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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.Mitochondrion|February 5, 2011
Mitochondrial DNA variations associated with recurrent pregnancy loss among Indian womenAyyasamy Vanniarajan, Periyasamy Govindaraj, S Justin Carlus, et al.HGG Advances|April 5, 2026
Novel MC1R variants cause red hair and lighter skin colourDeepak K Kashyap, Srashti J Agrawal, Meenakshisundaram Karthikeyan, 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.American Journal of Human Genetics|July 12, 2011
Indian Siddis: African descendants with Indian admixtureAnish M Shah, Rakesh Tamang, Priya Moorjani, 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.Scientific Reports|October 30, 2015
Genome-wide analysis correlates Ayurveda PrakritiPeriyasamy Govindaraj, Sheikh Nizamuddin, Anugula Sharath, et al.Human Genetics|January 23, 2018
Reconstructing the demographic history of the Himalayan and adjoining populationsRakesh Tamang, Gyaneshwer Chaubey, Amrita Nandan, et al.Journal of Translational Medicine|May 9, 2015
DNA methylation analysis of phenotype specific stratified Indian populationHarish Rotti, Sandeep Mallya, Shama Prasada Kabekkodu, et al.Pageof 7