Thulasi, V., Veerapandiyan, A., Pletcher, B. A., Tong, C. M., & Ming, X. (2017). A Case of Brown-Vialetto-Van Laere Syndrome Due To a Novel Mutation in SLC52A3 Gene: Clinical Course and Response to Riboflavin. Child Neurol Open.

Thulasi, Venkatraman, Aravindhan Veerapandiyan, Beth A. Pletcher, Chun M. Tong, i Xue Ming. "A Case of Brown-Vialetto-Van Laere Syndrome Due To a Novel Mutation in SLC52A3 Gene: Clinical Course and Response to Riboflavin." Child Neurol Open 2017.

Thulasi, Venkatraman, et al. "A Case of Brown-Vialetto-Van Laere Syndrome Due To a Novel Mutation in SLC52A3 Gene: Clinical Course and Response to Riboflavin." Child Neurol Open 2017.