Praveen Kumar Ramani
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Also affiliated: Arkansas Children's Hospital (2022–2026); Jordan University of Science and Technology (2026); Duke University (2026); University of Arkansas Medical Center (2020–2021); King Abdullah University Hospital (2026); Duke Medical Center (2025–2026); The University of Texas Southwestern Medical Center (2026)
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Biography and Research Information
OverviewAI-generated summary
Praveen Kumar Ramani's research focuses on child neurology, with recent publications addressing infantile epileptic spasms syndrome, epilepsy characteristics in muscular dystrophies, and KMT2B-related dystonia. He has also investigated pediatric myelodysplasia, developing a new prognostic scoring system, and explored Cogan syndrome in children. His work includes assessing sleep quality in children with migraines. Ramani has a total of 26 publications and 281 citations, with an h-index of 3. He has collaborated with several researchers at the University of Arkansas for Medical Sciences, including Aravindhan Veerapandiyan, Debopam Samanta, Sisira Yadala, and Raghu Ramakrishnaiah.
Metrics
- h-index: 3
- Publications: 26
- Citations: 27
Selected Publications
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Corpus callosotomy in Lennox-Gastaut syndrome: Effectiveness, safety, and predictors of outcome: A systematic review and meta-analysis (2026)
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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 PPP3CA (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
- Initial combination versus early sequential standard therapies for Infantile Epileptic Spasms Syndrome—Feedback from stakeholders
- Corpus callosotomy in Lennox-Gastaut syndrome: Effectiveness, safety, and predictors of outcome: A systematic review and meta-analysis
- 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
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