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Journal of Neuromuscular Diseases|December 13, 2021
Homozygous N-terminal missense variant in PLEKHG5 associated with intermediate CMT: A case reportDanique Beijer, Kiran Polavarapu, Veeramani Preethish-Kumar, et al.Neurology India|August 5, 2015
A prospective study on the immunophenotypic characterization of limb girdle muscular dystrophies 2 in IndiaAtchayaram Nalini, Kiran Polavarapu, Balaraju Sunitha, 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.The American Journal of Tropical Medicine and Hygiene|January 19, 2018
Case Report: Neurobrucellosis with Plastered Spinal Arachnoiditis: A Magnetic Resonance Imaging-Based ReportSaraswati Nashi, Veeramani Preethish-Kumar, Sayani Maji, 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.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.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.Acta Neurologica Scandinavica|November 29, 2021
Novel TBK1 variant associated with Frontotemporal Dementia overlap syndromeFaheem Arshad, Seena Vengalil, Atchayaram Nalini, 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.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.Pageof 12