J. Ponmalar

Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations

K. Thangaraj, P. Govindaraj, A. Taly, 2018, Clinical Neurology and Neurosurgery.

Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome

K. Thangaraj, K. Satyamoorthy, P. Govindaraj, 2021, Journal of Neurology.

Infantile Onset Encephalomyopathy, Heart Block, and Sensorineural Hearing Loss: RMND1-Associated Mitochondrial Disease

P. Govindaraj, A. Taly, S. Sinha, 2020, Journal of Pediatric Neurology.