| Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders G Novarino, AG Fenstermaker, MS Zaki, M Hofree, JL Silhavy, ... science 343 (6170), 506-511, 2014 | 565 | 2014 |
| Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery EM Scott, A Halees, Y Itan, EG Spencer, Y He, MA Azab, SB Gabriel, ... Nature genetics 48 (9), 1071-1076, 2016 | 366 | 2016 |
| Management of generalised convulsive status epilepticus (SE): A prospective randomised controlled study of combined treatment with intravenous lorazepam with either phenytoin … RC Mundlamuri, S Sinha, DK Subbakrishna, PV Prathyusha, M Nagappa, ... Epilepsy research 114, 52-58, 2015 | 118 | 2015 |
| Neurosyphilis: MRI features and their phenotypic correlation in a cohort of 35 patients from a tertiary care university hospital M Nagappa, S Sinha, AB Taly, SL Rao, S Nagarathna, PS Bindu, ... Neuroradiology 55, 379-388, 2013 | 105 | 2013 |
| Clinical, electrophysiological, imaging, and ultrastructural description in 68 patients with neuronal ceroid lipofuscinoses and its subtypes RH Jadav, S Sinha, TC Yasha, H Aravinda, N Gayathri, S Rao, PS Bindu, ... Pediatric neurology 50 (1), 85-95, 2014 | 82 | 2014 |
| Hyperemesis gravidarum induced Wernicke's encephalopathy: serial clinical, electrophysiological and MR imaging observations M Netravathi, S Sinha, AB Taly, PS Bindu, RD Bharath Journal of the neurological sciences 284 (1-2), 214-216, 2009 | 61 | 2009 |
| Therapeutic strategies for mitochondrial disorders J Finsterer, PS Bindu Pediatric neurology 52 (3), 302-313, 2015 | 52 | 2015 |
| Peripheral neuropathy in metachromatic leucodystrophy. A study of 40 cases from south India PS Bindu, A Mahadevan, AB Taly, R Christopher, N Gayathri, SK Shankar Journal of Neurology, Neurosurgery & Psychiatry 76 (12), 1698-1701, 2005 | 45 | 2005 |
| Cranial MRI in acute hyperammonemic encephalopathy PS Bindu, S Sinha, AB Taly, R Christopher, JME Kovoor Pediatric neurology 41 (2), 139-142, 2009 | 42 | 2009 |
| Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish L Southgate, D Dafou, J Hoyle, N Li, E Kinning, P Critchley, AH Németh, ... Neurogenetics 11, 379-389, 2010 | 39 | 2010 |
| Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism … S Kapoor, MH Shah, N Singh, MI Rather, V Bhat, S Gopinath, PS Bindu, ... PLoS One 11 (5), e0155605, 2016 | 36 | 2016 |
| Tumefactive demyelination: clinical, imaging and follow‐up observations in thirty‐nine patients M Nagappa, AB Taly, S Sinha, RD Bharath, A Mahadevan, PS Bindu, ... Acta Neurologica Scandinavica 128 (1), 39-47, 2013 | 36 | 2013 |
| Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome S Chakrabarty, P Govindaraj, BP Sankaran, M Nagappa, SP Kabekkodu, ... Journal of neurology 268, 2192-2207, 2021 | 35 | 2021 |
| Clinical features, therapeutic response, and follow-up in pediatric anti-N-methyl-D-aspartate receptor encephalitis: experience from a tertiary care university hospital in India M Nagappa, PS Bindu, A Mahadevan, S Sinha, PS Mathuranath, AB Taly Neuropediatrics 47 (01), 024-032, 2016 | 35 | 2016 |
| Clinical and imaging observations in isolated sulfite oxidase deficiency PS Bindu, R Christopher, A Mahadevan, RD Bharath Journal of Child Neurology 26 (8), 1036-1040, 2011 | 35 | 2011 |
| 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 | 33 | 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 | 32 | 2016 |
| Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations K Sonam, NA Khan, PS Bindu, AB Taly, N Gayathri, MMS Bharath, ... Brain and Development 36 (9), 807-812, 2014 | 32 | 2014 |
| Clinical, neuroimaging and pathological features of 5-nitroimidazole-induced encephalo-neuropathy in two patients: Insights into possible pathogenesis J Chacko, K Pramod, S Sinha, J Saini, A Mahadevan, RD Bharath, ... Neurology India 59 (5), 743-747, 2011 | 32 | 2011 |
| Evolution of MRI changes in Rasmussen's encephalitis K Pradeep, S Sinha, J Saini, A Mahadevan, A Arivazhagan, RD Bharath, ... Acta Neurologica Scandinavica 130 (4), 253-259, 2014 | 31 | 2014 |
