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| 37929431 | Characterisation of Patients with <i>SH3TC2</i> Associated Neuropathy in an Indian Cohort. | Neurol India | 2023 |
| 34663487 | Leukodystrophy Due to <i>eIF2B</i> Mutations in Adults. | Can J Neurol Sci | 2022 |
| 35499206 | Novel insights into the genetic profile of hereditary spastic paraplegia in India. | J Neurogenet | 2022 |
| 36537422 | Spectrum of Sensory Conduction Abnormalities in Guillain Barre Syndrome. | Neurol India | 2022 |
| 35936615 | Genetic Spectrum of Inherited Neuropathies in India. | Ann Indian Acad Neurol | 2022 |
| 36352595 | Insights from Magnetic Evoked Field Analysis in Patients with Wilson's Disease. | Neurol India | 2022 |
| 34447004 | Spectrum and Evolution of EEG Changes in Anti-NMDAR Encephalitis. | Ann Indian Acad Neurol | 2021 |
| 33740698 | Role of pulse methylprednisolone in epileptic encephalopathy: A retrospective observational analysis. | Epilepsy Res | 2021 |
| 32395712 | Variable treatment response in a patient with pyridoxal <i>N</i> phosphate oxidase (PNPO) deficiency- understanding the paradox. | Epilepsy Behav Rep | 2020 |
| 31993930 | PMP22 Gene-Associated Neuropathies: Phenotypic Spectrum in a Cohort from India. | J Mol Neurosci | 2020 |
| 31808207 | Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report. | Neuropathology | 2020 |
| 32021380 | Sjogren-Larsson Syndrome: Mechanisms and Management. | Appl Clin Genet | 2020 |
| 33109857 | Genetically Established Familial Amyloidotic Polyneuropathy from India: Narrating the Diagnostic "Odyssey" and a Mini Review. | Neurol India | 2020 |
| 30693486 | Autoantibodies in acquired myasthenia gravis: Clinical phenotype and immunological correlation. | Acta Neurol Scand | 2019 |
| 31640787 | Identification and functional characterization of two novel mutations in KCNJ10 and PI4KB in SeSAME syndrome without electrolyte imbalance. | Hum Genomics | 2019 |
| 31059521 | Genetic analysis of ATP7B in 102 south Indian families with Wilson disease. | PLoS One | 2019 |
| 30682680 | Comparing the efficacy of sodium valproate and levetiracetam following initial lorazepam in elderly patients with generalized convulsive status epilepticus (GCSE): A prospective randomized controlled pilot study. | Seizure | 2019 |
| 29272804 | Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations. | Clin Neurol Neurosurg | 2018 |
| 30212743 | Exome sequencing in adult neurology practice: Challenges and rewards in a mixed resource setting. | Clin Neurol Neurosurg | 2018 |
| 30232999 | Pediatric opsoclonus-myoclonus-ataxia syndrome: Experience from a tertiary care university hospital. | Neurol India | 2018 |
| 30196825 | Th17 pathway signatures in a large Indian cohort of Guillain Barré syndrome. | J Neuroimmunol | 2018 |
| 30348860 | Clinical Reasoning: West syndrome, pontocerebellar hypoplasia, and hypomyelination in a 6-month-old boy. | Neurology | 2018 |
| 30430072 | Comparison of Cheiloscopy and Rugoscopy in Karnataka, Kerala, and Manipuri Population. | J Int Soc Prev Community Dent | 2018 |
| 29424033 | Mitochondrial dysfunction in human skeletal muscle biopsies of lipid storage disorder. | J Neurochem | 2018 |
| 29353736 | Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children? | Mult Scler Relat Disord | 2018 |
| 29704819 | Comprehensive cytokine profiling provides evidence for a multi-lineage Th responses in Guillain Barré Syndrome. | Cytokine | 2018 |
| 29249217 | Palatal Tremor Revisited: Disorder with Nosological Diversity and Etiological Heterogeneity. | Can J Neurol Sci | 2018 |
| 29346803 | Author Response: Penetrance of the LHON Mutation m.11778G>A May Depend on Factors Other Than Haplotype or Heteroplasmy Rate. | Invest Ophthalmol Vis Sci | 2018 |
| 28025403 | Child Neurology: Sjögren-Larsson syndrome. | Neurology | 2017 |
| 28374236 | Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency. | Metab Brain Dis | 2017 |
| 28466389 | Erratum to: Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency. | Metab Brain Dis | 2017 |
| 28768321 | Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India. | Invest Ophthalmol Vis Sci | 2017 |
| 28841275 | Neuropsychiatric Manifestations of Pediatric NMDA Receptor Autoimmune Encephalitis: A Case Series From a Tertiary Care Center in India. | Prim Care Companion CNS Disord | 2017 |
| 28890042 | Guillain Barre Syndrome in the elderly: Experience from a tertiary-care hospital in India. | J Clin Neurosci | 2017 |
| 28009770 | Fatal Morvan Syndrome Associated With Myasthenia Gravis. | Neurologist | 2017 |
| 27596361 | Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene. | Brain Dev | 2017 |
| 27826120 | Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India. | Mitochondrion | 2017 |
| 26122629 | Improvement of Diffusion Tensor Imaging (DTI) Parameters with Decoppering Treatment in Wilson's Disease. | JIMD Rep | 2016 |
| 26675623 | Clinical, electrophysiological, imaging, pathological and therapeutic observations among 18 patients with Rasmussen's encephalitis. | J Clin Neurosci | 2016 |
| 27600858 | Reply to Letter to the Editor: Hearing impairment in m.3243A>G carriers requires comprehensive work- and follow-up. | Clin Neurol Neurosurg | 2016 |
| 27306358 | Huppke-Brendel syndrome in a seven months old boy with a novel 2-bp deletion in SLC33A1. | Metab Brain Dis | 2016 |
| 27359089 | Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome. | Clin Neurol Neurosurg | 2016 |
| 27196560 | Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex. | PLoS One | 2016 |
| 27011649 | Tangier's disease: An uncommon cause of facial weakness and non-length dependent demyelinating neuropathy. | Ann Indian Acad Neurol | 2016 |
| 26765764 | Non-Wilsonian hepatolenticular degeneration: Clinical and MRI observations in four families from south India. | J Clin Neurosci | 2016 |
| 26762927 | Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India. | Mitochondrion | 2016 |
| 27056375 | Combined MEG-EEG source localisation in patients with sub-acute sclerosing pan-encephalitis. | Neurol Sci | 2016 |
| 26727295 | 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. | Neuropediatrics | 2016 |
| 25038122 | Etiologic spectrum of biopsy-proven peripheral neuropathies in childhood from a resource-poor setting. | J Child Neurol | 2015 |
| 30363534 | Palatal Tremor in <i>POLG</i>-Associated Ataxia. | Mov Disord Clin Pract | 2015 |