Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome
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
Published in Journal of neurology (01.06.2021)
Published in Journal of neurology (01.06.2021)
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Child Neurology: Ethylmalonic encephalopathy
Govindaraj, Periyasamy, Parayil Sankaran, Bindu, Nagappa, Madhu, Arvinda, Hanumanthapura R, Deepha, Sekar, Jessiena Ponmalar, J N, Sinha, Sanjib, Gayathri, Narayanappa, Taly, Arun B
Published in Neurology (24.03.2020)
Published in Neurology (24.03.2020)
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Serum fibroblast growth factor 21 and growth differentiation factor 15: Two sensitive biomarkers in the diagnosis of mitochondrial disorders
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
Published in Mitochondrion (01.09.2021)
Published in Mitochondrion (01.09.2021)
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Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations
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.
Published in Clinical neurology and neurosurgery (01.01.2018)
Published in Clinical neurology and neurosurgery (01.01.2018)
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Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency
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.
Published in Metabolic brain disease (01.08.2017)
Published in Metabolic brain disease (01.08.2017)
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Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children?
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.
Published in Multiple sclerosis and related disorders (01.02.2018)
Published in Multiple sclerosis and related disorders (01.02.2018)
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Erratum to: Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency
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.
Published in Metabolic brain disease (01.08.2017)
Published in Metabolic brain disease (01.08.2017)
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