| Mitochondrial leukoencephalopathies: a border zone between acquired and inherited white matter disorders in children? PS Bindu, K Sonam, S Chiplunkar, P Govindaraj, M Nagappa, ... Multiple sclerosis and related disorders 20, 84-92, 2018 | 32 | 2018 |
| Huppke-Brendel syndrome in a seven months old boy with a novel 2-bp deletion in SLC33A1 S Chiplunkar, PS Bindu, M Nagappa, C Bineesh, P Govindaraj, ... Metabolic brain disease 31, 1195-1198, 2016 | 30 | 2016 |
| Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: a study from south India PS Bindu, H Arvinda, AB Taly, C Govindaraju, K Sonam, S Chiplunkar, ... Mitochondrion 25, 6-16, 2015 | 27 | 2015 |
| Mitochondrial oxidative phosphorylation disorders in children: phenotypic, genotypic and biochemical correlations in 85 patients from South India K Sonam, PS Bindu, MMS Bharath, P Govindaraj, N Gayathri, HR Arvinda, ... Mitochondrion 32, 42-49, 2017 | 26 | 2017 |
| Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations PS Bindu, K Sonam, P Govindaraj, C Govindaraju, S Chiplunkar, ... Clinical Neurology and Neurosurgery 164, 182-189, 2018 | 23 | 2018 |
| Child Neurology: Sjögren-Larsson syndrome M Nagappa, PS Bindu, S Chiplunkar, N Gupta, S Sinha, PS Mathuranath, ... Neurology 88 (1), e1-e4, 2017 | 19 | 2017 |
| Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome VP Vandana, PS Bindu, K Sonam, P Govindaraj, AB Taly, N Gayathri, ... Clinical Neurology and Neurosurgery 148, 17-21, 2016 | 19 | 2016 |
| Leukodystrophies and genetic leukoencephalopathies in children specified by exome sequencing in an expanded gene panel B Parayil Sankaran, M Nagappa, S Chiplunkar, S Kothari, P Govindaraj, ... Journal of Child Neurology 35 (7), 433-441, 2020 | 18 | 2020 |
| Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene M Nagappa, PS Bindu, S Chiplunkar, P Govindaraj, G Narayanappa, ... Brain and Development 39 (2), 161-165, 2017 | 14 | 2017 |
| Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India PS Bindu, C Govindaraju, K Sonam, M Nagappa, S Chiplunkar, R Kumar, ... Mitochondrion 27, 1-5, 2016 | 12 | 2016 |
| Serum fibroblast growth factor 21 and growth differentiation factor 15: Two sensitive biomarkers in the diagnosis of mitochondrial disorders A Huddar, P Govindaraj, S Chiplunkar, S Deepha, JNJ Ponmalar, M Philip, ... Mitochondrion 60, 170-177, 2021 | 11 | 2021 |
| Clinico-pathological and molecular spectrum of mitochondrial polymerase γ mutations in a cohort from India S Deepha, P Govindaraj, BP Sankaran, S Chiplunkar, C Kashinkunti, ... Journal of Molecular Neuroscience, 1-10, 2021 | 6 | 2021 |
| Child neurology: hereditary folate malabsorption A Huddar, S Chiplunkar, M Nagappa, P Govindaraj, S Sinha, AB Taly, ... Neurology 97 (1), 40-43, 2021 | 5 | 2021 |
| Huppke-Brendel Syndrome PS Bindu, S Chiplunkar, VP Vandana, M Nagappa, P Govindaraj, A Taly | 4 | 2019 |
| Palatal Tremor in POLG‐Associated Ataxia M Nagappa, PS Bindu, AB Taly, K Sonam, C Shwetha, R Kumar, ... Movement Disorders Clinical Practice 2 (3), 318, 2015 | 3 | 2015 |
| Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency S Chiplunkar, PS Bindu, M Nagappa, BB Panikulam, HR Arvinda, ... Metabolic brain disease 32, 967-970, 2017 | 2 | 2017 |
| Clinical Reasoning: West syndrome, pontocerebellar hypoplasia, and hypomyelination in a 6-month-old boy PS Bindu, M Nagappa, S Chiplunkar, P Govindaraj, PS Mathuranath, ... Neurology 91 (17), e1652-e1656, 2018 | 1 | 2018 |
| Differenzialdiagnose des Morbus Wilson W Hermann, C Tinta Nervenheilkunde 37 (10), 679-688, 2018 | 1 | 2018 |
| Paroxysmal Dystonia in a Child with Enoyl-CoA Hydratase Short-Chain 1 (ECHS1) Mutations A Huddar, P Govindaraj, S Chiplunkar, M Nagappa, AB Taly, ... Journal of Pediatric Neurology 21 (05), 408-410, 2023 | | 2023 |
| Infantile Onset Encephalomyopathy, Heart Block, and Sensorineural Hearing Loss: RMND1-Associated Mitochondrial Disease M Nagappa, VP Vandana, S Chiplunkar, P Govindaraj, JNJ Ponmalar, ... Journal of Pediatric Neurology 19 (03), 183-188, 2021 | | 2021 |
Periyasamy GovindarajAssistant Professor在 nimhans.ac.in 的电子邮件经过验证
Periyasamy GovindarajAssistant Professor在 nimhans.ac.in 的电子邮件经过验证