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Molecular Autism|December 28, 2019
Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literatureAlexander Kolevzon, Elsa Delaby, Elizabeth Berry-Kravis, et al.
Journal of Autism and Developmental Disorders|March 29, 2008
Characterization of potential outcome measures for future clinical trials in fragile X syndromeElizabeth Berry-Kravis, Allison Sumis, Ok-Kyung Kim, et al.
Journal of Autism and Developmental Disorders|March 14, 2026
Discourse Marker Use in Mothers of Autistic Individuals and FMR1 Premutation CarriersNell Maltman, Gary E Martin, Jamie Barstein, et al.
Clinical Parkinsonism & Related Disorders|April 20, 2026
Essential tremor-like phenotype in Fragile X carrier womenDeborah A Hall, Danuta Loesch, Tyler Svymbersky, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|March 27, 2020
TECPR2 mutation-associated respiratory dysregulation: more than central apneaPallavi P Patwari, Lisa F Wolfe, Girish D Sharma, et al.
Annals of Neurology|December 29, 2004
Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivationElizabeth Berry-Kravis, Kristina Potanos, Dahlia Weinberg, et al.
ACS Chemical Neuroscience|December 8, 2022
Emerging Therapeutic Strategies for Fragile X Syndrome: Q&AGhassan Alusi, Elizabeth Berry-Kravis, David Nelson, et al.
Journal of Inherited Metabolic Disease|August 15, 2025
Biomarker Validation in NPC1: Foundations for Clinical Trials and Regulatory AlignmentKrista Casazza, Stephanie M Cologna, Elizabeth Berry-Kravis, et al.
Archives of Neurology|August 18, 2004
Genetic polymorphisms in Parkinson disease subjects with and without hallucinations: an analysis of the cholecystokinin systemJennifer G Goldman, Christopher G Goetz, Elizabeth Berry-Kravis, et al.
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