Praveen Kumar Ramani
This is a likely match — the affiliation was inferred from OpenAlex, ORCID, and web sources but has not been fully confirmed. Treat with appropriate caution.
Researcher
Also affiliated: Arkansas Children's Hospital (2022–2024); Mahindra Group (India) (2019); Duke University (2026); University of Arkansas Medical Center (2020–2024); Duke Medical Center (2025); Epilepsy Foundation (2026); Child Neurology Associates (2022)
Faculty Researcher
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Praveen Kumar Ramani's research focuses on pediatric neurological disorders, including infantile epileptic spasms syndrome, dystonia, and epilepsy in muscular dystrophies. He has investigated treatment strategies for refractory seizures in conditions such as tuberous sclerosis and explored the characteristics of epilepsy in Duchenne and Becker muscular dystrophies. Ramani has also contributed to understanding rare genetic disorders, including KMT2B-related dystonia and Tay-Sachs disease, and has examined sleep quality in children with migraines. His work extends to autoimmune conditions affecting children, such as pediatric Cogan syndrome, and genetic conditions like Charcot-Marie-Tooth disease. Ramani collaborates with researchers at the University of Arkansas for Medical Sciences, including Aravindhan Veerapandiyan, Debopam Samanta, Sisira Yadala, and Raghu Ramakrishnaiah, with whom he has co-authored multiple publications.
Metrics
- h-index: 3
- Publications: 22
- Citations: 278
Selected Publications
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First-Line Rituximab in Pediatric-Onset Multiple Sclerosis: Clinical and MRI Outcomes in a Retrospective Cohort (2026)
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Photosensitive infantile spasms in a preterm infant with 4q22.3–q24 deletion involving <i>PPP3CA</i> (2026)
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Charcot‐Marie‐Tooth disease in children (2024)
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Initial combination versus early sequential standard therapies for Infantile Epileptic Spasms Syndrome—Feedback from stakeholders (2024)
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Paediatric Cogan Syndrome masquerading as IgA vasculitis (2023)
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Epilepsy Characteristics in Duchenne and Becker Muscular Dystrophies (2023)
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Everolimus for Treatment of Refractory Seizures in Tuberous Sclerosis (P3-8.002) (2022)
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Case Report: SATB2-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two Cases (2021)
Collaboration Network
Top Collaborators
- Epilepsy Characteristics in Duchenne and Becker Muscular Dystrophies
- Charcot‐Marie‐Tooth disease in children
- Case Report: SATB2-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two Cases
- Case Report: SATB2-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two Cases
- Case Report: SATB2-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two Cases
- Case Report: SATB2-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two Cases
- Case Report: SATB2-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two Cases
- Case Report: SATB2-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two Cases
- Case Report: SATB2-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two Cases
- Case Report: SATB2-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two Cases
- Case Report: SATB2-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two Cases
- Epilepsy Characteristics in Duchenne and Becker Muscular Dystrophies
- Epilepsy Characteristics in Duchenne and Becker Muscular Dystrophies
- Epilepsy Characteristics in Duchenne and Becker Muscular Dystrophies
- Epilepsy Characteristics in Duchenne and Becker Muscular Dystrophies
- Paediatric Cogan Syndrome masquerading as IgA vasculitis
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