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 (61-70 of 122) with videos related to

Pageof 13
Sort By:
Human Molecular Genetics|January 31, 2015
Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgeneMeagan R Pitcher, José A Herrera, Shelly A Buffington, et al.
The Journal of Genetic Psychology|February 20, 2025
Shared Environment - Different Genes: Speech-Language Development in a Pair of Dizygotic Twins with and Without <i>MECP2</i> MutationSigrun Lang, Peter B Marschik, Zuzanna Laudańska, et al.
Med (New York, N.Y.)|June 25, 2024
Trofinetide for the treatment of Rett syndrome: Results from the open-label extension LILAC studyAlan K Percy, Jeffrey L Neul, Timothy A Benke, et al.
Brain : a Journal of Neurology|December 24, 2016
Longitudinal course of epilepsy in Rett syndrome and related disordersDaniel C Tarquinio, Wei Hou, Anne Berg, et al.
Journal of Autism and Developmental Disorders|January 30, 2017
Assessment of Caregiver Inventory for Rett SyndromeJane B Lane, Amber R Salter, Nancy E Jones, et al.
Neurology|March 29, 2019
Double-blind, randomized, placebo-controlled study of trofinetide in pediatric Rett syndromeDaniel G Glaze, Jeffrey L Neul, Walter E Kaufmann, et al.
Nature Medicine|June 8, 2023
Trofinetide for the treatment of Rett syndrome: a randomized phase 3 studyJeffrey L Neul, Alan K Percy, Timothy A Benke, et al.
Pediatric Neurology|January 17, 2024
Trofinetide Treatment Demonstrates a Benefit Over Placebo for the Ability to Communicate in Rett SyndromeJeffrey L Neul, Alan K Percy, Timothy A Benke, et al.
American Journal of Medical Genetics. Part A|June 14, 2025
Medical Biases and Misconceptions Impact Diagnoses in Males With Loss of Function MECP2 VariantsTalia Thompson, Dennis Gurfinkel, Lori Silveira, et al.
Brain & Development|September 16, 2018
Behavioral profiles in Rett syndrome: Data from the natural history studyCaroline B Buchanan, Jennifer L Stallworth, Alexandra E Scott, et al.
Pageof 13

Showing results (61-70 of 122) with videos related to

Sort By:
Pageof 13
Human Molecular Genetics|January 31, 2015
Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgeneMeagan R Pitcher, José A Herrera, Shelly A Buffington, et al.
The Journal of Genetic Psychology|February 20, 2025
Shared Environment - Different Genes: Speech-Language Development in a Pair of Dizygotic Twins with and Without <i>MECP2</i> MutationSigrun Lang, Peter B Marschik, Zuzanna Laudańska, et al.
Med (New York, N.Y.)|June 25, 2024
Trofinetide for the treatment of Rett syndrome: Results from the open-label extension LILAC studyAlan K Percy, Jeffrey L Neul, Timothy A Benke, et al.
Brain : a Journal of Neurology|December 24, 2016
Longitudinal course of epilepsy in Rett syndrome and related disordersDaniel C Tarquinio, Wei Hou, Anne Berg, et al.
Journal of Autism and Developmental Disorders|January 30, 2017
Assessment of Caregiver Inventory for Rett SyndromeJane B Lane, Amber R Salter, Nancy E Jones, et al.
Neurology|March 29, 2019
Double-blind, randomized, placebo-controlled study of trofinetide in pediatric Rett syndromeDaniel G Glaze, Jeffrey L Neul, Walter E Kaufmann, et al.
Nature Medicine|June 8, 2023
Trofinetide for the treatment of Rett syndrome: a randomized phase 3 studyJeffrey L Neul, Alan K Percy, Timothy A Benke, et al.
Pediatric Neurology|January 17, 2024
Trofinetide Treatment Demonstrates a Benefit Over Placebo for the Ability to Communicate in Rett SyndromeJeffrey L Neul, Alan K Percy, Timothy A Benke, et al.
American Journal of Medical Genetics. Part A|June 14, 2025
Medical Biases and Misconceptions Impact Diagnoses in Males With Loss of Function MECP2 VariantsTalia Thompson, Dennis Gurfinkel, Lori Silveira, et al.
Brain & Development|September 16, 2018
Behavioral profiles in Rett syndrome: Data from the natural history studyCaroline B Buchanan, Jennifer L Stallworth, Alexandra E Scott, et al.
Pageof 13