Dalal P, Leslie ND, Lindor NM, Gilbert DL, Espay AJ. Motor tics, stereotypies, and self-flagellation in Primrose Syndrome. Neurology 2010; 75:284-286.
Ridel KR, Lipps, TD, Gilbert DL. The Prevalence of Neuropsychiatric Disorders in Children Diagnosed with Sydenham’s Chorea: a long-term follow-up of a clinic-based sample. Pediatric Neurology 2010;42:243-248.
Hopkins SE, Somoza A, Gilbert DL. Rare Autosomal Dominant POLG1 mutation in a family with Metabolic Strokes, Posterior Column Spinal Degeneration, and Multiendocrine Disease. Journal of Child Neurology 2009. October 18 Epub ahead of print.
Gilbert DL, Leslie EJ, Keddache M, Leslie ND. A Novel Hereditary Spastic Paraplegia with Dystonia linked to chromosome 2q24-2q31. Movement Disorders 2009; 24: 364-370.
Wong LJ, Naviaux RK, Brunetti-Pierri N, Zhang Q, Schmitt ES, Truong C, et al. Molecular and clinical genetics of mitochondrial diseases due to POLG mutations. Hum Mutat 2008; 29:E150-E172.
Giles LL, Delbello MP, Gilbert DL, Stanford KE, Shear PK, Strakowski SM. Cerebellar ataxia in youth at risk for Bipolar Disorder. Bipolar Disorders 2008; 10:733-737.