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Neurology India|July 22, 2022
Inflammatory Myositis in a Child due to Anti-NXP2 Antibody, First Case Report from IndiaAshok V Reddy Taallapalli, Sumanth Shivaram, Manisha Gupta, et al.Annals of Indian Academy of Neurology|August 13, 2025
Chronic Inflammatory Demyelinating Polyradiculoneuropathy: A Comparative Study of Magnetic Resonance Neurography and High-Resolution Nerve Ultrasound in the Assessment of Brachial PlexusS S Jayanth, Seena Vengalil, Dipti Baskar, et al.Neurology India|November 8, 2021
Lead Encephalopathy with Distinctive Brain Magnetic Resonance Imaging FindingsAmeya Patwardhan, Nalini Atchayaram, Jitender Saini, et al.Journal of Neuromuscular Diseases|September 30, 2025
An interesting report of POPDC3 limb girdle muscular dystrophy R26 from IndiaDipti Baskar, Kiran Polavarapu, Ananthapadmanabha Kotambail, et al.Acta Neurologica Scandinavica|November 29, 2021
Novel TBK1 variant associated with Frontotemporal Dementia overlap syndromeFaheem Arshad, Seena Vengalil, Atchayaram Nalini, et al.Neurology India|July 25, 2018
Hirayama disease/cervical flexion-induced myelopathy progressing to spastic paraparesis: A report on three cases with literature reviewVeeramani Preethish-Kumar, Kiran Polavarapu, Saraswati Nashi, et al.Journal of Clinical Neurology (Seoul, Korea)|January 13, 2017
Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large CohortSeena Vengalil, Veeramani Preethish-Kumar, Kiran Polavarapu, et al.Neuromuscular Disorders : NMD|September 27, 2016
Muscle MRI in Duchenne muscular dystrophy: Evidence of a distinctive patternKiran Polavarapu, Mahadevappa Manjunath, Veeramani Preethish-Kumar, et al.Neuromuscular Disorders : NMD|September 21, 2017
Fatty acid oxidation defects presenting as primary myopathy and prominent dropped head syndromeSeena Vengalil, Veeramani Preethish-Kumar, Kiran Polavarapu, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 25, 2026
Early cardiac and autonomic markers and their genotype-phenotype associations in Duchenne muscular dystrophyR Rashmi, I K Sangeetha, K Sridharan, et al.Pageof 14