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Mitochondrion|September 6, 2015
Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south IndiaParayil Sankaran Bindu, Hanumanthapura Arvinda, Arun B Taly, et al.Mitochondrion|January 15, 2016
Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south IndiaParayil Sankaran Bindu, Chikanna Govindaraju, Kothari Sonam, et al.Journal of Neurology|January 23, 2021
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndromeSanjiban Chakrabarty, Periyasamy Govindaraj, Bindu Parayil Sankaran, et al.Journal of Neurochemistry|August 13, 2017
Manganese- and 1-methyl-4-phenylpyridinium-induced neurotoxicity display differences in morphological, electrophysiological and genome-wide alterations: implications for idiopathic Parkinson's diseaseRajeswara Babu Mythri, Narayana Reddy Raghunath, Santosh Chandrakant Narwade, 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 5