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Journal of Child Neurology|June 28, 2015
Survey of the Child Neurology Program Coordinator Association: Workforce Issues and Readiness for the Next Accreditation SystemTerri B Feist, Julia L Campbell, Julie A LaBare, et al.Journal of Child Neurology|December 28, 2016
Challenges in Implementation of the New Accreditation SystemTerri B Feist, Julia L Campbell, Julie A LaBare, et al.Pediatric Neurology|July 31, 2016
The Clinical Predictors That Facilitate a Clinician's Decision to Order Genetic Testing for Rett SyndromeVinita Misra Knight, Paul S Horn, Donald L Gilbert, et al.Case Reports in Medicine|January 14, 2010
Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplicationRaymond A Clarke, Zhi Ming Fang, Ashish D Diwan, et al.Journal of Child Neurology|January 26, 2018
An Atypical Rett Syndrome Phenotype Due to a Novel Missense Mutation in CACNA1AMadison V Epperson, Michael E Haws, Shannon M Standridge, et al.Pediatric Neurology|October 18, 2011
When should clinicians order genetic testing for Dravet syndrome?Jamie K Fountain-Capal, Katherine D Holland, Donald L Gilbert, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2009
Immunopathogenic mechanisms in tourette syndrome: A critical reviewDavide Martino, Russell C Dale, Donald L Gilbert, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|February 17, 2017
GNAO1-associated epileptic encephalopathy and movement disorders: c.607G>A variant represents a probable mutation hotspot with a distinct phenotypeRavindra Arya, Christine Spaeth, Donald L Gilbert, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 30, 2026
The burden of bone disease in Duchenne muscular dystrophy: age-specific prevalence of osteoporosis and low bone densityNat Nasomyont, Cuixia Tian, Lindsey Hornung, et al.American Journal of Medical Genetics. Part A|July 28, 2023
An evaluation of clinical presentation and genetic testing approaches for patients with neuromuscular disordersAmanda Rosenberg, Cuixia Tian, Hua He, et al.Pageof 21