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Page 1
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. Among authors: paramasivam a. 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
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: paramasivam a. 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: paramasivam a. Mitochondrion. 2016 Mar;27:1-5. doi: 10.1016/j.mito.2015.12.009. Epub 2016 Jan 4. Mitochondrion. 2016. PMID: 26762927
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: paramasivam a. Mitochondrion. 2017 Jan;32:42-49. doi: 10.1016/j.mito.2016.11.002. Epub 2016 Nov 5. Mitochondrion. 2017. PMID: 27826120
Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial disease.
Bugiardini E, Poole OV, Manole A, Pittman AM, Horga A, Hargreaves I, Woodward CE, Sweeney MG, Holton JL, Taanman JW, Plant GT, Poulton J, Zeviani M, Ghezzi D, Taylor J, Smith C, Fratter C, Kanikannan MA, Paramasivam A, Thangaraj K, Spinazzola A, Holt IJ, Houlden H, Hanna MG, Pitceathly RDS. Bugiardini E, et al. Among authors: paramasivam a. Neurol Genet. 2017 May 2;3(3):e149. doi: 10.1212/NXG.0000000000000149. eCollection 2017 Jun. Neurol Genet. 2017. PMID: 28508084 Free PMC article.
Palatal Tremor in POLG-Associated Ataxia.
Nagappa M, Bindu PS, Taly AB, Sonam K, Shwetha C, Kumar R, Gayathri N, Srinivas-Bharath MM, Arvinda HR, Sinha S, Paramasivam A, Thangaraj K. Nagappa M, et al. Among authors: paramasivam a. Mov Disord Clin Pract. 2015 Jun 30;2(3):318-320. doi: 10.1002/mdc3.12195. eCollection 2015 Sep. Mov Disord Clin Pract. 2015. PMID: 30363534 Free PMC article. No abstract available.
80 results