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Neuropharmacology|September 24, 2021
Clinical and therapeutic significance of genetic variation in the GRIN gene family encoding NMDARsTim A Benke, Kristen Park, Ilona Krey, et al.Developmental Medicine and Child Neurology|May 24, 2021
Cerebral visual impairment in CDKL5 deficiency disorder: vision as an outcome measureHeather E Olson, Julia G Costantini, Lindsay C Swanson, et al.Neuron|November 26, 1999
Hippocampal LTD expression involves a pool of AMPARs regulated by the NSF-GluR2 interactionA Lüthi, R Chittajallu, F Duprat, et al.International Journal of Language & Communication Disorders|August 14, 2024
Parent-reported outcome measures evaluating communication in individuals with rare neurodevelopmental disorders: A systematic reviewJacinta M Saldaris, Jeremiah Ayalde, Samali Kankanange, et al.American Journal of Medical Genetics. Part A|March 1, 2024
Communication of individuals with CDKL5 deficiency disorder as observed by caregivers: A descriptive qualitative studyJessica Keeley, Sofia Benson-Goldberg, Jacinta Saldaris, et al.Journal of Child Neurology|September 3, 2025
Content Validation of the Communication Inventory Disability-Observer Reported (CID-OR)Jessica Keeley, Jacinta Saldaris, Sofia Benson-Goldberg, et al.American Journal of Medical Genetics. Part A|May 22, 2024
Rett syndrome diagnostic odyssey: Limitations of NextGen sequencingMegan Abbott, Katie Angione, Emily Forbes, et al.Contemporary Clinical Trials|February 12, 2022
Design and outcome measures of LAVENDER, a phase 3 study of trofinetide for Rett syndromeJeffrey L Neul, Alan K Percy, Timothy A Benke, et al.Nature Medicine|October 18, 2005
NKCC1 transporter facilitates seizures in the developing brainVolodymyr I Dzhala, Delia M Talos, Dan A Sdrulla, et al.Journal of Autism and Developmental Disorders|March 4, 2024
Psychometric Assessment of the Rett Syndrome Caregiver Assessment of Symptom Severity (RCASS)Melissa Raspa, Angela Gwaltney, Carla Bann, et al.Pageof 14