Dr. Soumya V C
Consultant
MBBS, MD( Paediatrics), DM (Neurology), Post Doctoral fellowship in Epilepsy, International Sleep Specialist ( WSS)
1. Ashalatha R, Menon RN, Chandran A, Thomas SV, Vilanilam G, Abraham M, et al. Do auras predict seizure outcome after temporal lobe epilepsy surgery? Epilepsy Research. 2018;147:109-14.
2. Chandrasekharan SV, Menon R, Cherian A, Radhakrishnan A. Effect of seizure viewing on psychological outcome in persons with epilepsy. Epilepsy Behav. 2021;114(Pt A):107605.
3. Chandrasekharan SV, Sundaram S, Malaichamy S, Poyuran R, Nair SS. Myoneuropathic presentation of limb girdle muscular dystrophy R8 with a novel TRIM32 mutation. Neuromuscul Disord. 2021.
4. Sundaram S, Chandrasekharan SV, Nair SS. Metachromatic leukodystrophy: molecular mechanism and therapeutic effect. In: Neurochemistry of Metabolic Diseases: Lysosomal Storage Diseases,
Phenylketonuria, and Canavan Disease. 3rd Edition
5. Vijay Kumar Boddu, Alex Rebello, Soumya V. Chandrasekharan, Pavan Kumar Rudrabhatla, Anuvitha Chandran, Swathy Ravi, Gopeekrishnan Unnithan, Ramshekhar N. Menon, Ajith Cherian, Ashalatha
Radhakrishnan, How does “locus of control” affect persons with epilepsy?,Epilepsy & Behavior,2021,Volume 123
6. Chandrasekharan S.V., Nair S.S., Ganapathy, A. et al. Charcot-Marie-Tooth disease type 2S: identical novel missense mutation of IGHMBP2 gene in two unrelated families. Neurol Sci (2021)
7. Menon Ramshekhar N, Chandrasekharan Soumya V. Atypical Variants of Benign Rolandic Epilepsy. IAN Reviews in Neurology 2022: Epilepsy-Innovations and Advances,Ch14
8 Alfiya, F., Jose, M., Chandrasekharan, S.V. et al. C12orf57 pathogenic variants: a unique cause of developmental encephalopathy in a south Indian child. J Genet 101, 30 (2022).
9. Rebello A, Chandrasekharan SV, Kumar Rudrabhatla P, Vincent SJ, Menon RN, Radhakrishnan A. Satisfaction among persons with epilepsy towards physical consultation versus online video consultation for
follow up. Epilepsy Behav. 2023 Mar;140:109081.
10. Fazal A, Jose M, Rudrabhatla PK, Chandrasekharan SV, Sundaram S, Radhakrishnan A, Banerjee M, Menon RN. Visual-sensitive epilepsy in GLUT-1 deficiency syndrome: Expanding the phenotype. Epileptic
Disord. 2023 Apr;25(2):265-268.
11. Jose M, Alfiya F, Harini P, Kumar Rudrabhatla P, Chandrasekharan SV, Jithu J, Banerjee M, Soumya Sundaram, Menon RN, Radhakrishnan A. Metabolic causes of pediatric developmental & epileptic
encephalopathies (DEE)- genetic variant analysis in a south Indian cohort (Ahead of print)
Dr. Soumya V C
Consultant
Neurology
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HOD - Senior Consultant
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