-Wooi Wan, Daniel R Connolly, et al.
Journal of Neurodevelopmental Disorders|September 17, 2021
Current neurologic treatment and emerging therapies in CDKL5 deficiency disorderHeather E Olson, Carolyn I Daniels, Isabel Haviland, et al.
Therapeutic Advances in Rare Disease|July 14, 2025
Finding buried genetic test results in the electronic health record is inefficient and variable across institutionsOlivia J Veatch, Jomol Mathew, Shira Rockowitz, et al.
Disease Models & Mechanisms|November 2, 2012
Preclinical research in Rett syndrome: setting the foundation for translational successDavid M Katz, Joanne E Berger-Sweeney, James H Eubanks, et al.
Journal of Neurodevelopmental Disorders|May 15, 2022
Anxiety-like behavior and anxiolytic treatment in the Rett syndrome natural history studyCaroline B Buchanan, Jennifer L Stallworth, Aubin E Joy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 19, 2006
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed malesDaniela del Gaudio, Ping Fang, Fernando Scaglia, et al.
Pediatric Neurology|August 13, 2021
Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental SyndromesOlivia J Veatch, Beth A Malow, Hye-Seung Lee, et al.
Neuroscience and Biobehavioral Reviews|August 24, 2019
Towards a consensus on developmental regressionDajie Zhang, Francesco Bedogni, Sofie Boterberg, et al.
Nature|May 22, 2015
Wild-type microglia do not reverse pathology in mouse models of Rett syndromeJieqi Wang, Jan Eike Wegener, Teng-Wei Huang, et al.
Pageof 13