Vimala Elumalai
Researcher
Also affiliated: Arkansas Children's Hospital (2021–2022)
Unknown Researcher
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Vimala Elumalai's research focuses on understanding and improving health outcomes for children with epilepsy and hereditary spastic paraplegia. Her work has investigated barriers and facilitators to epilepsy self-management among Black children and caregivers in Arkansas, a topic explored in a qualitative study. Elumalai has also examined physicians' perspectives on shared decision-making in pediatric epilepsy surgery and the conceptualization of interdisciplinary clinics for drug-resistant epilepsy, particularly during the COVID-19 pandemic. Her research extends to understanding seizures in rare genetic syndromes like Malan syndrome and epilepsy associated with the NIPA1 gene. Elumalai has contributed to studies on caregiver reports of seizures and has explored educational methodologies, such as asynchronous learning in flipped classrooms for online environments. She has collaborated with researchers from the University of Arkansas for Medical Sciences, including Debopam Samanta, Geoffrey Curran, Aravindhan Veerapandiyan, and Akilandeswari Aravindhan.
Metrics
- h-index: 3
- Publications: 8
- Citations: 47
Selected Publications
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Understanding Seizures in Malan Syndrome Through Caregiver Reports: A Cross-Sectional Study (2025)
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Understanding Seizures in Malan Syndrome Through Caregiver Reports: A Cross-Sectional Study (2025)
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Epilepsy in hereditary spastic paraplegia associated with NIPA1 gene (2022)
Collaboration Network
Top Collaborators
- Understanding Seizures in Malan Syndrome Through Caregiver Reports: A Cross-Sectional Study
- Understanding Seizures in Malan Syndrome Through Caregiver Reports: A Cross-Sectional Study
- Understanding Seizures in Malan Syndrome Through Caregiver Reports: A Cross-Sectional Study
- Understanding Seizures in Malan Syndrome Through Caregiver Reports: A Cross-Sectional Study
- Understanding Seizures in Malan Syndrome Through Caregiver Reports: A Cross-Sectional Study
- Understanding Seizures in Malan Syndrome Through Caregiver Reports: A Cross-Sectional Study
- Understanding Seizures in Malan Syndrome Through Caregiver Reports: A Cross-Sectional Study
- Understanding Seizures in Malan Syndrome Through Caregiver Reports: A Cross-Sectional Study
- Epilepsy in hereditary spastic paraplegia associated with NIPA1 gene
- Epilepsy in hereditary spastic paraplegia associated with NIPA1 gene
- Epilepsy in hereditary spastic paraplegia associated with NIPA1 gene
- Epilepsy in hereditary spastic paraplegia associated with NIPA1 gene
- Understanding Seizures in Malan Syndrome Through Caregiver Reports: A Cross-Sectional Study
- Understanding Seizures in Malan Syndrome Through Caregiver Reports: A Cross-Sectional Study
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