Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome by Chakrabarty, Sanjiban, Govindaraj, Periyasamy, Sankaran, Bindu Parayil, Nagappa, Madhu, Kabekkodu, Shama Prasada, Jayaram, Pradyumna, Mallya, Sandeep, Deepha, Sekar, Ponmalar, J. N. Jessiena, Arivinda, Hanumanthapura R., Meena, Angamuthu Kanikannan, Jha, Rajan Kumar, Sinha, Sanjib, Gayathri, Narayanappa, Taly, Arun B., Thangaraj, Kumarasamy, Satyamoorthy, Kapaettu

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Serum fibroblast growth factor 21 and growth differentiation factor 15: Two sensitive biomarkers in the diagnosis of mitochondrial disorders by Huddar, Akshata, Govindaraj, Periyasamy, Chiplunkar, Shwetha, Deepha, Sekar, Jessiena Ponmalar, J.N., Philip, Mariyamma, Nagappa, Madhu, Narayanappa, Gayathri, Mahadevan, Anita, Sinha, Sanjib, Taly, Arun B., Parayil Sankaran, Bindu

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Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations by Bindu, Parayil Sankaran, Sonam, Kothari, Govindaraj, Periyasamy, Govindaraju, Chikkanna, Chiplunkar, Shwetha, Nagappa, Madhu, Kumar, Rakesh, Vekhande, Chetan Chandrakanth, Arvinda, Hanumanthapura R., Gayathri, Narayanappa, Srinivas Bharath, M.M., Ponmalar, J.N. Jessiena, Philip, Mariyamma, Vandana, V.P., Khan, Nahid Akhtar, Nunia, Vandana, Paramasivam, Arumugam, Sinha, Sanjib, Thangaraj, Kumarasamy, Taly, Arun B.

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Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency by Chiplunkar, Shwetha, Bindu, Parayil Sankaran, Nagappa, Madhu, Panikulam, Bobby Baby, Arvinda, Hanumanthapura R, Govindaraj, Periyasamy, Srinivas Bharath, MM, Gayathri, Narayanappa, Jessiena Ponmalar, JN, Mathuranath, Pavagada S, Sinha, Sanjib, Taly, Arun B.

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Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children? by Bindu, Parayil Sankaran, Sonam, Kothari, Chiplunkar, Shwetha, Govindaraj, Periyasamy, Nagappa, Madhu, Vekhande, Chetan Chandrakanth, Aravinda, Hanumanthapura R., Ponmalar, JN Jessiena, Mahadevan, Anita, Gayathri, Narayanappa, Bharath, MM Srinivas, Sinha, Sanjib, Taly, Arun B.

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Erratum to: Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency by Chiplunkar, Shwetha, Bindu, Parayil Sankaran, Nagappa, Madhu, Panikulam, Bobby Baby, Arvinda, Hanumanthapura R, Govindaraj, Periyasamy, Srinivas Bharath, MM, Gayathri, Narayanappa, Jessiena Ponmalar, JN, Mathuranath, Pavagada S, Sinha, Sanjib, Taly, Arun B.

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