| The SARS‐CoV‐2/COVID‐19 pandemic and challenges in stroke care in India PN Sylaja, MVP Srivastava, S Shah, R Bhatia, D Khurana, A Sharma, ... Annals of the New York Academy of Sciences 1473 (1), 3-10, 2020 | 47 | 2020 |
| Metabolic syndrome in young adults with epilepsy SS Nair, S Harikrishnan, PS Sarma, SV Thomas Seizure 37, 61-64, 2016 | 42 | 2016 |
| Relapsing lumbosacral myeloradiculitis: an unusual presentation of MOG antibody disease S Sundaram, SS Nair, D Jaganmohan, G Unnikrishnan, M Nair Multiple Sclerosis Journal 26 (4), 509-511, 2020 | 41 | 2020 |
| Atypical meningioma: a clinicopathological analysis E Joseph, S Sandhyamani, MB Rao, S Nair, VV Radhakrishnan Neurology India 48 (4), 338-342, 2000 | 31 | 2000 |
| Genotype–phenotype correlations in valosin-containing protein disease: a retrospective muticentre study M Schiava, C Ikenaga, RN Villar-Quiles, M Caballero-Ávila, A Topf, ... Journal of Neurology, Neurosurgery & Psychiatry 93 (10), 1099-1111, 2022 | 23 | 2022 |
| Tumefactive demyelinating lesions: a clinicopathological correlative study R Neelima, K Krishnakumar, MD Nair, C Kesavadas, DR Hingwala, ... Indian Journal of Pathology and Microbiology 55 (4), 496-500, 2012 | 22 | 2012 |
| Consensus statement on immune modulation in multiple sclerosis and related disorders during the COVID-19 pandemic: expert group on behalf of the Indian Academy of Neurology R Bhatia, MVP Srivastava, D Khurana, L Pandit, T Mathew, S Gupta, ... Annals of Indian Academy of Neurology 23 (Suppl 1), S5-S14, 2020 | 18 | 2020 |
| Autoimmune encephalitis: Clinical diagnosis versus antibody confirmation AC Cyril, SS Nair, A Mathai, S Kannoth, SV Thomas Annals of Indian Academy of Neurology 18 (4), 408-411, 2015 | 17 | 2015 |
| Novel immunotherapies for myasthenia gravis SS Nair, S Jacob ImmunoTargets and therapy, 25-45, 2023 | 14 | 2023 |
| Maintenance of normoglycemia may improve outcome in acute ischemic stroke SS Nair, PN Sylaja, SE Sreedharan, S Sarma Annals of Indian Academy of Neurology 20 (2), 122-126, 2017 | 11 | 2017 |
| Rapidly progressive dementia, parkinsonism and myoclonus: an unusual presentation of dural arteriovenous fistula SA Jagtap, SS Nair, N Jain, MD Nair Neurology India 62 (1), 107-110, 2014 | 11 | 2014 |
| Clinical and Genetic Profile of Autism Spectrum Disorder–Epilepsy (ASD-E) Phenotype: Two Sides of the Same Coin! S Karunakaran, RN Menon, SS Nair, S Santhakumar, M Nair, ... Clinical EEG and Neuroscience 51 (6), 390-398, 2020 | 10 | 2020 |
| Congenital myasthenic syndrome: ten years clinical experience from a quaternary care south-Indian hospital V Wadwekar, SS Nair, V Tandon, A Kuruvilla, M Nair Journal of Clinical Neuroscience 72, 238-243, 2020 | 9 | 2020 |
| Persistent post-stroke dysphagia treated with cricopharyngeal myotomy SS Nair, AJ Surendaran, JR Menon, SE Sreedharan, PN Sylaja Annals of Indian Academy of Neurology 19 (2), 249-251, 2016 | 9 | 2016 |
| Electroneurography and advanced neuroimaging profile in pediatric-onset metachromatic leukodystrophy A Raina, SS Nair, C Nagesh, B Thomas, M Nair, S Sundaram Journal of Pediatric Neurosciences 14 (2), 70-75, 2019 | 8 | 2019 |
| A case-control study of risk factors for ischemic heart disease in patients attending tertiary care hospitals in India R Kapoor, S Vyas, P Patel, H Mehta, P Mehta, J Modi, S Nair South East Asia Journal of Public Health 3 (1), 57-60, 2014 | 8 | 2014 |
| Pregnancy‐associated respiratory failure in muscle specific kinase congenital myasthenic syndrome V Wadwekar, RR Pillai, S Sesh, SS Nair, M Nair Muscle & Nerve 59 (4), E24-E26, 2019 | 7 | 2019 |
| Impact of the COVID-19 pandemic on the frequency, clinical spectrum and outcomes of pediatric Guillain-Barré syndrome in India: a multicentric ambispective cohort study D Garg, RK Dhamija, A Choudhary, R Shree, S Kumar, P Samal, A Pathak, ... Annals of Indian Academy of Neurology 25 (1), 60-67, 2022 | 6 | 2022 |
| Quantitative susceptibility-weighted imaging in predicting disease activity in multiple sclerosis S Vinayagamani, S Sabarish, SS Nair, V Tandon, C Kesavadas, ... Neuroradiology 63, 1061-1069, 2021 | 6 | 2021 |
| Homozygous sequestosome 1 (SQSTM1) mutation: a rare cause for childhood-onset progressive cerebellar ataxia with vertical gaze palsy V Vedartham, S Sundaram, SS Nair, A Ganapathy, A Mannan, R Menon Ophthalmic Genetics 40 (4), 376-379, 2019 | 6 | 2019 |
