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Cephalalgia : an International Journal of Headache|March 18, 2022
The spectrum of indomethacin-responsive headaches in children and adolescentsKenneth A Myers, Rebecca Barmherzig, Nichelle R Raj, et al.
BMJ Open|February 16, 2022
Healthy food prescription incentive programme for adults with type 2 diabetes who are experiencing food insecurity: protocol for a randomised controlled trial, modelling and implementation studiesDana Lee Olstad, Reed Beall, Eldon Spackman, et al.
Epilepsia|February 13, 2023
WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality riskKaren L Oliver, Marina Trivisano, Simone A Mandelstam, et al.
Neurology. Genetics|October 30, 2023
mTOR Pathway Somatic Pathogenic Variants in Focal Malformations of Cortical Development: Novel Variants, Topographic Mapping, and Clinical OutcomesEric Krochmalnek, Andrea Accogli, Judith St-Onge, et al.
Pediatric Neurology|July 3, 2026
Examining Epilepsy in Angelman Syndrome: Insights From Caregiver-Reported Data in the Linking Angelman and Dup15q Data for Expanded Research DatabaseSarah Nelson Potter, Carlos Petzold, Katie Garbarini, et al.
Pediatric Neurology|November 5, 2021
Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability SyndromeJacqueline L Steele, Michelle M Morrow, Harvey B Sarnat, et al.
Epilepsia|March 14, 2020
KCNT1-related epilepsy: An international multicenter cohort of 27 pediatric casesFelippe Borlot, Ahmed Abushama, Nadine Morrison-Levy, et al.
Brain : a Journal of Neurology|July 28, 2025
Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatoniaHarsha Murthy, Ny Hoang, Jamie C Stark, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 24, 2023
Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor betaVéronique Caron, Nicolas Chassaing, Nicola Ragge, et al.
American Journal of Human Genetics|May 30, 2024
MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignatureRemzi Karayol, Maria Carla Borroto, Sadegheh Haghshenas, et al.
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