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Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India.
Sonam K, Bindu PS, Srinivas Bharath MM, Govindaraj P, Gayathri N, Arvinda HR, Chiplunkar S, Nagappa M, Sinha S, Khan NA, Nunia V, Paramasivam A, Thangaraj K, Taly AB. Sonam K, et al. Among authors: bindu ps. Mitochondrion. 2017 Jan;32:42-49. doi: 10.1016/j.mito.2016.11.002. Epub 2016 Nov 5. Mitochondrion. 2017. PMID: 27826120
Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations.
Bindu PS, Sonam K, Govindaraj P, Govindaraju C, Chiplunkar S, Nagappa M, Kumar R, Vekhande CC, Arvinda HR, Gayathri N, Srinivas Bharath MM, Ponmalar JNJ, Philip M, Vandana VP, Khan NA, Nunia V, Paramasivam A, Sinha S, Thangaraj K, Taly AB. Bindu PS, et al. Clin Neurol Neurosurg. 2018 Jan;164:182-189. doi: 10.1016/j.clineuro.2017.12.010. Epub 2017 Dec 9. Clin Neurol Neurosurg. 2018. PMID: 29272804
Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in India.
Khan NA, Govindaraj P, Soumittra N, Srilekha S, Ambika S, Vanniarajan A, Meena AK, Uppin MS, Sundaram C, Taly AB, Bindu PS, Gayathri N, Thangaraj K. Khan NA, et al. Among authors: bindu ps. Invest Ophthalmol Vis Sci. 2013 Jun 10;54(6):3999-4005. doi: 10.1167/iovs.13-11925. Invest Ophthalmol Vis Sci. 2013. PMID: 23674761
Giant axonal neuropathy.
Vijaykumar K, Bindu PS, Taly AB, Mahadevan A, Bharath RD, Gayathri N, Nagappa M, Sinha S. Vijaykumar K, et al. Among authors: bindu ps. J Child Neurol. 2015 Jun;30(7):912-5. doi: 10.1177/0883073814547721. Epub 2014 Sep 11. J Child Neurol. 2015. PMID: 25213662
119 results