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Child Neurology Open|February 27, 2023
Epilepsy Characteristics in Duchenne and Becker Muscular DystrophiesPraveen Kumar Ramani, Kindann Fawcett, Debra Guntrum, et al.Muscle & Nerve|November 28, 2019
Nusinersen for older patients with spinal muscular atrophy: A real-world clinical setting experienceAravindhan Veerapandiyan, Katy Eichinger, Debra Guntrum, et al.Child Neurology Open|November 24, 2022
Miyoshi Muscular Dystrophy Due to Novel Splice Site Variants in DYSF GeneGrace Bryant, Steven A Moore, James S Nix, et al.Muscle & Nerve|November 25, 2010
Pseudometabolic presentation of dystrophinopathy due to a missense mutationAravindhan Veerapandiyan, Vandana Shashi, Yong-Hui Jiang, et al.Child Neurology Open|May 13, 2022
Limb-Girdle Muscular Dystrophy R9 due to a Novel Complex Insertion/Duplication Variant in FKRP GeneErin Willis, Steven A Moore, Mary O Cox, et al.Epilepsy & Behavior : E&B|July 4, 2012
Electroencephalographic and seizure manifestations in two patients with folate receptor autoimmune antibody-mediated primary cerebral folate deficiencySonya U Steele, Sue Mei Cheah, Aravindhan Veerapandiyan, et al.Epilepsia|March 15, 2011
Oculogyric crises secondary to lamotrigine overdosageAravindhan Veerapandiyan, William B Gallentine, Sara A Winchester, et al.Cureus|January 16, 2026
Assessing Delays in Time to Diagnosis of Duchenne Muscular Dystrophy: A Survey of Current Primary Care PracticesAravindhan Veerapandiyan, Joseph F Hagan, Paul Lipkin, et al.Children (Basel, Switzerland)|November 27, 2021
COVID-19 in Pediatric Inpatients: A Multi-Center Observational Study of Factors Associated with Negative Short-Term OutcomesSara Rubenstein, Emily Grew, Katharine Clouser, et al.Journal of Personalized Medicine|September 28, 2021
Molecular Dysregulation in Autism Spectrum DisorderPritmohinder S Gill, Jeffery L Clothier, Aravindhan Veerapandiyan, et al.Pageof 6