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The Indian Journal of Medical Research|April 11, 2015
Mitochondrial disorders: challenges in diagnosis & treatmentNahid Akhtar Khan, Periyasamy Govindaraj, Angamuthu Kannan Meena, et al.Molecular Vision|June 28, 2013
Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathyNahid Akhtar Khan, Periyasamy Govindaraj, Vuskamalla Jyothi, et al.Mitochondrion|February 20, 2013
Mitochondrial DNA variations in Madras motor neuron diseasePeriyasamy Govindaraj, Atchayaram Nalini, Nithin Krishna, et al.Journal of Child Neurology|April 20, 2013
The "double panda" sign in Leigh diseaseKothari Sonam, P S Bindu, Narayanappa Gayathri, et al.Mitochondrion|February 8, 2011
Mitochondrial dysfunction and genetic heterogeneity in chronic periodontitisPeriyasamy Govindaraj, Nahid Akhtar Khan, Praturi Gopalakrishna, et al.Mitochondrion|November 13, 2013
Mitochondrial DNA variations associated with hypertrophic cardiomyopathyPeriyasamy Govindaraj, Nahid Akhtar Khan, Bindu Rani, 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.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.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.Clinical Neurology and Neurosurgery|December 23, 2017
Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlationsParayil Sankaran Bindu, Kothari Sonam, Periyasamy Govindaraj, et al.Pageof 1