Clinico-pathological and Molecular Spectrum of Mitochondrial Polymerase γ Mutations in a Cohort from India
Deepha, Sekar, Govindaraj, Periyasamy, Sankaran, Bindu Parayil, Chiplunkar, Shwetha, Kashinkunti, Chetan, Nunia, Vandana, Nagappa, Madhu, Sinha, Sanjib, Khanna, Tripti, Thangaraj, Kumarasamy, Taly, Arun B., Gayathri, Narayanappa
Published in Journal of molecular neuroscience (01.11.2021)
Published in Journal of molecular neuroscience (01.11.2021)
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Journal Article
Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene
Nagappa, Madhu, Bindu, Parayil Sankaran, Chiplunkar, Shwetha, Govindaraj, Periasamy, Narayanappa, Gayathri, Krishnan, Ayyappan, Bharath, M.M. Srinivas, Swaminathan, Aarthi, Saini, Jitender, Arvinda, Hanumanthapura R, Sinha, Sanjib, Mathuranath, Pavagada S, Taly, Arun B
Published in Brain & development (Tokyo. 1979) (01.02.2017)
Published in Brain & development (Tokyo. 1979) (01.02.2017)
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Journal Article
Reply to Letter to the Editor: Hearing impairment in m.3243A > G carriers requires comprehensive work- and follow-up
Vandana, V.P., PhD, Bindu, Parayil Sankaran, Sonam, Kothari, MBBS, Govindaraj, Periyasamy, PhD, Chiplunkar, Shwetha, MBBS, Gayathri, Narayanappa, PhD, Govindraj, Chikkanna, MD, Arvinda, H.R., MD, DM, Sinha, Sanjib, MD, DM, Nagappa, Madhu, DM, Thangaraj, K., PhD, Taly, Arun B., MD, DM
Published in Clinical neurology and neurosurgery (01.11.2016)
Published in Clinical neurology and neurosurgery (01.11.2016)
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Journal Article
Child Neurology: Hereditary Folate Malabsorption
Huddar, Akshata, Chiplunkar, Shwetha, Nagappa, Madhu, Govindaraj, Periyasamy, Sinha, Sanjib, Taly, Arun B, Parayil Sankaran, Bindu
Published in Neurology (06.07.2021)
Published in Neurology (06.07.2021)
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Journal Article
Leukodystrophies and Genetic Leukoencephalopathies in Children Specified by Exome Sequencing in an Expanded Gene Panel
Parayil Sankaran, Bindu, Nagappa, Madhu, Chiplunkar, Shwetha, Kothari, Sonam, Govindaraj, Periyasamy, Sinha, Sanjib, Taly, Arun B
Published in Journal of child neurology (01.06.2020)
Published in Journal of child neurology (01.06.2020)
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Journal Article
Clinical Reasoning: West syndrome, pontocerebellar hypoplasia, and hypomyelination in a 6-month-old boy
Bindu, Parayil Sankaran, Nagappa, Madhu, Chiplunkar, Shwetha, Govindaraj, Periyasamy, Mathuranath, Pavagada S, Sinha, Sanjib, Taly, Arun B
Published in Neurology (23.10.2018)
Published in Neurology (23.10.2018)
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Journal Article
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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Journal Article
Child Neurology: Sjögren-Larsson syndrome
Nagappa, Madhu, Bindu, Parayil S, Chiplunkar, Shwetha, Gupta, Neelesh, Sinha, Sanjib, Mathuranath, Pavagada S, Bharath, Rose D, Taly, Arun B
Published in Neurology (03.01.2017)
Published in Neurology (03.01.2017)
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Journal Article
Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south India
Bindu, Parayil Sankaran, Arvinda, Hanumanthapura, Taly, Arun B, Govindaraju, Chikanna, Sonam, Kothari, Chiplunkar, Shwetha, Kumar, Rakesh, Gayathri, Narayanappa, Bharath Mm, Srinivas, Nagappa, Madhu, Sinha, Sanjib, Khan, Nahid Akthar, Govindaraj, Periyasamy, Nunia, Vandana, Paramasivam, Arumugam, Thangaraj, Kumarasamy
Published in Mitochondrion (01.11.2015)
