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Annals of Indian Academy of Neurology|December 7, 2025
An Unusual Case of Extrapontine Myelinolysis in a Post-partum Woman with HypernatremiaAbhishek Rathore, Atchayaram Nalini, M Netravathi, et al.
BMC Medical Genetics|June 15, 2017
MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from IndiaSekar Deepha, Seena Vengalil, Veeramani Preethish-Kumar, et al.
The Journal of Spinal Cord Medicine|April 13, 2017
Ventral longitudinal intraspinal fluid collection: Rare presentation as brachial amyotrophy and intracranial hypotensionVeeramani Preethish-Kumar, Seena Vengalil, Sarbesh Tiwari, et al.
Indian Journal of Pediatrics|November 6, 2016
Ankle-Foot Orthosis in Duchenne Muscular Dystrophy: A 4 year Experience in a Multidisciplinary Neuromuscular Disorders ClinicAnupam Gupta, Atchayaram Nalini, Shanti Prakash Arya, et al.
Neuromuscular Disorders : NMD|December 3, 2019
GNE myopathy - A cross-sectional study on spatio-temporal gait characteristicsGaurav Gomez, Meeka Khanna, Anupam Gupta, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 7, 2016
Proximal and proximo-distal bimelic amyotrophy: Evidence of cervical flexion induced myelopathyVeeramani Preethish-Kumar, Kiran Polavarapu, Ravinder Jeet Singh, et al.
Neurocase|January 5, 2022
Novel CSF1R variant in adult-onset leukoencephalopathy masquerading as frontotemporal dementia: a follow-up studyFaheem Arshad, Seena Vengalil, Silambarasan Maskomani, et al.
Clinical Neurology and Neurosurgery|March 29, 2025
Anti-neurofascin-186 associated combined central and peripheral demyelination (CCPD): A novel entityAradhya Sekhar Bagchi, A Nalini, M Netravathi, et al.
Disability and Rehabilitation|August 24, 2024
The struggle to belong: a qualitative exploration of challenges in social spaces faced by children with Duchenne muscular dystrophy attending neuromuscular disorders clinicDinesh Kumar, Priya Treesa Thomas, Gargi S Kumar, et al.
Annals of Indian Academy of Neurology|July 5, 2021
Utility of Immunohistochemistry and Western Blot in Profiling Clinically Suspected Cases of Congenital Muscular DystrophyRadhika Mhatre, Deepha Sekar, Jessiena Ponmalar, et al.
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