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Page 1
Genetic Spectrum of Inherited Neuropathies in India.
Sharma S, Govindaraj P, Chickabasaviah YT, Siram R, Shroti A, Seshagiri DV, Debnath M, Bindu PS, Taly AB, Nagappa M. Sharma S, et al. Among authors: govindaraj p. Ann Indian Acad Neurol. 2022 May-Jun;25(3):407-416. doi: 10.4103/aian.aian_269_22. Epub 2022 Jun 14. Ann Indian Acad Neurol. 2022. PMID: 35936615 Free PMC article.
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: govindaraj p. Invest Ophthalmol Vis Sci. 2013 Jun 10;54(6):3999-4005. doi: 10.1167/iovs.13-11925. Invest Ophthalmol Vis Sci. 2013. PMID: 23674761
Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south India.
Bindu PS, Arvinda H, Taly AB, Govindaraju C, Sonam K, Chiplunkar S, Kumar R, Gayathri N, Bharath Mm S, Nagappa M, Sinha S, Khan NA, Govindaraj P, Nunia V, Paramasivam A, Thangaraj K. Bindu PS, et al. Among authors: govindaraj p. Mitochondrion. 2015 Nov;25:6-16. doi: 10.1016/j.mito.2015.08.002. Epub 2015 Sep 1. Mitochondrion. 2015. PMID: 26341968
Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India.
Bindu PS, Govindaraju C, Sonam K, Nagappa M, Chiplunkar S, Kumar R, Gayathri N, Bharath MM, Arvinda HR, Sinha S, Khan NA, Govindaraj P, Nunia V, Paramasivam A, Thangaraj K, Taly AB. Bindu PS, et al. Among authors: govindaraj p. Mitochondrion. 2016 Mar;27:1-5. doi: 10.1016/j.mito.2015.12.009. Epub 2016 Jan 4. Mitochondrion. 2016. PMID: 26762927
Reply to Letter to the Editor: Hearing impairment in m.3243A>G carriers requires comprehensive work- and follow-up.
Vandana VP, Bindu PS, Sonam K, Govindaraj P, Chiplunkar S, Gayathri N, Govindaraj C, Arvinda HR, Nagappa M, Sinha S, Thangaraj K, Taly AB. Vandana VP, et al. Among authors: govindaraj p, govindaraj c. Clin Neurol Neurosurg. 2016 Nov;150:198-199. doi: 10.1016/j.clineuro.2016.08.030. Epub 2016 Aug 31. Clin Neurol Neurosurg. 2016. PMID: 27600858 No abstract available.
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: govindaraj p. Mitochondrion. 2017 Jan;32:42-49. doi: 10.1016/j.mito.2016.11.002. Epub 2016 Nov 5. Mitochondrion. 2017. PMID: 27826120
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