Published in Mitochondrion (01.11.2015)
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Journal Article
Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India
Sonam, Kothari, Bindu, Parayil Sankaran, Srinivas Bharath, M M, Govindaraj, Periyasamy, Gayathri, Narayanappa, Arvinda, Hanumanthapura R, Chiplunkar, Shwetha, Nagappa, Madhu, Sinha, Sanjib, Khan, Nahid Akhtar, Nunia, Vandana, Paramasivam, Arumugam, Thangaraj, Kumarasamy, Taly, Arun B
Published in Mitochondrion (01.01.2017)
Published in Mitochondrion (01.01.2017)
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Journal Article
Huppke-Brendel syndrome in a seven months old boy with a novel 2-bp deletion in SLC33A1
Chiplunkar, Shwetha, Bindu, Parayil Sankaran, Nagappa, Madhu, Bineesh, Cheminikara, Govindaraj, Periyasamy, Gayathri, Narayanappa, Bharath, M. M. Srinivas, Arvinda, Hanumanthapura R., Mathuranath, Pavagada S., Sinha, Sanjib, Taly, Arun B.
Published in Metabolic brain disease (01.10.2016)
Published in Metabolic brain disease (01.10.2016)
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Journal Article
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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Journal Article
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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Journal Article
Audiological Manifestations in Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke like Episodes (MELAS) Syndrome
Vandana, V.P, Bindu, Parayil Sankaran, Sonam, Kothari, Govindaraj, Periyasamy, Taly, Arun B, Gayathri, Narayanappa, Chiplunkar, Shwetha, Govindraju, Chikkanna, Arvinda, H.R, Nagappa, Madhu, Sinha, Sanjib, Thangaraj, K
Published in Clinical neurology and neurosurgery (01.09.2016)
Published in Clinical neurology and neurosurgery (01.09.2016)
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Journal Article
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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Journal Article
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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Journal Article
Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India
Bindu, Parayil Sankaran, Govindaraju, Chikanna, Sonam, Kothari, Nagappa, Madhu, Chiplunkar, Shwetha, Kumar, Rakesh, Gayathri, Narayanappa, Bharath, M M Srinivas, Arvinda, Hanumanthapura R, Sinha, Sanjib, Khan, Nahid Akthar, Govindaraj, Periyasamy, Nunia, Vandana, Paramasivam, Arumugam, Thangaraj, Kumarasamy, Taly, Arun B
Published in Mitochondrion (01.03.2016)
Published in Mitochondrion (01.03.2016)
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Journal Article
Palatal Tremor in POLG‐Associated Ataxia
Nagappa, Madhu, Bindu, Parayil Sankaran, Taly, Arun B., Sonam, Kothari, Shwetha, Chiplunkar, Kumar, Rakesh, Gayathri, Narayanappa, Srinivas‐Bharath, M.M., Arvinda, Hanumanthapura R., Sinha, Sanjib, Paramasivam, Arumugam, Thangaraj, Kumarasamy
Published in Movement disorders clinical practice (Hoboken, N.J.) (01.09.2015)
Published in Movement disorders clinical practice (Hoboken, N.J.) (01.09.2015)
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Journal Article
Palatal Tremor in POLG-Associated Ataxia
Nagappa, Madhu, Bindu, Parayil Sankaran, Taly, Arun B, Sonam, Kothari, Shwetha, Chiplunkar, Kumar, Rakesh, Gayathri, Narayanappa, Srinivas-Bharath, M M, Arvinda, Hanumanthapura R, Sinha, Sanjib, Paramasivam, Arumugam, Thangaraj, Kumarasamy
Published in Movement disorders clinical practice (01.09.2015)
Published in Movement disorders clinical practice (01.09.2015)
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