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Journal of Neurology|September 10, 2021
Disrupted structural connectome and neurocognitive functions in Duchenne muscular dystrophy: classifying and subtyping based on Dp140 dystrophin isoformVeeramani Preethish-Kumar, Apurva Shah, Kiran Polavarapu, et al.Journal of Neurogenetics|July 8, 2024
Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathyShivani Sharma, Anita Mahadevan, Gayathri Narayanappa, et al.Investigative Ophthalmology & Visual Science|May 16, 2013
Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in IndiaNahid Akhtar Khan, Periyasamy Govindaraj, Nagasamy Soumittra, et al.Multiple Sclerosis and Related Disorders|January 23, 2018
Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children?Parayil Sankaran Bindu, Kothari Sonam, Shwetha Chiplunkar, et al.Investigative Ophthalmology & Visual Science|August 3, 2017
Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in IndiaNahid Akhtar Khan, Periyasamy Govindaraj, Nagasamy Soumittra, et al.Metabolic Brain Disease|April 5, 2017
Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiencyShwetha Chiplunkar, Parayil Sankaran Bindu, Madhu Nagappa, et al.Neuromuscular Disorders : NMD|August 22, 2021
Whole exome sequencing reveals a homozygous C1QBP deletion as the cause of progressive external ophthalmoplegia and multiple mtDNA deletionsLe Guo, Periyasamy Govindaraj, Mariëlle Kievit, et al.Mitochondrion|November 10, 2016
Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South IndiaKothari Sonam, Parayil Sankaran Bindu, M M Srinivas Bharath, et al.Toxicology Reports|December 15, 2022
A proteomic study to unveil lead toxicity-induced memory impairments invoked by synaptic dysregulationNivedha Mohanraj, Neha S Joshi, Roshni Poulose, et al.Mitochondrion|March 27, 2019
Mitochondrial genome variations in idiopathic dilated cardiomyopathyPeriyasamy Govindaraj, Bindu Rani, Pandarisamy Sundaravadivel, et al.Pageof 7